Gibran Hemani
#157,413
Most Influential Person Now
Researcher ORCID ID = 0000-0003-0920-1055
Gibran Hemani's AcademicInfluence.com Rankings
Gibran Hemanibiology Degrees
Biology
#12206
World Rank
#15667
Historical Rank
Bioinformatics
#146
World Rank
#148
Historical Rank
Biotechnology
#214
World Rank
#216
Historical Rank
Computational Biology
#265
World Rank
#266
Historical Rank
Download Badge
Biology
Gibran Hemani's Degrees
- PhD Genetics University of Oxford
- Bachelors Biotechnology University of Oxford
Why Is Gibran Hemani Influential?
(Suggest an Edit or Addition)Gibran Hemani's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- The MR-Base platform supports systematic causal inference across the human phenome (2018) (2168)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
- Mendelian randomization: genetic anchors for causal inference in epidemiological studies (2014) (1609)
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2018) (1090)
- 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 (2016) (775)
- Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index (2015) (666)
- Improved heritability estimation from genome-wide SNPs. (2012) (612)
- Orienting the causal relationship between imprecisely measured traits using GWAS summary data (2017) (536)
- Evaluating the potential role of pleiotropy in Mendelian randomization studies (2018) (530)
- Collider bias undermines our understanding of COVID-19 disease risk and severity (2020) (528)
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) (451)
- Systematic identification of genetic influences on methylation across the human life course (2016) (427)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- Genome-wide associations for birth weight and correlations with adult disease (2016) (371)
- Statistical inference in two-sample summary-data Mendelian randomization using robust adjusted profile score (2018) (362)
- Detecting epistasis in human complex traits (2014) (357)
- Recent Developments in Mendelian Randomization Studies (2017) (341)
- Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples (2014) (315)
- Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study (2017) (302)
- Two-sample Mendelian randomization: avoiding the downsides of a powerful, widely applicable but potentially fallible technique (2016) (301)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) (284)
- Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2018) (269)
- Contribution of genetic variation to transgenerational inheritance of DNA methylation (2014) (236)
- The MRC IEU OpenGWAS data infrastructure (2020) (227)
- Population genetic differentiation of height and body mass index across Europe (2015) (224)
- Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study (2019) (223)
- Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis (2019) (207)
- Detection and replication of epistasis influencing transcription in humans (2014) (193)
- MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations (2016) (190)
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2019) (183)
- Prenatal and early life influences on epigenetic age in children: a study of mother–offspring pairs from two cohort studies (2015) (177)
- Dominance genetic variation contributes little to the missing heritability for human complex traits. (2015) (175)
- Meffil: efficient normalization and analysis of very large DNA methylation datasets (2018) (147)
- Directional dominance on stature and cognition in diverse human populations (2015) (144)
- Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances (2018) (144)
- An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome (2018) (143)
- Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits (2018) (139)
- Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study (2017) (128)
- Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
- Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
- An Evolutionary Perspective on Epistasis and the Missing Heritability (2013) (126)
- Understanding the consequences of education inequality on cardiovascular disease: mendelian randomisation study (2019) (125)
- Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation (2020) (125)
- Invited Commentary: Detecting Individual and Global Horizontal Pleiotropy in Mendelian Randomization—A Job for the Humble Heterogeneity Statistic? (2018) (110)
- Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis (2016) (110)
- Telomere Length and Risk of Cancer and Non-neoplastic Diseases: Is Survivin the Ariadne's Thread?-Reply. (2017) (106)
- Population phenomena inflate genetic associations of complex social traits (2019) (98)
- Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis (2019) (98)
- Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs. (2013) (98)
- EpiGPU: exhaustive pairwise epistasis scans parallelized on consumer level graphics cards (2011) (97)
- Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies (2019) (92)
- Challenges and novel approaches for investigating molecular mediation (2016) (88)
- Congruence of Additive and Non-Additive Effects on Gene Expression Estimated from Pedigree and SNP Data (2013) (86)
- Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle (2019) (83)
- UK Biobank Genetic Data: MRC-IEU Quality Control, version 2 (2019) (79)
- Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. (2018) (79)
