|Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls|
Wellcome Trust Case Control Consortium
Nature 447 (7145), 661, 2007
|Genome-wide association study identifies eight loci associated with blood pressure|
C Newton-Cheh, T Johnson, V Gateva, MD Tobin, M Bochud, L Coin, ...
Nature genetics 41 (6), 666, 2009
|Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants|
PR Burton, DG Clayton, LR Cardon, N Craddock, P Deloukas, ...
Nature genetics 39 (11), 1329, 2007
|Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A|
S Nejentsev, JMM Howson, NM Walker, J Szeszko, SF Field, HE Stevens, ...
Nature 450 (7171), 887, 2007
|Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia|
C Wallace, SJ Newhouse, P Braund, F Zhang, M Tobin, M Falchi, ...
The American Journal of Human Genetics 82 (1), 139-149, 2008
|SLC2A9 is a high-capacity urate transporter in humans|
MJ Caulfield, PB Munroe, D O'Neill, K Witkowska, FJ Charchar, ...
PLoS medicine 5 (10), e197, 2008
|Genome-wide mapping of human loci for essential hypertension|
M Caulfield, P Munroe, J Pembroke, N Samani, A Dominiczak, M Brown, ...
The Lancet 361 (9375), 2118-2123, 2003
|Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci|
R Saxena, CC Elbers, Y Guo, I Peter, TR Gaunt, JL Mega, MB Lanktree, ...
The American Journal of Human Genetics 90 (3), 410-425, 2012
|Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci|
FW Asselbergs, Y Guo, S Sivapalaratnam, V Tragante, MB Lanktree, ...
The American Journal of Human Genetics 91 (5), 823-838, 2012
|Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study|
A Shatunov, K Mok, S Newhouse, ME Weale, B Smith, C Vance, ...
The Lancet Neurology 9 (10), 986-994, 2010
|Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations|
E Org, S Eyheramendy, P Juhanson, C Gieger, P Lichtner, N Klopp, ...
Human molecular genetics 18 (12), 2288-2296, 2009
|Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways|
T Network, C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, ...
Nature neuroscience 18 (2), 199, 2015
|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, 2014
|Blood pressure loci identified with a gene-centric array|
T Johnson, TR Gaunt, SJ Newhouse, S Padmanabhan, M Tomaszewski, ...
The American Journal of Human Genetics 89 (6), 688-700, 2011
|The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder|
BN Smith, S Newhouse, A Shatunov, C Vance, S Topp, L Johnson, ...
European Journal of Human Genetics 21 (1), 102, 2013
|Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip|
PJ Talmud, F Drenos, S Shah, T Shah, J Palmen, C Verzilli, TR Gaunt, ...
The American journal of human genetics 85 (5), 628-642, 2009
|Microarray, qPCR, and KCNJ5 Sequencing of Aldosterone-Producing Adenomas Reveal Differences in Genotype and Phenotype between Zona Glomerulosa- and …|
EAB Azizan, BYH Lam, SJ Newhouse, J Zhou, RE Kuc, J Clarke, ...
The Journal of Clinical Endocrinology 97 (5), E819-E829, 2012
|Association of WNK1 Gene Polymorphisms and Haplotypes With Ambulatory Blood Pressure in the General Population|
MD Tobin, SM Raleigh, S Newhouse, P Braund, C Bodycote, J Ogleby, ...
Circulation 112 (22), 3423-3429, 2005
|Candidate blood proteome markers of Alzheimer's disease onset and progression: a systematic review and replication study|
SJ Kiddle, M Sattlecker, P Proitsi, A Simmons, E Westman, C Bazenet, ...
Journal of Alzheimer's Disease 38 (3), 515-531, 2014
|Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height|
MB Lanktree, Y Guo, M Murtaza, JT Glessner, SD Bailey, ...
The American Journal of Human Genetics 88 (1), 6-18, 2011