| Year |
Citation |
Score |
| 2024 |
McDonagh EM, Trynka G, McCarthy M, Holzinger ER, Khader S, Nakic N, Hu X, Cornu H, Dunham I, Hulcoop D. Human Genetics and Genomics for Drug Target Identification and Prioritization: Open Targets' Perspective. Annual Review of Biomedical Data Science. PMID 38608311 DOI: 10.1146/annurev-biodatasci-102523-103838 |
0.626 |
|
| 2022 |
Soskic B, Cano-Gamez E, Smyth DJ, Ambridge K, Ke Z, Matte JC, Bossini-Castillo L, Kaplanis J, Ramirez-Navarro L, Lorenc A, Nakic N, Esparza-Gordillo J, Rowan W, Wille D, Tough DF, ... ... Trynka G, et al. Immune disease risk variants regulate gene expression dynamics during CD4 T cell activation. Nature Genetics. PMID 35618845 DOI: 10.1038/s41588-022-01066-3 |
0.371 |
|
| 2022 |
Bossini-Castillo L, Glinos DA, Kunowska N, Golda G, Lamikanra AA, Spitzer M, Soskic B, Cano-Gamez E, Smyth DJ, Cattermole C, Alasoo K, Mann A, Kundu K, Lorenc A, Soranzo N, ... ... Trynka G, et al. Immune disease variants modulate gene expression in regulatory CD4 T cells. Cell Genomics. 2: None. PMID 35591976 DOI: 10.1016/j.xgen.2022.100117 |
0.399 |
|
| 2020 |
Nasrallah R, Imianowski CJ, Bossini-Castillo L, Grant FM, Dogan M, Placek L, Kozhaya L, Kuo P, Sadiyah F, Whiteside SK, Mumbach MR, Glinos D, Vardaka P, Whyte CE, Lozano T, ... ... Trynka G, et al. A distal enhancer at risk locus 11q13.5 promotes suppression of colitis by T cells. Nature. PMID 32499651 DOI: 10.1038/S41586-020-2296-7 |
0.477 |
|
| 2020 |
Cano-Gamez E, Trynka G. From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases. Frontiers in Genetics. 11: 424. PMID 32477401 DOI: 10.3389/Fgene.2020.00424 |
0.583 |
|
| 2020 |
Cano-Gamez E, Soskic B, Roumeliotis TI, So E, Smyth DJ, Baldrighi M, Willé D, Nakic N, Esparza-Gordillo J, Larminie CGC, Bronson PG, Tough DF, Rowan WC, Choudhary JS, Trynka G. Single-cell transcriptomics identifies an effectorness gradient shaping the response of CD4 T cells to cytokines. Nature Communications. 11: 1801. PMID 32286271 DOI: 10.1038/S41467-020-15543-Y |
0.301 |
|
| 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, et al. The single-cell eQTLGen consortium. Elife. 9. PMID 32149610 DOI: 10.7554/Elife.52155 |
0.496 |
|
| 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, 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 |
0.538 |
|
| 2019 |
Soskic B, Cano-Gamez E, Smyth DJ, Rowan WC, Nakic N, Esparza-Gordillo J, Bossini-Castillo L, Tough DF, Larminie CGC, Bronson PG, Willé D, Trynka G. Chromatin activity at GWAS loci identifies T cell states driving complex immune diseases. Nature Genetics. PMID 31548716 DOI: 10.1038/S41588-019-0493-9 |
0.421 |
|
| 2018 |
Simovski B, Kanduri C, Gundersen S, Titov D, Domanska D, Bock C, Bossini-Castillo L, Chikina M, Favorov A, Layer RM, Mironov AA, Quinlan AR, Sheffield NC, Trynka G, Sandve GK. Coloc-stats: a unified web interface to perform colocalization analysis of genomic features. Nucleic Acids Research. PMID 29873782 DOI: 10.1093/Nar/Gky474 |
0.32 |
|
| 2017 |
Trynka G. Enhancers looping to target genes. Nature Genetics. 49: 1564-1565. PMID 29074944 DOI: 10.1038/Ng.3982 |
0.413 |
|
| 2017 |
Glinos DA, Soskic B, Trynka G. Immunogenomic approaches to understand the function of immune disease variants. Immunology. 152: 527-535. PMID 28718505 DOI: 10.1111/Imm.12796 |
0.563 |
|
| 2017 |
Huang H, Fang M, Jostins L, Umićević Mirkov M, Boucher G, Anderson CA, Andersen V, Cleynen I, Cortes A, Crins F, D'Amato M, Deffontaine V, Dmitrieva J, Docampo E, Elansary M, ... ... Trynka G, et al. Fine-mapping inflammatory bowel disease loci to single-variant resolution. Nature. PMID 28658209 DOI: 10.1038/Nature22969 |
0.635 |
|
| 2017 |
Wain LV, Shrine N, Artigas MS, Erzurumluoglu AM, Noyvert B, Bossini-Castillo L, Obeidat M, Henry AP, Portelli MA, Hall RJ, Billington CK, Rimington TL, Fenech AG, John C, Blake T, ... ... Trynka G, et al. Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nature Genetics. PMID 28166213 DOI: 10.1038/Ng.3787 |
0.433 |
|
| 2016 |
Gusev A, Shi H, Kichaev G, Pomerantz M, Li F, Long HW, Ingles SA, Kittles RA, Strom SS, Rybicki BA, Nemesure B, Isaacs WB, Zheng W, Pettaway CA, Yeboah ED, ... ... Trynka G, et al. Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation. Nature Communications. 7: 10979. PMID 27052111 DOI: 10.1038/Ncomms10979 |
0.6 |
|
| 2015 |
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 |
0.684 |
|
| 2015 |
Hayes JE, Trynka G, Vijai J, Offit K, Raychaudhuri S, Klein RJ. Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements. Plos One. 10: e0139360. PMID 26422229 DOI: 10.1371/Journal.Pone.0139360 |
0.629 |
|
| 2015 |
Finucane HK, Bulik-Sullivan B, Gusev A, Trynka G, Reshef Y, Loh PR, Anttila V, Xu H, Zang C, Farh K, Ripke S, Day FR, et al. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nature Genetics. PMID 26414678 DOI: 10.1038/Ng.3404 |
0.681 |
|
| 2015 |
Gutierrez-Achury J, Romanos J, Bakker SF, Kumar V, de Haas EC, Trynka G, Ricaño-Ponce I, Steck A, Chen WM, Onengut-Gumuscu S, Simsek S, Rewers M, Mulder CJ, et al. Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity. Diabetes Care. 38: S37-44. PMID 26405070 DOI: 10.2337/Dcs15-2007 |
0.536 |
|
| 2015 |
Trynka G, Westra HJ, Slowikowski K, Hu X, Xu H, Stranger BE, Klein RJ, Han B, Raychaudhuri S. Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci. American Journal of Human Genetics. 97: 139-52. PMID 26140449 DOI: 10.1016/J.Ajhg.2015.05.016 |
0.772 |
|
| 2015 |
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, 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 |
0.56 |
|
| 2015 |
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, 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 |
0.518 |
|
| 2015 |
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 |
0.646 |
|
| 2015 |
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, ... ... Trynka G, 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 |
0.51 |
|
| 2015 |
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 |
0.521 |
|
| 2015 |
Hayes JE, Trynka G, Vijai J, Offit K, Raychaudhuri S, Klein RJ. Overlap of lymphoma risk SNPs with regulatory regions in GM12878. Plos One. DOI: 10.1371/Journal.Pone.0139360.G002 |
0.57 |
|
| 2014 |
Gusev A, Lee SH, Trynka G, Finucane H, Vilhjálmsson BJ, Xu H, Zang C, Ripke S, Bulik-Sullivan B, Stahl E, Kähler AK, Hultman CM, Purcell SM, et al. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. American Journal of Human Genetics. 95: 535-52. PMID 25439723 DOI: 10.1016/J.Ajhg.2014.10.004 |
0.729 |
|
| 2014 |
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, 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 |
0.663 |
|
| 2014 |
Hu X, Kim H, Raj T, Brennan PJ, Trynka G, Teslovich N, Slowikowski K, Chen WM, Onengut S, Baecher-Allan C, De Jager PL, Rich SS, Stranger BE, Brenner MB, Raychaudhuri S. Regulation of gene expression in autoimmune disease loci and the genetic basis of proliferation in CD4+ effector memory T cells. Plos Genetics. 10: e1004404. PMID 24968232 DOI: 10.1371/Journal.Pgen.1004404 |
0.798 |
|
| 2014 |
Okada Y, Diogo D, Greenberg JD, Mouassess F, Achkar WA, Fulton RS, Denny JC, Gupta N, Mirel D, Gabriel S, Li G, Kremer JM, Pappas DA, Carroll RJ, Eyler AE, ... Trynka G, et al. Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. Plos One. 9: e87645. PMID 24520335 DOI: 10.1371/Journal.Pone.0087645 |
0.639 |
|
| 2014 |
Okada Y, Wu D, Trynka G, Raj T, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Yoshida S, Graham RR, Manoharan A, Ortmann W, Bhangale T, Denny JC, et al. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature. 506: 376-81. PMID 24390342 DOI: 10.1038/Nature12873 |
0.751 |
|
| 2014 |
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, 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 |
0.747 |
|
| 2014 |
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 |
0.498 |
|
| 2014 |
de Rooy DP, Zhernakova A, Tsonaka R, Willemze A, Kurreeman BA, Trynka G, van Toorn L, Toes RE, Huizinga TW, Houwing-Duistermaat JJ, Gregersen PK, van der Helm-van Mil AH. A genetic variant in the region of MMP-9 is associated with serum levels and progression of joint damage in rheumatoid arthritis. Annals of the Rheumatic Diseases. 73: 1163-9. PMID 23696630 DOI: 10.1136/Annrheumdis-2013-203375 |
