| Year |
Citation |
Score |
| 2023 |
Kentistou KA, Kaisinger LR, Stankovic S, Vaudel M, de Oliveira EM, Messina A, Walters RG, Liu X, Busch AS, Helgason H, Thompson DJ, Santon F, Petricek KM, Zouaghi Y, Huang-Doran I, ... ... Franke LH, et al. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Medrxiv : the Preprint Server For Health Sciences. PMID 37503126 DOI: 10.1101/2023.06.14.23291322 |
0.335 |
|
| 2023 |
Kellmann AJ, Lanting P, Franke L, van Enckevort EJ, Swertz MA. Semi-automatic translation of medicine usage data (in Dutch, free-text) from Lifelines COVID-19 questionnaires to ATC codes. Database : the Journal of Biological Databases and Curation. 2023. PMID 37114804 DOI: 10.1093/database/baad019 |
0.475 |
|
| 2023 |
Li S, Schmid KT, de Vries DH, Korshevniuk M, Losert C, Oelen R, van Blokland IV, Groot HE, Swertz MA, van der Harst P, Westra HJ, van der Wijst MGP, Heinig M, Franke L. Identification of genetic variants that impact gene co-expression relationships using large-scale single-cell data. Genome Biology. 24: 80. PMID 37072791 DOI: 10.1186/s13059-023-02897-x |
0.819 |
|
| 2023 |
Cato LD, Li R, Lu HY, Yu F, Wissman M, Mkumbe BS, Ekwattanakit S, Deelen P, Mwita L, Sangeda RZ, Suksangpleng T, Riolueang S, Bronson PG, Paul DS, Kawabata E, ... ... Franke L, et al. Genetic regulation of fetal hemoglobin across global populations. Medrxiv : the Preprint Server For Health Sciences. PMID 36993312 DOI: 10.1101/2023.03.24.23287659 |
0.816 |
|
| 2023 |
Boahen CK, Oelen R, Le K, Netea MG, Franke L, van der Wijst MGP, Kumar V. Integration of -induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. Frontiers in Immunology. 14: 1069379. PMID 36865558 DOI: 10.3389/fimmu.2023.1069379 |
0.314 |
|
| 2023 |
de Klein N, Tsai EA, Vochteloo M, Baird D, Huang Y, Chen CY, van Dam S, Oelen R, Deelen P, Bakker OB, El Garwany O, Ouyang Z, Marshall EE, Zavodszky MI, van Rheenen W, ... ... Franke L, et al. Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature Genetics. PMID 36823318 DOI: 10.1038/s41588-023-01300-6 |
0.804 |
|
| 2023 |
Boulogne F, Claus LR, Wiersma H, Oelen R, Schukking F, de Klein N, Li S, Westra HJ, van der Zwaag B, van Reekum F, Sierks D, Schönauer R, Li Z, Bijlsma EK, Bos WJW, ... ... Franke L, et al. KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease. European Journal of Human Genetics : Ejhg. PMID 36807342 DOI: 10.1038/s41431-023-01296-x |
0.82 |
|
| 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 |
0.817 |
|
| 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, ... ... Franke L, 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 |
0.645 |
|
| 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 |
0.569 |
|
| 2022 |
Porcu E, Claringbould A, Weihs A, Lepik K, Richardson TG, Völker U, Santoni FA, Teumer A, Franke L, Reymond A, Kutalik Z. Limited evidence for blood eQTLs in human sexual dimorphism. Genome Medicine. 14: 89. PMID 35953856 DOI: 10.1186/s13073-022-01088-w |
0.312 |
|
| 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 |
0.604 |
|
| 2022 |
Oelen R, de Vries DH, Brugge H, Gordon MG, Vochteloo M, Ye CJ, Westra HJ, Franke L, van der Wijst MGP. Single-cell RNA-sequencing of peripheral blood mononuclear cells reveals widespread, context-specific gene expression regulation upon pathogenic exposure. Nature Communications. 13: 3267. PMID 35672358 DOI: 10.1038/s41467-022-30893-5 |
0.777 |
|
| 2022 |
Warmerdam CAR, Wiersma HH, Lanting P, Ani A, Dijkema MXL, Snieder H, Vonk JM, Boezen HM, Deelen P, Franke LH. Increased genetic contribution to wellbeing during the COVID-19 pandemic. Plos Genetics. 18: e1010135. PMID 35588108 DOI: 10.1371/journal.pgen.1010135 |
0.778 |
|
| 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, ... ... Franke L, ... ... Franke L, ... ... Franke L, 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 |
0.804 |
|
| 2022 |
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, ... ... Franke L, et al. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. PMID 35102318 DOI: 10.1038/s41588-022-01020-3 |
0.815 |
|
| 2021 |
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, ... ... Franke L, et al. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. 53: 1636-1648. PMID 34873335 DOI: 10.1038/s41588-021-00973-1 |
0.831 |
|
| 2021 |
Warmerdam R, Lanting P, Deelen P, Franke L. Idéfix: identifying accidental sample mix-ups in biobanks using polygenic scores. Bioinformatics (Oxford, England). PMID 34792549 DOI: 10.1093/bioinformatics/btab783 |