- Automating Mendelian randomization through machine learning to construct a putative causal map of the human phenome (2017) (77)
- Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. (2019) (77)
- Education, intelligence and Alzheimer’s disease: evidence from a multivariable two-sample Mendelian randomization study (2018) (75)
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2018) (74)
- Within-family studies for Mendelian randomization: avoiding dynastic, assortative mating, and population stratification biases (2019) (74)
- Novel Risk Loci for Rheumatoid Arthritis in Han Chinese and Congruence With Risk Variants in Europeans (2014) (70)
- The EWAS Catalog: a database of epigenome-wide association studies. (2021) (62)
- Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (62)
- Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk (2017) (61)
- 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 (2017) (61)
- Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. (2016) (59)
- Another Explanation for Apparent Epistasis (2014) (59)
- Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects (2022) (59)
- Within-sibship GWAS improve estimates of direct genetic effects (2021) (58)
- Genome-wide genetic homogeneity between sexes and populations for human height and body mass index. (2015) (58)
- Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (58)
- Causal effects of lifetime smoking on risk for depression and schizophrenia: Evidence from a Mendelian randomisation study (2018) (56)
- The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects (2015) (55)
- C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis (2015) (52)
- Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging (2021) (48)
- Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease (2018) (47)
- A transcriptome-wide Mendelian randomization study to uncover tissue-dependent regulatory mechanisms across the human phenome (2019) (46)
- High COVID-19 transmission potential associated with re-opening universities can be mitigated with layered interventions (2020) (45)
- Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. (2016) (45)
- PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statistics (2017) (43)
- The variant call format provides efficient and robust storage of GWAS summary statistics (2020) (42)
- Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero (2018) (42)
- Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2 (2016) (41)
- Appraising the causal relevance of DNA methylation for risk of lung cancer (2018) (41)
- Genome-wide meta-analysis of depression in 807,553 individuals identifies 102 independent variants with replication in a further 1,507,153 individuals (2018) (40)
- Genetic evidence for assortative mating on alcohol consumption in the UK Biobank (2019) (39)
- Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. (2019) (37)
- Bayesian reassessment of the epigenetic architecture of complex traits (2018) (37)
- Using the MR-Base platform to investigate risk factors and drug targets for thousands of phenotypes. (2019) (34)
- Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology (2018) (34)
- A Mendelian Randomization dictionary: Useful definitions and descriptions for undertaking, understanding and interpreting Mendelian Randomization studies (2019) (33)
- Genome-wide analysis of epistasis in body mass index using multiple human populations (2012) (32)
- Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework (2020) (31)
- The Parkinson's Disease Mendelian Randomization Research Portal (2019) (31)
- Strengthening Causal Inference for Complex Disease Using Molecular Quantitative Trait Loci. (2019) (31)
- Common genetic variants and health outcomes appear geographically structured in the UK Biobank sample: Old concerns returning and their implications (2018) (31)
- MRC IEU UK Biobank GWAS pipeline version 1 (2017) (30)
- The Effect of Plasma Lipids and Lipid‐Lowering Interventions on Bone Mineral Density: A Mendelian Randomization Study (2020) (29)
- Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
- Using the MR-Base platform to investigate risk factors and drug targets for thousands of phenotypes (2019) (28)
- The use of negative control outcomes in Mendelian randomization to detect potential population stratification (2021) (28)
- Causal inference for heritable phenotypic risk factors using heterogeneous genetic instruments (2020) (27)
- Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association Studies (2019) (26)
- Pathways between early‐life adversity and adolescent self‐harm: the mediating role of inflammation in the Avon Longitudinal Study of Parents and Children (2019) (26)
- Orienting the causal relationship between imprecisely measured traits using genetic instruments (2017) (25)
- Genome-wide association study of blood lead shows multiple associations near ALAD. (2015) (25)
- COVID-19 transmission in a university setting: a rapid review of modelling studies (2020) (24)
- Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color (2021) (24)
- Meffil: efficient normalisation and analysis of very large DNA methylation samples (2017) (24)
- Identifying drug targets for neurological and psychiatric disease via genetics and the brain transcriptome (2021) (23)
- A Phenome-Wide Mendelian Randomization Study of Pancreatic Cancer Using Summary Genetic Data (2019) (23)
