Следене
Tom Gaunt
Tom Gaunt
MRC Integrative Epidemiology Unit, University of Bristol
Потвърден имейл адрес: bristol.ac.uk - Начална страница
Заглавие
Позовавания
Позовавания
Година
The MR-Base platform supports systematic causal inference across the human phenome
G Hemani, J Zheng, B Elsworth, KH Wade, V Haberland, D Baird, ...
elife 7, 2018
20352018
Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies
S Rodriguez, TR Gaunt, INM Day
American journal of epidemiology 169 (4), 505-514, 2009
12942009
Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models
HA Shihab, J Gough, DN Cooper, PD Stenson, GLA Barker, KJ Edwards, ...
Human mutation 34 (1), 57-65, 2013
10342013
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic …
J Zheng, AM Erzurumluoglu, BL Elsworth, JP Kemp, L Howe, PC Haycock, ...
Bioinformatics 33 (2), 272-279, 2017
7912017
DNA methylation in newborns and maternal smoking in pregnancy: genome-wide consortium meta-analysis
BR Joubert, JF Felix, P Yousefi, KM Bakulski, AC Just, C Breton, ...
The American Journal of Human Genetics 98 (4), 680-696, 2016
7002016
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
MV Holmes, CE Dale, L Zuccolo, RJ Silverwood, Y Guo, Z Ye, ...
Bmj 349, g4164, 2014
6842014
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
S Wahl, A Drong, B Lehne, M Loh, WR Scott, S Kunze, PC Tsai, JS Ried, ...
Nature 541 (7635), 81-86, 2017
6752017
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials
DI Swerdlow, D Preiss, KB Kuchenbaecker, MV Holmes, JEL Engmann, ...
The Lancet 385 (9965), 351-361, 2015
6402015
Mendelian randomization of blood lipids for coronary heart disease
MV Holmes, FW Asselbergs, TM Palmer, F Drenos, MB Lanktree, ...
European heart journal 36 (9), 539-550, 2015
6272015
Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts
P Würtz, AS Havulinna, P Soininen, T Tynkkynen, D Prieto-Merino, T Tillin, ...
Circulation 131 (9), 774-785, 2015
5262015
An integrative approach to predicting the functional effects of non-coding and coding sequence variation
HA Shihab, MF Rogers, J Gough, M Mort, DN Cooper, INM Day, TR Gaunt, ...
Bioinformatics 31 (10), 1536-1543, 2015
5192015
Systematic identification of genetic influences on methylation across the human life course
TR Gaunt, HA Shihab, G Hemani, JL Min, G Woodward, O Lyttleton, ...
Genome biology 17 (1), 1-14, 2016
4692016
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies
Nature 478 (7367), 103, 2011
4262011
C-reactive protein and its role in metabolic syndrome: mendelian randomisation study
NJ Timpson, DA Lawlor, RM Harbord, TR Gaunt, INM Day, LJ Palmer, ...
The Lancet 366 (9501), 1954-1959, 2005
4162005
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7 (1), 1-19, 2016
3972016
Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study
JC Chambers, M Loh, B Lehne, A Drong, J Kriebel, V Motta, S Wahl, ...
The lancet Diabetes & endocrinology 3 (7), 526-534, 2015
3722015
Association between telomere length and risk of cancer and non-neoplastic diseases: a Mendelian randomization study
PC Haycock, S Burgess, A Nounu, J Zheng, GN Okoli, J Bowden, ...
JAMA oncology 3 (5), 636-651, 2017
3562017
Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC)
RC Richmond, AJ Simpkin, G Woodward, TR Gaunt, O Lyttleton, ...
Human molecular genetics 24 (8), 2201-2217, 2015
3492015
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 1-9, 2015
3482015
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci
FW Asselbergs, Y Guo, EPA Van Iperen, S Sivapalaratnam, V Tragante, ...
The American Journal of Human Genetics 91 (5), 823-838, 2012
3022012
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