0.775 |
|
| 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, 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 |
0.623 |
|
| 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, ... ... Franke L, 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 |
0.83 |
|
| 2021 |
Hemani G, Shakhbazov K, Westra HJ, Esko T, Henders AK, McRae AF, Yang J, Gibson G, Martin NG, Metspalu A, Franke L, Montgomery GW, Visscher PM, Powell JE. Retraction Note: Detection and replication of epistasis influencing transcription in humans. Nature. 596: 306. PMID 34381240 DOI: 10.1038/s41586-021-03766-y |
0.711 |
|
| 2021 |
Hemani G, Powell JE, Wang H, Shakhbazov K, Westra HJ, Esko T, Henders AK, McRae AF, Martin NG, Metspalu A, Franke L, Montgomery GW, Goddard ME, Gibson G, Yang J, et al. Phantom epistasis between unlinked loci. Nature. 596: E1-E3. PMID 34381229 DOI: 10.1038/s41586-021-03765-z |
0.76 |
|
| 2021 |
van Blokland IV, Lanting P, Ori APS, Vonk JM, Warmerdam RCA, Herkert JC, Boulogne F, Claringbould A, Lopera-Maya EA, Bartels M, Hottenga JJ, Ganna A, Karjalainen J, ... ... Franke LH, et al. Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility. Plos One. 16: e0255402. PMID 34379666 DOI: 10.1371/journal.pone.0255402 |
0.791 |
|
| 2021 |
Ruth KS, Day FR, Hussain J, Martínez-Marchal A, Aiken CE, Azad A, Thompson DJ, Knoblochova L, Abe H, Tarry-Adkins JL, Gonzalez JM, Fontanillas P, Claringbould A, Bakker OB, Sulem P, ... ... Franke L, et al. Genetic insights into biological mechanisms governing human ovarian ageing. Nature. PMID 34349265 DOI: 10.1038/s41586-021-03779-7 |
0.78 |
|
| 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, ... ... Franke L, 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 |
0.597 |
|
| 2021 |
Zhang Z, van Dijk F, de Klein N, van Gijn ME, Franke LH, Sinke RJ, Swertz MA, van der Velde KJ. Feasibility of predicting allele specific expression from DNA sequencing using machine learning. Scientific Reports. 11: 10606. PMID 34012022 DOI: 10.1038/s41598-021-89904-y |
0.54 |
|
| 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, ... ... Franke L, 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 |
Pellegrino-Coppola D, Claringbould A, Stutvoet M, Boomsma DI, Ikram MA, Slagboom PE, Westra HJ, Franke L. Correction for both common and rare cell types in blood is important to identify genes that correlate with age. Bmc Genomics. 22: 184. PMID 33722199 DOI: 10.1186/s12864-020-07344-w |
0.739 |
|
| 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, ... ... Franke L, 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 |
0.838 |
|
| 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, ... Franke L, 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 |
0.615 |
|
| 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, ... Franke L, 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 |
0.48 |
|
| 2020 |
Folkersen L, Gustafsson S, Wang Q, Hansen DH, Hedman ÅK, Schork A, Page K, Zhernakova DV, Wu Y, Peters J, Eriksson N, Bergen SE, Boutin TS, Bretherick AD, Enroth S, ... ... Franke L, et al. Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Nature Metabolism. 2: 1135-1148. PMID 33067605 DOI: 10.1038/s42255-020-00287-2 |
0.743 |
|
| 2020 |
Lu X, Fraszczyk E, van der Meer TP, van Faassen M, Bloks VW, Kema IP, van Beek AP, Li S, Franke L, Westra HJ, Xu X, Huo X, Snieder H, Wolffenbuttel BHR, et al. An epigenome-wide association study identifies multiple DNA methylation markers of exposure to endocrine disruptors. Environment International. 144: 106016. PMID 32916427 DOI: 10.1016/J.Envint.2020.106016 |
0.762 |
|
| 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 |
0.838 |
|
| 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, ... ... Franke L, 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 |
0.802 |
|
| 2020 |
Huang Y, Ollikainen M, Muniandy M, Zhang T, van Dongen J, Hao G, van der Most PJ, Pan Y, Pervjakova N, Sun YV, Hui Q, Lahti J, Fraszczyk E, Lu X, Sun D, ... ... Franke L, et al. Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure. Hypertension (Dallas, Tex. : 1979). 76: 195-205. PMID 32520614 DOI: 10.1161/Hypertensionaha.120.14973 |
0.387 |
|
| 2020 |
Bangma A, Voskuil MD, Uniken Venema WTC, Brugge H, Hu S, Lanting P, Franke L, Dijkstra G, Festen EAM, Weersma RK. Predicted efficacy of a pharmacogenetic passport for inflammatory bowel disease. Alimentary Pharmacology & Therapeutics. PMID 32363635 DOI: 10.1111/Apt.15762 |
0.316 |
|
