WILLIAM NEWMAN
WILLIAM NEWMAN
Professor of Translational Genomic Medicine, University of Manchester
Verified email at manchester.ac.uk - Homepage
Title
Cited by
Cited by
Year
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
36772012
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
25622010
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
13762011
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
12532015
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
8232010
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
4872009
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
4602012
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
4442017
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
3062007
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
2861993
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
2672019
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
2102015
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
1982013
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
1862014
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
1722008
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
1692014
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
1632013
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
1532013
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
1482008
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