Gibran Hemani

发表

Recent Developments in Mendelian Randomization Studies

George Davey Smith, Jack Bowden, Jie Zheng, 2017, Current Epidemiology Reports.

The MRC IEU OpenGWAS data infrastructure

Valeriia Haberland, Peter Matthews, Tom R. Gaunt, 2020, bioRxiv.

EpiGraphDB: a database and data mining platform for health data science.

Valeriia Haberland, Jie Zheng, Yi Liu, 2020, Bioinformatics.

The MR-Base platform supports systematic causal inference across the human phenome

Valeriia Haberland, Jack Bowden, Tom R. Gaunt, 2018, eLife.

EpiGraphDB: a database and data mining platform for health data science

Valeriia Haberland, Tom R. Gaunt, Jie Zheng, 2020, bioRxiv.

Orienting the causal relationship between imprecisely measured traits using genetic instruments

George Davey Smith, Kate Tilling, Gibran Hemani, 2017, bioRxiv.

The variant call format provides efficient and robust storage of GWAS summary statistics

Tom R. Gaunt, Tom R Gaunt, Gibran Hemani, 2020, Genome Biology.

EpiGPU: exhaustive pairwise epistasis scans parallelized on consumer level graphics cards

Chris S. Haley, Wenhua Wei, Gibran Hemani, 2011, Bioinform..

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

Archie Campbell, Peter M Visscher, Gibran Hemani, 2020, Nature Communications.

Detection and replication of epistasis influencing transcription in humans

Joseph E. Powell, Andres Metspalu, Peter M. Visscher, 2014, Nature.

Using the MR-Base platform to investigate risk factors and drug targets for thousands of phenotypes

Neil M Davies, Tom R. Gaunt, Jie Zheng, 2019, Wellcome open research.

Invited Commentary Invited Commentary: Detecting Individual andGlobal Horizontal Pleiotropy in Mendelian Randomization—A Job for the Humble Heterogeneity Statistic?

Jack Bowden, Gibran Hemani, George Davey Smith, 2018 .

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 correlation analysis

Tom R. Gaunt, Jie Zheng, Alkes L. Price, 2016, bioRxiv.

Erratum to: EpiGraphDB: a database and data mining platform for health data science

Valeriia Haberland, Jie Zheng, Yi Liu, 2021, Bioinform..

Modelling pooling strategies for SARS-CoV-2 testing in a university setting

Ellen Brooks-Pollock, Gibran Hemani, Leon Danon, 2021 .

Improved heritability estimation from genome-wide SNPs.

Doug Speed, David J Balding, Gibran Hemani, 2012, American journal of human genetics.

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

Valeriia Haberland, Stephen Burgess, Jie Zheng, 2020, Nature genetics.

Novel Risk Loci for Rheumatoid Arthritis in Han Chinese and Congruence With Risk Variants in Europeans

Yi Wang, Tao Yue, Mengtao Li, 2014, Arthritis & rheumatology.

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 correlation analysis

Tom R. Gaunt, Jie Zheng, Alkes L. Price, 2016 .

MRC IEU UK Biobank GWAS pipeline version 1

Tom R. Gaunt, Gibran Hemani, Benjamin Elsworth, 2017 .

Directional dominance on stature and cognition in diverse human populations

Laura J. Scott, Claude Bouchard, Christian Gieger, 2015, Nature.

Population phenomena inflate genetic associations of complex social traits

Neil M Davies, Gibran Hemani, George Davey Smith, 2019, Science Advances.

Causal epigenome-wide association study identifies CpG sites that influence cardiovascular disease risk

Tom R. Gaunt, Jie Zheng, N J Timpson, 2017, bioRxiv.

LD hub and MR-base: online platforms for preforming LD score regression and Mendelian randomization analysis using GWAS summary data

Tom R. Gaunt, Jie Zheng, Alkes L. Price, 2016 .

Shared genetic control of expression and methylation in peripheral blood

Joseph E. Powell, Peter M. Visscher, Nicholas G. Martin, 2016, BMC Genomics.

Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples

Naomi R. Wray, Sang Hong Lee, Peter M. Visscher, 2014, PLoS genetics.

Genome-wide genetic homogeneity between sexes and populations for human height and body mass index.

Andres Metspalu, Reedik Mägi, Jian Yang, 2015, Human molecular genetics.

Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk

Tom R. Gaunt, Jie Zheng, Nicholas J Timpson, 2017, American journal of human genetics.

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

Mark R. Hurle, Valeriia Haberland, Tom R. Gaunt, 2019, bioRxiv.

Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates

Chris S. Haley, Sara A. Knott, Igor Rudan, 2011, PloS one.

Contribution of genetic variation to transgenerational inheritance of DNA methylation

Nicholas G Martin, Peter M Visscher, Gibran Hemani, 2014, Genome Biology.

Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease

Tom R. Gaunt, Jie Zheng, Nicholas J Timpson, 2018, Human molecular genetics.

Congruence of Additive and Non-Additive Effects on Gene Expression Estimated from Pedigree and SNP Data

Joseph E. Powell, Peter M. Visscher, Emmanouil T. Dermitzakis, 2013, PLoS genetics.

Detecting epistasis in human complex traits

Chris S. Haley, Gibran Hemani, C. Haley, 2014, Nature Reviews Genetics.