| 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 |
0.661 |
|
| 2020 |
de Vries DH, Matzaraki V, Bakker OB, Brugge H, Westra HJ, Netea MG, Franke L, Kumar V, van der Wijst MGP. Integrating GWAS with bulk and single-cell RNA-sequencing reveals a role for LY86 in the anti-Candida host response. Plos Pathogens. 16: e1008408. PMID 32251450 DOI: 10.1371/Journal.Ppat.1008408 |
0.761 |
|
| 2020 |
van der Wijst MG, de Vries DH, Groot HE, Trynka G, Hon CC, Bonder MJ, Stegle O, Nawijn M, Idaghdour Y, van der Harst P, Ye CJ, Powell J, Theis FJ, Mahfouz A, Heinig M, ... Franke L, et al. The single-cell eQTLGen consortium. Elife. 9. PMID 32149610 DOI: 10.7554/Elife.52155 |
0.464 |
|
| 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 |
0.558 |
|
| 2019 |
van Rooij J, Mandaviya PR, Claringbould A, Felix JF, van Dongen J, Jansen R, Franke L, 't Hoen PAC, Heijmans B, van Meurs JBJ. Evaluation of commonly used analysis strategies for epigenome- and transcriptome-wide association studies through replication of large-scale population studies. Genome Biology. 20: 235. PMID 31727104 DOI: 10.1186/S13059-019-1878-X |
0.319 |
|
| 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, ... ... Franke L, 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 |
0.799 |
|
| 2019 |
Ouwens KG, Jansen R, Nivard MG, van Dongen J, Frieser MJ, Hottenga JJ, Arindrarto W, Claringbould A, van Iterson M, Mei H, Franke L, Heijmans BT, A C 't Hoen P, van Meurs J, Brooks AI, et al. A characterization of cis- and trans-heritability of RNA-Seq-based gene expression. European Journal of Human Genetics : Ejhg. PMID 31558840 DOI: 10.1038/S41431-019-0511-5 |
0.389 |
|
| 2019 |
van Arensbergen J, Pagie L, FitzPatrick VD, de Haas M, Baltissen MP, Comoglio F, van der Weide RH, Teunissen H, Võsa U, Franke L, de Wit E, Vermeulen M, Bussemaker HJ, van Steensel B. High-throughput identification of human SNPs affecting regulatory element activity. Nature Genetics. PMID 31253979 DOI: 10.1038/S41588-019-0455-2 |
0.401 |
|
| 2019 |
Deelen P, van Dam S, Herkert JC, Karjalainen JM, Brugge H, Abbott KM, van Diemen CC, van der Zwaag PA, Gerkes EH, Zonneveld-Huijssoon E, Boer-Bergsma JJ, Folkertsma P, Gillett T, van der Velde KJ, Kanninga R, ... ... Franke L, et al. Improving the diagnostic yield of exome- sequencing by predicting gene-phenotype associations using large-scale gene expression analysis. Nature Communications. 10: 2837. PMID 31253775 DOI: 10.1038/S41467-019-10649-4 |
0.821 |
|
| 2019 |
Jadhav B, Monajemi R, Gagalova KK, Ho D, Draisma HHM, van de Wiel MA, Franke L, Heijmans BT, van Meurs J, Jansen R, 't Hoen PAC, Sharp AJ, Kiełbasa SM. RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting. Bmc Biology. 17: 50. PMID 31234833 DOI: 10.1186/S12915-019-0674-0 |
0.37 |
|
| 2019 |
Zeng B, Lloyd-Jones LR, Montgomery GW, Metspalu A, Esko T, Franke L, Vosa U, Claringbould A, Brigham KL, Quyyumi AA, Idaghdour Y, Yang J, Visscher PM, Powell JE, Gibson G. Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation. Genetics. PMID 31123039 DOI: 10.1534/Genetics.119.302091 |
0.436 |
|
| 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, ... ... Franke L, et al. Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine. Neurology. PMID 30944236 DOI: 10.1212/Wnl.0000000000007313 |
0.526 |
|
| 2019 |
Schlicht K, Nyczka P, Caliebe A, Freitag-Wolf S, Claringbould A, Franke L, Võsa U, Kardia SLR, Smith JA, Zhao W, Gieger C, Peters A, Prokisch H, Strauch K, et al. The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus. Human Genetics. PMID 30852652 DOI: 10.1007/S00439-019-01994-X |
0.497 |
|
| 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, 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 |
0.638 |
|
| 2019 |
Moore R, Casale FP, Jan Bonder M, Horta D, Franke L, Barroso I, Stegle O. A linear mixed-model approach to study multivariate gene-environment interactions. Nature Genetics. 51: 180-186. PMID 30478441 DOI: 10.1038/S41588-018-0271-0 |
0.303 |
|
| 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 |
0.655 |
|
| 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, ... ... Franke L, 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 |
0.689 |
|
| 2018 |
van der Wijst MGP, de Vries DH, Brugge H, Westra HJ, Franke L. An integrative approach for building personalized gene regulatory networks for precision medicine. Genome Medicine. 10: 96. PMID 30567569 DOI: 10.1186/S13073-018-0608-4 |
0.772 |
|
| 2018 |
