Andrew R. Wood
Reproducibility track record
2
assessed papers
95/100
mean reproducibility
2
reproduced (C1–C2)
0
flagged
310
total citations
flag rate:
0%
(0/2)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
Funders
—
Frequent co-authors
Uwe Völker 2Andres Metspalu 2Mathieu Platteel 1David Melzer 1Antoine Weihs 1Thomas Meitinger 1Jingyuan Fu 1Tōnu Esko 1Juha Karjalainen 1Kaido Lepik 1
Institutions
University of Tartu 2University of Exeter 2Universitätsmedizin Greifswald 2National Institute on Aging 2German Centre for Cardiovascular Research 2SIB Swiss Institute of Bioinformatics 1
Geography (author institutions)
EE 2GB 2DE 2IT 2US 2CH 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (2)
Complete publication record (344)
Request a reproduction →2 assessed by us (2 reproduced) · 342 not yet assessed — every PubMed paper on record, linked below.
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Genetic and lifestyle modifiers of haemochromatosis-related clinical outcomes in HFE C282Y homozygotes ↗JHEP Reports · 2026 · PMID 41951274not yet assessed
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Rare Coding Variants Reveal Distinct Genetic Architectures Across Multidimensional Sleep Phenotypes ↗medRxiv · 2026 · PMID 42369502not yet assessed
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Evidence of bidirectional relationship between type 2 diabetes and depression; a Mendelian randomization study ↗Molecular Psychiatry · 2025 · PMID 40595333not yet assessed
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Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels ↗Nature Genetics · 2025 · PMID 39994471not yet assessed
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Streamlining large-scale genomic data management: Insights from the UK Biobank whole-genome sequencing data ↗Cell Genomics · 2025 · PMID 40972583not yet assessed
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Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling ↗Nature Communications · 2025 · PMID 39809772not yet assessed
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Clinical utility of self-reported sleep duration and insomnia symptoms in type 2 diabetes prediction ↗Diabetologia · 2025 · PMID 40753283not yet assessed
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Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome ↗Genetics in Medicine · 2025 · PMID 40476350not yet assessed
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Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height ↗npj Genomic Medicine · 2025 · PMID 40016231not yet assessed
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Streamlining Large-Scale Genomic Data Management: Insights from the UK Biobank Whole-Genome Sequencing Data ↗medRxiv · 2025 · PMID 39974066not yet assessed
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Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025not yet assessed
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From Normal Variation in Sleep to Clinical Sleep Disorders: Genetic Insights from Over One Million Individuals ↗medRxiv · 2025 · PMID 41332830not yet assessed
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Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome ↗medRxiv · 2025not yet assessed
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not yet assessed
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Sleep and circadian health in the UK Biobank: Report on the 2023 sleep questionnaire enhancement ↗medRxiv · 2025not yet assessed
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Genotype-level quality control substantially reduces error rates in population-scale whole-genome sequencing ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025not yet assessed
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Genetic modifiers of rare variants in monogenic developmental disorder loci ↗Nature Genetics · 2024 · PMID 38637616not yet assessed
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Genetic links between ovarian ageing, cancer risk and de novo mutation rates ↗Nature · 2024 · PMID 39261734not yet assessed
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Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height ↗Nature Communications · 2024 · PMID 39362880not yet assessed
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Iron and risk of dementia: Mendelian randomisation analysis in UK Biobank ↗Journal of Medical Genetics · 2024 · PMID 38191510not yet assessed
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Hyperglycaemia is a causal risk factor for upper limb pathologies ↗International Journal of Epidemiology · 2024 · PMID 38205890not yet assessed
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Colorectal cancer risk stratification using a polygenic risk score in symptomatic primary care patients—a UK Biobank retrospective cohort study ↗European Journal of Human Genetics · 2024 · PMID 39090236not yet assessed
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SMIM1 absence is associated with reduced energy expenditure and excess weight ↗Med · 2024 · PMID 38906141not yet assessed
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The power of genetic diversity in genome-wide association studies of lipids ↗UNC Libraries · 2024not yet assessed
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Sleep inertia, not chronotype, is a marker of circadian misalignment and a risk factor for psychiatric disorders: genetic and epidemiological evidence ↗Sleep Medicine · 2024not yet assessed
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Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling ↗medRxiv · 2024 · PMID 38633783not yet assessed
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Penetrance of Pathogenic Genetic Variants Associated With Premature Ovarian Insufficiency ↗Obstetrical & Gynecological Survey · 2024not yet assessed
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Response to Penetrance estimates of hereditary cancers in a population setting using UK Biobank data ↗BJC Reports · 2024 · PMID 39516645not yet assessed
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ↗UNC Libraries · 2024not yet assessed
