Stephanie M. Gogarten

Amazon Research Foundation — Brazil

Biochemistry, Genetics and Molecular Biology · Life Sciences

50h-index15.6kcitations168works5.32yr avg
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Research Topics

Genetic Associations and Epidemiology(68), Genomics and Rare Diseases(18), Epigenetics and DNA Methylation(14), Galaxies: Formation, Evolution, Phenomena(13), Genetic Mapping and Diversity in Plants and Animals(13)

Publications139 total

Mitochondrial insertions/deletions (INDELs) burden in Parkinson's disease: an analysis from a Brazilian cohort
Parkinsonism & Related Disorders·2026Open Access
Molecular analysis of mitochondrial complex I in the levodopa short duration response in Parkinson's disease
Parkinsonism & Related Disorders·2026Open Access
Novel mitochondrial variants associated with Parkinson’s disease reveal a high heteroplasmy-weighted polygenic risk score in Brazilians
2026Open Access
The mitogenome mutation repertoire affects progression of Parkinson’s Disease
Genetics and Molecular Biology·2026Open Access
Recommendations for responsible use of population descriptors in polygenic risk score development
Nature Genetics·2025· 1 citedOpen Access
Human Genome Diversity Project data use and implications for the governance of legacy genomic data
Nature Genetics·2025
Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations
UNC Libraries·2025Open Access
Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of 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
Multi‐ancestry meta‐analysis identifies genetic modifiers of age‐at‐onset of Alzheimer's disease at known and novel loci
Alzheimer s & Dementia·2025· 1 citedOpen Access
A data model for population descriptors in genomic research
The American Journal of Human Genetics·2025
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
UNC Libraries·2025· 1 citedOpen Access
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
UNC Libraries·2025Open Access
The PRIMED Consortium: Reducing disparities in polygenic risk assessment
UNC Libraries·2024Open Access
The PRIMED Consortium: Reducing disparities in polygenic risk assessment
The American Journal of Human Genetics·2024· 29 citedOpen Access
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas
UNC Libraries·2024Open Access
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas
Cell Genomics·2024· 23 citedOpen Access
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
PubMed·2024· 2 citedOpen Access
Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations
Bioinformatics·2024· 15 citedOpen Access
Abstract B109: Guidelines from the PRIMED Consortium on the use of population descriptors in polygenic risk model development and application
Cancer Epidemiology Biomarkers & Prevention·2023
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Frequent Co-authors

Cathy C. Laurie(19), Matthew P. Conomos(13), Cecelia Laurie(12), Tamar Sofer(11), Xiuqing Guo(9), Kenneth Rice(9), Anil C. Seth(9), Jerome I. Rotter(9), Michael H. Cho(8), Susan R. Heckbert(8), Charles Kooperberg(8), Edwin K. Silverman(8), Ramachandran S. Vasan(8), L. Adrienne Cupples(8), Sarah C. Nelson(8), Julianne J. Dalcanton(8), Adrienne M. Stilp(8), David Levine(7), Bruce S. Weir(7), Brian E. Cade(7)