Shvetsova E, Sofronova A, Monajemi R, Gagalova K, Draisma HHM, White SJ, Santen GWE, Chuva de Sousa Lopes SM, Heijmans BT, van Meurs J, Jansen R, Franke L, Kiełbasa SM, den Dunnen JT, 't Hoen PAC, et al. Skewed X-inactivation is common in the general female population. European Journal of Human Genetics : Ejhg. PMID 30552425 DOI: 10.1038/S41431-018-0291-3 |
0.316 |
|
| 2018 |
Iotchkova V, Huang J, Morris JA, Jain D, Barbieri C, Walter K, Min JL, Chen L, Astle W, Cocca M, Deelen P, Elding H, Farmaki AE, Franklin CS, Franberg M, ... ... Franke L, et al. Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. Nature Genetics. PMID 30390057 DOI: 10.1038/S41588-018-0276-8 |
0.804 |
|
| 2018 |
Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T, Naderi E, Rose LM, Wu Y, Karlsson R, Barbalic M, Lin H, Pool R, ... ... Franke L, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics. 103: 691-706. PMID 30388399 DOI: 10.1016/J.Ajhg.2018.09.009 |
0.453 |
|
| 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 |
0.78 |
|
| 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, 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 |
0.822 |
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| 2018 |
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van Sommeren S, Janse M, Karjalainen J, Fehrmann R, Franke L, Fu J, Weersma RK. Extraintestinal manifestations and complications in inflammatory bowel disease: from shared genetics to shared biological pathways. Inflammatory Bowel Diseases. 20: 987-94. PMID 24739630 DOI: 10.1097/Mib.0000000000000032 |
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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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Hemani G, Shakhbazov K, Westra HJ, Esko T, Henders AK, McRae AF, Yang J, Gibson G, Martin NG, Metspalu A, Franke L, Montgomery GW, Visscher PM, Powell JE. Detection and replication of epistasis influencing transcription in humans. Nature. 508: 249-53. PMID 24572353 DOI: 10.1038/Nature13005 |
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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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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, ... ... Franke L, 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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Horvatovich P, Franke L, Bischoff R. Proteomic studies related to genetic determinants of variability in protein concentrations Journal of Proteome Research. 13: 5-14. PMID 24237071 DOI: 10.1021/Pr400765Y |
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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, 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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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, ... ... Franke L, 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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Westra HJ, Peters MJ, Esko T, Yaghootkar H, Schurmann C, Kettunen J, Christiansen MW, Fairfax BP, Schramm K, Powell JE, Zhernakova A, Zhernakova DV, Veldink JH, Van den Berg LH, Karjalainen J, ... ... Franke L, et al. Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics. 45: 1238-43. PMID 24013639 DOI: 10.1038/Ng.2756 |
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Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Westra HJ, Shakhbazov K, Abdellaoui A, Agrawal A, Albrecht E, Alizadeh BZ, Amin N, Barnard J, Baumeister SE, ... ... Franke L, et al. GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (New York, N.Y.). 340: 1467-71. PMID 23722424 DOI: 10.1126/Science.1235488 |
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Li G, Diogo D, Wu D, Spoonamore J, Dancik V, Franke L, Kurreeman F, Rossin EJ, Duclos G, Hartland C, Zhou X, Li K, Liu J, De Jager PL, Siminovitch KA, et al. Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. Plos Genetics. 9: e1003487. PMID 23696745 DOI: 10.1371/Journal.Pgen.1003487 |
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Trouw LA, Daha N, Kurreeman FA, Böhringer S, Goulielmos GN, Westra HJ, Zhernakova A, Franke L, Stahl EA, Levarht EW, Stoeken-Rijsbergen G, Verduijn W, Roos A, Li Y, Houwing-Duistermaat JJ, et al. Genetic variants in the region of the C1q genes are associated with rheumatoid arthritis. Clinical and Experimental Immunology. 173: 76-83. PMID 23607884 DOI: 10.1111/Cei.12097 |
