Deborah A. Nickerson

University of North Carolina at Chapel Hill — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

121h-index101.5kcitations670works3.62yr avg
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Research Topics

Genetic Associations and Epidemiology(131), Genomics and Rare Diseases(110), Genomic variations and chromosomal abnormalities(63), RNA modifications and cancer(44), Genetics and Neurodevelopmental Disorders(37)

Publications588 total

Integration of DNA sequencing with population pharmacokinetics to improve the prediction of irinotecan exposure in cancer patients
UNC Libraries·2025Open Access
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
UNC Libraries·2025Open Access
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
UNC Libraries·2025Open Access
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans
UNC Libraries·2025Open Access
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed
2025· 12 citedOpen Access
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
UNC Libraries·2024Open Access
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
UNC Libraries·2024Open Access
Remote surveillance and detection of SARS-CoV-2 transmission among household members in King County, Washington
BMC Infectious Diseases·2024· 1 citedOpen Access
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data
UNC Libraries·2024Open Access
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
UNC Libraries·2024Open Access
SARS-CoV-2 diversity and transmission on a university campus across two academic years during the pandemic
2024Open Access
Effect of sickle cell trait and apol1 genotype on the association of soluble upar with kidney function measures in black americans
UNC Libraries·2024Open Access
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
Nature Cardiovascular Research·2023· 17 citedOpen Access
The functional impact of rare variation across the regulatory cascade
Cell Genomics·2023· 13 citedOpen Access
Rare variants in <i>ANO1</i>, encoding a calcium-activated chloride channel, predispose to moyamoya disease
Brain·2023· 21 citedOpen Access
Structural variation across 138,134 samples in the TOPMed consortium
2023· 8 citedOpen Access
Structural variation across 138,134 samples in the TOPMed consortium
2023· 16 citedOpen Access
The Genetic Landscape of Familial Pulmonary Fibrosis
American Journal of Respiratory and Critical Care Medicine·2023· 41 citedOpen Access
Sentinel Surveillance System Implementation and Evaluation for SARS-CoV-2 Genomic Data, Washington, USA, 2020–2021
Emerging infectious diseases·2023· 15 citedOpen Access
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
Nature Communications·2022· 16 citedOpen Access
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Frequent Co-authors

Mark J. Rieder(20), Jay Shendure(16), Evan E. Eichler(13), Michael J. Bamshad(12), Eric Boerwinkle(10), Joshua D. Smith(10), David Altshuler(8), Gonçalo R. Abecasis(7), Stacey Gabriel(7), Choli Lee(7), Sarah Ng(6), Christopher S. Carlson(6), Andrew G. Clark(5), Brian J. O’Roak(5), Emily H. Turner(5), Joshua M. Akey(5), Abigail W. Bigham(5), Holly K. Tabor(5), Suzanne M. Leal(5), Michael A. Eberle(5)