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Adebowale Adeyemo

National Institutes of Health · US
Area of research
Genetics · Endocrinology, Diabetes and Metabolism
Research interest
Research interests include Genetic Associations and Epidemiology, Diabetes, Cardiovascular Risks, and Lipoproteins, Cleft Lip and Palate Research, and Genomics and Rare Diseases.
h-index
77
citations
32,058
works
535
NIH funding
primary concept
Medicine
email

Recent publications

KidneyGenAfrica, a pan-African partnership to deliver research and training excellence in genomics of kidney disease
Nature Genetics 2025cited by 1position: middledoi
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Nature 2024cited by 485position: middledoi
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Cell Genomics 2023cited by 19position: middledoi
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Nature Genetics 2022cited by 728position: middledoi
The Lancet Nigeria Commission: investing in health and the future of the nation
The Lancet 2022cited by 338position: middledoi
Vitamin D Deficiency and Its Association with Iron Deficiency in African Children
Nutrients 2022cited by 38position: middledoi
Polygenic Prediction of Type 2 Diabetes in Africa
Diabetes Care 2022cited by 25position: middledoi
Association of lipid profile biomarkers with breast cancer by molecular subtype: analysis of the MEND study
Scientific Reports 2022cited by 13position: middledoi
Polygenic risk scores for CARDINAL study
Nature Genetics 2022cited by 13position: middledoi
Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps
Nature Medicine 2021cited by 435position: middledoi
Meta-analyses identify DNA methylation associated with kidney function and damage
Nature Communications 2021cited by 78position: middledoi
Prevalence and predictors of vitamin D deficiency in young African children
BMC Medicine 2021cited by 42position: middledoi
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
The American Journal of Human Genetics 2021cited by 34position: middledoi
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus
Nature Communications 2021cited by 27position: middledoi
Epigenetic-age acceleration in the emerging burden of cardiometabolic diseases among migrant and non-migrant African populations: a population-based cross-sectional RODAM substudy
The Lancet Healthy Longevity 2021cited by 20position: middledoi
DNA Methylation as the Link between Migration and the Major Noncommunicable Diseases: the RODAM Study
Epigenomics 2021cited by 13position: middledoi
Genome-wide DNA methylation analysis on C-reactive protein among Ghanaians suggests molecular links to the emerging risk of cardiovascular diseases
npj Genomic Medicine 2021cited by 9position: middledoi
High-depth African genomes inform human migration and health
Nature 2020cited by 362position: middledoi
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Cell 2019cited by 283position: middledoi
Associations of autozygosity with a broad range of human phenotypes
Nature Communications 2019cited by 182position: middledoi
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Nature Genetics 2019cited by 151position: middledoi
<i>HLA</i>and autoantibodies define scleroderma subtypes and risk in African and European Americans and suggest a role for molecular mimicry
Proceedings of the National Academy of Sciences 2019cited by 74position: middledoi
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome
Journal of the American Society of Nephrology 2019cited by 62position: middledoi
Epigenome-wide association study in whole blood on type 2 diabetes among sub-Saharan African individuals: findings from the RODAM study
International Journal of Epidemiology 2018cited by 119position: middledoi
Genomic analyses in African populations identify novel risk loci for cleft palate
Human Molecular Genetics 2018cited by 86position: lastdoi
Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia
PLoS ONE 2018cited by 51position: middledoi
Brief Report: Whole‐Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans
Arthritis & Rheumatology 2018cited by 15position: middledoi
Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms
Cell 2017cited by 158position: middledoi
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
PLoS Genetics 2017cited by 130position: middledoi
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
PLoS Genetics 2017cited by 123position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Karlijn Meeks · National Human Genome Research Institute8 papers (2016–2021) · 8 papers (2016–2021)Liam Smeeth · Qatar University7 papers (2016–2021)Silver Bahendeka · Uganda Martyrs University7 papers (2016–2021)Ina Danquah · University of Bonn7 papers (2016–2021)Charles N. Rotimi · National Human Genome Research Institute6 papers (2012–2022)Ellis Owusu‐Dabo · Kwame Nkrumah University of Science and Technology6 papers (2016–2021)Frank P. Mockenhaupt · Humboldt-Universität zu Berlin6 papers (2016–2021)Joachim Spranger · Max Rubner Institut6 papers (2016–2021)Kerstin Klipstein‐Grobusch · University of Tübingen6 papers (2016–2021)Charles Agyemang · University of Alabama at Birmingham6 papers (2016–2021) · 5 papers (2017–2021) · 5 papers (2016–2018) · 5 papers (2016–2021)Juliet Addo · University of London5 papers (2016–2018)Matthias B. Schulze · Robert Bosch (Germany)5 papers (2016–2018) · 4 papers (2017–2021)Ana Requena‐Méndez · Karolinska University Hospital3 papers (2021–2021)Segun Fatumo · Institut thématique Génétique, génomique et bioinformatique3 papers (2021–2022) · 3 papers (2016–2018)