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Genetic Determinants of High Bp in Three Racial Groups

Funding type: cooperative_agreement
Funder scheme: U10
Start date: 1995-09-05
End date: 2000-08-31
Investigator: STEPHEN T TURNER
Institution: MAYO CLINIC COLL OF MEDICINE, ROCHESTER
Funded outputs count: 47
Funder award ID: U10HL054464
OpenAlex ID: G1938656707
Improved multiancestry fine-mapping identifies cis-regulatory variants underlying molecular traits and disease risk
2025 · Zeyun Lu, Xinran Wang, et al. · Nature Genetics · 17
Powerful mapping of cis -genetic effects on gene expression across diverse populations reveals novel disease-critical genes
2024 · Kai Akamatsu, Stephen Golzari, et al. · medRxiv · 1
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Improved multi-ancestry fine-mapping identifies cis -regulatory variants underlying molecular traits and disease risk
2024 · Zeyun Lu, Xinran Wang, et al. · medRxiv · 5
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Unappreciated subcontinental admixture in Europeans and European Americans and implications for genetic epidemiology studies
2023 · Mateus H. Gouveia, Amy R. Bentley, et al. · Nature Communications · 28
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Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
2023 · Sara M. Willems, Natasha H. J. Ng, et al. · Wellcome Open Research · 7
Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk
2023 · Xue Liu, Xianbang Sun, et al. · Journal of the American Heart Association · 34
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Structural variation across 138,134 samples in the TOPMed consortium
2023 · Goo Jun, Adam C English, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 24
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Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies
2022 · Zeyun Lu, Shyamalika Gopalan, et al. · The American Journal of Human Genetics · 58
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
2022 · Daniel DiCorpo, Sheila M. Gaynor, et al. · Communications Biology · 22
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Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts
2022 · Daniel DiCorpo, Jessica LeClair, et al. · Diabetes Care · 66
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Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes
2021 · Yingchang Lu, Latchezar Dimitrov, et al. · Circulation Genomic and Precision Medicine · 10
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A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program
2021 · Adrienne M Stilp, Leslie S Emery, et al. · American Journal of Epidemiology · 56
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Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
2021 · Vasiliki Lagou, Reedik Mägi, et al. · Nature Communications · 163
A Noncoding Variant Near PPP1R3B Promotes Liver Glycogen Storage and MetS, but Protects Against Myocardial Infarction
2020 · Bratati Kahali, Yue Chen, et al. · The Journal of Clinical Endocrinology & Metabolism · 16
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose
2020 · Peitao Wu, Denis Rybin, et al. · PLoS ONE · 41
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A Peripheral Blood DNA Methylation Signature of Hepatic Fat Reveals a Potential Causal Pathway for Nonalcoholic Fatty Liver Disease
2019 · Jiantao Ma, Jana Nano, et al. · Diabetes · 59
Longitudinal analysis of epigenome-wide DNA methylation reveals novel smoking-related loci in African Americans
2019 · Jiaxuan Liu, Wei Zhao, et al. · Epigenetics · 8
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Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
2019 · Karen Y. He, Xiaoyin Li, et al. · Human Genetics · 28
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
2019 · Paul S de Vries, Michael R Brown, et al. · American Journal of Epidemiology · 116
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Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31
2018 · Heming Wang, Priyanka Nandakumar, et al. · European Journal of Human Genetics · 5
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DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis
2018 · Cavin K. Ward-Caviness, Jennifer E. Huffman, et al. · Blood · 21
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Hormone therapy and urine protein excretion: a multiracial cohort study, systematic review, and meta-analysis
2018 · Andrea G. Kattah, Maria L.G. Suarez, et al. · Menopause The Journal of The North American Menopause Society · 30
Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry
2017 · Priyanka Nandakumar, Dongwon Lee, et al. · Journal of Hypertension · 20
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans
2015 · E Olfson, N L Saccone, et al. · Molecular Psychiatry · 43
GWAS for executive function and processing speed suggests involvement of the CADM2 gene
2015 · C A Ibrahim-Verbaas, J Bressler, et al. · Molecular Psychiatry · 147
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