about
Mendelian randomization: genetic anchors for causal inference in epidemiological studiesShared genetic control of expression and methylation in peripheral bloodGenome-wide association study of blood lead shows multiple associations near ALADThe association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjectsDirectional dominance on stature and cognition in diverse human populationsAssociation Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data.Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples.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.Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study.Contribution of genetic variation to transgenerational inheritance of DNA methylationEpiGPU: exhaustive pairwise epistasis scans parallelized on consumer level graphics cards.Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolatesDefining the role of common variation in the genomic and biological architecture of adult human height.Population genetic differentiation of height and body mass index across Europe.An evolutionary perspective on epistasis and the missing heritabilityGenome-wide associations for birth weight and correlations with adult diseaseGenetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index.The role of common genetic variation in educational attainment and income: evidence from the National Child Development Study.Prenatal and early life influences on epigenetic age in children: a study of mother-offspring pairs from two cohort studies.Improved heritability estimation from genome-wide SNPs.Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2.Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysisSystematic identification of genetic influences on methylation across the human life course.Collapsed methylation quantitative trait loci analysis for low frequency and rare variants.Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs.Detection and replication of epistasis influencing transcription in humans.Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.Challenges and novel approaches for investigating molecular mediation.The role of glycaemic and lipid risk factors in mediating the effect of BMI on coronary heart disease: a two-step, two-sample Mendelian randomisation study.Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood.Two-sample Mendelian randomization: avoiding the downsides of a powerful, widely applicable but potentially fallible technique.Hemani et al. reply.Response to Lee et al.: SNP-based heritability analysis with dense dataOrienting the causal relationship between imprecisely measured traits using GWAS summary data.Recent Developments in Mendelian Randomization Studies.Correction: Orienting the causal relationship between imprecisely measured traits using GWAS summary data.Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices.Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk.C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.
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description
researcher ORCID ID = 0000-0003-0920-1055
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wetenschapper
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name
Gibran Hemani
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Gibran Hemani
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Gibran Hemani
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Gibran Hemani
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label
Gibran Hemani
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Gibran Hemani
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Gibran Hemani
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Gibran Hemani
@nl
prefLabel
Gibran Hemani
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Gibran Hemani
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Gibran Hemani
@es
Gibran Hemani
@nl
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38861712000
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P496
0000-0003-0920-1055