| Year |
Citation |
Score |
| 2024 |
Moerkens R, Mooiweer J, Ramírez-Sánchez AD, Oelen R, Franke L, Wijmenga C, Barrett RJ, Jonkers IH, Withoff S. An iPSC-derived small intestine-on-chip with self-organizing epithelial, mesenchymal, and neural cells. Cell Reports. 43: 114247. PMID 38907996 DOI: 10.1016/j.celrep.2024.114247 |
0.57 |
|
| 2024 |
Lincoln MR, Connally N, Axisa PP, Gasperi C, Mitrovic M, van Heel D, Wijmenga C, Withoff S, Jonkers IH, Padyukov L, Rich SS, Graham RR, Gaffney PM, Langefeld CD, Vyse TJ, et al. Genetic mapping across autoimmune diseases reveals shared associations and mechanisms. Nature Genetics. 56: 838-845. PMID 38741015 DOI: 10.1038/s41588-024-01732-8 |
0.344 |
|
| 2024 |
Zhernakova DV, Wang D, Liu L, Andreu-Sánchez S, Zhang Y, Ruiz-Moreno AJ, Peng H, Plomp N, Del Castillo-Izquierdo Á, Gacesa R, Lopera-Maya EA, Temba GS, Kullaya VI, van Leeuwen SS, Xavier RJ, ... ... Wijmenga C, et al. Host genetic regulation of human gut microbial structural variation. Nature. PMID 38172637 DOI: 10.1038/s41586-023-06893-w |
0.303 |
|
| 2023 |
Kiryluk K, Sanchez-Rodriguez E, Zhou XJ, Zanoni F, Liu L, Mladkova N, Khan A, Marasa M, Zhang JY, Balderes O, Sanna-Cherchi S, Bomback AS, Canetta PA, Appel GB, Radhakrishnan J, ... ... Wijmenga C, et al. Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy. Nature Genetics. PMID 37337107 DOI: 10.1038/s41588-023-01422-x |
0.334 |
|
| 2023 |
Lopera-Maya EA, Li S, de Brouwer R, Nolte IM, van Breen J, Jongbloed JDH, Swertz MA, Snieder H, Franke L, Wijmenga C, de Boer RA, Deelen P, van der Zwaag PA, Sanna S. Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA Carriers. Journal of Cardiovascular Translational Research. PMID 36622581 DOI: 10.1007/s12265-022-10347-5 |
0.81 |
|
| 2022 |
Zhou W, Kanai M, Wu KH, Rasheed H, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Lo Faro V, Lopera-Maya EA, Läll K, ... ... Wijmenga C, et al. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192. PMID 36777996 DOI: 10.1016/j.xgen.2022.100192 |
0.697 |
|
| 2022 |
Lepamets M, Auwerx C, Nõukas M, Claringbould A, Porcu E, Kals M, Jürgenson T, Morris AP, Võsa U, Bochud M, Stringhini S, Wijmenga C, Franke L, Peterson H, Vilo J, et al. Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations. Hgg Advances. 3: 100133. PMID 36035246 DOI: 10.1016/j.xhgg.2022.100133 |
0.634 |
|
| 2022 |
Lopera-Maya EA, Kurilshikov A, van der Graaf A, Hu S, Andreu-Sánchez S, Chen L, Vila AV, Gacesa R, Sinha T, Collij V, Klaassen MAY, Bolte LA, Gois MFB, Neerincx PBT, Swertz MA, ... ... Wijmenga C, et al. Author Correction: Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Nature Genetics. PMID 35879415 DOI: 10.1038/s41588-022-01164-2 |
0.507 |
|
| 2022 |
Andreu-Sánchez S, Aubert G, Ripoll-Cladellas A, Henkelman S, Zhernakova DV, Sinha T, Kurilshikov A, Cenit MC, Jan Bonder M, Franke L, Wijmenga C, Fu J, van der Wijst MGP, Melé M, Lansdorp P, et al. Genetic, parental and lifestyle factors influence telomere length. Communications Biology. 5: 565. PMID 35681050 DOI: 10.1038/s42003-022-03521-7 |
0.658 |
|
| 2022 |
Hop PJ, Zwamborn RAJ, Hannon E, Shireby GL, Nabais MF, Walker EM, van Rheenen W, van Vugt JJFA, Dekker AM, Westeneng HJ, Tazelaar GHP, van Eijk KR, Moisse M, Baird D, Al Khleifat A, ... ... Wijmenga C, et al. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. Science Translational Medicine. 14: eabj0264. PMID 35196023 DOI: 10.1126/scitranslmed.abj0264 |
0.799 |
|
| 2022 |
Lopera-Maya EA, Kurilshikov A, van der Graaf A, Hu S, Andreu-Sánchez S, Chen L, Vila AV, Gacesa R, Sinha T, Collij V, Klaassen MAY, Bolte LA, Gois MFB, Neerincx PBT, Swertz MA, ... ... Wijmenga C, et al. Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Nature Genetics. 54: 143-151. PMID 35115690 DOI: 10.1038/s41588-021-00992-y |
0.603 |
|
| 2021 |
Matzaraki V, Le KTT, Jaeger M, Aguirre-Gamboa R, Johnson MD, Sanna S, Rosati D, Franke L, Zhernakova A, Fu J, Withoff S, Jonkers I, Li Y, Joosten LAB, Netea MG, ... Wijmenga C, et al. Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Frontiers in Immunology. 12: 662171. PMID 34512620 DOI: 10.3389/fimmu.2021.662171 |
0.677 |
|
| 2021 |
Võsa U, Claringbould A, Westra HJ, Bonder MJ, Deelen P, Zeng B, Kirsten H, Saha A, Kreuzhuber R, Yazar S, Brugge H, Oelen R, de Vries DH, van der Wijst MGP, Kasela S, ... ... Wijmenga C, et al. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nature Genetics. PMID 34475573 DOI: 10.1038/s41588-021-00913-z |
0.817 |
|
| 2021 |
Chu X, Jaeger M, Beumer J, Bakker OB, Aguirre-Gamboa R, Oosting M, Smeekens SP, Moorlag S, Mourits VP, Koeken VACM, de Bree C, Jansen T, Mathews IT, Dao K, Najhawan M, ... ... Wijmenga C, et al. Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease. Genome Biology. 22: 198. PMID 34229738 DOI: 10.1186/s13059-021-02413-z |
0.661 |
|
| 2021 |
Mc Intyre K, Lanting P, Deelen P, Wiersma HH, Vonk JM, Ori APS, Jankipersadsing SA, Warmerdam R, van Blokland I, Boulogne F, Dijkema MXL, Herkert JC, Claringbould A, Bakker O, Lopera Maya EA, ... ... Wijmenga C, et al. Lifelines COVID-19 cohort: investigating COVID-19 infection and its health and societal impacts in a Dutch population-based cohort. Bmj Open. 11: e044474. PMID 33737436 DOI: 10.1136/bmjopen-2020-044474 |
0.772 |
|
| 2021 |
Kurilshikov A, Medina-Gomez C, Bacigalupe R, Radjabzadeh D, Wang J, Demirkan A, Le Roy CI, Raygoza Garay JA, Finnicum CT, Liu X, Zhernakova DV, Bonder MJ, Hansen TH, Frost F, Rühlemann MC, ... ... Wijmenga C, et al. Large-scale association analyses identify host factors influencing human gut microbiome composition. Nature Genetics. PMID 33462485 DOI: 10.1038/s41588-020-00763-1 |
0.833 |
|
| 2020 |
van der Graaf A, Zorro MM, Claringbould A, Võsa U, Aguirre-Gamboa R, Li C, Mooiweer J, Ricaño-Ponce I, Borek Z, Koning F, Kooy-Winkelaar Y, Sollid LM, Qiao SW, Kumar V, Li Y, ... ... Wijmenga C, et al. Systematic Prioritization of Candidate Genes in Disease Loci Identifies as a Master Regulator of IFNγ Signaling in Celiac Disease. Frontiers in Genetics. 11: 562434. PMID 33569077 DOI: 10.3389/fgene.2020.562434 |
0.676 |
|
| 2020 |
Lanting P, Drenth E, Boven L, van Hoek A, Hijlkema A, Poot E, van der Vries G, Schoevers R, Horwitz E, Gans R, Kosterink J, Plantinga M, van Langen I, Ranchor A, Wijmenga C, et al. Practical Barriers and Facilitators Experienced by Patients, Pharmacists and Physicians to the Implementation of Pharmacogenomic Screening in Dutch Outpatient Hospital Care-An Explorative Pilot Study. Journal of Personalized Medicine. 10. PMID 33371313 DOI: 10.3390/jpm10040293 |
0.572 |
|
| 2020 |
van den Akker EB, Trompet S, Barkey Wolf JJH, Beekman M, Suchiman HED, Deelen J, Asselbergs FW, Boersma E, Cats D, Elders PM, Geleijnse JM, Ikram MA, Kloppenburg M, Mei H, Meulenbelt I, ... ... Wijmenga C, et al. Metabolic Age Based on the BBMRI-NL H-NMR Metabolomics Repository as Biomarker of Age-related Disease. Circulation. Genomic and Precision Medicine. 13: 541-547. PMID 33079603 DOI: 10.1161/CIRCGEN.119.002610 |
0.503 |
|
| 2020 |
van der Graaf A, Claringbould A, Rimbert A, Westra HJ, Li Y, Wijmenga C, Sanna S. Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids. Nature Communications. 11: 4930. PMID 33004804 DOI: 10.1038/s41467-020-18716-x |
0.751 |
|
| 2020 |
Chen L, Collij V, Jaeger M, van den Munckhof ICL, Vich Vila A, Kurilshikov A, Gacesa R, Sinha T, Oosting M, Joosten LAB, Rutten JHW, Riksen NP, Xavier RJ, Kuipers F, Wijmenga C, et al. Gut microbial co-abundance networks show specificity in inflammatory bowel disease and obesity. Nature Communications. 11: 4018. PMID 32782301 DOI: 10.1038/S41467-020-17840-Y |
0.32 |
|
| 2020 |
Hu S, Vich Vila A, Gacesa R, Collij V, Stevens C, Fu JM, Wong I, Talkowski ME, Rivas MA, Imhann F, Bolte L, van Dullemen H, Dijkstra G, Visschedijk MC, Festen EA, ... ... Wijmenga C, et al. Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD. Gut. PMID 32651235 DOI: 10.1136/Gutjnl-2019-319706 |
0.371 |
|
| 2020 |
Lopera Maya EA, van der Graaf A, Lanting P, van der Geest M, Fu J, Swertz M, Franke L, Wijmenga C, Deelen P, Zhernakova A, Sanna S. Lack of Association Between Genetic Variants at and Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes. Frontiers in Genetics. 11: 613. PMID 32582302 DOI: 10.3389/Fgene.2020.00613 |
0.831 |
|
| 2020 |
Aguirre-Gamboa R, de Klein N, di Tommaso J, Claringbould A, van der Wijst MG, de Vries D, Brugge H, Oelen R, Võsa U, Zorro MM, Chu X, Bakker OB, Borek Z, Ricaño-Ponce I, Deelen P, ... ... Wijmenga C, et al. Deconvolution of bulk blood eQTL effects into immune cell subpopulations. Bmc Bioinformatics. 21: 243. PMID 32532224 DOI: 10.1186/S12859-020-03576-5 |
0.794 |
|
| 2020 |
Peters V, Tigchelaar-Feenstra EF, Imhann F, Dekens JAM, Swertz MA, Franke LH, Wijmenga C, Weersma RK, Alizadeh BZ, Dijkstra G, Campmans-Kuijpers MJE. Habitual dietary intake of IBD patients differs from population controls: a case-control study. European Journal of Nutrition. PMID 32333097 DOI: 10.1007/S00394-020-02250-Z |
0.707 |
|
| 2019 |
Vojinovic D, Radjabzadeh D, Kurilshikov A, Amin N, Wijmenga C, Franke L, Ikram MA, Uitterlinden AG, Zhernakova A, Fu J, Kraaij R, van Duijn CM. Relationship between gut microbiota and circulating metabolites in population-based cohorts. Nature Communications. 10: 5813. PMID 31862950 DOI: 10.1038/S41467-019-13721-1 |
0.633 |
|
| 2019 |
Clark DW, Okada Y, Moore KHS, Mason D, Pirastu N, Gandin I, Mattsson H, Barnes CLK, Lin K, Zhao JH, Deelen P, Rohde R, Schurmann C, Guo X, Giulianini F, ... ... Wijmenga C, et al. Associations of autozygosity with a broad range of human phenotypes. Nature Communications. 10: 4957. PMID 31673082 DOI: 10.1038/S41467-019-12283-6 |
0.792 |
|
| 2019 |
López-Isac E, Acosta-Herrera M, Kerick M, Assassi S, Satpathy AT, Granja J, Mumbach MR, Beretta L, Simeón CP, Carreira P, Ortego-Centeno N, Castellvi I, Bossini-Castillo L, Carmona FD, Orozco G, ... ... Wijmenga C, et al. GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways. Nature Communications. 10: 4955. PMID 31672989 DOI: 10.1038/S41467-019-12760-Y |
0.454 |
|
| 2019 |
Ricaño-Ponce I, Gutierrez-Achury J, Costa AF, Deelen P, Kurilshikov A, Zorro MM, Platteel M, van der Graaf A, Sanna S, Daffra O, Zhernakova A, Fu J, Trynka G, Smecuol E, ... ... Wijmenga C, et al. Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease. European Journal of Human Genetics : Ejhg. PMID 31591516 DOI: 10.1038/S41431-019-0520-4 |
0.82 |
|
| 2019 |
Le KTT, Matzaraki V, Netea MG, Wijmenga C, Moser J, Kumar V. Functional Annotation of Genetic Loci Associated With Sepsis Prioritizes Immune and Endothelial Cell Pathways. Frontiers in Immunology. 10: 1949. PMID 31475010 DOI: 10.3389/Fimmu.2019.01949 |
0.466 |
|
| 2019 |
Edwards RA, Vega AA, Norman HM, Ohaeri M, Levi K, Dinsdale EA, Cinek O, Aziz RK, McNair K, Barr JJ, Bibby K, Brouns SJJ, Cazares A, de Jonge PA, Desnues C, ... ... Wijmenga C, et al. Global phylogeography and ancient evolution of the widespread human gut virus crAssphage. Nature Microbiology. PMID 31285584 DOI: 10.1038/S41564-019-0494-6 |
0.335 |
|
| 2019 |
Jaeger M, Matzaraki V, Aguirre-Gamboa R, Gresnigt MS, Chu X, Johnson MD, Oosting M, Smeekens SP, Withoff S, Jonkers I, Perfect JR, van de Veerdonk FL, Kullberg BJ, Joosten LAB, Li Y, ... Wijmenga C, et al. A Genome-Wide Functional Genomics Approach Identifies Susceptibility Pathways to Fungal Bloodstream Infection in Humans. The Journal of Infectious Diseases. PMID 31241743 DOI: 10.1093/Infdis/Jiz206 |
0.343 |
|
| 2019 |
Jaeger M, Pinelli M, Borghi M, Constantini C, Dindo M, van Emst L, Puccetti M, Pariano M, Ricaño-Ponce I, Büll C, Gresnigt MS, Wang X, Gutierrez Achury J, Jacobs CWM, Xu N, ... ... Wijmenga C, et al. A systems genomics approach identifies as a susceptibility factor in recurrent vulvovaginal candidiasis. Science Translational Medicine. 11. PMID 31189718 DOI: 10.1126/Scitranslmed.Aar3558 |
0.421 |
|
| 2019 |
Moerkens R, Mooiweer J, Withoff S, Wijmenga C. Celiac disease-on-chip: Modeling a multifactorial disease in vitro. United European Gastroenterology Journal. 7: 467-476. PMID 31065364 DOI: 10.1177/2050640619836057 |
0.363 |
|
| 2019 |
Kurilshikov A, van den Munckhof IC, Chen L, Bonder MJ, Schraa K, Rutten J, Riksen NP, de Graaf J, Oosting M, Sanna S, Joosten LA, van der Graaf M, Brand T, Koonen DP, van Faassen MJ, ... ... Wijmenga C, et al. Gut Microbial Associations to Plasma Metabolites Linked to Cardiovascular Phenotypes and Risk: A Cross-Sectional Study. Circulation Research. PMID 30971183 DOI: 10.1161/Circresaha.118.314642 |
0.305 |
|
| 2019 |
Onderwater GLJ, Ligthart L, Bot M, Demirkan A, Fu J, van der Kallen CJH, Vijfhuizen LS, Pool R, Liu J, Vanmolkot FHM, Beekman M, Wen KX, Amin N, Thesing CS, Pijpers JA, ... ... Wijmenga C, et al. Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine. Neurology. PMID 30944236 DOI: 10.1212/Wnl.0000000000007313 |
0.601 |
|
| 2019 |
Zeevi D, Korem T, Godneva A, Bar N, Kurilshikov A, Lotan-Pompan M, Weinberger A, Fu J, Wijmenga C, Zhernakova A, Segal E. Structural variation in the gut microbiome associates with host health. Nature. PMID 30918406 DOI: 10.1038/S41586-019-1065-Y |
0.39 |
|
| 2019 |
Sanna S, van Zuydam NR, Mahajan A, Kurilshikov A, Vich Vila A, Võsa U, Mujagic Z, Masclee AAM, Jonkers DMAE, Oosting M, Joosten LAB, Netea MG, Franke L, Zhernakova A, Fu J, ... Wijmenga C, et al. Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases. Nature Genetics. PMID 30778224 DOI: 10.1038/S41588-019-0350-X |
0.688 |
|
| 2019 |
Collij V, Imhann F, Vich Vila A, Fu J, Dijkstra G, Festen EAM, Voskuil MD, Daly MJ, Xavier RJ, Wijmenga C, Zhernakova A, Weersma RK. SLC39A8 missense variant is associated with Crohn's disease but does not have a major impact on gut microbiome composition in healthy subjects. Plos One. 14: e0211328. PMID 30703110 DOI: 10.1371/Journal.Pone.0211328 |
0.392 |
|
| 2019 |
Márquez A, Kerick M, Zhernakova A, Gutierrez-Achury J, Chen W, Onengut-Gumuscu S, González-Álvaro I, Rodriguez-Rodriguez L, González-Gay MA, Mayes M, Raychaudhuri S, Rich SS, Wijmenga C, Ibanez JM. Op0190 Meta-Analysis Of Immunochip Data Of Four Autoimmune Diseases Reveals Novel Single-Disease And Cross-Phenotype Associations Annals of the Rheumatic Diseases. 78: 170-170. DOI: 10.1136/Annrheumdis-2019-Eular.402 |
0.604 |
|
| 2019 |
Hu S, Vich Vila A, Gacesa R, Collij V, Xavier R, Stevens C, Daly M, Wijmenga C, van Dullemen H, Dijkstra G, Visschedijk M, Festen E, Fu J, Kurilshikov A, Zhernakova A, et al. OP01 In-depth characterisation of host genetics and gut microbiome unravels novel host–microbiome interactions in inflammatory bowel disease Journal of Crohn's and Colitis. 13: S001-S001. DOI: 10.1093/Ecco-Jcc/Jjy222.000 |
0.352 |
|
| 2019 |
Peters V, Tigchelaar E, Imhann F, Dekens J, Swertz M, Franke L, Wijmenga C, Weersma RK, Alizadeh B, Dijkstra G, Campmans-Kuijpers MJ. Sa2029 – Habitual Dietary Intake of Dutch IBD Patients Differs from Population Controls: A Case-Control Study Gastroenterology. 156: S-477-S-478. DOI: 10.1016/S0016-5085(19)38052-7 |
0.701 |
|
| 2019 |
Hu S, Vila AV, Gacesa R, Collij V, Xavier R, Stevens C, Daly MJ, Wijmenga C, van Dullemen H, Dijkstra G, Visschedijk MC, Festen EA, Fu J, Kurilshikov A, Zhernakova A, et al. 149 – In-Depth Characterization of Host-Genetics and Gut Microbiome Unravels Novel Host-Microbiome Interactions in Inflammatory Bowel Disease Gastroenterology. 156: S-34. DOI: 10.1016/S0016-5085(19)36862-3 |
0.332 |
|
| 2018 |
Acosta-Herrera M, Kerick M, González-Serna D, Wijmenga C, Franke A, Gregersen PK, Padyukov L, Worthington J, Vyse TJ, Alarcón-Riquelme ME, Mayes MD, Martin J. Genome-wide meta-analysis reveals shared new in systemic seropositive rheumatic diseases. Annals of the Rheumatic Diseases. PMID 30573655 DOI: 10.1136/Annrheumdis-2018-214127 |
0.386 |
|
| 2018 |
Márquez A, Kerick M, Zhernakova A, Gutierrez-Achury J, Chen WM, Onengut-Gumuscu S, González-Álvaro I, Rodriguez-Rodriguez L, Rios-Fernández R, González-Gay MA, Mayes MD, ... ... Wijmenga C, et al. Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Genome Medicine. 10: 97. PMID 30572963 DOI: 10.1186/S13073-018-0604-8 |
0.58 |
|
| 2018 |
Vich Vila A, Imhann F, Collij V, Jankipersadsing SA, Gurry T, Mujagic Z, Kurilshikov A, Bonder MJ, Jiang X, Tigchelaar EF, Dekens J, Peters V, Voskuil MD, Visschedijk MC, van Dullemen HM, ... ... Wijmenga C, et al. Gut microbiota composition and functional changes in inflammatory bowel disease and irritable bowel syndrome. Science Translational Medicine. 10. PMID 30567928 DOI: 10.1126/Scitranslmed.Aap8914 |
0.733 |
|
| 2018 |
Franzosa EA, Sirota-Madi A, Avila-Pacheco J, Fornelos N, Haiser HJ, Reinker S, Vatanen T, Hall AB, Mallick H, McIver LJ, Sauk JS, Wilson RG, Stevens BW, Scott JM, Pierce K, ... ... Wijmenga C, et al. Gut microbiome structure and metabolic activity in inflammatory bowel disease. Nature Microbiology. PMID 30531976 DOI: 10.1038/S41564-018-0306-4 |
0.339 |
|
| 2018 |
Zhernakova DV, Le TH, Kurilshikov A, Atanasovska B, Bonder MJ, Sanna S, Claringbould A, Võsa U, Deelen P, Franke L, de Boer RA, Kuipers F, Netea MG, Hofker MH, Wijmenga C, et al. Author Correction: Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome. Nature Genetics. PMID 30341443 DOI: 10.1038/S41588-018-0275-9 |
0.777 |
|
| 2018 |
Zhernakova DV, Le TH, Kurilshikov A, Atanasovska B, Bonder MJ, Sanna S, Claringbould A, Võsa U, Deelen P, Franke L, de Boer RA, Kuipers F, Netea MG, ... ... Wijmenga C, et al. Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome. Nature Genetics. PMID 30250126 DOI: 10.1038/S41588-018-0224-7 |
0.816 |
|
| 2018 |
Luijk R, Wu H, Ward-Caviness CK, Hannon E, Carnero-Montoro E, Min JL, Mandaviya P, Müller-Nurasyid M, Mei H, van der Maarel SM, Relton C, Mill J, Waldenberger M, Bell JT, ... ... Wijmenga C, et al. Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation. Nature Communications. 9: 3738. PMID 30218040 DOI: 10.1038/S41467-018-05714-3 |
0.678 |
|
| 2018 |
Luijk R, Dekkers KF, van Iterson M, Arindrarto W, Claringbould A, Hop P, Boomsma DI, van Duijn CM, van Greevenbroek MMJ, Veldink JH, Wijmenga C, Franke L, 't Hoen PAC, Jansen R, et al. Genome-wide identification of directed gene networks using large-scale population genomics data. Nature Communications. 9: 3097. PMID 30082726 DOI: 10.1038/S41467-018-05452-6 |
0.696 |
|
| 2018 |
Wray NR, Wijmenga C, Sullivan PF, Yang J, Visscher PM. Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model. Cell. 173: 1573-1580. PMID 29906445 DOI: 10.1016/J.Cell.2018.05.051 |
0.367 |
|
| 2018 |
Wang J, Kurilshikov A, Radjabzadeh D, Turpin W, Croitoru K, Bonder MJ, Jackson MA, Medina-Gomez C, Frost F, Homuth G, Rühlemann M, Hughes D, Kim HN, Spector TD, ... ... Wijmenga C, et al. Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative. Microbiome. 6: 101. PMID 29880062 DOI: 10.1186/S40168-018-0479-3 |