- Navigating sample overlap, winner's curse and weak instrument bias in Mendelian randomization studies using the UK Biobank (2021) (23)
- Contacts and behaviours of university students during the COVID-19 pandemic at the start of the 2020/2021 academic year (2020) (23)
- Identification of loci where DNA methylation potentially mediates genetic risk of type 1 diabetes. (2018) (21)
- Correction: Orienting the causal relationship between imprecisely measured traits using GWAS summary data (2017) (20)
- The association of DNA methylation with body mass index: distinguishing between predictors and biomarkers (2019) (20)
- EpiGraphDB: a database and data mining platform for health data science (2020) (19)
- Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate (2019) (19)
- Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans (2018) (18)
- Genome-wide analysis of mitral valve disease in Cavalier King Charles Spaniels. (2012) (18)
- Is disrupted sleep a risk factor for Alzheimer’s disease? Evidence from a two-sample Mendelian randomization analysis (2019) (17)
- The role of common genetic variation in educational attainment and income: evidence from the National Child Development Study (2015) (17)
- Response to Lee et al.: SNP-based heritability analysis with dense data. (2013) (16)
- Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates (2011) (16)
- Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants (2022) (16)
- Identical twins carry a persistent epigenetic signature of early genome programming (2021) (15)
- UK Biobank Genetic Data: MRC-IEU Quality Control, Version 1 [Updated version at DOI: 10.5523/bris.1ovaau5sxunp2cv8rcy88688v] (2017) (15)
- Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease (2018) (15)
- Why are education, socioeconomic position and intelligence genetically correlated? (2019) (14)
- Investigating the role of insulin in increased adiposity: Bi-directional Mendelian randomization study (2017) (14)
- The Parkinson’s Disease Mendelian Randomization Research Portal (2019) (14)
- Prenatal alcohol exposure and facial morphology in a UK cohort. (2019) (13)
- Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing (2020) (12)
- An integrative approach to detect epigenetic mechanisms that putatively mediate the influence of lifestyle exposures on disease susceptibility (2019) (12)
- Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood (2018) (12)
- Schizophrenia risk and reproductive success: a Mendelian randomization study (2018) (12)
- Investigating the causal relationship between neuroticism and depression via Mendelian randomization (2019) (12)
- Meta-analyses identify DNA methylation associated with kidney function and damage (2021) (12)
- Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies (2020) (11)
- Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood (2017) (11)
- Shared genetic control of expression and methylation in peripheral blood (2016) (11)
- The causal effect of educational attainment on Alzheimer’s disease: A two-sample Mendelian randomization study (2017) (10)
- Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices (2017) (10)
- Genome wide analysis of mitral valve disease in Cavalier King Charles Spaniels (2011) (10)
- The effect of plasma lipids and lipid lowering interventions on bone mineral density: a Mendelian randomization study (2018) (9)
- MR-TRYX: Exploiting horizontal pleiotropy to infer novel causal pathways (2018) (9)
- Using genetic instruments to estimate interactions in Mendelian Randomization studies (2019) (9)
- Collapsed methylation quantitative trait loci analysis for low frequency and rare variants (2016) (9)
- Hemani et al. reply (2014) (8)
- Proteome-wide Mendelian randomization in global biobank meta-analysis reveals multi-ancestry drug targets for common diseases (2022) (8)
- LD hub and MR-base: online platforms for preforming LD score regression and Mendelian randomization analysis using GWAS summary data (2016) (7)
- Investigating the transparency of reporting in two-sample summary data Mendelian randomization studies using the MR-Base platform (2021) (7)
- MR-TRYX: A Mendelian randomization framework that exploits horizontal pleiotropy to infer novel causal pathways (2018) (7)
- An exploration of the genetic epidemiology of non-suicidal self-harm and suicide attempt (2021) (7)
- Causal epigenome-wide association study identifies CpG sites that influence cardiovascular disease risk (2017) (7)
- The use of negative control outcomes in Mendelian Randomisation to detect potential population stratification or selection bias (2020) (7)
- Phantom epistasis between unlinked loci (2021) (7)
- ACE Inhibitors, ARBs and Other Anti-Hypertensive Drugs and Novel COVID-19: An Association Study from the COVID Symptom Tracker App in 2,215,386 Individuals (2020) (7)
- Schizophrenia liability shares common molecular genetic risk factors with sleep duration and nightmares in childhood. (2019) (6)
- DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses (2021) (6)
- The spectre of Berkson's paradox: Collider bias in Covid‐19 research (2020) (6)
- Assortative mating and within-spouse pair comparisons (2020) (6)
- Systematic Mendelian randomization framework elucidates hundreds of genetic loci which may influence disease through changes in DNA methylation levels (2017) (6)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
- Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study (2020) (6)
- Tendency towards being a “Morning person” increases risk of Parkinson’s disease: evidence from Mendelian randomisation (2018) (6)
- Modelling pooling strategies for SARS-CoV-2 testing in a university setting (2021) (5)
- Using genetic instruments to estimate interactions in Mendelian randomization studies. (2019) (5)
- Lung function, COPD and cognitive function: a multivariable and two sample Mendelian randomization study (2021) (5)
- Investigating DNA methylation as a potential mediator between pigmentation genes, pigmentary traits and skin cancer (2020) (5)
- Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus (2021) (5)
- Comment on the Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank. (2019) (5)
- PhenoSpD: an atlas of phenotypic correlations and a multiple testing correction for the human phenome (2017) (5)
- Evaluating and implementing block jackknife resampling Mendelian randomization to mitigate bias induced by overlapping samples (2021) (4)
- Evaluating indirect genetic effects of siblings using singletons (2022) (4)
- The EWAS Catalog: a database of epigenome-wide association studies (2022) (4)
- The Norwegian Mother, Father, and Child cohort study (MoBa) genotyping data resource: MoBaPsychGen pipeline v.1 (2022) (4)
- Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis (2022) (4)
- Correction to: Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (4)
- Schizophrenia liability shares common molecular genetic risk factors with sleep duration and nightmares in childhood (2019) (4)
- We should be cautious about associations of patient characteristics with COVID-19 outcomes that are identified in hospitalised patients (2020) (3)
- Polygenic risks for joint developmental trajectories of internalizing and externalizing problems: findings from the ALSPAC cohort. (2021) (3)
- Systematic evaluation of the causal relationship between DNA methylation and C-reactive protein (2018) (3)
- An efficient and robust tool for colocalisation: Pair-wise Conditional and Colocalisation (PWCoCo) (2022) (3)
- Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms (2020) (3)
- The association of DNA methylation with body mass index: distinguishing between predictors and biomarkers (2020) (3)
- What explains the effect of education on cardiovascular disease? Applying Mendelian randomization to identify the consequences of education inequality (2018) (3)
- Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies (2019) (3)
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2020) (3)
- Alcohol consumption and mate choice in UK Biobank: comparing observational and Mendelian randomization estimates (2018) (3)
- Extensive QTL and association analyses of the QTLMAS2009 Data (2010) (3)
- Polygenic Risks for Joint Developmental Trajectories of Internalizing and Externalizing Problems: Findings from the ALSPAC Cohort (2021) (2)
- Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging (2021) (2)
- Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. (2016) (2)
- Systematic identification of genetic influences on methylation across the human life course (2016) (2)
- The Bristol CMIP6 Data Hackathon (2022) (2)
- Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2019) (2)
- Limits of lockdown: characterising essential contacts during strict physical distancing (2021) (2)
- Exploring the variance in complex traits captured by DNA methylation assays (2020) (1)
- Does Neuroticism Cause Depression? A Mendelian Randomization Study (2018) (1)
- gwas-vcf-performance (2020) (1)
- The bidirectional causal effects of brain morphology across the life course and risk of Alzheimers disease: A cross-cohort comparison and Mendelian randomization meta-analysis (2021) (1)
- Prenatal alcohol exposure and facial morphology in a UK cohort (2018) (1)
- The impact of fatty acids biosynthesis on the risk of cardiovascular diseases in Europeans and East Asians: a Mendelian randomization study (2022) (1)
- Impacts of vaccination and asymptomatic testing on SARS-CoV-2 transmission dynamics in a university setting (2021) (1)
- explodecomputer/covid-uob-pooling: Initial publication (2021) (1)
- Contribution of genetic variation to transgenerational inheritance of DNA methylation (2014) (1)
- Contact patterns before and during the UK's Autumn 2020 COVID-19 lockdown among university students and staff (2021) (1)
- Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization (2018) (1)
- University students and staff able to maintain low daily contact numbers during various COVID-19 guideline periods (2021) (1)
- ARIES mQTL results (2016) (1)
- DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses (2022) (1)
- Applying Mendelian randomization to appraise causality in relationships between nutrition and cancer (2021) (1)
- The variant call format provides efficient and robust storage of GWAS summary statistics (2021) (1)
- University of Southern Denmark Prenatal and early life influences on epigenetic age in children (2015) (1)
- Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits (2020) (1)
- Trans-ethnic genome-wide association study of kidney function provides novel insight into effector genes and causal effects on kidney-specific disease aetiologies (2018) (1)
- Review and further developments in statistical corrections for Winner’s Curse in genetic association studies (2022) (1)