0.53 |
|
| 2013 |
Trynka G, Raychaudhuri S. Using chromatin marks to interpret and localize genetic associations to complex human traits and diseases. Current Opinion in Genetics & Development. 23: 635-41. PMID 24287333 DOI: 10.1016/J.Gde.2013.10.009 |
0.666 |
|
| 2013 |
Cui J, Stahl EA, Saevarsdottir S, Miceli C, Diogo D, Trynka G, Raj T, Mirkov MU, Canhao H, Ikari K, Terao C, Okada Y, Wedrén S, Askling J, Yamanaka H, et al. Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Plos Genetics. 9: e1003394. PMID 23555300 DOI: 10.1371/Journal.Pgen.1003394 |
0.619 |
|
| 2013 |
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, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Plos Genetics. 9: e1003270. PMID 23459209 DOI: 10.1371/Journal.Pgen.1003270 |
0.513 |
|
| 2013 |
Trynka G, Sandor C, Han B, Xu H, Stranger BE, Liu XS, Raychaudhuri S. Chromatin marks identify critical cell types for fine mapping complex trait variants Nature Genetics. 45: 124-130. PMID 23263488 DOI: 10.1038/Ng.2504 |
0.637 |
|
| 2012 |
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, ... Trynka G, 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 |
0.805 |
|
| 2012 |
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, ... ... Trynka G, 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 |
0.486 |
|
| 2012 |
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 |
0.689 |
|
| 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, ... ... Trynka G, 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 |
0.493 |
|
| 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, 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 |
0.594 |
|
| 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, ... ... Trynka G, 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 |
0.736 |
|
| 2011 |
Sperandeo MP, Tosco A, Izzo V, Tucci F, Troncone R, Auricchio R, Romanos J, Trynka G, Auricchio S, Jabri B, Greco L. Potential celiac patients: a model of celiac disease pathogenesis. Plos One. 6: e21281. PMID 21760890 DOI: 10.1371/Journal.Pone.0021281 |
0.441 |
|
| 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 |
0.677 |
|
| 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, 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 |
0.789 |
|
| 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, 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 |
0.617 |
|
| 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 |
0.526 |
|
| 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, 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 |
0.465 |
|
| 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, et al. Multiple common variants for celiac disease influencing immune gene expression. Nature Genetics. 42: 295-302. PMID 20190752 DOI: 10.1038/Ng.543 |
0.595 |
|
| 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, et al. Erratum: Corrigendum: Multiple common variants for celiac disease influencing immune gene expression Nature Genetics. 42: 465-465. DOI: 10.1038/Ng0510-465 |
0.41 |
|
| 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, 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 |
0.621 |
|
| 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 |
0.361 |
|
| 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, 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 |
0.479 |
|
| 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 |
0.492 |
|
| 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 |
0.589 |
|
| 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 |
0.574 |
|
| 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 |
0.326 |
|
| 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 |
0.37 |
|
| 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 |
0.545 |
|
| 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 |
0.477 |
|
| 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, ... ... Trynka G, 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 |
0.54 |
|
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