0.688 |
|
| 2018 |
Nousiainen K, Kanduri K, Ricaño-Ponce I, Wijmenga C, Lahesmaa R, Kumar V, Lähdesmäki H. snpEnrichR: analyzing co-localization of SNPs and their proxies in genomic regions. Bioinformatics (Oxford, England). PMID 29878048 DOI: 10.1093/Bioinformatics/Bty460 |
0.37 |
|
| 2018 |
Hrdlickova B, Mulder CJ, Malamut G, Meresse B, Platteel M, Kamatani Y, Ricaño-Ponce I, van Wanrooij RLJ, Zorro MM, Jan Bonder M, Gutierrez-Achury J, Cellier C, Zhernakova A, Nijeboer P, Galan P, ... ... Wijmenga C, et al. A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease. European Journal of Gastroenterology & Hepatology. PMID 29787419 DOI: 10.1097/Meg.0000000000001168 |
0.336 |
|
| 2018 |
Bakker OB, Aguirre-Gamboa R, Sanna S, Oosting M, Smeekens SP, Jaeger M, Zorro M, Võsa U, Withoff S, Netea-Maier RT, Koenen HJPM, Joosten I, Xavier RJ, Franke L, Joosten LAB, ... ... Wijmenga C, et al. Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses. Nature Immunology. PMID 29784908 DOI: 10.1038/S41590-018-0121-3 |
0.661 |
|
| 2018 |
Bonfiglio F, Henström M, Nag A, Hadizadeh F, Zheng T, Cenit MC, Tigchelaar E, Williams F, Reznichenko A, Ek WE, Rivera NV, Homuth G, Aghdassi AA, Kacprowski T, Männikkö M, ... ... Wijmenga C, et al. A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome. Neurogastroenterology and Motility : the Official Journal of the European Gastrointestinal Motility Society. e13358. PMID 29673008 DOI: 10.1111/Nmo.13358 |
0.425 |
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| 2018 |
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Peters V, Tigchelaar E, Campmans-Kuijpers M, Sheedfar F, Imhann F, Dekens J, Wijmenga C, Swertz M, Franke L, Weersma R, Dijkstra G, Alizadeh B. P831 - Habitual dietary intake of Dutch IBD patients differs from population controls : A case-control study Journal of Crohns & Colitis. 12. DOI: 10.1093/Ecco-Jcc/Jjx180.958 |
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Klaassen M, Imhann F, Collij V, Vich Vila A, Gacesa R, Fu J, Zhernakova A, Wijmenga C, Weersma R. P102 Increased abundance of gut microbial virulence genes and pro-inflammatory pathways during Crohn’s disease exacerbations Journal of Crohn's and Colitis. 12: S145-S145. DOI: 10.1093/Ecco-Jcc/Jjx180.229 |
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Jonkers IH, Wijmenga C. Context-specific effects of genetic variants associated with autoimmune disease. Human Molecular Genetics. 26: R185-R192. PMID 28977443 DOI: 10.1093/Hmg/Ddx254 |
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Kurilshikov A, Wijmenga C, Fu J, Zhernakova A. Host Genetics and Gut Microbiome: Challenges and Perspectives. Trends in Immunology. PMID 28669638 DOI: 10.1016/J.It.2017.06.003 |
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Visser AE, Pazoki R, Pulit SL, van Rheenen W, Raaphorst J, van der Kooi AJ, Ricaño-Ponce I, Wijmenga C, Otten HG, Veldink JH, van den Berg LH. No association between gluten sensitivity and amyotrophic lateral sclerosis. Journal of Neurology. 264: 694-700. PMID 28168522 DOI: 10.1007/S00415-017-8400-8 |
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van der Velde KJ, de Boer EN, van Diemen CC, Sikkema-Raddatz B, Abbott KM, Knopperts A, Franke L, Sijmons RH, de Koning TJ, Wijmenga C, Sinke RJ, Swertz MA. GAVIN: Gene-Aware Variant INterpretation for medical sequencing. Genome Biology. 18: 6. PMID 28093075 DOI: 10.1186/S13059-016-1141-7 |
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Amini M, Bashirova D, Prins BP, Corpeleijn E, Bruinenberg M, Franke L, Harst PV, Navis G, Wolffenbuttel BH, Stolk RP, Wijmenga C, Postma DS, Koppelman GH, Boezen HM, et al. Eosinophil Count Is a Common Factor for Complex Metabolic and Pulmonary Traits and Diseases: The LifeLines Cohort Study. Plos One. 11: e0168480. PMID 27978545 DOI: 10.1371/Journal.Pone.0168480 |
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Imhann F, Bonder MJ, Vich Vila A, Fu J, Mujagic Z, Vork L, Tigchelaar EF, Jankipersadsing SA, Cenit MC, Harmsen HJ, Dijkstra G, Franke L, Xavier RJ, Jonkers D, Wijmenga C, et al. Proton pump inhibitors affect the gut microbiome. Gut. PMID 26657899 DOI: 10.1136/Gutjnl-2015-310376 |
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Atanasovska B, Kumar V, Fu J, Wijmenga C, Hofker MH. GWAS as a Driver of Gene Discovery in Cardiometabolic Diseases. Trends in Endocrinology and Metabolism: Tem. PMID 26596674 DOI: 10.1016/J.Tem.2015.10.004 |
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Gutierrez-Achury J, Zorro MM, Ricaño-Ponce I, Zhernakova DV, Diogo D, Raychaudhuri S, Franke L, Trynka G, Wijmenga C, Zhernakova A. Functional implications of disease-specific variants in loci jointly associated to coeliac disease and rheumatoid arthritis. Human Molecular Genetics. PMID 26546613 DOI: 10.1093/Hmg/Ddv455 |
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Cao Z, Conway KL, Heath RJ, Rush JS, Leshchiner ES, Ramirez-Ortiz ZG, Nedelsky NB, Huang H, Ng A, Gardet A, Cheng SC, Shamji AF, Rioux JD, Wijmenga C, Netea MG, et al. Ubiquitin Ligase TRIM62 Regulates CARD9-Mediated Anti-fungal Immunity and Intestinal Inflammation. Immunity. 43: 715-26. PMID 26488816 DOI: 10.1016/J.Immuni.2015.10.005 |
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Li YR, van Setten J, Verma SS, Lu Y, Holmes MV, Gao H, Lek M, Nair N, Chandrupatla H, Chang B, Karczewski KJ, Wong C, Mohebnasab M, Mukhtar E, Phillips R, ... ... Wijmenga C, et al. Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies. Genome Medicine. 7: 90. PMID 26423053 DOI: 10.1186/S13073-015-0211-X |
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Fu J, Bonder MJ, Cenit MC, Tigchelaar EF, Maatman A, Dekens JA, Brandsma E, Marczynska J, Imhann F, Weersma RK, Franke L, Poon TW, Xavier RJ, Gevers D, Hofker MH, ... Wijmenga C, et al. The Gut Microbiome Contributes to a Substantial Proportion of the Variation in Blood Lipids. Circulation Research. 117: 817-24. PMID 26358192 DOI: 10.1161/Circresaha.115.306807 |
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Tigchelaar EF, Zhernakova A, Dekens JA, Hermes G, Baranska A, Mujagic Z, Swertz MA, Muñoz AM, Deelen P, Cénit MC, Franke L, Scholtens S, Stolk RP, Wijmenga C, Feskens EJ. Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics. Bmj Open. 5: e006772. PMID 26319774 DOI: 10.1136/Bmjopen-2014-006772 |
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Lundin KE, Wijmenga C. Coeliac disease and autoimmune disease-genetic overlap and screening. Nature Reviews. Gastroenterology & Hepatology. 12: 507-15. PMID 26303674 DOI: 10.1038/Nrgastro.2015.136 |
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Lenz TL, Deutsch AJ, Han B, Hu X, Okada Y, Eyre S, Knapp M, Zhernakova A, Huizinga TW, Abecasis G, Becker J, Boeckxstaens GE, Chen WM, Franke A, Gladman DD, ... ... Wijmenga C, et al. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nature Genetics. PMID 26258845 DOI: 10.1038/Ng.3379 |
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van Leeuwen EM, Kanterakis A, Deelen P, Kattenberg MV, Slagboom PE, de Bakker PI, Wijmenga C, Swertz MA, Boomsma DI, van Duijn CM, Karssen LC, Hottenga JJ. Population-specific genotype imputations using minimac or IMPUTE2. Nature Protocols. 10: 1285-96. PMID 26226460 DOI: 10.1038/Nprot.2015.077 |
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Shah S, Bonder MJ, Marioni RE, Zhu Z, McRae AF, Zhernakova A, Harris SE, Liewald D, Henders AK, Mendelson MM, Liu C, Joehanes R, Liang L, Levy D, ... ... Wijmenga C, et al. Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations. American Journal of Human Genetics. 97: 75-85. PMID 26119815 DOI: 10.1016/J.Ajhg.2015.05.014 |
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Begun J, Lassen KG, Jijon HB, Baxt LA, Goel G, Heath RJ, Ng A, Tam JM, Kuo SY, Villablanca EJ, Fagbami L, Oosting M, Kumar V, Schenone M, Carr SA, ... ... Wijmenga C, et al. Integrated Genomics of Crohn's Disease Risk Variant Identifies a Role for CLEC12A in Antibacterial Autophagy. Cell Reports. 11: 1905-18. PMID 26095365 DOI: 10.1016/J.Celrep.2015.05.045 |
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Dobon B, Hassan HY, Laayouni H, Luisi P, Ricaño-Ponce I, Zhernakova A, Wijmenga C, Tahir H, Comas D, Netea MG, Bertranpetit J. The genetics of East African populations: a Nilo-Saharan component in the African genetic landscape. Scientific Reports. 5: 9996. PMID 26017457 DOI: 10.1038/Srep09996 |
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Francioli LC, Polak PP, Koren A, Menelaou A, Chun S, Renkens I, van Duijn CM, Swertz M, Wijmenga C, van Ommen G, Slagboom PE, Boomsma DI, Ye K, Guryev V, et al. Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics. PMID 25985141 DOI: 10.1038/Ng.3292 |
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Franke L, El Bannoudi H, Jansen DT, Kok K, Trynka G, Diogo D, Swertz M, Fransen K, Knevel R, Gutierrez-Achury J, Ärlestig L, Greenberg JD, Kremer J, Pappas DA, Kanterakis A, ... ... Wijmenga C, et al. Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes. European Journal of Human Genetics : Ejhg. PMID 25966632 DOI: 10.1038/Ejhg.2015.95 |
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Westra HJ, Arends D, Esko T, Peters MJ, Schurmann C, Schramm K, Kettunen J, Yaghootkar H, Fairfax BP, Andiappan AK, Li Y, Fu J, Karjalainen J, Platteel M, Visschedijk M, ... ... Wijmenga C, et al. Cell Specific eQTL Analysis without Sorting Cells. Plos Genetics. 11: e1005223. PMID 25955312 DOI: 10.1371/Journal.Pgen.1005223 |
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Deelen P, Zhernakova DV, de Haan M, van der Sijde M, Bonder MJ, Karjalainen J, van der Velde KJ, Abbott KM, Fu J, Wijmenga C, Sinke RJ, Swertz MA, Franke L. Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels. Genome Medicine. 7: 30. PMID 25954321 DOI: 10.1186/S13073-015-0152-4 |
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Coleman C, Quinn EM, Ryan AW, Conroy J, Trimble V, Mahmud N, Kennedy N, Corvin AP, Morris DW, Donohoe G, O'Morain C, MacMathuna P, Byrnes V, Kiat C, Trynka G, ... Wijmenga C, et al. Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. European Journal of Human Genetics : Ejhg. PMID 25920553 DOI: 10.1038/Ejhg.2015.87 |
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Gutierrez-Achury J, Zhernakova A, Pulit SL, Trynka G, Hunt KA, Romanos J, Raychaudhuri S, van Heel DA, Wijmenga C, de Bakker PI. Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease. Nature Genetics. 47: 577-8. PMID 25894500 DOI: 10.1038/Ng.3268 |
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Kloosterman WP, Francioli LC, Hormozdiari F, Marschall T, Hehir-Kwa JY, Abdellaoui A, Lameijer EW, Moed MH, Koval V, Renkens I, van Roosmalen MJ, Arp P, Karssen LC, Coe BP, Handsaker RE, ... ... Wijmenga C, et al. Characteristics of de novo structural changes in the human genome. Genome Research. 25: 792-801. PMID 25883321 DOI: 10.1101/Gr.185041.114 |
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van der Velde KJ, Kuiper J, Thompson BA, Plazzer JP, van Valkenhoef G, de Haan M, Jongbloed JD, Wijmenga C, de Koning TJ, Abbott KM, Sinke R, Spurdle AB, Macrae F, Genuardi M, Sijmons RH, et al. Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization. Human Mutation. 36: 712-9. PMID 25871441 DOI: 10.1002/Humu.22798 |
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Carmona FD, Mackie SL, Martín JE, Taylor JC, Vaglio A, Eyre S, Bossini-Castillo L, Castañeda S, Cid MC, Hernández-Rodríguez J, Prieto-González S, Solans R, Ramentol-Sintas M, González-Escribano MF, Ortiz-Fernández L, ... ... Wijmenga C, et al. A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility. American Journal of Human Genetics. 96: 565-80. PMID 25817017 DOI: 10.1016/J.Ajhg.2015.02.009 |
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van Leeuwen EM, Karssen LC, Deelen J, Isaacs A, Medina-Gomez C, Mbarek H, Kanterakis A, Trompet S, Postmus I, Verweij N, van Enckevort DJ, Huffman JE, White CC, Feitosa MF, Bartz TM, ... ... Wijmenga C, et al. Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Nature Communications. 6: 6065. PMID 25751400 DOI: 10.1038/Ncomms7065 |
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Wolfs MG, Gruben N, Rensen SS, Verdam FJ, Greve JW, Driessen A, Wijmenga C, Buurman WA, Franke L, Scheja L, Koonen DP, Shiri-Sverdlov R, van Haeften TW, Hofker MH, Fu J. Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesity. Nutrition & Diabetes. 5: e146. PMID 25664838 DOI: 10.1038/Nutd.2014.43 |
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Emilsson L, Wijmenga C, Murray JA, Ludvigsson JF. Autoimmune Disease in First-Degree Relatives and Spouses of Individuals With Celiac Disease. Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association. 13: 1271-1277.e2. PMID 25645875 DOI: 10.1016/J.Cgh.2015.01.026 |
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van Gerven NM, de Boer YS, Zwiers A, Verwer BJ, Drenth JP, van Hoek B, van Erpecum KJ, Beuers U, van Buuren HR, den Ouden JW, Verdonk RC, Koek GH, Brouwer JT, Guichelaar MM, Vrolijk JM, ... ... Wijmenga C, et al. HLA-DRB1*03:01 and HLA-DRB1*04:01 modify the presentation and outcome in autoimmune hepatitis type-1. Genes and Immunity. 16: 247-52. PMID 25611558 DOI: 10.1038/Gene.2014.82 |
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Fehrmann RS, Karjalainen JM, Krajewska M, Westra HJ, Maloney D, Simeonov A, Pers TH, Hirschhorn JN, Jansen RC, Schultes EA, van Haagen HH, de Vries EG, te Meerman GJ, Wijmenga C, van Vugt MA, et al. Gene expression analysis identifies global gene dosage sensitivity in cancer. Nature Genetics. 47: 115-25. PMID 25581432 DOI: 10.1038/Ng.3173 |
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Jaeger M, van der Lee R, Cheng SC, Johnson MD, Kumar V, Ng A, Plantinga TS, Smeekens SP, Oosting M, Wang X, Barchet W, Fitzgerald K, Joosten LA, Perfect JR, Wijmenga C, et al. The RIG-I-like helicase receptor MDA5 (IFIH1) is involved in the host defense against Candida infections. European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology. 34: 963-74. PMID 25579795 DOI: 10.1007/S10096-014-2309-2 |
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Scholtens S, Smidt N, Swertz MA, Bakker SJ, Dotinga A, Vonk JM, van Dijk F, van Zon SK, Wijmenga C, Wolffenbuttel BH, Stolk RP. Cohort Profile: LifeLines, a three-generation cohort study and biobank. International Journal of Epidemiology. 44: 1172-80. PMID 25502107 DOI: 10.1093/Ije/Dyu229 |
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Schaefer AS, Bochenek G, Jochens A, Ellinghaus D, Dommisch H, Güzeldemir-Akçakanat E, Graetz C, Harks I, Jockel-Schneider Y, Weinspach K, Meyle J, Eickholz P, Linden GJ, Cine N, Nohutcu R, ... ... Wijmenga C, et al. Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis. Circulation. Cardiovascular Genetics. 8: 159-67. PMID 25466412 DOI: 10.1161/Circgenetics.114.000554 |
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Palles C, Chegwidden L, Li X, Findlay JM, Farnham G, Castro Giner F, Peppelenbosch MP, Kovac M, Adams CL, Prenen H, Briggs S, Harrison R, Sanders S, MacDonald D, Haigh C, ... ... Wijmenga C, et al. Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus. Gastroenterology. 148: 367-78. PMID 25447851 DOI: 10.1053/J.Gastro.2014.10.041 |
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Kumar V, Gutierrez-Achury J, Kanduri K, Almeida R, Hrdlickova B, Zhernakova DV, Westra HJ, Karjalainen J, Ricaño-Ponce I, Li Y, Stachurska A, Tigchelaar EF, Abdulahad WH, Lähdesmäki H, Hofker MH, ... ... Wijmenga C, et al. Systematic annotation of celiac disease loci refines pathological pathways and suggests a genetic explanation for increased interferon-gamma levels. Human Molecular Genetics. 24: 397-409. PMID 25190711 DOI: 10.1093/Hmg/Ddu453 |
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Senapati S, Gutierrez-Achury J, Sood A, Midha V, Szperl A, Romanos J, Zhernakova A, Franke L, Alonso S, Thelma BK, Wijmenga C, Trynka G. Evaluation of European coeliac disease risk variants in a north Indian population. European Journal of Human Genetics : Ejhg. 23: 530-5. PMID 25052311 DOI: 10.1038/Ejhg.2014.137 |
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Rostami-Nejad M, Romanos J, Rostami K, Ganji A, Ehsani-Ardakani MJ, Bakhshipour AR, Zojaji H, Mohebbi SR, Zali MR, Wijmenga C. Allele and haplotype frequencies for HLA-DQ in Iranian celiac disease patients. World Journal of Gastroenterology. 20: 6302-8. PMID 24876751 DOI: 10.3748/Wjg.V20.I20.6302 |
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Bossini-Castillo L, de Kovel C, Kallberg H, van 't Slot R, Italiaander A, Coenen M, Tak PP, Posthumus MD, Wijmenga C, Huizinga T, van der Helm-van Mil AH, Stoeken-Rijsbergen G, Rodriguez-Rodriguez L, Balsa A, González-Álvaro I, et al. A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides. Annals of the Rheumatic Diseases. 74: e15. PMID 24532677 DOI: 10.1136/Annrheumdis-2013-204591 |
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van Gerven NM, de Boer YS, Zwiers A, Verwer B, Drenth JP, van Hoek B, Van Erpecum KJ, Beuers U, van Buuren HR, den Ouden JW, Verdonk R, Koek GH, Brouwer J, Guichelaar M, Vrolijk J, ... ... Wijmenga C, et al. Sa1677 HLA-DRB1*0301 and HLA-DRB1*0401 Modify the Presentation and Outcome in Autoimmune Hepatitis Type-1 Gastroenterology. 148: S-1009. DOI: 10.1016/S0016-5085(15)33445-4 |
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Kumar V, Wijmenga C, Xavier RJ. Genetics of immune-mediated disorders: from genome-wide association to molecular mechanism. Current Opinion in Immunology. 31: 51-7. PMID 25458995 DOI: 10.1016/J.Coi.2014.09.007 |
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Hrdlickova B, Kumar V, Kanduri K, Zhernakova DV, Tripathi S, Karjalainen J, Lund RJ, Li Y, Ullah U, Modderman R, Abdulahad W, Lähdesmäki H, Franke L, Lahesmaa R, Wijmenga C, et al. Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity. Genome Medicine. 6: 88. PMID 25419237 DOI: 10.1186/S13073-014-0088-0 |
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Bonder MJ, Kasela S, Kals M, Tamm R, Lokk K, Barragan I, Buurman WA, Deelen P, Greve JW, Ivanov M, Rensen SS, van Vliet-Ostaptchouk JV, Wolfs MG, Fu J, Hofker MH, ... Wijmenga C, et al. Genetic and epigenetic regulation of gene expression in fetal and adult human livers. Bmc Genomics. 15: 860. PMID 25282492 DOI: 10.1186/1471-2164-15-860 |
