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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ... Nature genetics 43 (12), 1193-1201, 2011 | 940 | 2011 |
Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014 | 710 | 2014 |
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ... PLoS genetics 6 (2), e1000841, 2010 | 458 | 2010 |
Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA RSN Fehrmann, RC Jansen, JH Veldink, HJ Westra, D Arends, ... PLoS genetics 7 (8), e1002197, 2011 | 434 | 2011 |
Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-κB signalling G Trynka, A Zhernakova, J Romanos, L Franke, KA Hunt, G Turner, ... Gut 58 (8), 1078-1083, 2009 | 243 | 2009 |
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Common and different genetic background for rheumatoid arthritis and coeliac disease MJH Coenen, G Trynka, S Heskamp, B Franke, CC van Diemen, ... Human molecular genetics 18 (21), 4195-4203, 2009 | 179 | 2009 |
Cell specific eQTL analysis without sorting cells HJ Westra, D Arends, T Esko, MJ Peters, C Schurmann, K Schramm, ... PLoS genetics 11 (5), e1005223, 2015 | 137 | 2015 |
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A high-quality human reference panel reveals the complexity and distribution of genomic structural variants JY Hehir-Kwa, T Marschall, WP Kloosterman, LC Francioli, JA Baaijens, ... Nature communications 7 (1), 1-10, 2016 | 104 | 2016 |
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Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels EM Van Leeuwen, LC Karssen, J Deelen, A Isaacs, C Medina-Gomez, ... Nature communications 6 (1), 6065, 2015 | 51 | 2015 |
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly A Kim, C Savary, C Dubourg, W Carré, C Mouden, H Hamdi-Roze, ... Brain 142 (1), 35-49, 2019 | 47 | 2019 |
PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype–phenotype associations MK Ten Kate, M Platteel, R Mulder, P Terpstra, GAF Nicolaes, PH Reitsma, ... Human mutation 29 (7), 939-947, 2008 | 41 | 2008 |
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Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease I Ricaño-Ponce, J Gutierrez-Achury, AF Costa, P Deelen, A Kurilshikov, ... European Journal of Human Genetics 28 (3), 313-323, 2020 | 30 | 2020 |
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