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Author Correction: The power of genetic diversity in genome-wide association studies of lipids ↗RePEc: Research Papers in Economics · 2024not yet assessed
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Effects of physical activity and sedentary time on depression, anxiety and well-being: a bidirectional Mendelian randomisation study ↗BMC Medicine · 2023 · PMID 38110912not yet assessed
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Penetrance of pathogenic genetic variants associated with premature ovarian insufficiency ↗Nature Medicine · 2023 · PMID 37349538not yet assessed
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Loci for insulin processing and secretion provide insight into type 2 diabetes risk ↗The American Journal of Human Genetics · 2023 · PMID 36693378not yet assessed
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Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood ↗Diabetologia · 2023 · PMID 37280435not yet assessed
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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH ↗Diabetologia · 2023 · PMID 37233759not yet assessed
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Identification and analysis of individuals who deviate from their genetically-predicted phenotype ↗PLoS Genetics · 2023 · PMID 37733769not yet assessed
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Correlates of Risk for Disinhibited Behaviors in the Million Veteran Program Cohort ↗JAMA Psychiatry · 2023 · PMID 37938835not yet assessed
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Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records ↗BMC Medical Genomics · 2023 · PMID 37784116not yet assessed
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Does physical activity moderate the association between shorter leukocyte telomere length and incident coronary heart disease? Data from 54,180 UK Biobank participants ↗GeroScience · 2023 · PMID 37544968not yet assessed
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#3118 ERECTILE DYSFUNCTION IS A HARBINGER OF CHRONIC KIDNEY DISEASE ↗Nephrology Dialysis Transplantation · 2023not yet assessed
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Author Correction: The power of genetic diversity in genome-wide association studies of lipids ↗Nature · 2023 · PMID 37237109not yet assessed
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Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Whole genome sequencing analysis identifies rare, large-effect non-coding variants and regions associated with circulating protein levels ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023not yet assessed
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Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion ↗medRxiv · 2023 · PMID 36798216not yet assessed
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Identification and analysis of individuals who deviate from their genetically-predicted phenotype ↗bioRxiv (Cold Spring Harbor Laboratory) · 2023 · PMID 36798175not yet assessed
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Additional file 28 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 21 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 25 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 18 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 27 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 10 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 29 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 19 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (UWA) · 2023not yet assessed
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Additional file 4 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 17 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 2 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 33 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 32 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 5 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 30 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 7 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 8 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 20 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 22 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Discovery Research Portal (University of Dundee) · 2023not yet assessed
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Additional file 23 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 1 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Additional file 12 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗UWA Profiles and Research Repository (University of Western Australia) · 2023not yet assessed
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Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts ↗The American Journal of Human Genetics · 2022 · PMID 36257325not yet assessed
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Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population ↗The American Journal of Human Genetics · 2022 · PMID 35700724not yet assessed
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ↗The American Journal of Human Genetics · 2022 · PMID 35931049not yet assessed
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗Genome biology · 2022 · PMID 36575460not yet assessed
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Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study ↗Diabetes Care · 2022 · PMID 35349659not yet assessed
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Prevalence of Fabry disease-causing variants in the UK Biobank ↗Journal of Medical Genetics · 2022 · PMID 35977816not yet assessed
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Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia, Bipolar Disorder, and Depression Among Adults in the US Veterans Affairs Health Care System ↗JAMA Psychiatry · 2022 · PMID 36103194not yet assessed
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Detection and characterization of male sex chromosome abnormalities in the UK Biobank study ↗Genetics in Medicine · 2022 · PMID 35687092not yet assessed
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Babies of South Asian and European Ancestry Show Similar Associations With Genetic Risk Score for Birth Weight Despite the Smaller Size of South Asian Newborns ↗Diabetes · 2022 · PMID 35061033not yet assessed
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Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies ↗The American Journal of Human Genetics · 2022 · PMID 36055212not yet assessed
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Recurrent 17q12 microduplications contribute to renal disease but not diabetes ↗Journal of Medical Genetics · 2022 · PMID 36109160not yet assessed
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The impact of Mendelian sleep and circadian genetic variants in a population setting ↗PLoS Genetics · 2022 · PMID 36137075not yet assessed
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Simulated distributions from negative experiments highlight the importance of the body mass index distribution in explaining depression–body mass index genetic risk score interactions ↗International Journal of Epidemiology · 2022 · PMID 35388897not yet assessed
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A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Correction: Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation ↗eLife · 2022 · PMID 35583923not yet assessed
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Genetic susceptibility to earlier ovarian ageing increases <i>de novo</i> mutation rate in offspring ↗medRxiv · 2022not yet assessed
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Study of the associations between short telomeres, sex hormones and pulmonary fibrosis ↗medRxiv · 2022not yet assessed
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not yet assessed
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The impact of Mendelian sleep and circadian genetic variants in a population setting ↗medRxiv · 2022not yet assessed
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Corrigendum to: A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio ↗Human Molecular Genetics · 2022 · PMID 35246685not yet assessed
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Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study ↗2022not yet assessed
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The role of accelerometer-derived sleep traits on glycated haemoglobin and glucose levels: a Mendelian randomization study ↗medRxiv · 2022not yet assessed
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Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study ↗2022not yet assessed
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Genomic insights into the mechanism of NK3R antagonists for treatment of menopausal vasomotor symptoms ↗medRxiv · 2022not yet assessed
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Genetically proxied therapeutic prolyl-hydroxylase inhibition and cardiovascular risk ↗Human Molecular Genetics · 2022 · PMID 36048866not yet assessed
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The power of genetic diversity in genome-wide association studies of lipids ↗Nature · 2021 · PMID 34887591not yet assessed
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The trans-ancestral genomic architecture of glycemic traits ↗Nature Genetics · 2021 · PMID 34059833not yet assessed
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Genetic determinants of daytime napping and effects on cardiometabolic health ↗Nature Communications · 2021 · PMID 33568662not yet assessed
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Genetic insights into biological mechanisms governing human ovarian ageing ↗Nature · 2021 · PMID 34349265not yet assessed
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Genetic predictors of participation in optional components of UK Biobank ↗Nature Communications · 2021 · PMID 33563987not yet assessed
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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptomeNature Communications · 2021 · PMID 34561431L1 100/100
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Genetic Evidence for Different Adiposity Phenotypes and Their Opposing Influences on Ectopic Fat and Risk of Cardiometabolic Disease ↗Diabetes · 2021 · PMID 33980691not yet assessed
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Higher adiposity and mental health: causal inference using Mendelian randomization ↗Human Molecular Genetics · 2021 · PMID 34270736not yet assessed
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A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor ↗PLoS Genetics · 2021 · PMID 34111113not yet assessed
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Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health ↗Molecular Psychiatry · 2021 · PMID 34099873not yet assessed
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Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation ↗eLife · 2021 · PMID 35074047not yet assessed
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Understanding Factors That Cause Tinnitus: A Mendelian Randomization Study in the UK Biobank ↗Ear and Hearing · 2021 · PMID 34108397not yet assessed
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Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile ↗Diabetologia · 2021 · PMID 34542646not yet assessed
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Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight ↗Human Molecular Genetics · 2021 · PMID 34897462not yet assessed
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Genetically defined favourable adiposity is not associated with a clinically meaningful difference in clinical course in people with type 2 diabetes but does associate with a favourable metabolic profile ↗Diabetic Medicine · 2021 · PMID 33501652not yet assessed
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not yet assessed
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Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ↗medRxiv · 2021not yet assessed
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not yet assessed
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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not yet assessed
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Associations of genetic scores for birth weight with newborn size and later anthropometric traits and cardiometabolic risk markers in South Asians ↗Research Square · 2021not yet assessed
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Rare genetic variants in dominant developmental disorder loci cause milder related phenotypes in the general population ↗medRxiv · 2021not yet assessed
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The trans-ancestral genomic architecture of glycemic traits. ↗UCL Discovery (University College London) · 2021not yet assessed
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Using genetics to uncouple higher adiposity from its adverse metabolic effects and understand its role in metabolic and non-metabolic disease. ↗Research Square · 2021not yet assessed
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Mendelian randomization to investigate the link between TSH and thyroid cancer ↗Endocrine Related Cancer · 2021not yet assessed
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Genetically defined favourable adiposity is not associated with a clinically meaningful difference in clinical course in people with type 2 diabetes but does associate with a favourable metabolic profilee-space (Manchester Metropolitan University) · 2021not yet assessed
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not yet assessed
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Using genetics to uncouple higher adiposity from its adverse metabolic effects and understand its role in metabolic and non-metabolic disease. ↗Research Square · 2021not yet assessed
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not yet assessed
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Using human genetics to understand the disease impacts of testosterone in men and women ↗Nature Medicine · 2020 · PMID 32042192not yet assessed
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Sleep characteristics across the lifespan in 1.1 million people from the Netherlands, United Kingdom and United States: a systematic review and meta-analysis ↗Nature Human Behaviour · 2020 · PMID 33199855not yet assessed
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Telomere length and risk of idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease: a mendelian randomisation study ↗The Lancet Respiratory Medicine · 2020 · PMID 33197388not yet assessed
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Does Obesity Cause Thyroid Cancer? A Mendelian Randomization Study ↗The Journal of Clinical Endocrinology & Metabolism · 2020 · PMID 32392279not yet assessed
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Quantification of the overall contribution of gene-environment interaction for obesity-related traits ↗Nature Communications · 2020 · PMID 32170055not yet assessed
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Mitochondrial genetic variation is enriched in G-quadruplex regions that stall DNA synthesis in vitro ↗Human Molecular Genetics · 2020 · PMID 32191790not yet assessed
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Is disrupted sleep a risk factor for Alzheimer’s disease? Evidence from a two-sample Mendelian randomization analysis ↗International Journal of Epidemiology · 2020 · PMID 33150399not yet assessed
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Genetic evidence that higher central adiposity causes gastro-oesophageal reflux disease: a Mendelian randomization study ↗International Journal of Epidemiology · 2020 · PMID 32588049not yet assessed
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Common maternal and fetal genetic variants show expected polygenic effects on risk of small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies ↗PLoS Genetics · 2020 · PMID 33284794not yet assessed
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A single nucleotide polymorphism genetic risk score to aid diagnosis of coeliac disease: a pilot study in clinical care ↗Alimentary Pharmacology & Therapeutics · 2020 · PMID 32790217not yet assessed
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A Mendelian Randomization Study Provides Evidence That Adiposity and Dyslipidemia Lead to Lower Urinary Albumin-to-Creatinine Ratio, a Marker of Microvascular Function ↗Diabetes · 2020 · PMID 31915152not yet assessed
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Clinical Features and Genetic Risk of Demyelination Following Anti-TNF Treatment ↗Journal of Crohn s and Colitis · 2020 · PMID 32497177not yet assessed
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Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity ↗The Journal of Clinical Endocrinology & Metabolism · 2020 · PMID 32944759not yet assessed
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Large Copy-Number Variants in UK Biobank Caused by Clonal Hematopoiesis May Confound Penetrance Estimates ↗The American Journal of Human Genetics · 2020 · PMID 32574563not yet assessed
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Mendelian randomization supports a causative effect of TSH on thyroid carcinoma ↗Endocrine Related Cancer · 2020 · PMID 32698144not yet assessed
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture ↗University of Regensburg Publication Server (University of Regensburg) · 2020not yet assessed
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Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics ↗UNC Libraries · 2020not yet assessed
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The genetic architecture of type 2 diabetes ↗UNC Libraries · 2020not yet assessed
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗UNC Libraries · 2020not yet assessed
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Mendelian randomization study of height and risk of colorectal cancer ↗UNC Libraries · 2020not yet assessed
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Genetic predictors of participation in optional components of UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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not yet assessed
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The Trans-Ancestral Genomic Architecture of Glycaemic Traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome ↗medRxiv · 2020not yet assessed
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not yet assessed
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not yet assessed
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Assessing the causal role of sleep traits on glycated haemoglobin: a Mendelian randomization study ↗medRxiv · 2020not yet assessed
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Common maternal and fetal genetic variants show expected polygenic effects on the probability of being born small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Genome-wide associations for birth weight and correlations with adult disease ↗UNC Libraries · 2020not yet assessed
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Mendelian randomization supports a causative effect of TSH on thyroid carcinoma ↗Endocrine Related Cancer · 2020 · PMID 33107437not yet assessed
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A genome wide association study of frozen shoulder identifies a common variant of <i>WNT7B</i> and diabetes as causal risk factors ↗medRxiv · 2020not yet assessed
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Quality control and conduct of genome-wide association meta-analyses ↗UNC Libraries · 2020not yet assessed
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Multiple Loci Are Associated with White Blood Cell Phenotypes ↗UNC Libraries · 2020not yet assessed
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans ↗UNC Libraries · 2020not yet assessed
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A reference panel of 64,976 haplotypes for genotype imputation ↗UNC Libraries · 2020not yet assessed
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Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗Digital Commons@Becker (Washington University School of Medicine) · 2020not yet assessed
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Defining the role of common variation in the genomic and biological architecture of adult human height ↗UNC Libraries · 2020not yet assessed
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Hundreds of variants clustered in genomic loci and biological pathways affect human height ↗UNC Libraries · 2020not yet assessed
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Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies ↗UNC Libraries · 2020not yet assessed
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Across-cohort QC analyses of GWAS summary statistics from complex traits ↗UNC Libraries · 2020not yet assessed
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New genetic loci link adipose and insulin biology to body fat distribution ↗White Rose Research Online (University of Leeds, The University of Sheffield, University of York) · 2020not yet assessed
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Genetic studies of body mass index yield new insights for obesity biology ↗UNC Libraries · 2020not yet assessed
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Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms ↗Nature Communications · 2019 · PMID 30696823not yet assessed
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Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates ↗Nature Communications · 2019 · PMID 30846698not yet assessed
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ↗Nature Genetics · 2019 · PMID 31043758not yet assessed
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Biological and clinical insights from genetics of insomnia symptoms ↗Nature Genetics · 2019 · PMID 30804566not yet assessed
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Development and Standardization of an Improved Type 1 Diabetes Genetic Risk Score for Use in Newborn Screening and Incident Diagnosis ↗Diabetes Care · 2019 · PMID 30655379not yet assessed
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Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour ↗Nature Communications · 2019 · PMID 30952852not yet assessed
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Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study ↗PLoS Medicine · 2019 · PMID 30703100not yet assessed
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Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes ↗Nature Communications · 2019 · PMID 31409809not yet assessed
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Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting ↗The American Journal of Human Genetics · 2019 · PMID 30665703not yet assessed
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Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank ↗BMJ · 2019 · PMID 30651232not yet assessed
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Investigating causal relations between sleep traits and risk of breast cancer in women: mendelian randomisation study ↗BMJ · 2019 · PMID 31243001not yet assessed
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Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms ↗Gut · 2019 · PMID 30661054not yet assessed
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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution ↗Nature Genetics · 2019 · PMID 30778226not yet assessed
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Effects of body mass index on relationship status, social contact and socio-economic position: Mendelian randomization and within-sibling study in UK Biobank ↗International Journal of Epidemiology · 2019 · PMID 31800047not yet assessed
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Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis ↗PLoS Medicine · 2019 · PMID 31211782not yet assessed
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Genome-Wide Association Study of Microscopic Colitis in the UK Biobank Confirms Immune-Related Pathogenesis ↗Journal of Crohn s and Colitis · 2019 · PMID 31125052not yet assessed
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A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio ↗Human Molecular Genetics · 2019 · PMID 31630189not yet assessed
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Assessment of <i>MTNR1B</i> Type 2 Diabetes Genetic Risk Modification by Shift Work and Morningness-Eveningness Preference in the UK Biobank ↗Diabetes · 2019 · PMID 31757795not yet assessed
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Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes ↗Sleep Medicine · 2019not yet assessed
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Methods for quick, accurate and cost-effective determination of the type 1 diabetes genetic risk score (T1D-GRS) ↗Clinical Chemistry and Laboratory Medicine (CCLM) · 2019 · PMID 31665112not yet assessed
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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2019not yet assessed
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Is disrupted sleep a risk factor for Alzheimer’s disease? Evidence from a two-sample Mendelian randomization analysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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Effects of body mass index on relationship status, social contact, and socioeconomic position: Mendelian Randomization study in UK Biobank ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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2DOES HIGH BMI IN THE ABSENCE OF METABOLIC CONSEQUENCES CAUSE DEPRESSION? ↗European Neuropsychopharmacology · 2019not yet assessed
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Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics ↗publish.UP (University of Potsdam) · 2019not yet assessed
-
Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry ↗Human Molecular Genetics · 2018 · PMID 30124842not yet assessed
-
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry ↗Human Molecular Genetics · 2018 · PMID 30239722not yet assessed
-
Estimating sleep parameters using an accelerometer without sleep diary ↗Scientific Reports · 2018 · PMID 30154500not yet assessed
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗Nature Genetics · 2018 · PMID 29632382not yet assessed
-
Using genetics to understand the causal influence of higher BMI on depression ↗International Journal of Epidemiology · 2018 · PMID 30423117not yet assessed
-
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics ↗Human Molecular Genetics · 2018 · PMID 29309628not yet assessed
-
Mosaic Turner syndrome shows reduced penetrance in an adult population study ↗Genetics in Medicine · 2018 · PMID 30181606not yet assessed
-
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology ↗The American Journal of Human Genetics · 2018 · PMID 30583798not yet assessed
-
Genome-Wide and Abdominal MRI Data Provide Evidence That a Genetically Determined Favorable Adiposity Phenotype Is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease, and Hypertension ↗Diabetes · 2018 · PMID 30352878not yet assessed
-
A Common Allele in FGF21 Associated with Sugar Intake Is Associated with Body Shape, Lower Total Body-Fat Percentage, and Higher Blood Pressure ↗Cell Reports · 2018 · PMID 29641994not yet assessed
-
DNA methylation and inflammation marker profiles associated with a history of depression ↗Human Molecular Genetics · 2018 · PMID 29790996not yet assessed
-
The Common <i>HNF1A</i> Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY ↗Diabetes · 2018 · PMID 29895593not yet assessed
-
Response to Prakash et al. ↗Genetics in Medicine · 2018 · PMID 30573795not yet assessed
-
not yet assessed
-
Meta-analysis of genome-wide association studies for height and body mass index in ∼700,000 individuals of European ancestry ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Estimating sleep parameters using an accelerometer without sleep diary ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
not yet assessed
-
Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body Fat Distribution ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Genetic studies of accelerometer-based sleep measures in 85,670 individuals yield new insights into human sleep behaviour ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2018 · PMID 29549329not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2018 · PMID 29549330not yet assessed
-
Biological and clinical insights from genetics of insomnia symptoms ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Assessing the pathogenicity, penetrance and expressivity of putative disease-causing variants in a population setting ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Evidence of a common causal relationship between body mass index and inflammatory skin disease: a Mendelian Randomization study ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls ↗Scientific Data · 2018not yet assessed
-
Investigating causal relationships between sleep traits and risk of breast cancer: a Mendelian randomization study ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. ↗Kölner Universitäts PublikationsServer (Universität zu Köln) · 2018not yet assessed
-
not yet assessed
-
A twin study of type 2 diabetes, brain structure, and function ↗Swinburne Research Bank (Swinburne University of Technology) · 2018not yet assessed
-
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
GWAS identifies novel risk locus for erectile dysfunction and implicates hypothalamic neurobiology and diabetes in etiology ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans ↗Diabetes · 2017 · PMID 28566273not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Nature · 2017 · PMID 28146470not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2017 · PMID 29273807not yet assessed
-
Genetic evidence of assortative mating in humans ↗Nature Human Behaviour · 2017not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017not yet assessed
-
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants ↗Diabetes · 2017 · PMID 28490609not yet assessed
-
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits ↗Nature Communications · 2017 · PMID 28963451not yet assessed
-
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers ↗PLoS ONE · 2017 · PMID 28957414not yet assessed
-
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk ↗Diabetes · 2017 · PMID 28341696not yet assessed
-
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees ↗Proceedings of the National Academy of Sciences · 2017 · PMID 29279374not yet assessed
-
Influence of cell distribution and diabetes status on the association between mitochondrial <scp>DNA</scp> copy number and aging phenotypes in the In<scp>CHIANTI</scp> study ↗Aging Cell · 2017 · PMID 29047204not yet assessed
-
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk ↗University of Southern Denmark Research Portal (University of Southern Denmark) · 2017not yet assessed
-
Assessment of sleep parameters from raw accelerometry data ↗Sleep Medicine · 2017not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Apollo (University of Cambridge) · 2017not yet assessed
-
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls ↗Scientific Data · 2017 · PMID 29257133not yet assessed
-
Red Blood Cell Distribution Width: genetic evidence for aging pathways in 116,666 volunteers ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Mosaic Turner syndrome shows reduced phenotypic penetrance in an adult population study compared to clinically ascertained cases ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Phenotypes associated with female X chromosome aneuploidy in UK Biobank: an unselected, adult, population-based cohort2017not yet assessed
-
Narrow-sense heritability estimation of complex traits using identity-by-descent information ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
A common allele in FGF21 associated with preference for sugar consumption lowers body fat in the lower body and increases blood pressure ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017not yet assessed
-
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. ↗Apollo (University of Cambridge) · 2017not yet assessed
-
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017not yet assessed
-
Red Blood Cell Distribution Width: genetic evidence for aging pathways in 116,666 volunteers: Genetic influences on Red Blood Cell variation2017not yet assessed
-
The genetic architecture of type 2 diabetes ↗Nature · 2016 · PMID 27398621not yet assessed
-
Genome-wide associations for birth weight and correlations with adult disease ↗Nature · 2016 · PMID 27680694not yet assessed
-
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci ↗PLoS Genetics · 2016 · PMID 27494321not yet assessed
-
Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank ↗BMJ · 2016 · PMID 26956984not yet assessed
-
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight ↗JAMA · 2016 · PMID 26978208not yet assessed
-
Gene–obesogenic environment interactions in the UK Biobank study ↗International Journal of Epidemiology · 2016 · PMID 28073954not yet assessed
-
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels ↗Nature Communications · 2016 · PMID 26833098not yet assessed
-
Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease ↗Diabetes · 2016 · PMID 27207519not yet assessed
-
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants ↗Aging · 2016 · PMID 27015805not yet assessed
-
Prosaposin is a regulator of progranulin levels and oligomerization ↗Nature Communications · 2016 · PMID 27356620not yet assessed
-
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ↗Molecular Psychiatry · 2016 · PMID 27184124not yet assessed
-
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19 ↗BMC Proceedings · 2016 · PMID 27980614not yet assessed
-
Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively ↗Diabetologia · 2016 · PMID 26961502not yet assessed
-
Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health ↗Human Reproduction · 2016 · PMID 26732621not yet assessed
-
Quantifying the extent to which index event biases influence large genetic association studies ↗Human Molecular Genetics · 2016 · PMID 28040731not yet assessed
-
Across-cohort QC analyses of GWAS summary statistics from complex traits ↗European Journal of Human Genetics · 2016 · PMID 27552965not yet assessed
-
Independent test assessment using the extreme value distribution theory ↗BMC Proceedings · 2016 · PMID 27980644not yet assessed
-
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight ↗Obstetrical & Gynecological Survey · 2016not yet assessed
-
Human Longevity is Influenced by Many Genetic Variants: Evidence from 75,000 UK Biobank Participants ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Genome-wide association analyses in > 119,000 individuals identifies thirteen morningness and two sleep duration loci ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Quantifying the extent to which index event biases influence large genetic association studies ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Evidence that lower socioeconomic position accentuates genetic susceptibility to obesity ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Causal Relationship between Obesity and Vitamin D Status2016not yet assessed
-
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels ↗University of Southern Denmark Research Portal (University of Southern Denmark) · 2016not yet assessed
-
The genetic architecture of type 2 diabetes. ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2016not yet assessed
-
Genetic studies of body mass index yield new insights for obesity biology ↗Nature · 2015 · PMID 25673413not yet assessed
-
New genetic loci link adipose and insulin biology to body fat distribution ↗Nature · 2015 · PMID 25673412not yet assessed
-
Biological interpretation of genome-wide association studies using predicted gene functions ↗Nature Communications · 2015 · PMID 25597830not yet assessed
-
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci ↗Nature Genetics · 2015 · PMID 26551672not yet assessed
-
Population genetic differentiation of height and body mass index across Europe ↗Nature Genetics · 2015 · PMID 26366552not yet assessed
-
Directional dominance on stature and cognition in diverse human populations ↗Nature · 2015 · PMID 26131930not yet assessed
-
Cell Specific eQTL Analysis without Sorting CellsPLoS Genetics · 2015 · PMID 25955312L1 90/100
-
Mendelian randomization study of height and risk of colorectal cancer ↗International Journal of Epidemiology · 2015 · PMID 25997436not yet assessed
-
Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at <i>CCND2</i> Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion ↗Diabetes · 2015 · PMID 25605810not yet assessed
-
Across-cohort QC analyses of genome-wide association study summary statistics from complex traits ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause, and impact reproductive health: a UK Biobank study ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
A reference panel of 64,976 haplotypes for genotype imputation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
and type 2 diabetes respectively2015not yet assessed
-
Directional dominance on stature and cognition in diverse human populations ↗Archive ouverte UNIGE (University of Geneva) · 2015not yet assessed
-
at menopause, and impact reproductive health: a UK Biobank study2015not yet assessed
-
Variants in the <i>FTO</i> and <i>CDKAL1</i> loci have recessive effects on risk of obesity and type 2 diabetes respectively ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2015not yet assessed
-
Cell Specific eQTL Analysis without Sorting CellsNorthumbria Research Link (Northumbria University) · 2015not yet assessed
-
Defining the role of common variation in the genomic and biological architecture of adult human height ↗Nature Genetics · 2014not yet assessed
-
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility ↗Nature Genetics · 2014 · PMID 24509480not yet assessed
-
Quality control and conduct of genome-wide association meta-analyses ↗Nature Protocols · 2014 · PMID 24762786not yet assessed
-
Rare variants in <i>PPARG</i> with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes ↗Proceedings of the National Academy of Sciences · 2014 · PMID 25157153not yet assessed
-
Defining the role of common variation in the genomic and biological architecture of adult human height. ↗PubMed · 2014 · PMID 25282103not yet assessed
-
Another explanation for apparent epistasis ↗Nature · 2014 · PMID 25279928not yet assessed
-
Targeted Allelic Expression Profiling in Human Islets Identifies <i>cis</i>-Regulatory Effects for Multiple Variants Identified by Type 2 Diabetes Genome-Wide Association Studies ↗Diabetes · 2014 · PMID 25392243not yet assessed
-
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes ↗Human Molecular Genetics · 2014 · PMID 25378555not yet assessed
-
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees ↗BMC Proceedings · 2014 · PMID 25519314not yet assessed
-
Cell specific eQTL analysis without sorting cells ↗bioRxiv (Cold Spring Harbor Laboratory) · 2014not yet assessed
-
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityUWA Profiles and Research Repository (University of Western Australia) · 2014not yet assessed
-
Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts ↗PLoS Medicine · 2013 · PMID 23393431not yet assessed
-
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture ↗Nature Genetics · 2013 · PMID 23563607not yet assessed
-
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗PLoS Genetics · 2013 · PMID 23754948not yet assessed
-
Genetic Variants Associated With Glycine Metabolism and Their Role in Insulin Sensitivity and Type 2 Diabetes ↗Diabetes · 2013 · PMID 23378610not yet assessed
-
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation ↗PLoS ONE · 2013 · PMID 23696881not yet assessed
-
Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics ↗The American Journal of Human Genetics · 2013 · PMID 23891470not yet assessed
-
The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts ↗BMC Genomics · 2013 · PMID 24044605not yet assessed
-
Comparison of the Effect of Insulin Glulisine to Insulin Aspart on Breakfast Postprandial Blood Glucose Levels in Children with Type 1 Diabetes Mellitus on Multiple Daily Injections ↗Endocrine Practice · 2013 · PMID 23425652not yet assessed
-
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗Tampere University Institutional Repository (Tampere University) · 2013not yet assessed
-
Supplementary Material 152013not yet assessed
-
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes ↗Nature Genetics · 2012 · PMID 22885922not yet assessed
-
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture ↗Nature Genetics · 2012 · PMID 22504420not yet assessed
-
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals ↗PLoS Genetics · 2012 · PMID 22479202not yet assessed
-
A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation ↗PLoS Genetics · 2012 · PMID 22829776not yet assessed
-
No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels ↗Diabetes · 2012 · PMID 22415877not yet assessed
-
Multiple genetic variants explain measurable variance in type 2 diabetes-related traits in Pakistanis ↗Diabetologia · 2012 · PMID 22538361not yet assessed
-
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2012not yet assessed
-
Text Clustering Using LucidWorks and Apache MahoutVTechWorks (Virginia Tech) · 2012not yet assessed
-
A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone-Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone RegulationTampere University Institutional Repository (Tampere University) · 2012not yet assessed
-
Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing ↗Aging Cell · 2011 · PMID 21668623not yet assessed
-
Multiple Loci Are Associated with White Blood Cell Phenotypes ↗PLoS Genetics · 2011 · PMID 21738480not yet assessed
-
Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies ↗Circulation Cardiovascular Genetics · 2011 · PMID 22199011not yet assessed
-
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association ↗Human Molecular Genetics · 2011 · PMID 21798870not yet assessed
-
Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗Nature Genetics · 2011not yet assessed
-
Identifying likely causal connections between gene expression levels using a Mendelian randomization approach ↗Clinical Biochemistry · 2011not yet assessed
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗Nature Genetics · 2010 · PMID 20935630not yet assessed
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height ↗Nature · 2010 · PMID 20881960not yet assessed
-
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗Nature Genetics · 2010not yet assessed
-
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. ↗PubMed · 2010 · PMID 20935629not yet assessed
-
Preparing mission students to do contextual theologyePlace - Preserving, Learning, and Creative Exchange (Asbury Theological Seminary) · 2009not yet assessed
-
Regulation of Metallothionein Gene Expression and Secretion in Rat Adipocytes Differentiated from Preadipocytes in Primary Culture ↗Hormone and Metabolic Research · 2000 · PMID 11246822not yet assessed
-
Marine Garbology: An Article of Trash.1989not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Wood A” paper on PubMed ↗