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Schaefer AS, Jochens A, Dommisch H, Graetz C, Jockel-Schneider Y, Harks I, Staufenbiel I, Meyle J, Eickholz P, Folwaczny M, Laine M, Noack B, Wijmenga C, Lieb W, Bruckmann C, et al. A large candidate-gene association study suggests genetic variants at IRF5 and PRDM1 to be associated with aggressive periodontitis. Journal of Clinical Periodontology. 41: 1122-31. PMID 25263394 DOI: 10.1111/Jcpe.12314 |
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Kumar V, Cheng SC, Johnson MD, Smeekens SP, Wojtowicz A, Giamarellos-Bourboulis E, Karjalainen J, Franke L, Withoff S, Plantinga TS, van de Veerdonk FL, van der Meer JW, Joosten LA, Sokol H, Bauer H, ... ... Wijmenga C, et al. Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia. Nature Communications. 5: 4675. PMID 25197941 DOI: 10.1038/Ncomms5675 |
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Steck AK, Dong F, Wong R, Fouts A, Liu E, Romanos J, Wijmenga C, Norris JM, Rewers MJ. Improving prediction of type 1 diabetes by testing non-HLA genetic variants in addition to HLA markers. Pediatric Diabetes. 15: 355-62. PMID 25075402 DOI: 10.1111/Pedi.12092 |
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Gockel I, Becker J, Wouters MM, Niebisch S, Gockel HR, Hess T, Ramonet D, Zimmermann J, Vigo AG, Trynka G, de León AR, de la Serna JP, Urcelay E, Kumar V, Franke L, ... ... Wijmenga C, et al. Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. Nature Genetics. 46: 901-4. PMID 24997987 DOI: 10.1038/Ng.3029 |
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Smolonska J, Koppelman GH, Wijmenga C, Vonk JM, Zanen P, Bruinenberg M, Curjuric I, Imboden M, Thun GA, Franke L, Probst-Hensch NM, Nürnberg P, Riemersma RA, van Schayck CP, Loth DW, et al. Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis. The European Respiratory Journal. 44: 860-72. PMID 24993907 DOI: 10.1183/09031936.00001914 |
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Simino J, Shi G, Bis JC, Chasman DI, Ehret GB, Gu X, Guo X, Hwang SJ, Sijbrands E, Smith AV, Verwoert GC, Bragg-Gresham JL, Cadby G, Chen P, Cheng CY, ... ... Wijmenga C, et al. Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. American Journal of Human Genetics. 95: 24-38. PMID 24954895 DOI: 10.1016/J.Ajhg.2014.05.010 |
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Loth DW, Artigas MS, Gharib SA, Wain LV, Franceschini N, Koch B, Pottinger TD, Smith AV, Duan Q, Oldmeadow C, Lee MK, Strachan DP, James AL, Huffman JE, Vitart V, ... ... Wijmenga C, et al. Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nature Genetics. 46: 669-77. PMID 24929828 DOI: 10.1038/Ng.3011 |
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Deelen P, Menelaou A, van Leeuwen EM, Kanterakis A, van Dijk F, Medina-Gomez C, Francioli LC, Hottenga JJ, Karssen LC, Estrada K, Kreiner-Møller E, Rivadeneira F, van Setten J, Gutierrez-Achury J, Westra HJ, ... ... Wijmenga C, et al. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. European Journal of Human Genetics : Ejhg. 22: 1321-6. PMID 24896149 DOI: 10.1038/Ejhg.2014.19 |
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Hofker MH, Fu J, Wijmenga C. The genome revolution and its role in understanding complex diseases. Biochimica Et Biophysica Acta. 1842: 1889-1895. PMID 24834846 DOI: 10.1016/J.Bbadis.2014.05.002 |
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de Boer YS, van Gerven NM, Zwiers A, Verwer BJ, van Hoek B, van Erpecum KJ, Beuers U, van Buuren HR, Drenth JP, den Ouden JW, Verdonk RC, Koek GH, Brouwer JT, Guichelaar MM, Vrolijk JM, ... ... Wijmenga C, et al. Genome-wide association study identifies variants associated with autoimmune hepatitis type 1. Gastroenterology. 147: 443-52.e5. PMID 24768677 DOI: 10.1053/J.Gastro.2014.04.022 |
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Li H, Chan L, Bartuzi P, Melton SD, Weber A, Ben-Shlomo S, Varol C, Raetz M, Mao X, Starokadomskyy P, van Sommeren S, Mokadem M, Schneider H, Weisberg R, Westra HJ, ... ... Wijmenga C, et al. Copper metabolism domain-containing 1 represses genes that promote inflammation and protects mice from colitis and colitis-associated cancer. Gastroenterology. 147: 184-195.e3. PMID 24727021 DOI: 10.1053/J.Gastro.2014.04.007 |
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Li N, van der Sijde MR, Bakker SJ, Dullaart RP, van der Harst P, Gansevoort RT, Elbers CC, Wijmenga C, Snieder H, Hofker MH, Fu J. Pleiotropic effects of lipid genes on plasma glucose, HbA1c, and HOMA-IR levels. Diabetes. 63: 3149-58. PMID 24722249 DOI: 10.2337/Db13-1800 |
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Fransen K, van Sommeren S, Westra HJ, Veenstra M, Lamberts LE, Modderman R, Dijkstra G, Fu J, Wijmenga C, Franke L, Weersma RK, van Diemen CC. Correlation of genetic risk and messenger RNA expression in a Th17/IL23 pathway analysis in inflammatory bowel disease. Inflammatory Bowel Diseases. 20: 777-82. PMID 24662057 DOI: 10.1097/Mib.0000000000000013 |
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Tragante V, Barnes MR, Ganesh SK, Lanktree MB, Guo W, Franceschini N, Smith EN, Johnson T, Holmes MV, Padmanabhan S, Karczewski KJ, Almoguera B, Barnard J, Baumert J, Chang YP, ... ... Wijmenga C, et al. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. American Journal of Human Genetics. 94: 349-60. PMID 24560520 DOI: 10.1016/J.Ajhg.2013.12.016 |
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Laayouni H, Oosting M, Luisi P, Ioana M, Alonso S, Ricaño-Ponce I, Trynka G, Zhernakova A, Plantinga TS, Cheng SC, van der Meer JW, Popp R, Sood A, Thelma BK, Wijmenga C, et al. Convergent evolution in European and Rroma populations reveals pressure exerted by plague on Toll-like receptors. Proceedings of the National Academy of Sciences of the United States of America. 111: 2668-73. PMID 24550294 DOI: 10.1073/Pnas.1317723111 |
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Kallionpää H, Elo LL, Laajala E, Mykkänen J, Ricaño-Ponce I, Vaarma M, Laajala TD, Hyöty H, Ilonen J, Veijola R, Simell T, Wijmenga C, Knip M, Lähdesmäki H, Simell O, et al. Innate immune activity is detected prior to seroconversion in children with HLA-conferred type 1 diabetes susceptibility. Diabetes. 63: 2402-14. PMID 24550192 DOI: 10.2337/Db13-1775 |
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Geremek M, Ziętkiewicz E, Bruinenberg M, Franke L, Pogorzelski A, Wijmenga C, Witt M. Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients. Plos One. 9: e88216. PMID 24516614 DOI: 10.1371/Journal.Pone.0088216 |
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Mayes MD, Bossini-Castillo L, Gorlova O, Martin JE, Zhou X, Chen WV, Assassi S, Ying J, Tan FK, Arnett FC, Reveille JD, Guerra S, Teruel M, Carmona FD, Gregersen PK, ... ... Wijmenga C, et al. Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. American Journal of Human Genetics. 94: 47-61. PMID 24387989 DOI: 10.1016/J.Ajhg.2013.12.002 |
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Manichaikul A, Hoffman EA, Smolonska J, Gao W, Cho MH, Baumhauer H, Budoff M, Austin JH, Washko GR, Carr JJ, Kaufman JD, Pottinger T, Powell CA, Wijmenga C, Zanen P, et al. Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. American Journal of Respiratory and Critical Care Medicine. 189: 408-18. PMID 24383474 DOI: 10.1164/Rccm.201306-1061Oc |
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Yoneyama S, Guo Y, Lanktree MB, Barnes MR, Elbers CC, Karczewski KJ, Padmanabhan S, Bauer F, Baumert J, Beitelshees A, Berenson GS, Boer JM, Burke G, Cade B, Chen W, ... ... Wijmenga C, et al. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. Human Molecular Genetics. 23: 2498-510. PMID 24345515 DOI: 10.1093/Hmg/Ddt626 |
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Almeida R, Ricaño-Ponce I, Kumar V, Deelen P, Szperl A, Trynka G, Gutierrez-Achury J, Kanterakis A, Westra HJ, Franke L, Swertz MA, Platteel M, Bilbao JR, Barisani D, Greco L, ... ... Wijmenga C, et al. Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant. Human Molecular Genetics. 23: 2481-9. PMID 24334606 DOI: 10.1093/Hmg/Ddt619 |
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Scholtens S, Postma DS, Moffatt MF, Panasevich S, Granell R, Henderson AJ, Melén E, Nyberg F, Pershagen G, Jarvis D, Ramasamy A, Wjst M, Svanes C, Bouzigon E, Demenais F, ... ... Wijmenga C, et al. Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure. The Journal of Allergy and Clinical Immunology. 133: 885-8. PMID 24315450 DOI: 10.1016/J.Jaci.2013.08.049 |
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Cleynen I, Vazeille E, Artieda M, Verspaget HW, Szczypiorska M, Bringer MA, Lakatos PL, Seibold F, Parnell K, Weersma RK, Mahachie John JM, Morgan-Walsh R, Staelens D, Arijs I, De Hertogh G, ... ... Wijmenga C, et al. Genetic and microbial factors modulating the ubiquitin proteasome system in inflammatory bowel disease. Gut. 63: 1265-74. PMID 24092863 DOI: 10.1136/Gutjnl-2012-303205 |
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Bondar C, Plaza-Izurieta L, Fernandez-Jimenez N, Irastorza I, Withoff S, Wijmenga C, Chirdo F, Bilbao JR. THEMIS and PTPRK in celiac intestinal mucosa: coexpression in disease and after in vitro gliadin challenge European Journal of Human Genetics. 22: 358-362. PMID 23820479 DOI: 10.1038/Ejhg.2013.136 |
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Boomsma DI, Wijmenga C, Slagboom EP, Swertz MA, Karssen LC, Abdellaoui A, Ye K, Guryev V, Vermaat M, Van Dijk F, Francioli LC, Hottenga JJ, Laros JFJ, Li Q, Li Y, et al. The Genome of the Netherlands: Design, and project goals European Journal of Human Genetics. 22: 221-227. PMID 23714750 DOI: 10.1038/Ejhg.2013.118 |
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Romanos J, Rosén A, Kumar V, Trynka G, Franke L, Szperl A, Gutierrez-Achury J, van Diemen CC, Kanninga R, Jankipersadsing SA, Steck A, Eisenbarth G, van Heel DA, Cukrowska B, Bruno V, ... ... Wijmenga C, et al. Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants. Gut. 63: 415-22. PMID 23704318 DOI: 10.1136/Gutjnl-2012-304110 |
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Stoffels M, Szperl A, Simon A, Netea MG, Plantinga TS, van Deuren M, Kamphuis S, Lachmann HJ, Cuppen E, Kloosterman WP, Frenkel J, van Diemen CC, Wijmenga C, van Gijn M, van der Meer JW. MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease. Annals of the Rheumatic Diseases. 73: 455-61. PMID 23505238 DOI: 10.1136/Annrheumdis-2012-202580 |
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Wijmenga C, Gutierrez-Achury J. Celiac Disease Genetics Journal of Pediatric Gastroenterology & Nutrition. 59: S4-S7. DOI: 10.1097/01.Mpg.0000450392.23156.10 |
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Deelen P, Menelaou A, Van Leeuwen EM, Kanterakis A, Van Dijk F, Medina-Gomez C, Francioli LC, Hottenga JJ, Karssen LC, Estrada K, Kreiner-Møller E, Rivadeneira F, Van Setten J, Gutierrez-Achury J, Westra HJ, ... ... Wijmenga C, et al. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of the Netherlands' European Journal of Human Genetics. 22: 1321-1326. DOI: 10.1038/ejhg.2014.19 |
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de Boer Y, van Gerven N, Verwer B, Zwiers A, van Hoek B, van Erpecum K, Beuers U, van Buuren H, Drenth J, den Ouden J, Verdonk R, Koek G, Brouwer J, Guichelaar M, Vrolijk J, ... ... Wijmenga C, et al. O131 GENOME-WIDE ASSOCIATION STUDY IN AUTOIMMUNE HEPATITIS IDENTIFIES RISK VARIANT IN THE SH2B3 REGION Journal of Hepatology. 60: S54. DOI: 10.1016/S0168-8278(14)60133-1 |
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Nijmeijer RM, van Santvoort HC, Zhernakova A, Teller S, Scheiber JA, de Kovel CG, Besselink MG, Visser JT, Lutgendorff F, Bollen TL, Boermeester MA, Rijkers GT, Weiss FU, Mayerle J, Lerch MM, ... ... Wijmenga C, et al. Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis. Plos One. 8: e85870. PMID 24386489 DOI: 10.1371/Journal.Pone.0085870 |
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Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, ... ... Wijmenga C, et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics. 45: 1274-83. PMID 24097068 DOI: 10.1038/Ng.2797 |
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Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, ... ... Wijmenga C, et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics. 45: 1345-52. PMID 24097064 DOI: 10.1038/Ng.2795 |
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Bradley DT, Hughes AE, Badger SA, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Grétarsdóttir S, Burnand K, Child AH, Clough RE, Cockerill G, Hafez H, Scott DJ, ... ... Wijmenga C, et al. A variant in LDLR is associated with abdominal aortic aneurysm. Circulation. Cardiovascular Genetics. 6: 498-504. PMID 24046328 DOI: 10.1161/Circgenetics.113.000165 |
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Zhernakova A, Withoff S, Wijmenga C. Clinical implications of shared genetics and pathogenesis in autoimmune diseases. Nature Reviews. Endocrinology. 9: 646-59. PMID 23959365 DOI: 10.1038/Nrendo.2013.161 |
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Ricaño-Ponce I, Wijmenga C. Mapping of immune-mediated disease genes. Annual Review of Genomics and Human Genetics. 14: 325-53. PMID 23834318 DOI: 10.1146/Annurev-Genom-091212-153450 |
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Zhernakova DV, de Klerk E, Westra HJ, Mastrokolias A, Amini S, Ariyurek Y, Jansen R, Penninx BW, Hottenga JJ, Willemsen G, de Geus EJ, Boomsma DI, Veldink JH, van den Berg LH, Wijmenga C, et al. DeepSAGE reveals genetic variants associated with alternative polyadenylation and expression of coding and non-coding transcripts. Plos Genetics. 9: e1003594. PMID 23818875 DOI: 10.1371/Journal.Pgen.1003594 |
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Ellinghaus D, Zhang H, Zeissig S, Lipinski S, Till A, Jiang T, Stade B, Bromberg Y, Ellinghaus E, Keller A, Rivas MA, Skieceviciene J, Doncheva NT, Liu X, Liu Q, ... ... Wijmenga C, et al. Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. Gastroenterology. 145: 339-47. PMID 23624108 DOI: 10.1053/J.Gastro.2013.04.040 |
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Liu JZ, Hov JR, Folseraas T, Ellinghaus E, Rushbrook SM, Doncheva NT, Andreassen OA, Weersma RK, Weismüller TJ, Eksteen B, Invernizzi P, Hirschfield GM, Gotthardt DN, Pares A, Ellinghaus D, ... ... Wijmenga C, et al. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nature Genetics. 45: 670-5. PMID 23603763 DOI: 10.1038/Ng.2616 |
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Schaefer AS, Bochenek G, Manke T, Nothnagel M, Graetz C, Thien A, Jockel-Schneider Y, Harks I, Staufenbiel I, Wijmenga C, Eberhard J, Guzeldemir-Akcakanat E, Cine N, Folwaczny M, Noack B, et al. Validation of reported genetic risk factors for periodontitis in a large-scale replication study. Journal of Clinical Periodontology. 40: 563-72. PMID 23587006 DOI: 10.1111/Jcpe.12092 |
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den Hoed M, Eijgelsheim M, Esko T, Brundel BJ, Peal DS, Evans DM, Nolte IM, Segrè AV, Holm H, Handsaker RE, Westra HJ, Johnson T, Isaacs A, Yang J, Lundby A, ... ... Wijmenga C, et al. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics. 45: 621-31. PMID 23583979 DOI: 10.1038/Ng.2610 |
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van Setten J, Isgum I, Smolonska J, Ripke S, de Jong PA, Oudkerk M, de Koning H, Lammers JW, Zanen P, Groen HJ, Boezen HM, Postma DS, Wijmenga C, Viergever MA, Mali WP, et al. Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction. Atherosclerosis. 228: 400-5. PMID 23561647 DOI: 10.1016/J.Atherosclerosis.2013.02.039 |
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Knevel R, de Rooy DP, Zhernakova A, Gröndal G, Krabben A, Steinsson K, Wijmenga C, Cavet G, Toes RE, Huizinga TW, Gregersen PK, van der Helm-van Mil AH. Association of variants in IL2RA with progression of joint destruction in rheumatoid arthritis. Arthritis and Rheumatism. 65: 1684-93. PMID 23529819 DOI: 10.1002/Art.37938 |
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Kiezun A, Pulit SL, Francioli LC, van Dijk F, Swertz M, Boomsma DI, van Duijn CM, Slagboom PE, van Ommen GJ, Wijmenga C, de Bakker PI, Sunyaev SR. Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency. Plos Genetics. 9: e1003301. PMID 23468643 DOI: 10.1371/Journal.Pgen.1003301 |
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Faraco J, Lin L, Kornum BR, Kenny EE, Trynka G, Einen M, Rico TJ, Lichtner P, Dauvilliers Y, Arnulf I, Lecendreux M, Javidi S, Geisler P, Mayer G, Pizza F, ... ... Wijmenga C, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Plos Genetics. 9: e1003270. PMID 23459209 DOI: 10.1371/Journal.Pgen.1003270 |
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Hughes T, Coit P, Adler A, Yilmaz V, Aksu K, Düzgün N, Keser G, Cefle A, Yazici A, Ergen A, Alpsoy E, Salvarani C, Casali B, Kötter I, Gutierrez-Achury J, ... Wijmenga C, et al. Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease. Nature Genetics. 45: 319-24. PMID 23396137 DOI: 10.1038/Ng.2551 |
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Mohamed Hoesein FA, Wauters E, Janssens W, Groen HJ, Smolonska J, Wijmenga C, Postma DS, Boezen HM, De Jong PA, Decramer M, Lammers JW, Lambrechts D, Zanen P. Variants in the 15q24/25 locus associate with lung function decline in active smokers. Plos One. 8: e53219. PMID 23349703 DOI: 10.1371/Journal.Pone.0053219 |
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Kumar V, Westra HJ, Karjalainen J, Zhernakova DV, Esko T, Hrdlickova B, Almeida R, Zhernakova A, Reinmaa E, Võsa U, Hofker MH, Fehrmann RS, Fu J, Withoff S, Metspalu A, ... ... Wijmenga C, et al. Human disease-associated genetic variation impacts large intergenic non-coding RNA expression. Plos Genetics. 9: e1003201. PMID 23341781 DOI: 10.1371/Journal.Pgen.1003201 |
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Gonzaludo N, Zheng HX, Wang J, Chanock SJ, Jin L, Scherer S, Wijmenga C, Kwok PY, Brookes AJ. HGV2012: Leveraging Next-Generation Technology and Large Datasets to Advance Disease Research Human Mutation. 34: 657-660. PMID 23315969 DOI: 10.1002/Humu.22270 |
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Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, ... ... Wijmenga C, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Human Molecular Genetics. 22: 1663-78. PMID 23303523 DOI: 10.1093/Hmg/Dds555 |
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Smeekens SP, Ng A, Kumar V, Johnson MD, Plantinga TS, van Diemen C, Arts P, Verwiel ET, Gresnigt MS, Fransen K, van Sommeren S, Oosting M, Cheng SC, Joosten LA, Hoischen A, ... ... Wijmenga C, et al. Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans. Nature Communications. 4: 1342. PMID 23299892 DOI: 10.1038/Ncomms2343 |
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Ellinghaus D, Folseraas T, Holm K, Ellinghaus E, Melum E, Balschun T, Laerdahl JK, Shiryaev A, Gotthardt DN, Weismüller TJ, Schramm C, Wittig M, Bergquist A, Björnsson E, Marschall HU, ... ... Wijmenga C, et al. Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4. Hepatology (Baltimore, Md.). 58: 1074-83. PMID 22821403 DOI: 10.1002/Hep.25977 |
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Nejad MR, Rostami K, Romanos J, Zojaji H, Zali MR, Wijmenga C. OC-090 Correlation between Distribution of HLA Haplotypes and Severity of Mucosal Damages Gut. 62: A39.1-A39. DOI: 10.1136/Gutjnl-2013-304907.089 |
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Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YPC, Elbers CC, Farrall M, Fischer ME, Gaunt NF, ... ... Wijmenga C, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array Human Molecular Genetics. 22: 3394-3395. DOI: 10.1093/Hmg/Ddt177 |
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Gockel I, Becker J, Wouters MM, Brun P, Vigo AG, Trynka G, Kumar V, Franke L, Westra H, Wijmenga C, Zaninotto G, Drescher DG, Niebisch S, Tack JF, Mueller M, et al. 815 An Insertion of Eight Amino Acids in HLA-DQA1 and Three Amino Acid Substitutions in HLA-DQA1 and HLA-DQB1 Confer Risk to Idiopathic Achalasia Gastroenterology. 144: S-142. DOI: 10.1016/S0016-5085(13)60510-7 |
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Hancock DB, Artigas MS, Gharib SA, Henry A, Manichaikul A, Ramasamy A, Loth DW, Imboden M, Koch B, McArdle WL, Smith AV, Smolonska J, Sood A, Tang W, Wilk JB, ... ... Wijmenga C, et al. Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. Plos Genetics. 8: e1003098. PMID 23284291 DOI: 10.1371/Journal.Pgen.1003098 |
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Duarri A, Jezierska J, Fokkens M, Meijer M, Schelhaas HJ, den Dunnen WF, van Dijk F, Verschuuren-Bemelmans C, Hageman G, van de Vlies P, Küsters B, van de Warrenburg BP, Kremer B, Wijmenga C, Sinke RJ, et al. Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19. Annals of Neurology. 72: 870-80. PMID 23280838 DOI: 10.1002/Ana.23700 |
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Eyre S, Bowes J, Diogo D, Lee A, Barton A, Martin P, Zhernakova A, Stahl E, Viatte S, McAllister K, Amos CI, Padyukov L, Toes RE, Huizinga TW, Wijmenga C, et al. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics. 44: 1336-40. PMID 23143596 DOI: 10.1038/Ng.2462 |
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Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, ... ... Wijmenga C, et al. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nature Genetics. 44: 1341-8. PMID 23143594 DOI: 10.1038/Ng.2467 |
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Jostins L, Ripke S, Weersma RK, Duerr RH, McGovern DP, Hui KY, Lee JC, Schumm LP, Sharma Y, Anderson CA, Essers J, Mitrovic M, Ning K, Cleynen I, Theatre E, ... ... Wijmenga C, et al. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature. 491: 119-24. PMID 23128233 DOI: 10.1038/Nature11582 |
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Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, ... ... Wijmenga C, et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics. 91: 823-38. PMID 23063622 DOI: 10.1016/J.Ajhg.2012.08.032 |
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Su Z, Gay LJ, Strange A, Palles C, Band G, Whiteman DC, Lescai F, Langford C, Nanji M, Edkins S, van der Winkel A, Levine D, Sasieni P, Bellenguez C, Howarth K, ... ... Wijmenga C, et al. Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nature Genetics. 44: 1131-6. PMID 22961001 DOI: 10.1038/Ng.2408 |
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Helgadottir A, Gretarsdottir S, Thorleifsson G, Holm H, Patel RS, Gudnason T, Jones GT, van Rij AM, Eapen DJ, Baas AF, Tregouet DA, Morange PE, Emmerich J, Lindblad B, Gottsäter A, ... ... Wijmenga C, et al. Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. Journal of the American College of Cardiology. 60: 722-9. PMID 22898070 DOI: 10.1016/J.Jacc.2012.01.078 |
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Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, ... ... Wijmenga C, et al. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American Journal of Respiratory and Critical Care Medicine. 186: 622-32. PMID 22837378 DOI: 10.1164/Rccm.201202-0366Oc |
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Netea MG, Wijmenga C, O'Neill LA. Genetic variation in Toll-like receptors and disease susceptibility. Nature Immunology. 13: 535-42. PMID 22610250 DOI: 10.1038/Ni.2284 |
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Kumar V, Wijmenga C, Withoff S. From genome-wide association studies to disease mechanisms: celiac disease as a model for autoimmune diseases. Seminars in Immunopathology. 34: 567-80. PMID 22580835 DOI: 10.1007/S00281-012-0312-1 |
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van Eerde AM, Duran K, van Riel E, de Kovel CG, Koeleman BP, Knoers NV, Renkema KY, van der Horst HJ, Bökenkamp A, van Hagen JM, van den Berg LH, Wolffenbuttel KP, van den Hoek J, Feitz WF, de Jong TP, ... ... Wijmenga C, et al. Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. Plos One. 7: e31327. PMID 22558067 DOI: 10.1371/Journal.Pone.0031327 |
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Folseraas T, Melum E, Rausch P, Juran BD, Ellinghaus E, Shiryaev A, Laerdahl JK, Ellinghaus D, Schramm C, Weismüller TJ, Gotthardt DN, Hov JR, Clausen OP, Weersma RK, Janse M, ... ... Wijmenga C, et al. Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci. Journal of Hepatology. 57: 366-75. PMID 22521342 DOI: 10.1016/J.Jhep.2012.03.031 |
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Dolmans GH, Werker PM, de Jong IJ, Nijman RJ, Wijmenga C, Ophoff RA. WNT2 locus is involved in genetic susceptibility of Peyronie's disease. The Journal of Sexual Medicine. 9: 1430-4. PMID 22489561 DOI: 10.1111/J.1743-6109.2012.02704.X |
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Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... ... Wijmenga C, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
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Stahl EA, Wegmann D, Trynka G, Gutierrez-Achury J, Do R, Voight BF, Kraft P, Chen R, Kallberg HJ, Kurreeman FA, Kathiresan S, Wijmenga C, Gregersen PK, et al. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nature Genetics. 44: 483-9. PMID 22446960 DOI: 10.1038/Ng.2232 |
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van Vliet-Ostaptchouk JV, van Haeften TW, Landman GW, Reiling E, Kleefstra N, Bilo HJ, Klungel OH, de Boer A, van Diemen CC, Wijmenga C, Boezen HM, Dekker JM, van 't Riet E, Nijpels G, Welschen LM, et al. Common variants in the type 2 diabetes KCNQ1 gene are associated with impairments in insulin secretion during hyperglycaemic glucose clamp. Plos One. 7: e32148. PMID 22403629 DOI: 10.1371/Journal.Pone.0032148 |
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Antó JM, Pinart M, Akdis M, Auffray C, Bachert C, Basagaña X, Carlsen KH, Guerra S, von Hertzen L, Illi S, Kauffmann F, Keil T, Kiley JP, Koppelman GH, Lupinek C, ... ... Wijmenga C, et al. Understanding the complexity of IgE-related phenotypes from childhood to young adulthood: a Mechanisms of the Development of Allergy (MeDALL) seminar. The Journal of Allergy and Clinical Immunology. 129: 943-54.e4. PMID 22386796 DOI: 10.1016/J.Jaci.2012.01.047 |
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Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, ... ... Wijmenga C, et al. Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American Journal of Human Genetics. 90: 410-25. PMID 22325160 DOI: 10.1016/J.Ajhg.2011.12.022 |
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| 2012 |
Fu J, Wolfs MG, Deelen P, Westra HJ, Fehrmann RS, Te Meerman GJ, Buurman WA, Rensen SS, Groen HJ, Weersma RK, van den Berg LH, Veldink J, Ophoff RA, Snieder H, van Heel D, ... ... Wijmenga C, et al. Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression. Plos Genetics. 8: e1002431. PMID 22275870 DOI: 10.1371/Journal.Pgen.1002431 |
0.812 |
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| 2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, ... ... Wijmenga C, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.728 |
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| 2012 |
Hunt KA, Smyth DJ, Balschun T, Ban M, Mistry V, Ahmad T, Anand V, Barrett JC, Bhaw-Rosun L, Bockett NA, Brand OJ, Brouwer E, Concannon P, Cooper JD, Dias KR, ... ... Wijmenga C, et al. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nature Genetics. 44: 3-5. PMID 22200769 DOI: 10.1038/Ng.1037 |
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| 2012 |
Kumar V, Wijmenga C. Celiac disease: update from the 14th International Celiac Disease Symposium 2011. Expert Review of Gastroenterology & Hepatology. 5: 685-7. PMID 22017696 DOI: 10.1586/Egh.11.70 |
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| 2012 |
Ruigrok YM, Baas AF, Medic J, Wijmenga C, Rinkel GJ. The transforming growth factor-β receptor genes and the risk of intracranial aneurysms. International Journal of Stroke : Official Journal of the International Stroke Society. 7: 645-8. PMID 21978186 DOI: 10.1111/J.1747-4949.2011.00615.X |
0.365 |
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| 2012 |
Lanktree M, Guo Y, Murtaza M, Glessner J, Bailey S, Onland-Moret N, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson C, Klopp N, Baumert J, Padmanabhan S, ... ... Wijmenga C, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height The American Journal of Human Genetics. 90: 1116-1117. DOI: 10.1016/J.Ajhg.2012.05.017 |
0.365 |
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| 2012 |
Saxena R, Elbers C, Guo Y, Peter I, Gaunt T, Mega J, Lanktree M, Tare A, Castillo B, Li Y, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight B, ... ... Wijmenga C, et al. Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci The American Journal of Human Genetics. 90: 753. DOI: 10.1016/J.Ajhg.2012.03.001 |
0.308 |
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| 2011 |
Trynka G, Hunt KA, Bockett NA, Romanos J, Mistry V, Szperl A, Bakker SF, Bardella MT, Bhaw-Rosun L, Castillejo G, de la Concha EG, de Almeida RC, Dias KR, van Diemen CC, Dubois PC, ... ... Wijmenga C, et al. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nature Genetics. 43: 1193-201. PMID 22057235 DOI: 10.1038/Ng.998 |
0.73 |
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| 2011 |
Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Gretarsdottir S, Badger SA, Bradley DT, Burnand K, Child AH, Clough RE, Cockerill G, Hafez H, Scott DJ, ... ... Wijmenga C, et al. Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. American Journal of Human Genetics. 89: 619-27. PMID 22055160 DOI: 10.1016/J.Ajhg.2011.10.002 |
0.406 |
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| 2011 |
Surakka I, Isaacs A, Karssen LC, Laurila PP, Middelberg RP, Tikkanen E, Ried JS, Lamina C, Mangino M, Igl W, Hottenga JJ, Lagou V, van der Harst P, Mateo Leach I, Esko T, ... ... Wijmenga C, et al. A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. Plos Genetics. 7: e1002333. PMID 22028671 DOI: 10.1371/Journal.Pgen.1002333 |
0.436 |
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| 2011 |
Soler Artigas M, Loth DW, Wain LV, Gharib SA, Obeidat M, Tang W, Zhai G, Zhao JH, Smith AV, Huffman JE, Albrecht E, Jackson CM, Evans DM, Cadby G, Fornage M, ... ... Wijmenga C, et al. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nature Genetics. 43: 1082-90. PMID 21946350 DOI: 10.1038/Ng.941 |
0.323 |
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| 2011 |
Fu J, Festen EA, Wijmenga C. Multi-ethnic studies in complex traits. Human Molecular Genetics. 20: R206-13. PMID 21890495 DOI: 10.1093/hmg/ddr386 |
0.315 |
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| 2011 |
Nijmeijer RM, Gadaleta RM, van Mil SW, van Bodegraven AA, Crusius JB, Dijkstra G, Hommes DW, de Jong DJ, Stokkers PC, Verspaget HW, Weersma RK, van der Woude CJ, Stapelbroek JM, Schipper ME, Wijmenga C, et al. Farnesoid X receptor (FXR) activation and FXR genetic variation in inflammatory bowel disease. Plos One. 6: e23745. PMID 21887309 DOI: 10.1371/Journal.Pone.0023745 |
0.314 |
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| 2011 |
Cotsapas C, Voight BF, Rossin E, Lage K, Neale BM, Wallace C, Abecasis GR, Barrett JC, Behrens T, Cho J, De Jager PL, Elder JT, Graham RR, Gregersen P, Klareskog L, ... ... Wijmenga C, et al. Pervasive sharing of genetic effects in autoimmune disease. Plos Genetics. 7: e1002254. PMID 21852963 DOI: 10.1371/Journal.Pgen.1002254 |
0.451 |
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| 2011 |
Fehrmann RS, Jansen RC, Veldink JH, Westra HJ, Arends D, Bonder MJ, Fu J, Deelen P, Groen HJ, Smolonska A, Weersma RK, Hofstra RM, Buurman WA, Rensen S, Wolfs MG, ... ... Wijmenga C, et al. Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. Plos Genetics. 7: e1002197. PMID 21829388 DOI: 10.1371/Journal.Pgen.1002197 |
0.832 |
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| 2011 |
Dolmans GH, Werker PM, Hennies HC, Furniss D, Festen EA, Franke L, Becker K, van der Vlies P, Wolffenbuttel BH, Tinschert S, Toliat MR, Nothnagel M, Franke A, Klopp N, Wichmann HE, ... ... Wijmenga C, et al. Wnt signaling and Dupuytren's disease. The New England Journal of Medicine. 365: 307-17. PMID 21732829 DOI: 10.1056/Nejmoa1101029 |
0.687 |
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| 2011 |
Westra HJ, Jansen RC, Fehrmann RS, te Meerman GJ, van Heel D, Wijmenga C, Franke L. MixupMapper: correcting sample mix-ups in genome-wide datasets increases power to detect small genetic effects. Bioinformatics (Oxford, England). 27: 2104-11. PMID 21653519 DOI: 10.1093/Bioinformatics/Btr323 |
0.795 |
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| 2011 |
Shi J, Zhou L, Zhernakova A, Qian J, Zhu F, Sun G, Zhu L, Ma X, Dijkstra G, Wijmenga C, Faber KN, Lu X, Weersma RK. Haplotype-based analysis of ulcerative colitis risk loci identifies both IL2 and IL21 as susceptibility genes in Han Chinese. Inflammatory Bowel Diseases. 17: 2472-9. PMID 21648020 DOI: 10.1002/Ibd.21652 |
0.389 |
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| 2011 |
Szperl A, Ricaño-Ponce I, Li J, Deelen P, Kanterakis A, Plagnol V, van Dijk F, Westra H, Trynka G, Mulder C, Swertz M, Wijmenga C, Zheng HC. Exome sequencing in a family segregating for celiac disease Clinical Genetics. 80: 138-147. PMID 21627641 DOI: 10.1111/J.1399-0004.2011.01714.X |
0.81 |
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| 2011 |
de Greef JC, Wang J, Balog J, den Dunnen JT, Frants RR, Straasheijm KR, Aytekin C, van der Burg M, Duprez L, Ferster A, Gennery AR, Gimelli G, Reisli I, Schuetz C, Schulz A, ... ... Wijmenga C, et al. Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2. American Journal of Human Genetics. 88: 796-804. PMID 21596365 DOI: 10.1016/J.Ajhg.2011.04.018 |
0.515 |
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| 2011 |
Hrdlickova B, Westra HJ, Franke L, Wijmenga C. Celiac disease: moving from genetic associations to causal variants. Clinical Genetics. 80: 203-313. PMID 21595655 DOI: 10.1111/j.1399-0004.2011.01707.x |
0.841 |
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| 2011 |
Janse M, Lamberts LE, Franke L, Raychaudhuri S, Ellinghaus E, Muri Boberg K, Melum E, Folseraas T, Schrumpf E, Bergquist A, Björnsson E, Fu J, Jan Westra H, Groen HJ, Fehrmann RS, ... ... Wijmenga C, et al. Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9. Hepatology (Baltimore, Md.). 53: 1977-85. PMID 21425313 DOI: 10.1002/Hep.24307 |
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| 2011 |
Gutierrez-Achury J, Coutinho de Almeida R, Wijmenga C. Shared genetics in coeliac disease and other immune-mediated diseases. Journal of Internal Medicine. 269: 591-603. PMID 21401738 DOI: 10.1111/J.1365-2796.2011.02375.X |
0.415 |
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| 2011 |
Zhernakova A, Stahl EA, Trynka G, Raychaudhuri S, Festen EA, Franke L, Westra HJ, Fehrmann RS, Kurreeman FA, Thomson B, Gupta N, Romanos J, McManus R, Ryan AW, Turner G, ... ... Wijmenga C, et al. Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. Plos Genetics. 7: e1002004. PMID 21383967 DOI: 10.1371/Journal.Pgen.1002004 |
0.826 |
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| 2011 |
Brown SJ, Asai Y, Cordell HJ, Campbell LE, Zhao Y, Liao H, Northstone K, Henderson J, Alizadehfar R, Ben-Shoshan M, Morgan K, Roberts G, Masthoff LJ, Pasmans SG, van den Akker PC, ... Wijmenga C, et al. Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy. The Journal of Allergy and Clinical Immunology. 127: 661-7. PMID 21377035 DOI: 10.1016/J.Jaci.2011.01.031 |
0.414 |
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| 2011 |
Szperl A, Saavalainen P, Weersma RK, Lappalainen M, Paavola-Sakki P, Halme L, Färkkilä M, Turunen U, Kontula K, Ponsioen CY, Wijmenga C, van Diemen CC. Functional polymorphism in IL12B promoter site is associated with ulcerative colitis. Inflammatory Bowel Diseases. 17: E38-40. PMID 21351215 DOI: 10.1002/Ibd.21670 |
0.309 |
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| 2011 |
Einarsdottir E, Bevova MR, Zhernakova A, Monsuur A, Koskinen LL, van't Slot R, Mulder C, Mearin ML, Korponay-Szabo IR, Kaukinen K, Kurppa K, Kere J, Mäki M, Wijmenga C, Saavalainen P. Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations. European Journal of Human Genetics : Ejhg. 19: 682-6. PMID 21326284 DOI: 10.1038/Ejhg.2011.2 |
0.433 |
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| 2011 |
Knauff EA, Blauw HM, Pearson PL, Kok K, Wijmenga C, Veldink JH, van den Berg LH, Bouchard P, Fauser BC, Franke L. Copy number variants on the X chromosome in women with primary ovarian insufficiency. Fertility and Sterility. 95: 1584-8.e1. PMID 21316664 DOI: 10.1016/J.Fertnstert.2011.01.018 |
0.616 |
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| 2011 |
van Disseldorp J, Franke L, Eijkemans R, Broekmans F, Macklon N, Wijmenga C, Fauser B. Genome-wide analysis shows no genomic predictors of ovarian response to stimulation by exogenous FSH for IVF. Reproductive Biomedicine Online. 22: 382-8. PMID 21316307 DOI: 10.1016/J.Rbmo.2010.12.006 |
0.684 |
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| 2011 |
Festen EA, Goyette P, Green T, Boucher G, Beauchamp C, Trynka G, Dubois PC, Lagacé C, Stokkers PC, Hommes DW, Barisani D, Palmieri O, Annese V, van Heel DA, Weersma RK, ... ... Wijmenga C, et al. A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease. Plos Genetics. 7: e1001283. PMID 21298027 DOI: 10.1371/Journal.Pgen.1001283 |