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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, ... ... Franke L, 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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Cvejic A, Haer-Wigman L, Stephens JC, Kostadima M, Smethurst PA, Frontini M, van den Akker E, Bertone P, Bielczyk-Maczyńska E, Farrow S, Fehrmann RS, Gray A, de Haas M, Haver VG, Jordan G, ... ... Franke L, et al. SMIM1 underlies the Vel blood group and influences red blood cell traits. Nature Genetics. 45: 542-5. PMID 23563608 DOI: 10.1038/Ng.2603 |
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Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR, Esko T, Fall T, Ferreira T, Gentilini D, Jackson AU, ... ... Franke L, et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics. 45: 501-12. PMID 23563607 DOI: 10.1038/Ng.2606 |
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Knevel R, Krabben A, Wilson AG, Brouwer E, Leijsma MK, Lindqvist E, de Rooy DP, Daha NA, van der Linden MP, Tsonaka S, Zhernakova A, Westra HJ, Franke L, Houwing-Duistermaat JJ, Toes RE, et al. A genetic variant in granzyme B is associated with progression of joint destruction in rheumatoid arthritis. Arthritis and Rheumatism. 65: 582-9. PMID 23440692 DOI: 10.1002/Art.37808 |
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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, ... Franke L, 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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Cozen W, Li D, Timofeeva M, Diepstra A, Hazelett D, Delahaye-Sourdeix M, Edlund CK, Rostgaard K, Berg DJVD, Franke L, Smedby KE, Glaser SL, Westra H, Robison LL, Mack TM, et al. A Meta-Analysis Of Hodgkin Lymphoma Reveals 19p13.3 (TCF3) As a Novel Susceptibility Loc Blood. 122: 626-626. DOI: 10.1182/Blood.V122.21.626.626 |
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Knevel R, Krabben A, Wilson G, Brouwer E, Lindqvist E, de Rooy D, Daha N, van der Linden M, Tsonaka R, Zhernakova S, Westra H, Franke L, Houwing-Duistermaat J, Toes R, Huizinga T, et al. THU0001 Variation in granzyme-b is associated with progression of joint destruction in rheumatoid arthritis Annals of the Rheumatic Diseases. 71: 154.1-154. DOI: 10.1136/Annrheumdis-2012-Eular.1966 |
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Loos R, Hoed Md, Eijgelsheim M, Esko T, Peal DS, Segrè AV, Handsaker RE, Westra H, Johnson T, Yang J, Lundby A, Visscher PM, Willer C, Franke L, Sibon OC, et al. Identification of heart rate-associated loci and genes Protocol Exchange. DOI: 10.1038/Protex.2013.041 |
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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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van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, ... ... Franke L, et al. Seventy-five genetic loci influencing the human red blood cell. Nature. 492: 369-75. PMID 23222517 DOI: 10.1038/Nature11677 |
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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, ... ... Franke L, 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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de Boer RA, Verweij N, van Veldhuisen DJ, Westra HJ, Bakker SJ, Gansevoort RT, Muller Kobold AC, van Gilst WH, Franke L, Mateo Leach I, van der Harst P. A genome-wide association study of circulating galectin-3. Plos One. 7: e47385. PMID 23056639 DOI: 10.1371/Journal.Pone.0047385 |
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Franceschini N, van Rooij FJ, Prins BP, Feitosa MF, Karakas M, Eckfeldt JH, Folsom AR, Kopp J, Vaez A, Andrews JS, Baumert J, Boraska V, Broer L, Hayward C, Ngwa JS, ... ... Franke L, et al. Discovery and fine mapping of serum protein loci through transethnic meta-analysis. American Journal of Human Genetics. 91: 744-53. PMID 23022100 DOI: 10.1016/J.Ajhg.2012.08.021 |
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Diekstra FP, Saris CG, van Rheenen W, Franke L, Jansen RC, van Es MA, van Vught PW, Blauw HM, Groen EJ, Horvath S, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Robberecht W, et al. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. Plos One. 7: e35333. PMID 22509407 DOI: 10.1371/Journal.Pone.0035333 |
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Demirkan A, van Duijn CM, Ugocsai P, Isaacs A, Pramstaller PP, Liebisch G, Wilson JF, Johansson Ã…, Rudan I, Aulchenko YS, Kirichenko AV, Janssens AC, Jansen RC, Gnewuch C, Domingues FS, ... ... Franke L, et al. Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. Plos Genetics. 8: e1002490. PMID 22359512 DOI: 10.1371/Journal.Pgen.1002490 |
