Gibran Hemani
Gibran Hemani
Research Fellow, University of Bristol
Verified email at
TitleCited byYear
Defining the role of common variation in the genomic and biological architecture of adult human height
AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ...
Nature genetics 46 (11), 1173, 2014
Mendelian randomization: genetic anchors for causal inference in epidemiological studies
G Davey Smith, G Hemani
Human molecular genetics 23 (R1), R89-R98, 2014
Improved heritability estimation from genome-wide SNPs
D Speed, G Hemani, MR Johnson, DJ Balding
The American Journal of Human Genetics 91 (6), 1011-1021, 2012
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
J Yang, A Bakshi, Z Zhu, G Hemani, AAE Vinkhuyzen, SH Lee, ...
Nature genetics 47 (10), 1114, 2015
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
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, e34408, 2018
Detecting epistasis in human complex traits
WH Wei, G Hemani, CS Haley
Nature Reviews Genetics 15 (11), 722-733, 2014
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), 61, 2016
Statistical power to detect genetic (co) variance of complex traits using SNP data in unrelated samples
PM Visscher, G Hemani, AAE Vinkhuyzen, GB Chen, SH Lee, NR Wray, ...
PLoS genetics 10 (4), e1004269, 2014
Genome-wide associations for birth weight and correlations with adult disease
M Horikoshi, RN Beaumont, FR Day, NM Warrington, MN Kooijman, ...
Nature 538 (7624), 248, 2016
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
Detection and replication of epistasis influencing transcription in humans
G Hemani, K Shakhbazov, HJ Westra, T Esko, AK Henders, AF McRae, ...
Nature 508 (7495), 249, 2014
Contribution of genetic variation to transgenerational inheritance of DNA methylation
AF McRae, JE Powell, AK Henders, L Bowdler, G Hemani, S Shah, ...
Genome biology 15 (5), R73, 2014
Population genetic differentiation of height and body mass index across Europe
MR Robinson, G Hemani, C Medina-Gomez, M Mezzavilla, T Esko, ...
Nature genetics 47 (11), 1357, 2015
An evolutionary perspective on epistasis and the missing heritability
G Hemani, S Knott, C Haley
PLoS genetics 9 (2), e1003295, 2013
Dominance genetic variation contributes little to the missing heritability for human complex traits
Z Zhu, A Bakshi, AAE Vinkhuyzen, G Hemani, SH Lee, IM Nolte, ...
The American Journal of Human Genetics 96 (3), 377-385, 2015
Directional dominance on stature and cognition in diverse human populations
PK Joshi, T Esko, H Mattsson, N Eklund, I Gandin, T Nutile, AU Jackson, ...
Nature 523 (7561), 459, 2015
EpiGPU: exhaustive pairwise epistasis scans parallelized on consumer level graphics cards
G Hemani, A Theocharidis, W Wei, C Haley
Bioinformatics 27 (11), 1462-1465, 2011
Two-sample Mendelian randomization: avoiding the downsides of a powerful, widely applicable but potentially fallible technique
FP Hartwig, NM Davies, G Hemani, G Davey Smith
International journal of epidemiology 45 (6), 1717-1726, 2016
Orienting the causal relationship between imprecisely measured traits using GWAS summary data
G Hemani, K Tilling, GD Smith
PLoS genetics 13 (11), e1007081, 2017
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