0.408 |
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| 2011 |
Anderson CA, Boucher G, Lees CW, Franke A, D'Amato M, Taylor KD, Lee JC, Goyette P, Imielinski M, Latiano A, Lagacé C, Scott R, Amininejad L, Bumpstead S, Baidoo L, ... ... Wijmenga C, et al. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nature Genetics. 43: 246-52. PMID 21297633 DOI: 10.1038/Ng.764 |
0.836 |
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| 2011 |
Diaz-Gallo LM, Espino-Paisán L, Fransen K, Gómez-GarcÃa M, van Sommeren S, Cardeña C, Rodrigo L, Mendoza JL, Taxonera C, Nieto A, Alcain G, Cueto I, López-Nevot MA, Bottini N, Barclay ML, ... ... Wijmenga C, et al. Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis. Inflammatory Bowel Diseases. 17: 2287-94. PMID 21287672 DOI: 10.1186/1479-5876-8-S1-P2 |
0.398 |
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| 2011 |
Bousquet J, Anto J, Auffray C, Akdis M, Cambon-Thomsen A, Keil T, Haahtela T, Lambrecht BN, Postma DS, Sunyer J, Valenta R, Akdis CA, Annesi-Maesano I, Arno A, Bachert C, ... ... Wijmenga C, et al. MeDALL (Mechanisms of the Development of ALLergy): an integrated approach from phenotypes to systems medicine. Allergy. 66: 596-604. PMID 21261657 DOI: 10.1111/J.1398-9995.2010.02534.X |
0.35 |
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| 2011 |
Szperl AM, Golachowska MR, Bruinenberg M, Prekeris R, Thunnissen AM, Karrenbeld A, Dijkstra G, Hoekstra D, Mercer D, Ksiazyk J, Wijmenga C, Wapenaar MC, Rings EH, van IJzendoorn SC. Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. Journal of Pediatric Gastroenterology and Nutrition. 52: 307-13. PMID 21206382 DOI: 10.1097/Mpg.0B013E3181Eea177 |
0.305 |
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| 2011 |
Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... ... Wijmenga C, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/J.Ajhg.2010.11.007 |
0.455 |
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| 2011 |
Melum E, Franke A, Schramm C, Weismüller TJ, Gotthardt DN, Offner FA, Juran BD, Laerdahl JK, Labi V, Björnsson E, Weersma RK, Henckaerts L, Teufel A, Rust C, Ellinghaus E, ... ... Wijmenga C, et al. Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. Nature Genetics. 43: 17-9. PMID 21151127 DOI: 10.1038/Ng.728 |
0.431 |
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| 2011 |
Windelinckx A, De Mars G, Huygens W, Peeters MW, Vincent B, Wijmenga C, Lambrechts D, Delecluse C, Roth SM, Metter EJ, Ferrucci L, Aerssens J, Vlietinck R, Beunen GP, Thomis MA. Comprehensive fine mapping of chr12q12-14 and follow-up replication identify activin receptor 1B (ACVR1B) as a muscle strength gene. European Journal of Human Genetics : Ejhg. 19: 208-15. PMID 21063444 DOI: 10.1038/Ejhg.2010.173 |
0.374 |
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| 2011 |
Dolmans G, Werker P, Hennies H, Furniss D, Festen E, Franke L, van der Vlies P, Wolffenbuttel B, Giele H, Ophoff R, Wijmenga C. 37: A FIRST GENOME-WIDE ASSOCIATION STUDY IN DUPUYTRENʼS DISEASE IDENTIFIES 9 SUSCEPTIBILITY LOCI AND SUGGESTS A MAJOR ROLE FOR WNT-SIGNALLING Plastic and Reconstructive Surgery. 127: 27. DOI: 10.1097/01.Prs.0000396724.48390.C3 |
0.701 |
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| 2011 |
Fu J, Festen EA, Wijmenga C. Multi-ethnic studies in complex traits Human Molecular Genetics. 20: R206-R213. DOI: 10.1093/Hmg/Ddr386 |
0.429 |
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| 2011 |
Anderson CA, Boucher G, Lees CW, Franke A, D'Amato M, Taylor KD, Lee JC, Goyette P, Imielinski M, Latiano A, Lagacé C, Scott R, Amininejad L, Bumpstead S, Baidoo L, ... ... Wijmenga C, et al. Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 Nature Genetics. 43: 919-919. DOI: 10.1038/Ng0911-919B |
0.8 |
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| 2011 |
McGovern DPB, Gardet A, Törkvist L, Goyette P, Essers J, Taylor KD, Neale BM, Ong RTH, Lagace C, Li C, Green T, Stevens CR, Beauchamp C, Fleshner PR, Carlson M, ... ... Wijmenga C, et al. Genome-wide association identifies multiple ulcerative colitis susceptibility loci (vol 42, pg 332, 2010) Nature Genetics. 43: 388-388. DOI: 10.1038/Ng0411-388C |
0.416 |
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| 2011 |
Folseraas T, Melum E, Juran B, Weersma R, Schramm C, Weismüller T, Gotthardt D, Boberg K, Janse M, Buchert E, Björnsson E, Henckaerts L, Rust C, Teufel A, Bergquist A, ... ... Wijmenga C, et al. 102 NOVEL SUSCEPTIBILITY LOCI FOR PRIMARY SCLEROSING CHOLANGITIS IDENTIFIED BY GENOME-WIDE ASSOCIATION AND REPLICATION ANALYSIS Journal of Hepatology. 54: S46. DOI: 10.1016/S0168-8278(11)60104-9 |
0.408 |
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| 2011 |
Janse M, Lamberts LE, Franke L, Raychaudhuri S, Ellinghaus E, Boberg KM, Melum E, Schrumpf E, Bergquist A, Bjornsson E, Porte RJ, Weismüller TJ, Wedemeyer J, Schramm C, Sterneck M, ... ... Wijmenga C, et al. Three Genetic Susceptibility Loci Indicate a Role for IL2, REL and CARD9 in Primary Sclerosing Cholangitis Gastroenterology. 140: S-906. DOI: 10.1016/S0016-5085(11)63761-X |
0.706 |
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| 2011 |
Cleynen I, Artieda M, Szczypiorska M, Verspaget HW, Lakatos PL, Seibold F, Ahmad T, Weersma RK, Müller S, Tordai A, Hommes DW, Parnell K, Wijmenga C, Van Steen K, Rutgeerts PJ, et al. The Protease Genes Cyld and USP40 Are Associated With Crohn's Disease: Results From a European Consortium Gastroenterology. 140: S-269. DOI: 10.1016/S0016-5085(11)61076-7 |
0.348 |
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van Sommeren S, Visschedijk MC, Festen EA, de Jong DJ, Ponsioen CY, Wijmenga C, Weersma RK. HNF4α and CDH1 are associated with ulcerative colitis in a Dutch cohort Inflammatory Bowel Diseases. 17: 1714-1718. DOI: 10.1002/Ibd.21541 |
0.409 |
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| 2010 |
van Sommeren S, Visschedijk MC, Festen EA, de Jong DJ, Ponsioen CY, Wijmenga C, Weersma RK. HNF4α and CDH1 are associated with ulcerative colitis in a Dutch cohort. Inflammatory Bowel Diseases. 17: 1714-8. PMID 21744425 DOI: 10.1002/ibd.21541 |
0.312 |
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| 2010 |
Hogen Esch CE, Rosén A, Auricchio R, Romanos J, Chmielewska A, Putter H, Ivarsson A, Szajewska H, Koning F, Wijmenga C, Troncone R, Mearin ML. The PreventCD Study design: towards new strategies for the prevention of coeliac disease. European Journal of Gastroenterology & Hepatology. 22: 1424-30. PMID 21389794 DOI: 10.1097/Meg.0B013E32833Fe9Ae |
0.335 |
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| 2010 |
Roberts RL, Hollis-Moffatt JE, Gómez-García M, Fransen K, Ponsioen CY, Crusius BA, Wijmenga C, Martín J, Weersma RK, Merriman TR, Barclay ML, Gearry RB, Alizadeh BZ. Association of the protein-tyrosine phosphatase nonreceptor type substrate 1 (PTPNS1) gene with inflammatory bowel disease. Inflammatory Bowel Diseases. 17: E19-21. PMID 21225905 DOI: 10.1002/Ibd.21470 |
0.34 |
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| 2010 |
Geremek M, Bruinenberg M, Ziętkiewicz E, Pogorzelski A, Witt M, Wijmenga C. Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes. Human Genetics. 129: 283-93. PMID 21136274 DOI: 10.1007/S00439-010-0922-4 |
0.352 |
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| 2010 |
Franke A, McGovern DP, Barrett JC, Wang K, Radford-Smith GL, Ahmad T, Lees CW, Balschun T, Lee J, Roberts R, Anderson CA, Bis JC, Bumpstead S, Ellinghaus D, Festen EM, ... ... Wijmenga C, et al. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nature Genetics. 42: 1118-25. PMID 21102463 DOI: 10.1038/Ng.717 |
0.621 |
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| 2010 |
Sotoodehnia N, Isaacs A, de Bakker PI, Dörr M, Newton-Cheh C, Nolte IM, van der Harst P, Müller M, Eijgelsheim M, Alonso A, Hicks AA, Padmanabhan S, Hayward C, Smith AV, Polasek O, ... ... Wijmenga C, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nature Genetics. 42: 1068-76. PMID 21076409 DOI: 10.1038/Ng.716 |
0.68 |
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| 2010 |
Trynka G, Wijmenga C, van Heel DA. A genetic perspective on coeliac disease. Trends in Molecular Medicine. 16: 537-50. PMID 20947431 DOI: 10.1016/J.Molmed.2010.09.003 |
0.468 |
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| 2010 |
Weersma RK, Crusius JB, Roberts RL, Koeleman BP, Palomino-Morales R, Wolfkamp S, Hollis-Moffatt JE, Festen EA, Meisneris S, Heijmans R, Noble CL, Gearry RB, Barclay ML, Gómez-Garcia M, Lopez-Nevot MA, ... ... Wijmenga C, et al. Association of FcgR2a, but not FcgR3a, with inflammatory bowel diseases across three Caucasian populations. Inflammatory Bowel Diseases. 16: 2080-9. PMID 20848524 DOI: 10.1002/Ibd.21342 |
0.365 |
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| 2010 |
Lu Y, Feskens EJ, Boer JM, Imholz S, Verschuren WM, Wijmenga C, Vaarhorst A, Slagboom E, Müller M, Dollé ME. Exploring genetic determinants of plasma total cholesterol levels and their predictive value in a longitudinal study. Atherosclerosis. 213: 200-5. PMID 20832063 DOI: 10.1016/J.Atherosclerosis.2010.08.053 |
0.328 |
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| 2010 |
Wolfs MG, Rensen SS, Bruin-Van Dijk EJ, Verdam FJ, Greve JW, Sanjabi B, Bruinenberg M, Wijmenga C, van Haeften TW, Buurman WA, Franke L, Hofker MH. Co-expressed immune and metabolic genes in visceral and subcutaneous adipose tissue from severely obese individuals are associated with plasma HDL and glucose levels: a microarray study. Bmc Medical Genomics. 3: 34. PMID 20687939 DOI: 10.1186/1755-8794-3-34 |
0.644 |
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| 2010 |
Gretarsdottir S, Baas AF, Thorleifsson G, Holm H, den Heijer M, de Vries JP, Kranendonk SE, Zeebregts CJ, van Sterkenburg SM, Geelkerken RH, van Rij AM, Williams MJ, Boll AP, Kostic JP, Jonasdottir A, ... ... Wijmenga C, et al. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nature Genetics. 42: 692-7. PMID 20622881 DOI: 10.1038/Ng.622 |
0.383 |
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| 2010 |
Fransen K, Visschedijk MC, van Sommeren S, Fu JY, Franke L, Festen EA, Stokkers PC, van Bodegraven AA, Crusius JB, Hommes DW, Zanen P, de Jong DJ, Wijmenga C, van Diemen CC, Weersma RK. Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease. Human Molecular Genetics. 19: 3482-8. PMID 20601676 DOI: 10.1093/Hmg/Ddq264 |
0.706 |
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| 2010 |
Voight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, Zeggini E, Huth C, Aulchenko YS, Thorleifsson G, McCulloch LJ, Ferreira T, Grallert H, Amin N, Wu G, ... ... Wijmenga C, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics. 42: 579-89. PMID 20581827 DOI: 10.1038/Ng.609 |
0.632 |
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| 2010 |
Zhernakova A, Elbers CC, Ferwerda B, Romanos J, Trynka G, Dubois PC, de Kovel CG, Franke L, Oosting M, Barisani D, Bardella MT, Joosten LA, Saavalainen P, van Heel DA, ... ... Wijmenga C, et al. Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection. American Journal of Human Genetics. 86: 970-7. PMID 20560212 DOI: 10.1016/J.Ajhg.2010.05.004 |
0.678 |
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| 2010 |
Stahl EA, Raychaudhuri S, Remmers EF, Xie G, Eyre S, Thomson BP, Li Y, Kurreeman FA, Zhernakova A, Hinks A, Guiducci C, Chen R, Alfredsson L, Amos CI, Ardlie KG, ... ... Wijmenga C, et al. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nature Genetics. 42: 508-14. PMID 20453842 DOI: 10.1038/Ng.582 |
0.584 |
|
| 2010 |
Krischek B, Tajima A, Akagawa H, Narita A, Ruigrok Y, Rinkel G, Wijmenga C, Feigl GC, Kim CJ, Hori T, Tatagiba M, Kasuya H, Inoue I. Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohort. Neuroscience. 169: 339-343. PMID 20452405 DOI: 10.1016/J.Neuroscience.2010.05.002 |
0.376 |
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| 2010 |
Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, Simon M, Krex D, Arlier Z, Nayak N, Ruigrok YM, Niemelä M, Tajima A, von und zu Fraunberg M, Dóczi T, ... ... Wijmenga C, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nature Genetics. 42: 420-5. PMID 20364137 DOI: 10.1038/Ng.563 |
0.363 |
|
| 2010 |
Persengiev S, Koeleman BP, Downes K, Valdigem G, van der Slik AR, Eerligh P, Monsuur A, Bruining GJ, Wijmenga C, Todd JA, Roep BO, Alizadeh BZ. Association analysis of myosin IXB and type 1 diabetes. Human Immunology. 71: 598-601. PMID 20303373 DOI: 10.1016/J.Humimm.2010.03.002 |
0.394 |
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| 2010 |
McGovern DP, Gardet A, Törkvist L, Goyette P, Essers J, Taylor KD, Neale BM, Ong RT, Lagacé C, Li C, Green T, Stevens CR, Beauchamp C, Fleshner PR, Carlson M, ... ... Wijmenga C, et al. Genome-wide association identifies multiple ulcerative colitis susceptibility loci. Nature Genetics. 42: 332-7. PMID 20228799 DOI: 10.1038/Ng.549 |
0.467 |
|
| 2010 |
Dubois PC, Trynka G, Franke L, Hunt KA, Romanos J, Curtotti A, Zhernakova A, Heap GA, Adány R, Aromaa A, Bardella MT, van den Berg LH, Bockett NA, de la Concha EG, Dema B, ... ... Wijmenga C, et al. Multiple common variants for celiac disease influencing immune gene expression. Nature Genetics. 42: 295-302. PMID 20190752 DOI: 10.1038/Ng.543 |
0.733 |
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| 2010 |
Bauer F, Onland-Moret NC, Charlotte OM, Niehoff AG, Elbers CC, Grobbee DE, Wijmenga C, van der Schouw YT. PTPN1 polymorphisms are associated with total and low-density lipoprotein cholesterol. European Journal of Cardiovascular Prevention and Rehabilitation : Official Journal of the European Society of Cardiology, Working Groups On Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology. 17: 28-34. PMID 20177231 DOI: 10.1097/Hjr.0B013E32832D30C4 |
0.313 |
|
| 2010 |
Baas AF, Medic J, van't Slot R, de Vries JP, van Sambeek MR, Geelkerken BH, Boll BP, Grobbee DE, Wijmenga C, Ruigrok YM, Blankensteijn JD. Association study of single nucleotide polymorphisms on chromosome 19q13 with abdominal aortic aneurysm. Angiology. 61: 243-7. PMID 20156811 DOI: 10.1177/0003319709354752 |
0.334 |
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| 2010 |
Wolters VM, Alizadeh BZ, Weijerman ME, Zhernakova A, van Hoogstraten IM, Mearin ML, Wapenaar MC, Wijmenga C, Schreurs MW. Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability. Human Immunology. 71: 392-6. PMID 20096742 DOI: 10.1016/J.Humimm.2010.01.016 |
0.372 |
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| 2010 |
Baas AF, Medic J, van't Slot R, de Vries JP, van Sambeek MR, Verhoeven EL, Boll BP, Grobbee DE, Wijmenga C, Blankensteijn JD, Ruigrok YM. The intracranial aneurysm susceptibility genes HSPG2 and CSPG2 are not associated with abdominal aortic aneurysm. Angiology. 61: 238-42. PMID 20053631 DOI: 10.1177/0003319709354751 |
0.33 |
|
| 2010 |
van der Heide F, Nolte IM, Kleibeuker JH, Wijmenga C, Dijkstra G, Weersma RK. Differences in genetic background between active smokers, passive smokers, and non-smokers with Crohn's disease. The American Journal of Gastroenterology. 105: 1165-72. PMID 19953089 DOI: 10.1038/Ajg.2009.659 |
0.319 |
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| 2010 |
Karlsen TH, Franke A, Melum E, Kaser A, Hov JR, Balschun T, Lie BA, Bergquist A, Schramm C, Weismüller TJ, Gotthardt D, Rust C, Philipp EE, Fritz T, Henckaerts L, ... ... Wijmenga C, et al. Genome-wide association analysis in primary sclerosing cholangitis. Gastroenterology. 138: 1102-11. PMID 19944697 DOI: 10.1053/J.Gastro.2009.11.046 |
0.42 |
|
| 2010 |
Buizer-Voskamp JE, Franke L, Staal WG, van Daalen E, Kemner C, Ophoff RA, Vorstman JA, van Engeland H, Wijmenga C. Systematic genotype-phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism. European Journal of Human Genetics : Ejhg. 18: 588-95. PMID 19935830 DOI: 10.1038/Ejhg.2009.206 |
0.682 |
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| 2010 |
Festen EA, Stokkers PC, van Diemen CC, van Bodegraven AA, Boezen HM, Crusius BJ, Hommes DW, van der Woude CJ, van der Woude JC, Balschun T, Verspaget HW, Schreiber S, de Jong DJ, Franke A, Dijkstra G, ... Wijmenga C, et al. Genetic analysis in a Dutch study sample identifies more ulcerative colitis susceptibility loci and shows their additive role in disease risk. The American Journal of Gastroenterology. 105: 395-402. PMID 19861958 DOI: 10.1038/Ajg.2009.576 |
0.461 |
|
| 2010 |
Kurreeman FA, Goulielmos GN, Alizadeh BZ, Rueda B, Houwing-Duistermaat J, Sanchez E, Bevova M, Radstake TR, Vonk MC, Galanakis E, Ortego N, Verduyn W, Zervou MI, Roep BO, Dema B, ... ... Wijmenga C, et al. The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases. Annals of the Rheumatic Diseases. 69: 696-9. PMID 19433411 DOI: 10.1136/Ard.2008.106567 |
0.378 |
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| 2010 |
Crippa A, Magli MC, Robles F, Capoti A, Ferraretti AP, Gianaroli L, Gallina A, Bonaparte E, Moretti M, Colpi GM, Nerva F, Contalbi G, Vacalluzzo L, Tabano S, Grati FR, ... ... Wijmenga C, et al. Posters * Reproductive Genetics (PGD/PGS) Human Reproduction. 25: i321-i332. DOI: 10.1093/humrep/de.25.s1.534 |
0.622 |
|
| 2010 |
Dubois PCA, Trynka G, Franke L, Hunt KA, Romanos J, Curtotti A, Zhernakova A, Heap GAR, Ádány R, Aromaa A, Bardella MT, van den Berg LH, Bockett NA, de la Concha EG, Dema B, ... ... Wijmenga C, et al. Erratum: Corrigendum: Multiple common variants for celiac disease influencing immune gene expression Nature Genetics. 42: 465-465. DOI: 10.1038/Ng0510-465 |
0.683 |
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| 2010 |
Festen EA, Goyette P, Green T, Beauchamp C, Lagace C, Boucher G, Trynka G, Dubois PC, Stokkers P, Hommes DW, Barisani D, Palmieri O, Annese V, van Heel D, Weersma RK, ... ... Wijmenga C, et al. 34 A Meta-Analysis of Genome Wide Association Scans Identifies TAGAP and Pus10 as Shared Risk Loci for Crohn's Disease and Celiac Disease Gastroenterology. 138: S-7. DOI: 10.1016/S0016-5085(10)60028-5 |
0.415 |
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| 2009 |
Lambrechts D, Buysschaert I, Zanen P, Coolen J, Lays N, Cuppens H, Groen HJ, Dewever W, van Klaveren RJ, Verschakelen J, Wijmenga C, Postma DS, Decramer M, Janssens W. The 15q24/25 susceptibility variant for lung cancer and chronic obstructive pulmonary disease is associated with emphysema. American Journal of Respiratory and Critical Care Medicine. 181: 486-93. PMID 20007924 DOI: 10.1164/Rccm.200909-1364Oc |
0.318 |
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| 2009 |
Wolfs MGM, Hofker MH, Wijmenga C, Haeften TWv. Type 2 Diabetes Mellitus: New Genetic Insights will Lead to New Therapeutics. Current Genomics. 10: 110-118. PMID 19794883 DOI: 10.2174/138920209787847023 |
0.339 |
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| 2009 |
Elbers CC, de Kovel CG, van der Schouw YT, Meijboom JR, Bauer F, Grobbee DE, Trynka G, van Vliet-Ostaptchouk JV, Wijmenga C, Onland-Moret NC. Variants in neuropeptide Y receptor 1 and 5 are associated with nutrient-specific food intake and are under recent selection in Europeans. Plos One. 4: e7070. PMID 19759915 DOI: 10.1371/Journal.Pone.0007070 |
0.323 |
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| 2009 |
Vliet-Ostaptchouk vJ, Hofker MH, Schouw YTvd, Wijmenga C, Onland-Moret NC. Genetic variation in the hypothalamic pathways and its role on obesity. Obesity Reviews. 10: 593-609. PMID 19712437 DOI: 10.1111/J.1467-789X.2009.00597.X |
0.336 |
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| 2009 |
Bauer F, Elbers CC, Adan RA, Loos RJ, Onland-Moret NC, Grobbee DE, van Vliet-Ostaptchouk JV, Wijmenga C, van der Schouw YT. Obesity genes identified in genome-wide association studies are associated with adiposity measures and potentially with nutrient-specific food preference. The American Journal of Clinical Nutrition. 90: 951-9. PMID 19692490 DOI: 10.3945/Ajcn.2009.27781 |
0.323 |
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| 2009 |
Baas AF, Medic J, van 't Slot R, de Kovel CG, Zhernakova A, Geelkerken RH, Kranendonk SE, van Sterkenburg SM, Grobbee DE, Boll AP, Wijmenga C, Blankensteijn JD, Ruigrok YM. Association of the TGF-beta receptor genes with abdominal aortic aneurysm. European Journal of Human Genetics : Ejhg. 18: 240-4. PMID 19672284 DOI: 10.1038/Ejhg.2009.141 |
0.361 |
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| 2009 |
van den Berg SW, Dollé ME, Imholz S, van der A DL, van 't Slot R, Wijmenga C, Verschuren WM, Strien C, Siezen CL, Hoebee B, Feskens EJ, Boer JM. Genetic variations in regulatory pathways of fatty acid and glucose metabolism are associated with obesity phenotypes: a population-based cohort study. International Journal of Obesity (2005). 33: 1143-52. PMID 19652658 DOI: 10.1038/Ijo.2009.152 |
0.403 |
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| 2009 |
Coenen MJ, Trynka G, Heskamp S, Franke B, van Diemen CC, Smolonska J, van Leeuwen M, Brouwer E, Boezen MH, Postma DS, Platteel M, Zanen P, Lammers JW, Groen HJ, Mali WP, ... ... Wijmenga C, et al. Common and different genetic background for rheumatoid arthritis and coeliac disease. Human Molecular Genetics. 18: 4195-203. PMID 19648290 DOI: 10.1093/Hmg/Ddp365 |
0.34 |
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| 2009 |
Forabosco P, Neuhausen SL, Greco L, Naluai AT, Wijmenga C, Saavalainen P, Houlston RS, Ciclitira PJ, Babron M, Lewis CM. Meta-analysis of genome-wide linkage studies in celiac disease. Human Heredity. 68: 223-230. PMID 19622889 DOI: 10.1159/000228920 |
0.433 |
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| 2009 |
Smolonska J, Wijmenga C, Postma DS, Boezen HM. Meta-analyses on suspected chronic obstructive pulmonary disease genes: a summary of 20 years' research. American Journal of Respiratory and Critical Care Medicine. 180: 618-31. PMID 19608716 DOI: 10.1164/Rccm.200905-0722Oc |
0.308 |
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| 2009 |
Festen EA, Szperl AM, Weersma RK, Wijmenga C, Wapenaar MC. Inflammatory bowel disease and celiac disease: overlaps in the pathology and genetics, and their potential drug targets. Endocrine, Metabolic & Immune Disorders Drug Targets. 9: 199-218. PMID 19519468 DOI: 10.2174/187153009788452426 |
0.324 |
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| 2009 |
Knauff EA, Franke L, van Es MA, van den Berg LH, van der Schouw YT, Laven JS, Lambalk CB, Hoek A, Goverde AJ, Christin-Maitre S, Hsueh AJ, Wijmenga C, Fauser BC. Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. Human Reproduction (Oxford, England). 24: 2372-8. PMID 19508998 DOI: 10.1093/Humrep/Dep197 |
0.698 |
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| 2009 |
van der Zwaag B, Franke L, Poot M, Hochstenbach R, Spierenburg HA, Vorstman JA, van Daalen E, de Jonge MV, Verbeek NE, Brilstra EH, van 't Slot R, Ophoff RA, van Es MA, Blauw HM, Veldink JH, ... ... Wijmenga C, et al. Gene-network analysis identifies susceptibility genes related to glycobiology in autism. Plos One. 4: e5324. PMID 19492091 DOI: 10.1371/Journal.Pone.0005324 |
0.69 |
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| 2009 |
Romanos J, van Diemen CC, Nolte IM, Trynka G, Zhernakova A, Fu J, Bardella MT, Barisani D, McManus R, van Heel DA, Wijmenga C. Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease. Gastroenterology. 137: 834-40, 840.e1-3. PMID 19454285 DOI: 10.1053/J.Gastro.2009.05.040 |
0.374 |
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| 2009 |
Koskinen L, Romanos J, Kaukinen K, Mustalahti K, Korponay-Szabo I, Barisani D, Bardella MT, Ziberna F, Vatta S, Széles G, Pocsai Z, Karell K, Haimila K, Adány R, Not T, ... ... Wijmenga C, et al. Cost-effective HLA typing with tagging SNPs predicts celiac disease risk haplotypes in the Finnish, Hungarian, and Italian populations. Immunogenetics. 61: 247-56. PMID 19255754 DOI: 10.1007/S00251-009-0361-3 |
0.406 |
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| 2009 |
Trynka G, Zhernakova A, Romanos J, Franke L, Hunt KA, Turner G, Bruinenberg M, Heap GA, Platteel M, Ryan AW, de Kovel C, Holmes GK, Howdle PD, Walters JR, Sanders DS, ... ... Wijmenga C, et al. Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. Gut. 58: 1078-83. PMID 19240061 DOI: 10.1136/Gut.2008.169052 |
0.713 |
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| 2009 |
Elbers CC, van Eijk KR, Franke L, Mulder F, van der Schouw YT, Wijmenga C, Onland-Moret NC. Using genome-wide pathway analysis to unravel the etiology of complex diseases. Genetic Epidemiology. 33: 419-31. PMID 19235186 DOI: 10.1002/Gepi.20395 |
0.708 |
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| 2009 |
Festen EA, Goyette P, Scott R, Annese V, Zhernakova A, Lian J, Lefèbvre C, Brant SR, Cho JH, Silverberg MS, Taylor KD, de Jong DJ, Stokkers PC, Mcgovern D, Palmieri O, ... ... Wijmenga C, et al. Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis. Gut. 58: 799-804. PMID 19201773 DOI: 10.1136/Gut.2008.166918 |
0.305 |
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| 2009 |
Hofker M, Wijmenga C. A supersized list of obesity genes. Nature Genetics. 41: 139-40. PMID 19174833 DOI: 10.1038/Ng0209-139 |
0.357 |
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| 2009 |
Weersma RK, Stokkers PC, Cleynen I, Wolfkamp SC, Henckaerts L, Schreiber S, Dijkstra G, Franke A, Nolte IM, Rutgeerts P, Wijmenga C, Vermeire S. Confirmation of multiple Crohn's disease susceptibility loci in a large Dutch-Belgian cohort. The American Journal of Gastroenterology. 104: 630-8. PMID 19174780 DOI: 10.1038/Ajg.2008.112 |
0.408 |
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| 2009 |
Heap GA, Trynka G, Jansen RC, Bruinenberg M, Swertz MA, Dinesen LC, Hunt KA, Wijmenga C, Vanheel DA, Franke L. Complex nature of SNP genotype effects on gene expression in primary human leucocytes. Bmc Medical Genomics. 2: 1. PMID 19128478 DOI: 10.1186/1755-8794-2-1 |
0.783 |
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| 2009 |
Romanos J, Wijmenga C. Comment on: Barker et al. (2008) Two single nucleotide polymorphisms identify the highest-risk diabetes HLA genotype: Diabetes 57:3152-3155, 2008. Diabetes. 58: e1; author reply e2. PMID 19114716 DOI: 10.2337/Db08-1312 |
0.322 |
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| 2009 |
Zhernakova A, van Diemen CC, Wijmenga C. Detecting shared pathogenesis from the shared genetics of immune-related diseases. Nature Reviews. Genetics. 10: 43-55. PMID 19092835 DOI: 10.1038/nrg2489 |
0.305 |
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| 2009 |
Weersma RK, Stokkers PC, van Bodegraven AA, van Hogezand RA, Verspaget HW, de Jong DJ, van der Woude CJ, Oldenburg B, Linskens RK, Festen EA, van der Steege G, Hommes DW, Crusius JB, Wijmenga C, Nolte IM, et al. Molecular prediction of disease risk and severity in a large Dutch Crohn's disease cohort. Gut. 58: 388-95. PMID 18824555 DOI: 10.1136/Gut.2007.144865 |
0.381 |
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| 2009 |
Elbers CC, van der Schouw YT, Wijmenga C, Onland-Moret NC. Comment on: Perry et al. (2009) Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach. Diabetes;58:1463-1467 Diabetes. 58: e9-e9. DOI: 10.2337/Db09-0766 |
0.321 |
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| 2009 |
Zhernakova A, van Diemen CC, Wijmenga C. Detecting shared pathogenesis from the shared genetics of immune-related diseases Nature Reviews Genetics. 10: 43-55. DOI: 10.1038/Nrg2489 |
0.42 |
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| 2009 |
Nijmeijer RM, van Santvoort HC, Zhernakova A, Besselink MG, Wapenaar MC, Boermeester MA, Gooszen HG, Akkermans LM, Wijmenga C. S1814 Genetic Variants of Myosin IXB and Pard3 Predispose to Acute Pancreatitis Gastroenterology. 136: A-275. DOI: 10.1016/S0016-5085(09)61256-7 |
0.304 |
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| 2009 |
Dubois PC, Trynka G, Heap GA, Hunt KA, Franke L, van Heel D, Gwilliam R, Deloukas P, McManus R, Saavalainen P, Wijmenga C. S1751 Copy Number Variant and Extended SNP Genome Wide Association Study in Celiac Disease Gastroenterology. 136: A-263. DOI: 10.1016/S0016-5085(09)61195-1 |
0.649 |
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| 2009 |
Weersma RK, Crusius B, Koeleman BP, Roberts RL, Palomino-Morales RJ, Wolfkamp SC, Hollis-Moffatt JE, Festen EA, Meisner S, Heijmans R, Gearry RB, Barclay ML, Gomez-Garcia M, Lopez-Nevot MA, Nieto A, ... ... Wijmenga C, et al. S1172 The Differential Association of the FcgR2a and FcgR3a Genes in Inflammatory Bowel Diseases Across Three Caucasian Populations Gastroenterology. 136: A-206. DOI: 10.1016/S0016-5085(09)60922-7 |
0.364 |
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| 2009 |
Golachowska MR, Szperl A, Bruineberg M, Prekeris R, Thunnissen AW, Hoekstra D, Wijmenga C, Ksiazyk J, Rings EH, Wapenaar MC, IJzendoorn SC. 393 Apical Recycling Endosome-Associated Myosin Vb Is Mutated in Microvillus Inclusion Disease and Is Involved in Intestinal Brush Border Development Gastroenterology. 136: A-66. DOI: 10.1016/S0016-5085(09)60296-1 |
0.347 |
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| 2009 |
Szperl A, van Diemen C, Zhernakova A, Wijmenga C. F.22. Identifying Causal Variants in Shared Immune-related Diseases Genes by High-throughput Sequencing Clinical Immunology. 131: S100. DOI: 10.1016/J.Clim.2009.03.290 |
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| 2009 |
Zhernakova A, Diemen Cv, Wijmenga C. F.19. The Shared Genetics of Immune-related Diseases - What Genome-wide Association Studies Reveal Clinical Immunology. 131: S98-S99. DOI: 10.1016/J.Clim.2009.03.287 |
0.404 |
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| 2009 |
van Diemen C, Romanos J, Nolte I, Barisani D, McManus R, van Heel D, Wijmenga C. OR.68. Genetic Risk Model for Celiac Disease Helps Identify High-risk Individuals Clinical Immunology. 131: S28-S29. DOI: 10.1016/J.Clim.2009.03.080 |
0.34 |
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| 2008 |
Romanos J, Rybak A, Wijmenga C, Wapenaar MC. Molecular diagnosis of celiac disease: are we there yet? Expert Opinion On Medical Diagnostics. 2: 399-416. PMID 23495707 DOI: 10.1517/17530059.2.4.399 |
0.43 |
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| 2008 |
Koskinen LL, Einarsdottir E, Dukes E, Heap GA, Dubois P, Korponay-Szabo IR, Kaukinen K, Kurppa K, Ziberna F, Vatta S, Not T, Ventura A, Sistonen P, Adány R, Pocsai Z, ... ... Wijmenga C, et al. Association study of the IL18RAP locus in three European populations with coeliac disease. Human Molecular Genetics. 18: 1148-55. PMID 19103669 DOI: 10.1093/Hmg/Ddn438 |
0.474 |
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| 2008 |
Smyth DJ, Plagnol V, Walker NM, Cooper JD, Downes K, Yang JH, Howson JM, Stevens H, McManus R, Wijmenga C, Heap GA, Dubois PC, Clayton DG, Hunt KA, van Heel DA, et al. Shared and distinct genetic variants in type 1 diabetes and celiac disease. The New England Journal of Medicine. 359: 2767-77. PMID 19073967 DOI: 10.1056/Nejmoa0807917 |
0.398 |
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| 2008 |
Bilguvar K, Yasuno K, Niemelä M, Ruigrok YM, von Und Zu Fraunberg M, van Duijn CM, van den Berg LH, Mane S, Mason CE, Choi M, Gaál E, Bayri Y, Kolb L, Arlier Z, Ravuri S, ... ... Wijmenga C, et al. Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nature Genetics. 40: 1472-7. PMID 18997786 DOI: 10.1038/Ng.240 |
0.345 |
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| 2008 |
van Loo KM, Dejaegere T, van Zweeden M, van Schijndel JE, Wijmenga C, Trip MD, Martens GJ. Male-specific association between a gamma-secretase polymorphism and premature coronary atherosclerosis. Plos One. 3: e3662. PMID 18987747 DOI: 10.1371/Journal.Pone.0003662 |
0.384 |
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| 2008 |
Bauer F, Onland-Moret NC, Niehoff AG, Elbers CC, Grobbee DE, Wijmenga C, van der Schouw YT. No association of PTPN1 polymorphisms with macronutrient intake and measures of adiposity. Obesity (Silver Spring, Md.). 16: 2767-71. PMID 18846048 DOI: 10.1038/Oby.2008.426 |
0.331 |
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| 2008 |
Franke A, Balschun T, Karlsen TH, Sventoraityte J, Nikolaus S, Mayr G, Domingues FS, Albrecht M, Nothnagel M, Ellinghaus D, Sina C, Onnie CM, Weersma RK, Stokkers PCF, Wijmenga C, et al. Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility Nature Genetics. 40: 1319-1323. PMID 18836448 DOI: 10.1038/Ng.221 |
0.398 |
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| 2008 |
Romanos J, Barisani D, Trynka G, Zhernakova A, Bardella MT, Wijmenga C. Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease. Journal of Medical Genetics. 46: 60-3. PMID 18805825 DOI: 10.1136/Jmg.2008.061457 |
0.332 |
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| 2008 |
Lu Y, Dollé ME, Imholz S, van 't Slot R, Verschuren WM, Wijmenga C, Feskens EJ, Boer JM. Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations. Journal of Lipid Research. 49: 2582-9. PMID 18660489 DOI: 10.1194/Jlr.M800232-Jlr200 |
0.329 |
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| 2008 |
Orozco G, Alizadeh BZ, Delgado-Vega AM, González-Gay MA, Balsa A, Pascual-Salcedo D, Fernández-Gutierrez B, González-Escribano MF, Petersson IF, van Riel PL, Barrera P, Coenen MJ, Radstake TR, van Leeuwen MA, Wijmenga C, et al. Association of STAT4 with rheumatoid arthritis: a replication study in three European populations. Arthritis and Rheumatism. 58: 1974-80. PMID 18576336 DOI: 10.1002/Art.23549 |
0.334 |
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| 2008 |
Festen EA, Zhernakova A, Wijmenga C, Weersma RK. Association of DLG5 variants with gluten-sensitive enteropathy. Gut. 57: 1027-8. PMID 18559397 DOI: 10.1136/Gut.2007.144857 |
0.415 |
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| 2008 |
Franke L, de Kovel CG, Aulchenko YS, Trynka G, Zhernakova A, Hunt KA, Blauw HM, van den Berg LH, Ophoff R, Deloukas P, van Heel DA, Wijmenga C. Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays. American Journal of Human Genetics. 82: 1316-33. PMID 18519066 DOI: 10.1016/J.Ajhg.2008.05.008 |
0.705 |
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| 2008 |
Monsuur AJ, de Bakker PI, Zhernakova A, Pinto D, Verduijn W, Romanos J, Auricchio R, Lopez A, van Heel DA, Crusius JB, Wijmenga C. Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms. Plos One. 3: e2270. PMID 18509540 DOI: 10.1371/Journal.Pone.0002270 |
0.373 |
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| 2008 |
Hunt KA, Franke L, Deloukas P, Wijmenga C, van Heel DA. No evidence in a large UK collection for celiac disease risk variants reported by a Spanish study. Gastroenterology. 134: 1629-30; author repl. PMID 18471539 DOI: 10.1053/J.Gastro.2008.03.068 |
0.722 |
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| 2008 |
Meex SJ, van Vliet-Ostaptchouk JV, van der Kallen CJ, van Greevenbroek MM, Schalkwijk CG, Feskens EJ, Blaak EE, Wijmenga C, Hofker MH, Stehouwer CD, de Bruin TW. Upstream transcription factor 1 (USF1) in risk of type 2 diabetes: association study in 2000 Dutch Caucasians. Molecular Genetics and Metabolism. 94: 352-5. PMID 18445538 DOI: 10.1016/J.Ymgme.2008.03.011 |
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| 2008 |
Zhernakova A, Festen EM, Franke L, Trynka G, van Diemen CC, Monsuur AJ, Bevova M, Nijmeijer RM, van 't Slot R, Heijmans R, Boezen HM, van Heel DA, van Bodegraven AA, Stokkers PC, Wijmenga C, et al. Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP. American Journal of Human Genetics. 82: 1202-10. PMID 18439550 DOI: 10.1016/J.Ajhg.2008.03.016 |
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| 2008 |
Hunt KA, Zhernakova A, Turner G, Heap GA, Franke L, Bruinenberg M, Romanos J, Dinesen LC, Ryan AW, Panesar D, Gwilliam R, Takeuchi F, McLaren WM, Holmes GK, Howdle PD, ... ... Wijmenga C, et al. Newly identified genetic risk variants for celiac disease related to the immune response. Nature Genetics. 40: 395-402. PMID 18311140 DOI: 10.1038/Ng.102 |
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| 2008 |
Ruigrok YM, Wijmenga C, Rinkel GJ, van't Slot R, Baas F, Wolfs M, Westerveld A, Roos YB. Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32. Stroke; a Journal of Cerebral Circulation. 39: 1096-102. PMID 18309175 DOI: 10.1161/Strokeaha.107.495168 |
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Geremek M, Schoenmaker F, Zietkiewicz E, Pogorzelski A, Diehl S, Wijmenga C, Witt M. Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q. European Journal of Human Genetics : Ejhg. 16: 688-95. PMID 18270537 DOI: 10.1038/Ejhg.2008.5 |
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| 2008 |
van Vliet-Ostaptchouk JV, Onland-Moret NC, van Haeften TW, Franke L, Elbers CC, Shiri-Sverdlov R, van der Schouw YT, Hofker MH, Wijmenga C. HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort. European Journal of Human Genetics : Ejhg. 16: 652-6. PMID 18231124 DOI: 10.1038/Sj.Ejhg.5202008 |
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| 2008 |
Wolters VM, Wijmenga C. Genetic background of celiac disease and its clinical implications. The American Journal of Gastroenterology. 103: 190-5. PMID 18184122 DOI: 10.1111/J.1572-0241.2007.01471.X |
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van Vliet-Ostaptchouk JV, Onland-Moret NC, Shiri-Sverdlov R, van Gorp PJJ, Custers A, Peeters PHM, Wijmenga C, Hofker MH, Van der Schouw YT. Polymorphisms of the TUB gene are associated with body composition and eating behavior in middle-aged women Plos One. 3. PMID 18183286 DOI: 10.1371/Journal.Pone.0001405 |
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Helgadottir A, Thorleifsson G, Magnusson KP, Grétarsdottir S, Steinthorsdottir V, Manolescu A, Jones GT, Rinkel GJ, Blankensteijn JD, Ronkainen A, Jääskeläinen JE, Kyo Y, Lenk GM, Sakalihasan N, Kostulas K, ... ... Wijmenga C, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nature Genetics. 40: 217-24. PMID 18176561 DOI: 10.1038/Ng.72 |
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| 2008 |
van Es MA, van Vught PW, Blauw HM, Franke L, Saris CG, Van den Bosch L, de Jong SW, de Jong V, Baas F, van't Slot R, Lemmens R, Schelhaas HJ, Birve A, Sleegers K, Van Broeckhoven C, ... ... Wijmenga C, et al. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Nature Genetics. 40: 29-31. PMID 18084291 DOI: 10.1038/Ng.2007.52 |
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Weersma RK, Zhernakova A, Nolte IM, Lefebvre C, Rioux JD, Mulder F, van Dullemen HM, Kleibeuker JH, Wijmenga C, Dijkstra G. ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands. The American Journal of Gastroenterology. 103: 621-7. PMID 18047540 DOI: 10.1111/J.1572-0241.2007.01660.X |
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| 2008 |
Wapenaar MC, Monsuur AJ, van Bodegraven AA, Weersma RK, Bevova MR, Linskens RK, Howdle P, Holmes G, Mulder CJ, Dijkstra G, van Heel DA, Wijmenga C. Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis. Gut. 57: 463-7. PMID 17989107 DOI: 10.1136/Gut.2007.133132 |
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Jungerius BJ, Bakker SC, Monsuur AJ, Sinke RJ, Kahn RS, Wijmenga C. Is MYO9B the missing link between schizophrenia and celiac disease? American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 351-5. PMID 17948900 DOI: 10.1002/Ajmg.B.30605 |
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| 2008 |
Friedman JI, Vrijenhoek T, Markx S, Janssen IM, van der Vliet WA, Faas BH, Knoers NV, Cahn W, Kahn RS, Edelmann L, Davis KL, Silverman JM, Brunner HG, van Kessel AG, Wijmenga C, et al. CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. Molecular Psychiatry. 13: 261-6. PMID 17646849 DOI: 10.1038/Sj.Mp.4002049 |
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Van Eerde AM, Lu W, De Jong TP, Wijmenga C, Giltay JC. Candidate Genes for Vesico-Ureteral Reflux Journal of Pediatric Urology. 4: S73. DOI: 10.1016/J.Jpurol.2008.01.144 |
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| 2007 |
Koskinen LL, Korponay-Szabo IR, Viiri K, Juuti-Uusitalo K, Kaukinen K, Lindfors K, Mustalahti K, Kurppa K, Adány R, Pocsai Z, Széles G, Einarsdottir E, Wijmenga C, Mäki M, Partanen J, et al. Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association. Journal of Medical Genetics. 45: 222-7. PMID 18077767 DOI: 10.1136/Jmg.2007.053991 |
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Zhernakova A, Alizadeh BZ, Bevova M, van Leeuwen MA, Coenen MJ, Franke B, Franke L, Posthumus MD, van Heel DA, van der Steege G, Radstake TR, Barrera P, Roep BO, Koeleman BP, Wijmenga C. Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases. American Journal of Human Genetics. 81: 1284-8. PMID 17999365 DOI: 10.1086/522037 |
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Wolters VM, Verbeek WH, Zhernakova A, Onland-Moret C, Schreurs MW, Monsuur AJ, Verduijn W, Wijmenga C, Mulder CJ. The MYO9B gene is a strong risk factor for developing refractory celiac disease. Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association. 5: 1399-405, 1405.e1-2. PMID 17967566 DOI: 10.1016/J.Cgh.2007.08.018 |
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| 2007 |
Jungerius BJ, Hoogendoorn ML, Bakker SC, Van't Slot R, Bardoel AF, Ophoff RA, Wijmenga C, Kahn RS, Sinke RJ. An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia. Molecular Psychiatry. 13: 1060-8. PMID 17893707 DOI: 10.1038/Sj.Mp.4002080 |
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| 2007 |
Saunders CL, Chiodini BD, Sham P, Lewis CM, Abkevich V, Adeyemo AA, de Andrade M, Arya R, Berenson GS, Blangero J, Boehnke M, Borecki IB, Chagnon YC, Chen W, Comuzzie AG, ... ... Wijmenga C, et al. Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring, Md.). 15: 2263-75. PMID 17890495 DOI: 10.1038/Oby.2007.269 |
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van Es MA, Van Vught PW, Blauw HM, Franke L, Saris CG, Andersen PM, Van Den Bosch L, de Jong SW, van 't Slot R, Birve A, Lemmens R, de Jong V, Baas F, Schelhaas HJ, Sleegers K, ... ... Wijmenga C, et al. ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. The Lancet. Neurology. 6: 869-77. PMID 17827064 DOI: 10.1016/S1474-4422(07)70222-3 |
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Alizadeh BZ, Valdigem G, Coenen MJ, Zhernakova A, Franke B, Monsuur A, van Riel PL, Barrera P, Radstake TR, Roep BO, Wijmenga C, Koeleman BP. Association analysis of functional variants of the FcgRIIa and FcgRIIIa genes with type 1 diabetes, celiac disease and rheumatoid arthritis. Human Molecular Genetics. 16: 2552-9. PMID 17652100 DOI: 10.1093/Hmg/Ddm194 |
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Gudmundsson J, Sulem P, Steinthorsdottir V, Bergthorsson JT, Thorleifsson G, Manolescu A, Rafnar T, Gudbjartsson D, Agnarsson BA, Baker A, Sigurdsson A, Benediktsdottir KR, Jakobsdottir M, Blondal T, Stacey SN, ... ... Wijmenga C, et al. Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. Nature Genetics. 39: 977-83. PMID 17603485 DOI: 10.1038/Ng2062 |
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Sánchez E, Alizadeh BZ, Valdigem G, Ortego-Centeno N, Jiménez-Alonso J, de Ramón E, García A, López-Nevot MA, Wijmenga C, Martín J, Koeleman BP. MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population. Human Immunology. 68: 610-5. PMID 17584584 DOI: 10.1016/J.Humimm.2007.03.006 |
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van Heel DA, Franke L, Hunt KA, Gwilliam R, Zhernakova A, Inouye M, Wapenaar MC, Barnardo MC, Bethel G, Holmes GK, Feighery C, Jewell D, Kelleher D, Kumar P, Travis S, ... ... Wijmenga C, et al. A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. Nature Genetics. 39: 827-9. PMID 17558408 DOI: 10.1038/Ng2058 |
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van Eerde AM, Koeleman BP, van de Kamp JM, de Jong TP, Wijmenga C, Giltay JC. Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux. Pediatric Nephrology (Berlin, Germany). 22: 1129-33. PMID 17497182 DOI: 10.1007/S00467-007-0492-4 |
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Rustici G, van Bakel H, Lackner DH, Holstege FC, Wijmenga C, Bähler J, Brazma A. Global transcriptional responses of fission and budding yeast to changes in copper and iron levels: a comparative study. Genome Biology. 8: R73. PMID 17477863 DOI: 10.1186/Gb-2007-8-5-R73 |
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Steinthorsdottir V, Thorleifsson G, Reynisdottir I, Benediktsson R, Jonsdottir T, Walters GB, Styrkarsdottir U, Gretarsdottir S, Emilsson V, Ghosh S, Baker A, Snorradottir S, Bjarnason H, Ng MCY, Hansen T, ... ... Wijmenga C, et al. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes Nature Genetics. 39: 770-775. PMID 17460697 DOI: 10.1038/Ng2043 |
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Monsuur AJ, Wijmenga C. Understanding the molecular basis of celiac disease: what genetic studies reveal. Annals of Medicine. 38: 578-91. PMID 17438672 DOI: 10.1080/07853890600989054 |
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Lu W, van Eerde AM, Fan X, Quintero-Rivera F, Kulkarni S, Ferguson H, Kim HG, Fan Y, Xi Q, Li QG, Sanlaville D, Andrews W, Sundaresan V, Bi W, Yan J, ... ... Wijmenga C, et al. Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. American Journal of Human Genetics. 80: 616-32. PMID 17357069 DOI: 10.1086/512735 |
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Alizadeh BZ, Eerligh P, van der Slik AR, Shastry A, Zhernakova A, Valdigem G, Bruining JG, Sanjeevi CB, Wijmenga C, Roep BO, Koeleman BP. MICA marks additional risk factors for Type 1 diabetes on extended HLA haplotypes: an association and meta-analysis. Molecular Immunology. 44: 2806-12. PMID 17350686 DOI: 10.1016/J.Molimm.2007.01.032 |
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Diosdado B, van Bakel H, Strengman E, Franke L, van Oort E, Mulder CJ, Wijmenga C, Wapenaar MC. Neutrophil recruitment and barrier impairment in celiac disease: a genomic study. Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association. 5: 574-81. PMID 17336591 DOI: 10.1016/J.Cgh.2006.11.014 |
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Wapenaar MC, Monsuur AJ, Poell J, Slot Rv‘, Meijer JWR, Meijer GA, Mulder CJ, Mearin ML, Wijmenga C. The SPINK gene family and celiac disease susceptibility Immunogenetics. 59: 349-357. PMID 17333166 DOI: 10.1007/S00251-007-0199-5 |
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Oosting J, Lips EH, van Eijk R, Eilers PH, Szuhai K, Wijmenga C, Morreau H, van Wezel T. High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays. Genome Research. 17: 368-76. PMID 17267813 DOI: 10.1101/Gr.5686107 |
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Elbers CC, Onland-Moret NC, Franke L, Niehoff AG, van der Schouw YT, Wijmenga C. A strategy to search for common obesity and type 2 diabetes genes. Trends in Endocrinology and Metabolism: Tem. 18: 19-26. PMID 17126559 DOI: 10.1016/J.Tem.2006.11.003 |
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Vliet-Ostaptchouk JVv, Shiri-Sverdlov R, Zhernakova A, Strengman E, Haeften TWv, Hofker MH, Wijmenga C. Association of variants of transcription factor 7-like 2 (TCF7L2) with susceptibility to type 2 diabetes in the Dutch Breda cohort Diabetologia. 50: 59-62. PMID 17031610 DOI: 10.1007/S00125-006-0477-Z |
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Monsuur AJ, Stepniak D, Diosdado B, Wapenaar MC, Mearin ML, Koning F, Wijmenga C. Genetic and functional analysis of pyroglutamyl-peptidase I in coeliac disease. European Journal of Gastroenterology & Hepatology. 18: 637-44. PMID 16702853 DOI: 10.1097/00042737-200606000-00010 |
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van Bodegraven AA, Curley CR, Hunt KA, Monsuur AJ, Linskens RK, Onnie CM, Crusius JB, Annese V, Latiano A, Silverberg MS, Bitton A, Fisher SA, Steinhart AH, Forbes A, Sanderson J, ... ... Wijmenga C, et al. Genetic variation in myosin IXB is associated with ulcerative colitis. Gastroenterology. 131: 1768-74. PMID 17087940 DOI: 10.1053/J.Gastro.2006.09.011 |
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de Bakker PI, McVean G, Sabeti PC, Miretti MM, Green T, Marchini J, Ke X, Monsuur AJ, Whittaker P, Delgado M, Morrison J, Richardson A, Walsh EC, Gao X, Galver L, ... ... Wijmenga C, et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nature Genetics. 38: 1166-72. PMID 16998491 DOI: 10.1038/Ng1885 |
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Amundsen SS, Vatn M, Wijmenga C, Sollid LM, Lie BA. Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort Tissue Antigens. 68: 249-252. PMID 16948647 DOI: 10.1111/J.1399-0039.2006.00665.X |
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| 2006 |
Zhernakova A, Alizadeh BZ, Eerligh P, Hanifi-Moghaddam P, Schloot NC, Diosdado B, Wijmenga C, Roep BO, Koeleman BP. Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetes. Genes and Immunity. 7: 544-9. PMID 16855620 DOI: 10.1038/Sj.Gene.6364326 |
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| 2006 |
Curley CR, Monsuur AJ, Wapenaar MC, Rioux JD, Wijmenga C. A functional candidate screen for coeliac disease genes. European Journal of Human Genetics : Ejhg. 14: 1215-22. PMID 16835590 DOI: 10.1038/sj.ejhg.5201687 |
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Diosdado B, Monsuur AJ, Mearin ML, Mulder C, Wijmenga C. The downstream modulator of interferon- γ , STAT1 is not genetically associated to the Dutch coeliac disease population European Journal of Human Genetics. 14: 1120-1124. PMID 16773129 DOI: 10.1038/Sj.Ejhg.5201667 |
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Amundsen SS, Monsuur AJ, Wapenaar MC, Lie BA, Ek J, Gudjónsdóttir AH, Ascher H, Wijmenga C, Sollid LM. Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort. Human Immunology. 67: 341-5. PMID 16720215 DOI: 10.1016/J.Humimm.2006.03.020 |
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| 2006 |
Franke L, van Bakel H, Fokkens L, de Jong ED, Egmont-Petersen M, Wijmenga C. Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. American Journal of Human Genetics. 78: 1011-25. PMID 16685651 DOI: 10.1086/504300 |
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Shiri-Sverdlov R, Custers A, van Vliet-Ostaptchouk JV, van Gorp PJ, Lindsey PJ, van Tilburg JH, Zhernakova S, Feskens EJ, van der A DL, Dollé ME, van Haeften TW, Koeleman BP, Hofker MH, Wijmenga C. Identification of TUB as a novel candidate gene influencing body weight in humans. Diabetes. 55: 385-9. PMID 16443771 DOI: 10.2337/Diabetes.55.02.06.Db05-0997 |
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Hunt KA, Monsuur AJ, McArdle WL, Kumar PJ, Travis SP, Walters JR, Jewell DP, Strachan DP, Playford RJ, Wijmenga C, van Heel DA. Lack of association of MYO9B genetic variants with coeliac disease in a British cohort. Gut. 55: 969-72. PMID 16423886 DOI: 10.1136/Gut.2005.086769 |
0.456 |
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| 2006 |
Geremek M, Zietkiewicz E, Diehl SR, Alizadeh BZ, Wijmenga C, Witt M. Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24-25. Journal of Medical Genetics. 43: e1. PMID 16397065 DOI: 10.1136/Jmg.2005.031526 |
0.358 |
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| 2006 |
Lips EH, Dierssen JW, van Eijk R, Oosting J, Eilers PH, Tollenaar RA, de Graaf EJ, van't Slot R, Wijmenga C, Morreau H, van Wezel T. Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays. Cancer Research. 65: 10188-91. PMID 16288005 DOI: 10.1158/0008-5472.Can-05-2486 |
0.33 |
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| 2006 |
Ruigrok YM, Rinkel GJ, Wijmenga C. The Versican Gene and the Risk of Intracranial Aneurysms Neurosurgery. 58: 396. DOI: 10.1161/01.Str.0000236499.55301.09 |
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| 2006 |
Diosdado B, van Bakel H, Wapenaar M, Franke L, Meijer J, Mearin M, Mulder C, Wijmenga C. Expression profiles of coeliac disease biopsies during mucosa recovery European Journal of Gastroenterology & Hepatology. 18: A34-A35. DOI: 10.1097/00042737-200601000-00123 |
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| 2006 |
Monsuur A, Lavrijsen I, Zhernakova A, Franke L, Wijmenga C. Fine-mapping of the coeliac disease linkage region on chromosome 19p13 reveals a new player in the field European Journal of Gastroenterology & Hepatology. 18: A34. DOI: 10.1097/00042737-200601000-00121 |
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| 2006 |
Ruigrok YM, Rinkel GJ, van't Slot R, Wolfs M, Tang S, Wijmenga C. Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms Human Molecular Genetics. 15: 3361-3368. DOI: 10.1093/Hmg/Ddl412 |
0.367 |
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| 2006 |
Curley CR, Monsuur AJ, Wapenaar MC, Rioux JD, Wijmenga C. A functional candidate screen for coeliac disease genes European Journal of Human Genetics. 14: 1215-1222. DOI: 10.1038/Sj.Ejhg.5201687 |
0.437 |
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| 2005 |
Van Vught PW, Sutedja NA, Veldink JH, Koeleman BP, Groeneveld GJ, Wijmenga C, Uitdehaag BM, de Jong JM, Baas F, Wokke JH, Van den Berg LH. Lack of association between VEGF polymorphisms and ALS in a Dutch population. Neurology. 65: 1643-5. PMID 16301496 DOI: 10.1212/01.Wnl.0000184514.39853.56 |
0.31 |
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| 2005 |
Forman OP, Boursnell ME, Dunmore BJ, Stendall N, van den Sluis B, Fretwell N, Jones C, Wijmenga C, Rothuizen J, van Oost BA, Holmes NG, Binns MM, Jones P. Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers. Animal Genetics. 36: 497-501. PMID 16293123 DOI: 10.1111/J.1365-2052.2005.01360.X |
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| 2005 |
Monsuur AJ, de Bakker PI, Alizadeh BZ, Zhernakova A, Bevova MR, Strengman E, Franke L, van't Slot R, van Belzen MJ, Lavrijsen IC, Diosdado B, Daly MJ, Mulder CJ, Mearin ML, Meijer JW, ... ... Wijmenga C, et al. Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect. Nature Genetics. 37: 1341-4. PMID 16282976 DOI: 10.1038/Ng1680 |
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Diosdado B, van Oort E, Wijmenga C. "Coelionomics": towards understanding the molecular pathology of coeliac disease. Clinical Chemistry and Laboratory Medicine. 43: 685-95. PMID 16207126 DOI: 10.1515/Cclm.2005.117 |
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| 2005 |
Wijmenga C. Expressing the differences between Crohn disease and ulcerative colitis. Plos Medicine. 2: e230; quiz e304. PMID 16120009 DOI: 10.1371/Journal.Pmed.0020230 |
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| 2005 |
Koning F, Gilissen L, Wijmenga C. Gluten: a two-edged sword. Immunopathogenesis of celiac disease. Springer Seminars in Immunopathology. 27: 217-32. PMID 16091925 DOI: 10.1007/S00281-005-0203-9 |
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| 2005 |
Kok HS, van Asselt KM, van der Schouw YT, Peeters PH, Wijmenga C. Genetic studies to identify genes underlying menopausal age. Human Reproduction Update. 11: 483-93. PMID 16024548 DOI: 10.1093/Humupd/Dmi024 |
0.395 |
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| 2005 |
Wapenaar MC, Wijmenga C. A combined genetics and genomics approach to unravelling molecular pathways in coeliac disease. Novartis Foundation Symposium. 267: 113-34; discussion 1. PMID 15999804 |
0.368 |
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| 2005 |
van Heel DA, Hunt K, Greco L, Wijmenga C. Genetics in coeliac disease. Best Practice & Research. Clinical Gastroenterology. 19: 323-39. PMID 15925839 DOI: 10.1016/J.Bpg.2005.01.001 |
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| 2005 |
Diosdado B, Stepniak DT, Monsuur AJ, Franke L, Wapenaar MC, Mearin ML, Koning F, Wijmenga C. No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population. American Journal of Physiology. Gastrointestinal and Liver Physiology. 289: G495-500. PMID 15890709 DOI: 10.1152/Ajpgi.00056.2005 |
0.706 |
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| 2005 |
Zhernakova A, Eerligh P, Wijmenga C, Barrera P, Roep BO, Koeleman BP. Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population. Genes and Immunity. 6: 459-61. PMID 15875058 DOI: 10.1038/Sj.Gene.6364220 |
0.359 |
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| 2005 |
Ruigrok YM, Slooter AJC, Bardoel A, Frijns CJM, Rinkel GJE, Wijmenga C. Genes and outcome after aneurysmal subarachnoid haemorrhage Journal of Neurology. 252: 417-422. PMID 15726267 DOI: 10.1007/S00415-005-0661-Y |
0.31 |
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| 2005 |
Ruigrok YM, Rinkel GJE, Wijmenga C. Genetics of intracranial aneurysms. Lancet Neurology. 4: 179-189. PMID 15721828 DOI: 10.1016/S1474-4422(05)01015-X |
0.365 |
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| 2005 |
Monsuur A, Lavrijsen I, Zhernakova A, Franke L, Wijmenga C. FINE-MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD Journal of Pediatric Gastroenterology and Nutrition. 40: 616. DOI: 10.1097/00042737-200601000-00121 |
0.638 |
|
| 2005 |
Diosdado B, Bakel HV, Wapenaar M, Franke L, Meijer J, Mearin M, Mulder C, Wijmenga C. EXPRESSION PROFILES OF COELIAC DISEASE BIOPSIES DURING MUCOSA RECOVERY Journal of Pediatric Gastroenterology and Nutrition. 40: 631. DOI: 10.1097/00005176-200505000-00063 |
0.639 |
|
| 2005 |
Zhernakova A, Eerligh P, Barrera P, Weseloy JZ, Huizinga TWJ, Roep BO, Wijmenga C, Koeleman BPC. CTLA4 is differentially associated with autoimmune diseases in the Dutch population Human Genetics. 118: 58-66. DOI: 10.1007/S00439-005-0006-Z |
0.373 |
|
| 2005 |
Wapenaar MC, Wijmenga C. A combined genetics and genomics approach to unravelling molecular pathways in coeliac disease. Novartis Foundation Symposium. 267: 113-144. DOI: 10.1002/047002139X.Ch9 |
0.473 |
|
| 2004 |
Ruigrok YM, Seitz U, Wolterink S, Rinkel GJ, Wijmenga C, Urbán Z. Association of polymorphisms and haplotypes in the elastin gene in Dutch patients with sporadic aneurysmal subarachnoid hemorrhage. Stroke. 35: 2064-8. PMID 15297630 DOI: 10.1161/01.Str.0000139380.50649.5C |
0.365 |
|
| 2004 |
van Belzen MJ, Mulder CJ, Zhernakova A, Pearson PL, Houwen RH, Wijmenga C. CTLA4 +49 A/G and CT60 polymorphisms in Dutch coeliac disease patients. European Journal of Human Genetics : Ejhg. 12: 782-5. PMID 15199380 DOI: 10.1038/Sj.Ejhg.5201165 |
0.382 |
|
| 2004 |
Diosdado B, Wapenaar MC, Franke L, Duran KJ, Goerres MJ, Hadithi M, Crusius JB, Meijer JW, Duggan DJ, Mulder CJ, Holstege FC, Wijmenga C. A microarray screen for novel candidate genes in coeliac disease pathogenesis. Gut. 53: 944-51. PMID 15194641 DOI: 10.1136/Gut.2003.018374 |
0.677 |
|
| 2004 |
Franke L, van Bakel H, Diosdado B, van Belzen M, Wapenaar M, Wijmenga C. TEAM: a tool for the integration of expression, and linkage and association maps. European Journal of Human Genetics : Ejhg. 12: 633-8. PMID 15114375 DOI: 10.1038/Sj.Ejhg.5201215 |
0.702 |
|
| 2004 |
van Belzen MJ, Vrolijk MM, Meijer JW, Crusius JB, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9. The American Journal of Gastroenterology. 99: 466-71. PMID 15056087 DOI: 10.1111/J.1572-0241.2004.04072.X |
0.401 |
|
| 2004 |
Kok HS, van Asselt KM, Peeters PH, van der Schouw YT, Grobbee DE, Pearson PL, Wijmenga C. Age at natural menopause is not linked with the follicle-stimulating hormone receptor region: a sib-pair study. Fertility and Sterility. 81: 611-6. PMID 15037410 DOI: 10.1016/J.Fertnstert.2003.08.017 |
0.329 |
|
| 2004 |
van Belzen MJ, Koeleman BP, Crusius JB, Meijer JW, Bardoel AF, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients. Genes and Immunity. 5: 215-20. PMID 15014431 DOI: 10.1038/Sj.Gene.6364061 |
0.421 |
|
| 2004 |
van Asselt KM, Kok HS, Putter H, Wijmenga C, Peeters PH, van der Schouw YT, Grobbee DE, te Velde ER, Mosselman S, Pearson PL. Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative trait loci influencing variation in human menopausal age. American Journal of Human Genetics. 74: 444-53. PMID 14872408 DOI: 10.1086/382136 |
0.351 |
|
| 2004 |
Seegers D, Borm ME, van Belzen MJ, Mulder CJ, Bailing J, Crusius JB, Meijer JW, Wijmenga C, Peña AS, Bouma G. IL12B and IRF1 gene polymorphisms and susceptibility to celiac disease. European Journal of Immunogenetics : Official Journal of the British Society For Histocompatibility and Immunogenetics. 30: 421-5. PMID 14675396 DOI: 10.1111/J.1365-2370.2003.00428.X |
0.406 |
|
| 2004 |
Wapenaar MC, van Belzen MJ, Fransen JH, Fariña Sarasqueta A, Houwen RH, Meijer JW, Mulder CJ, Wijmenga C. The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility Journal of Autoimmunity. 23: 183-190. DOI: 10.1016/J.Jaut.2004.05.004 |
0.389 |
|
| 2003 |
van Tilburg JH, Sandkuijl LA, Franke L, Strengman E, Pearson PL, van Haeften TW, Wijmenga C. Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population. European Journal of Clinical Investigation. 33: 1070-4. PMID 14636289 DOI: 10.1111/J.1365-2362.2003.01276.X |
0.637 |
|
| 2003 |
van Tilburg JH, Sandkuijl LA, Strengman E, Pearson PL, van Haeften TW, Wijmenga C. Variance-component analysis of obesity in type 2 diabetes confirms loci on chromosomes 1q and 11q. Obesity Research. 11: 1290-4. PMID 14627748 DOI: 10.1038/Oby.2003.175 |
0.301 |
|
| 2003 |
Van Belzen MJ, Meijer JW, Sandkuijl LA, Bardoel AF, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. A major non-HLA locus in celiac disease maps to chromosome 19. Gastroenterology. 125: 1032-41. PMID 14517787 DOI: 10.1016/S0016-5085(03)01205-8 |
0.414 |
|
| 2003 |
Tao TY, Liu F, Klomp L, Wijmenga C, Gitlin JD. The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein. The Journal of Biological Chemistry. 278: 41593-6. PMID 12968035 DOI: 10.1074/Jbc.C300391200 |
0.311 |
|
| 2003 |
Sluis Bvd, Peter AT, Wijmenga C. Indirect Molecular Diagnosis of Copper Toxicosis in Bedlington Terriers Is Complicated by Haplotype Diversity Journal of Heredity. 94: 256-259. PMID 12816967 DOI: 10.1093/Jhered/Esg030 |
0.339 |
|
| 2003 |
van Tilburg JH, Sandkuijl LA, Strengman E, van Someren H, Rigters-Aris CA, Pearson PL, van Haeften TW, Wijmenga C. A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13. The Journal of Clinical Endocrinology and Metabolism. 88: 2223-30. PMID 12727978 DOI: 10.1210/Jc.2002-021252 |
0.341 |
|
| 2003 |
Freimer NB, Heutink P, Wijmenga C. Lodewijk A. Sandkuijl, M.D. (July 31, 1953–December 4, 2002) The American Journal of Human Genetics. 72: 781-784. DOI: 10.1086/374381 |
0.347 |
|
| 2003 |
Van Belzen M, Meijer JW, Sandkuijl LA, Bardoel AF, Mulder CJ, Pearson PL, Wijmenga C, Houwen RH. A major non-HLA locus in celiac disease maps to chromosome 19 Gastroenterology. 124: A656. DOI: 10.1016/S0016-5085(03)83324-3 |
0.434 |
|
| 2003 |
Diosdado B, Wapenaar MC, Duran KJ, Franke L, Meijer JW, Holstege FC, Wijmenga C, Mulder CJ. Identification of novel candidate genes in celiac disease pathogenesis using microarrays Gastroenterology. 124: A376. DOI: 10.1016/S0016-5085(03)81903-0 |
0.677 |
|
| 2002 |
Peña AS, Wijmenga C. Genetic factors underlying gluten-sensitive enteropathy. Current Allergy and Asthma Reports. 1: 526-33. PMID 11892082 DOI: 10.1007/S11882-001-0061-Z |
0.454 |
|
| 2002 |
van De Sluis B, Rothuizen J, Pearson PL, van Oost BA, Wijmenga C. Identification of a new copper metabolism gene by positional cloning in a purebred dog population. Human Molecular Genetics. 11: 165-73. PMID 11809725 DOI: 10.1093/Hmg/11.2.165 |
0.369 |
|
| 2001 |
van Belzen MJ, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. The tissue transglutaminase gene is not a primary factor predisposing to celiac disease. The American Journal of Gastroenterology. 96: 3337-40. PMID 11774946 DOI: 10.1016/S0002-9270(01)03897-7 |
0.389 |
|
| 2001 |
Papadopoulos GK, Wijmenga C, Koning F. Interplay between genetics and the environment in the development of celiac disease: perspectives for a healthy life. The Journal of Clinical Investigation. 108: 1261-6. PMID 11696566 DOI: 10.1172/Jci14344 |
0.336 |
|
| 2001 |
van Tilburg J, van Haeften TW, Pearson P, Wijmenga C. Defining the genetic contribution of type 2 diabetes mellitus. Journal of Medical Genetics. 38: 569-78. PMID 11546824 DOI: 10.1136/Jmg.38.9.569 |
0.325 |
|
| 2000 |
Müller T, Wijmenga C, Phillips AD, Janecke A, Houwen RH, Fischer H, Ellemunter H, Frühwirth M, Offner F, Hofer S, Müller W, Booth IW, Heinz-Erian P. Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes. Gastroenterology. 119: 1506-13. PMID 11113072 DOI: 10.1053/Gast.2000.20514 |
0.363 |
|
| 2000 |
Hansen RS, Stöger R, Wijmenga C, Stanek AM, Canfield TK, Luo P, Matarazzo MR, D'Esposito M, Feil R, Gimelli G, Weemaes CM, Laird CD, Gartler SM. Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant. Human Molecular Genetics. 9: 2575-87. PMID 11063717 DOI: 10.1093/Hmg/9.18.2575 |
0.317 |
|
| 1999 |
Hansen RS, Wijmenga C, Luo P, Stanek AM, Canfield TK, Weemaes CM, Gartler SM. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. Proceedings of the National Academy of Sciences of the United States of America. 96: 14412-7. PMID 10588719 DOI: 10.1073/Pnas.96.25.14412 |
0.302 |
|
| 1999 |
van de Sluis BJ, Breen M, Nanji M, van Wolferen M, de Jong P, Binns MM, Pearson PL, Kuipers J, Rothuizen J, Cox DW, Wijmenga C, van Oost BA. Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16. Human Molecular Genetics. 8: 501-7. PMID 9949209 DOI: 10.1093/Hmg/8.3.501 |
0.353 |
|
| 1999 |
van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Mühlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, et al. Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered. Oncogene. 18: 543-50. PMID 9927211 DOI: 10.1038/Sj.Onc.1202321 |
0.331 |
|
| 1999 |
Müller T, Sluis Bvd, Müller W, Pearson P, Wijmenga C. Non-Indian childhood cirrhosis. European Journal of Medical Research. 4: 293-297. DOI: 10.1007/978-1-59259-288-3_22 |
0.432 |
|
| 1998 |
Wijmenga C, Müller T, Murli IS, Brunt T, Feichtinger H, Schönitzer D, Houwen RH, Müller W, Sandkuijl LA, Pearson PL. Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease. European Journal of Human Genetics : Ejhg. 6: 624-8. PMID 9887382 DOI: 10.1038/Sj.Ejhg.5200235 |
0.418 |
|
| 1998 |
Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Localization of the ICF syndrome to chromosome 20 by homozygosity mapping. American Journal of Human Genetics. 63: 803-9. PMID 9718351 DOI: 10.1086/302021 |
0.316 |
|
| 1998 |
Giltay JC, Brunt T, Beemer FA, Wit JM, van Amstel HK, Pearson PL, Wijmenga C. Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite. American Journal of Human Genetics. 62: 937-40. PMID 9529354 DOI: 10.1086/301796 |
0.38 |
|
| 1996 |
Castilla LH, Wijmenga C, Wang Q, Stacy T, Speck NA, Eckhaus M, Marín-Padilla M, Collins FS, Wynshaw-Boris A, Liu PP. Failure of embryonic hematopoiesis and lethal hemorrhages in mouse embryos heterozygous for a knocked-in leukemia gene CBFB-MYH11. Cell. 87: 687-96. PMID 8929537 DOI: 10.1016/S0092-8674(00)81388-4 |
0.695 |
|
| 1996 |
Bakker E, Van der Wielen MJ, Voorhoeve E, Ippel PF, Padberg GW, Frants RR, Wijmenga C. Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases. Journal of Medical Genetics. 33: 29-35. PMID 8825045 DOI: 10.1136/Jmg.33.1.29 |
0.574 |
|
| 1996 |
Liu PP, Wijmenga C, Hajra A, Blake TB, Kelley CA, Adelstein RS, Bagg A, Rector J, Cotelingam J, Willman CL, Collins FS. Identification of the chimeric protein product of the CBFB-MYH11 fusion gene in inv(16) leukemia cells. Genes, Chromosomes & Cancer. 16: 77-87. PMID 8818654 DOI: 10.1002/(Sici)1098-2264(199606)16:2<77::Aid-Gcc1>3.0.Co;2-# |
0.447 |
|
| 1996 |
Wijmenga C, Gregory PE, Hajra A, Schröck E, Ried T, Eils R, Liu PP, Collins FS. Core binding factor beta-smooth muscle myosin heavy chain chimeric protein involved in acute myeloid leukemia forms unusual nuclear rod-like structures in transformed NIH 3T3 cells. Proceedings of the National Academy of Sciences of the United States of America. 93: 1630-5. PMID 8643682 DOI: 10.1073/Pnas.93.4.1630 |
0.42 |
|
| 1995 |
Liu PP, Hajra A, Wijmenga C, Collins FS. Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia Blood. 85: 2289-2302. PMID 7727763 DOI: 10.1182/Blood.V85.9.2289.Bloodjournal8592289 |
0.517 |
|
| 1995 |
Wijmenga C, Speck NA, Dracopoli NC, Hofker MH, Liu P, Collins FS. Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter. Genomics. 26: 611-4. PMID 7607690 DOI: 10.1016/0888-7543(95)80185-O |
0.451 |
|
| 1995 |
Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Facioscapulohumeral muscular dystrophy in the dutch population Muscle & Nerve. 18: S81-S84. DOI: 10.1002/Mus.880181315 |
0.645 |
|
| 1995 |
Padberg GW, Brouwer OF, de Keizer RJW, Dijkman G, Wijmenga C, Grote JJ, Frants RR. On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy Muscle & Nerve. 18: S73-S80. DOI: 10.1002/Mus.880181314 |
0.63 |
|
| 1995 |
Brouwer OF, Padberg GW, Bakker E, Wijmenga C, Frants RR. Early onset facioscapulohumeral muscular dystrophy Muscle & Nerve. 18: S67-S72. DOI: 10.1002/Mus.880181313 |
0.652 |
|
| 1995 |
Bakker E, Wijmenga C, Vossen RHAM, Padberg GW, Hewitt J, van Der Wielen M, Rasmussen K, Frants RR. The FSHD-linked locus D4F104S1 (p13E-11) ON 4q35 has a homologue on 10qter Muscle & Nerve. 18: S39-S44. DOI: 10.1002/Mus.880181309 |
0.676 |
|
| 1995 |
van Deutekom JCT, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35 Muscle & Nerve. 18: S19-S26. DOI: 10.1002/Mus.880181306 |
0.662 |
|
| 1995 |
Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR. Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35 Muscle & Nerve. 18: S14-S18. DOI: 10.1002/Mus.880181305 |
0.656 |
|
| 1994 |
Brouwer OF, Padberg GW, Wijmenga C, Frants RR. Facioscapulohumeral muscular dystrophy in early childhood. Archives of Neurology. 51: 387-94. PMID 8155016 DOI: 10.1001/Archneur.1994.00540160085011 |
0.622 |
|
| 1994 |
Hewitt JE, Lyle R, Clark LN, Valleley EM, Wright TJ, Wijmenga C, van Deutekom JC, Francis F, Sharpe PT, Hofker M. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Human Molecular Genetics. 3: 1287-95. PMID 7987304 DOI: 10.1093/Hmg/3.8.1287 |
0.328 |
|
| 1994 |
Cacurri S, Deidda G, Piazzo N, Novelletto A, La Cesa I, Servidei S, Galluzzi G, Wijmenga C, Frants RR, Felicetti L. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD). Human Genetics. 94: 367-74. PMID 7927331 DOI: 10.1007/Bf00201595 |
0.514 |
|
| 1994 |
Wijmenga C, van Deutekom JC, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions. Genomics. 19: 21-6. PMID 7910579 DOI: 10.1006/Geno.1994.1006 |
0.677 |
|
| 1993 |
Passos-Bueno MR, Wijmenga C, Takata RE, Marie SK, Vainzof M, Pavanello RC, Hewitt JE, Bakker E, Carvalho A, Akiyama J. No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers. Human Molecular Genetics. 2: 557-62. PMID 8518794 DOI: 10.1093/Hmg/2.5.557 |
0.349 |
|
| 1993 |
Upadhyaya M, Jardine P, Maynard J, Farnham J, Sarfarazi M, Wijmenga C, Hewitt JE, Frants R, Harper PS, Lunt PW. Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements. Human Molecular Genetics. 2: 981-7. PMID 8364581 DOI: 10.1093/Hmg/2.7.981 |
0.541 |
|
| 1993 |
Wijmenga C, Wright TJ, Baan MJ, Padberg GW, Williamson R, van Ommen GJ, Hewitt JE, Hofker MH, Frants RR. Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region. Human Molecular Genetics. 2: 1667-72. PMID 8268920 DOI: 10.1093/Hmg/2.10.1667 |
0.668 |
|
| 1993 |
Cobben JM, Scheffer H, De Visser M, Osinga J, Frants R, van der Steege G, Wijmenga C, ten Kate LP, van Ommen GJ, Buys CH. Linkage and apparent heterogeneity in proximal spinal muscular atrophies. Neuromuscular Disorders : Nmd. 3: 327-33. PMID 8268730 DOI: 10.1016/0960-8966(93)90026-G |
0.454 |
|
| 1993 |
Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ. Molecular genetics of facioscapulohumeral muscular dystrophy. Neuromuscular Disorders : Nmd. 3: 487-91. PMID 8186699 |
0.488 |
|
| 1993 |
Wijmenga C, Hofker MH, Padberg GW, Frants RR. Genetic mapping of facioscapulohumeral muscular dystrophy. Molecular and Cell Biology of Human Diseases Series. 3: 111-38. PMID 8111536 DOI: 10.1007/978-94-011-1528-5_5 |
0.54 |
|
| 1993 |
van Deutekom JC, Wijmenga C, van Tienhoven EA, Gruter AM, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. Human Molecular Genetics. 2: 2037-42. PMID 8111371 DOI: 10.1093/HMG/2.12.2037 |
0.546 |
|
| 1993 |
Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, Wasmuth JJ, Murray JC, Hofker MH, Frants RR. The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus. Human Genetics. 92: 198-203. PMID 8103757 DOI: 10.1007/Bf00219692 |
0.682 |
|
| 1993 |
Weiffenbach B, Dubois J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell JR, Winokur S, Altherr MR, Schultz P, Olandt S, Frants RR, Pericak-Vance MA, Griggs RC. Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events Nature Genetics. 4: 165-169. PMID 8102297 DOI: 10.1038/Ng0693-165 |
0.55 |
|
| 1993 |
Brouwer OF, Wijmenga C, Frants RR, Padberg GW. Facioscapulohumeral muscular dystrophy: the impact of genetic research. Clinical Neurology and Neurosurgery. 95: 9-21. PMID 8095870 DOI: 10.1016/0303-8467(93)90086-V |
0.707 |
|
| 1993 |
Wright TJ, Wijmenga C, Clark LN, Frants RR, Williamson R, Hewitt JE. Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11. Human Molecular Genetics. 2: 1673-8. PMID 7903581 DOI: 10.1093/Hmg/2.10.1673 |
0.51 |
|
| 1992 |
Wijmenga C, Deaven L, Frants RR. Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35. Nucleic Acids Research. 20: 1161. PMID 1549496 DOI: 10.1093/Nar/20.5.1161 |
0.497 |
|
| 1992 |
Wijmenga C, Brouwer OF, Padberg GW, Frants RR. Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophy. Lancet (London, England). 340: 985-6. PMID 1357400 DOI: 10.1016/0140-6736(92)92885-J |
0.541 |
|
| 1992 |
Padberg G, Wijmenga C, Upadhyaya M, Weiffenbach B, Brouwer O, Murray J, Pericak-Vance M, Lunt P, Frants R, Harper P, Sarfarazi M. 17. Regional mapping of the facioscapulohumeral muscular dystrophy gene on 4q35: linkage analysis of the International Consortium Clinical Neurology and Neurosurgery. 94: 79. DOI: 10.1016/0303-8467(92)90142-P |
0.638 |
|
| 1991 |
Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. Genomics. 9: 570-5. PMID 2037288 DOI: 10.1016/0888-7543(91)90348-I |
0.602 |
|
| 1990 |
Wijmenga C, Frants RR, Brouwer OF, van der Klift HM, Khan PM, Padberg GW. Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5 Journal of the Neurological Sciences. 95: 225-229. PMID 2157824 DOI: 10.1016/0022-510X(90)90245-I |
0.657 |
|
| 1990 |
Wijmenga C, Frants RR, Brouwer OF, Moerer P, Weber JL, Padberg GW. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4. Lancet (London, England). 336: 651-3. PMID 1975852 DOI: 10.1016/0140-6736(90)92148-B |
0.685 |
|
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