Cathy C. Laurie

University of North Carolina at Chapel Hill — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

82h-index29.0kcitations253works3.02yr avg
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Research Topics

Genetic Associations and Epidemiology(114), Genetic Mapping and Diversity in Plants and Animals(34), Epigenetics and DNA Methylation(20), Genetic and phenotypic traits in livestock(20), Genomics and Rare Diseases(15)

Publications204 total

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
UNC Libraries·2025Open Access
African Ancestry–Specific Alleles and Kidney Disease Risk in Hispanics/Latinos
UNC Libraries·2025Open Access
Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
UNC Libraries·2025Open Access
A Genome-Wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos
UNC Libraries·2025Open Access
Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos
UNC Libraries·2025Open Access
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
UNC Libraries·2024Open Access
Data from Evaluating Genetic Risk for Prostate Cancer among Japanese and Latinos
2023Open Access
Supplementary Table 1 from Evaluating Genetic Risk for Prostate Cancer among Japanese and Latinos
2023Open Access
Data from Evaluating Genetic Risk for Prostate Cancer among Japanese and Latinos
2023Open Access
Supplementary Table 1 from Evaluating Genetic Risk for Prostate Cancer among Japanese and Latinos
2023Open Access
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program
Circulation Genomic and Precision Medicine·2023· 11 citedOpen Access
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension
Hypertension·2022· 27 citedOpen Access
Protein prediction for trait mapping in diverse populations
2021· 3 citedOpen Access
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
The American Journal of Human Genetics·2021· 11 citedOpen Access
Protein prediction for trait mapping in diverse populations
Zenodo (CERN European Organization for Nuclear Research)·2021Open Access
Protein prediction for trait mapping in diverse populations
Zenodo (CERN European Organization for Nuclear Research)·2021Open Access
Protein prediction for trait mapping in diverse populations
Zenodo (CERN European Organization for Nuclear Research)·2021Open Access
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
The American Journal of Human Genetics·2021· 49 citedOpen Access
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program
American Journal of Epidemiology·2021· 66 citedOpen Access
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Nature Communications·2021· 49 citedOpen Access
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Frequent Co-authors

Kimberly F. Doheny(13), Stephanie M. Gogarten(11), Cecelia Laurie(11), Kenneth Rice(10), Stephen S. Rich(10), Eric Boerwinkle(9), Matthew P. Conomos(9), Myriam Fornage(9), Bruce M. Psaty(9), Jerome I. Rotter(9), Bruce S. Weir(8), Charles Kooperberg(8), Daniel B. Mirel(8), David Levine(7), Elizabeth Pugh(7), Kari E. North(6), Caitlin McHugh(6), Mary L. Marazita(6), Eleanor Feingold(6), Tamar Sofer(6)