Donna K. Arnett

University of Kentucky — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

111h-index99.5kcitations952works5.82yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genetic Associations and Epidemiology(270), Blood Pressure and Hypertension Studies(96), Cardiovascular Function and Risk Factors(95), Epigenetics and DNA Methylation(91), Birth, Development, and Health(62)

Publications891 total

Genetic diversity fuels gene discovery for tobacco and alcohol use
UNC Libraries·2025Open Access
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
UNC Libraries·2025Open Access
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
UNC Libraries·2025Open Access
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
UNC Libraries·2025Open Access
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
UNC Libraries·2025Open Access
DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation
UNC Libraries·2025Open Access
Coffee consumption and calcified atherosclerotic plaques in the coronary arteries: The NHLBI Family Heart Study
UNC Libraries·2025Open Access
Sugar-Sweetened Beverage Consumption and Calcified Atherosclerotic Plaques in the Coronary Arteries: The NHLBI Family Heart Study
UNC Libraries·2025Open Access
Influence of Ancestral and Geographic Factors on Intracerebral Hemorrhage Risks Among Africans and Americans
Stroke·2025
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals
Genome biology·2025· 1 citedOpen Access
Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Human Genetics and Genomics Advances·2025Open Access
Genome‐wide meta‐analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans
UNC Libraries·2025Open Access
Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants
2025Open Access
Antecedent sedative use is independently associated with stroke occurrence among west Africans: Evidence from the SIREN case-control study
eNeurologicalSci·2025Open Access
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
UNC Libraries·2025· 1 citedOpen Access
Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids
UNC Libraries·2025Open Access
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
UNC Libraries·2025Open Access
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
UNC Libraries·2025Open Access
cellSTAAR: Incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of non-coding regions
2025· 2 citedOpen Access
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Nature Communications·2025· 3 citedOpen Access
page 1 of 45Next →

Frequent Co-authors

Myriam Fornage(14), Marguerite R. Irvin(12), Eric Boerwinkle(12), Salim S. Virani(9), Sharon L. R. Kardia(9), Daniel Levy(9), Joshua C. Bis(9), Emelia J. Benjamin(8), Jennifer A. Smith(8), Dariush Mozaffarian(7), Mary Cushman(7), Virginia J. Howard(7), Paul D. Sorlie(7), Hemant K. Tiwari(7), James S. Pankow(7), Devin Absher(7), Michael Mendelson(7), André G. Uitterlinden(7), Bruce M. Psaty(7), Xiuqing Guo(7)