- DNA methylation mediates genetic liability to non-syndromic cleft lip/palate (2018) (1)
- Design and quality control of large-scale two-sample Mendelian randomisation studies (2021) (1)
- Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits (2020) (1)
- Implications of selection bias for the COVID Symptom Tracker Study (2020) (1)
- Increased BMI May Protect against Parkinson's Disease: Evidence From Mendelian Randomisation Study (2017) (0)
- DNA co-methylation has a stable structure and is related to specific aspects of genome regulation (2022) (0)
- INFERENCE IN TWO-SAMPLE SUMMARY-DATA MENDELIAN RANDOMIZATION USING ROBUST ADJUSTED PROFILE SCORE By (2019) (0)
- Identification of loci where DNA methylation potentially mediates genetic risk of type 1 diabetes (2018) (0)
- for Blood Pressure Genome-Wide Association Studies, (2018). Genetic association of albuminuria with cardiometabolic disease and blood pressure. Human Genetics (2018) (0)
- A Comparison of CPU and OpenCL Parallelization Methods for Correlation and Graph Layout Algorithms used in the Network Analysis of High Dimensional Data (2013) (0)
- Detecting parent of origin effects using GREML of transmitted genotypes (2016) (0)
- Shared genetic control of expression and methylation in peripheral blood (2016) (0)
- Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis (2019) (0)
- Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices (2017) (0)
- Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework (2020) (0)
- Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (0)
- Retraction Note: Detection and replication of epistasis influencing transcription in humans (2021) (0)
- A comparison of the genes and genesets identified by GWAS and EWAS of fifteen complex traits (2022) (0)
- PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment (2023) (0)
- Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2 Ware, (2016) (0)
- Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at (2016) (0)
- Genetic studies of birth weight give biological insights into links with adult disease (2016) (0)
- Evaluating the potential benefits and pitfalls of combining protein and expression quantitative trait loci in evidencing drug targets (2022) (0)
- (2019). Parkinson’s Disease Mendelian Randomization Research (2019) (0)
- Incorrect Institutional Affiliations of Authors in the Article by Jiang et al (Arthritis Rheumatol, May 2014) (2014) (0)
- Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies (2018) (0)
- eQTLGen Consortium (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. (2018) (0)
- Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2019) (0)
- Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association Studies (2019) (0)
- Is schizophrenia risk related to disordered niacin metabolism? Evidence from an Indian 1 genome-wide association study 2 (2020) (0)
- Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2019) (0)
- Erratum to: EpiGraphDB: a database and data mining platform for health data science (2021) (0)
- Review Strengthening Causal Inference for Complex Disease Using Molecular 2 Quantitative Trait Loci 3 (2019) (0)
- Collection of genetic data at scale for a nationally representative population: the UK Millennium Cohort Study. (2021) (0)
- The association between genetically elevated polyunsaturated fatty acids and risk of cancer (2023) (0)
- Genetic influences on alcohol flushing in East Asian populations (2023) (0)
- Use of genetic correlations to examine selection bias (2023) (0)
- Detecting Individual and Global Horizontal Pleiotropy in Mendelian Randomization—A Job for the Humble Heterogeneity Statistic? American Journal of Epidemiology, 187(12), 2681-2685. [kwy185] (2018) (0)
- between early-life adversity and adolescent self-harm: the mediating role inflammation in the Longitudinal Study of and (2019) (0)
- Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (0)
- Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2019). Investigating the causal relationship between neuroticism and depression via Mendelian randomization. Acta , 395-397. (2019) (0)
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2019) (0)
- Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
- Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort (2021) (0)
- Dissecting genetic interactions in complex traits (2012) (0)
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2018) (0)
- Trans-ancestry meta-analysis improves performance of genetic scores for multiple adiposity-related traits in East Asian populations (2022) (0)
- Collider bias from selecting disease samples distorts causal inferences (2022) (0)
- Evidence of positive and negative selection associated with DNA methylation (2021) (0)
- Use of non-invasive methods to collect DNA for genome wide analysis from companion animals (2011) (0)
- Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood (2017) (0)
- Alcohol consumption and mate choice in UK Biobank : comparing 1 observational and Mendelian randomization estimates 2 (2019) (0)
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) (0)
- Correction to: Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (0)
This paper list is powered by the following services:
Other Resources About Gibran Hemani
What Schools Are Affiliated With Gibran Hemani?
Gibran Hemani is affiliated with the following schools:
