| Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease L Jostins, S Ripke, RK Weersma, RH Duerr, DP McGovern, KY Hui, ... Nature 491 (7422), 119-124, 2012 | 3677 | 2012 |
| Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci A Franke, DPB McGovern, JC Barrett, K Wang, GL Radford-Smith, ... Nature genetics 42 (12), 1118-1125, 2010 | 2562 | 2010 |
| Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 CA Anderson, G Boucher, CW Lees, A Franke, M D'Amato, KD Taylor, ... Nature genetics 43 (3), 246-252, 2011 | 1376 | 2011 |
| Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations JZ Liu, S Van Sommeren, H Huang, SC Ng, R Alberts, A Takahashi, ... Nature genetics 47 (9), 979-986, 2015 | 1253 | 2015 |
| Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls N Craddock, ME Hurles, N Cardin, RD Pearson, V Plagnol, S Robson, ... Nature 464 (7289), 713, 2010 | 823 | 2010 |
| Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region JC Barrett, JC Lee, CW Lees, NJ Prescott, CA Anderson, A Phillips, ... Nature genetics 41 (12), 1330, 2009 | 487 | 2009 |
| International IBD Genetics Consortium (IIBDGC). Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease L Jostins, S Ripke, RK Weersma, RH Duerr, DP McGovern, KY Hui, ... Nature 491 (7422), 119-124, 2012 | 460 | 2012 |
| Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease KM De Lange, L Moutsianas, JC Lee, CA Lamb, Y Luo, NA Kennedy, ... Nature genetics 49 (2), 256-261, 2017 | 444 | 2017 |
| Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome G Rice, WG Newman, J Dean, T Patrick, R Parmar, K Flintoff, P Robins, ... The American Journal of Human Genetics 80 (4), 811-815, 2007 | 306 | 2007 |
| Expression of VCAM-1 and E-selectin in an in vivo model of endothelial activation. JW Fries, AJ Williams, RC Atkins, W Newman, MF Lipscomb, T Collins The American journal of pathology 143 (3), 725, 1993 | 286 | 1993 |
| Polygenic risk scores for prediction of breast cancer and breast cancer subtypes N Mavaddat, K Michailidou, J Dennis, M Lush, L Fachal, A Lee, JP Tyrer, ... The American Journal of Human Genetics 104 (1), 21-34, 2019 | 267 | 2019 |
| Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease N Wolf, M Quaranta, NJ Prescott, M Allen, R Smith, AD Burden, ... Journal of medical genetics 45 (2), 114-116, 2008 | 239* | 2008 |
| High-density mapping of the MHC identifies a shared role for HLA-DRB1* 01: 03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis P Goyette, G Boucher, D Mallon, E Ellinghaus, L Jostins, H Huang, ... Nature genetics 47 (2), 172-179, 2015 | 210 | 2015 |
| Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway JC Lee, M Espéli, CA Anderson, MA Linterman, JM Pocock, NJ Williams, ... Cell 155 (1), 57-69, 2013 | 198 | 2013 |
| Germline Mutations in SUFU Cause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated With PTCH1 Mutations MJ Smith, C Beetz, SG Williams, SS Bhaskar, J O'Sullivan, B Anderson, ... Journal of Clinical Oncology 32 (36), 4155-4161, 2014 | 186 | 2014 |
| Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis KD Hadfield, WG Newman, NL Bowers, A Wallace, C Bolger, A Colley, ... Journal of medical genetics 45 (6), 332-339, 2008 | 172 | 2008 |
| CYP2D6 Genotype and Adjuvant Tamoxifen: Meta‐Analysis of Heterogeneous Study Populations MA Province, MP Goetz, H Brauch, DA Flockhart, JM Hebert, R Whaley, ... Clinical Pharmacology & Therapeutics 95 (2), 216-227, 2014 | 169 | 2014 |
| Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas MJ Smith, J O'Sullivan, SS Bhaskar, KD Hadfield, G Poke, J Caird, ... Nature genetics 45 (3), 295-298, 2013 | 163 | 2013 |
| Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease EM Jenkinson, AU Rehman, T Walsh, J Clayton-Smith, K Lee, RJ Morell, ... The American Journal of Human Genetics 92 (4), 605-613, 2013 | 153 | 2013 |
| Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin HC Hennies, U Kornak, H Zhang, J Egerer, X Zhang, W Seifert, ... Nature genetics 40 (12), 1410-1412, 2008 | 148 | 2008 |