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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, ... ... Franke L, 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 |
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Johnson T, Gaunt TR, Newhouse SJ, Padmanabhan S, Tomaszewski M, Kumari M, Morris RW, Tzoulaki I, O'Brien ET, Poulter NR, Sever P, Shields DC, Thom S, Wannamethee SG, Whincup PH, ... ... Franke L, et al. Blood pressure loci identified with a gene-centric array. American Journal of Human Genetics. 89: 688-700. PMID 22100073 DOI: 10.1016/J.Ajhg.2011.10.013 |
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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, ... ... Franke L, 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 |
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Sampietro ML, Trompet S, Verschuren JJ, Talens RP, Deelen J, Heijmans BT, de Winter RJ, Tio RA, Doevendans PA, Ganesh SK, Nabel EG, Westra HJ, Franke L, van den Akker EB, Westendorp RG, et al. A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention. Human Molecular Genetics. 20: 4748-57. PMID 21878436 DOI: 10.1093/Hmg/Ddr389 |
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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, ... ... Franke L, 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 |
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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, et al. Wnt signaling and Dupuytren's disease. The New England Journal of Medicine. 365: 307-17. PMID 21732829 DOI: 10.1056/Nejmoa1101029 |
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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 |
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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 |
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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, 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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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, 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 |
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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 |
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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 |
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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, ... ... Franke L, 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 |
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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 |
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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, ... ... Franke L, 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 |
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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, 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 |
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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, ... ... Franke L, 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 |
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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 |
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Martín JE, Alizadeh BZ, González-Gay MA, Balsa A, Pascual-Salcedo D, Fernández-Gutiérrez B, Raya E, Franke L, van't Slot R, Coenen MJ, van Riel P, Radstake TR, Koeleman BP, Martín J. Identification of the oxidative stress-related gene MSRA as a rheumatoid arthritis susceptibility locus by genome-wide pathway analysis. Arthritis and Rheumatism. 62: 3183-90. PMID 20617525 DOI: 10.1002/Art.27648 |
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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 |
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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, 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 |
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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, et al. Multiple common variants for celiac disease influencing immune gene expression. Nature Genetics. 42: 295-302. PMID 20190752 DOI: 10.1038/Ng.543 |
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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 |
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Heap GA, Yang JH, Downes K, Healy BC, Hunt KA, Bockett N, Franke L, Dubois PC, Mein CA, Dobson RJ, Albert TJ, Rodesch MJ, Clayton DG, Todd JA, van Heel DA, et al. Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing. Human Molecular Genetics. 19: 122-34. PMID 19825846 DOI: 10.1093/Hmg/Ddp473 |
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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, ... ... Franke L, et al. Posters * Reproductive Genetics (PGD/PGS) Human Reproduction. 25: i321-i332. DOI: 10.1093/humrep/de.25.s1.534 |
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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, et al. Erratum: Corrigendum: Multiple common variants for celiac disease influencing immune gene expression Nature Genetics. 42: 465-465. DOI: 10.1038/Ng0510-465 |
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Franke L, Jansen RC. eQTL analysis in humans. Methods in Molecular Biology (Clifton, N.J.). 573: 311-28. PMID 19763935 DOI: 10.1007/978-1-60761-247-6_17 |
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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 |
0.652 |
|
| 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, 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 |
0.638 |
|
| 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, 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 |
0.668 |
|
| 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 |
0.666 |
|
| 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 |
0.767 |
|
| 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 |
0.582 |
|
| 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 |
0.661 |
|
| 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 |
0.68 |
|
| 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 |
0.617 |
|
| 2008 |
Blauw HM, Veldink JH, van Es MA, van Vught PW, Saris CG, van der Zwaag B, Franke L, Burbach JP, Wokke JH, Ophoff RA, van den Berg LH. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen. The Lancet. Neurology. 7: 319-26. PMID 18313986 DOI: 10.1016/S1474-4422(08)70048-6 |
0.428 |
|
| 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, 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 |
0.662 |
|
| 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 |
0.643 |
|
| 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, 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 |
0.658 |
|
| 2007 |
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 |
0.608 |
|
| 2007 |
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, 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 |
0.615 |
|
| 2007 |
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, 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 |
0.616 |
|
| 2007 |
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 |
0.62 |
|
| 2007 |
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 |
0.583 |
|
| 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 |
0.631 |
|
| 2006 |
Vorstman JAS, Staal WG, Van Daalen E, Van Engeland H, Hochstenbach PFR, Franke L. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism Molecular Psychiatry. 11: 18-28. PMID 16205736 DOI: 10.1038/Sj.Mp.4001781 |
0.34 |
|
| 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 |
0.568 |
|
| 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 |
0.506 |
|
| 2006 |
Vorstman JAS, Staal WG, Daalen Ev, Engeland Hv, Hochstenbach PFR, Franke L. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism Molecular Psychiatry. 11: 18-28. DOI: 10.1038/Sj.Mp.4001757 |
0.304 |
|
| 2006 |
Staal W, Franke L, Vorstman JAS, Hochstenbach R, Engeland HV. S.07.05 Autism candidate genes in cytogenetic regions of interest identified with a gene interaction network European Neuropsychopharmacology. 16. DOI: 10.1016/S0924-977X(06)70048-7 |
0.313 |
|
| 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, 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 |
0.634 |
|
| 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 |
0.652 |
|
| 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 |
0.556 |
|
| 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 |
0.568 |
|
| 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 |
0.614 |
|
| 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 |
0.657 |
|
| 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 |
0.57 |
|
| 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 |
0.613 |
|
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