| SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap AD Johnson, RE Handsaker, SL Pulit, MM Nizzari, CJ O'Donnell, ... Bioinformatics 24 (24), 2938-2939, 2008 | 1497 | 2008 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1360 | 2018 |
| Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ... Nature genetics 50 (4), 524-537, 2018 | 1232 | 2018 |
| The major genetic determinants of HIV-1 control affect HLA class I peptide presentation International HIV Controllers Study Science 330 (6010), 1551-1557, 2010 | 1109 | 2010 |
| Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry SL Pulit, C Stoneman, AP Morris, AR Wood, CA Glastonbury, J Tyrrell, ... Human molecular genetics 28 (1), 166-174, 2019 | 847 | 2019 |
| Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014 | 706 | 2014 |
| Multi-ethnic genome-wide association study for atrial fibrillation C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ... Nature genetics 50 (9), 1225-1233, 2018 | 603 | 2018 |
| Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nature genetics 48 (9), 1043-1048, 2016 | 588 | 2016 |
| Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1268-1283. e6, 2018 | 576 | 2018 |
| HLA-B*13:01 and the Dapsone Hypersensitivity Syndrome FR Zhang, H Liu, A Irwanto, XA Fu, Y Li, GQ Yu, YX Yu, MF Chen, HQ Low, ... New England Journal of Medicine 369 (17), 1620-1628, 2013 | 342 | 2013 |
| The Genome of the Netherlands: design, and project goals DI Boomsma, C Wijmenga, EP Slagboom, MA Swertz, LC Karssen, ... European journal of human genetics 22 (2), 221-227, 2014 | 323 | 2014 |
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ... Nature genetics 46 (8), 826-836, 2014 | 319 | 2014 |
| GWAS identifies 14 loci for device-measured physical activity and sleep duration A Doherty, K Smith-Byrne, T Ferreira, MV Holmes, C Holmes, SL Pulit, ... Nature communications 9 (1), 5257, 2018 | 304 | 2018 |
| Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1 A Cortes, SL Pulit, PJ Leo, JJ Pointon, PC Robinson, MH Weisman, ... Nature communications 6 (1), 7146, 2015 | 267 | 2015 |
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014 | 236 | 2014 |
| Association of Granulomatosis With Polyangiitis (Wegener's) With HLA–DPB1*04 and SEMA6A Gene Variants: Evidence From Genome‐Wide Analysis G Xie, D Roshandel, R Sherva, PA Monach, EY Lu, T Kung, K Carrington, ... Arthritis & Rheumatism 65 (9), 2457-2468, 2013 | 197 | 2013 |
| Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease J Gutierrez-Achury, A Zhernakova, SL Pulit, G Trynka, KA Hunt, ... Nature genetics 47 (6), 577-578, 2015 | 181 | 2015 |
| Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study SL Pulit, PF McArdle, Q Wong, R Malik, K Gwinn, S Achterberg, A Algra, ... The Lancet Neurology 15 (2), 174-184, 2016 | 170 | 2016 |
| Stroke genetics: discovery, biology, and clinical applications M Dichgans, SL Pulit, J Rosand The Lancet Neurology 18 (6), 587-599, 2019 | 161 | 2019 |
| Low-frequency and common genetic variation in ischemic stroke: the METASTROKE collaboration R Malik, M Traylor, SL Pulit, S Bevan, JC Hopewell, EG Holliday, W Zhao, ... Neurology 86 (13), 1217-1226, 2016 | 158 | 2016 |
Paul I W de BakkerVertex PharmaceuticalsVerified email at vrtx.com
