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Author Details

Stephanie M Gogarten
2011
55
26
PMIDPaper TitleJournal TitlePublished Year
37192819Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research.J Am Med Inform Assoc2023
37745480Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.bioRxiv2023
37873338Admix-kit: An Integrated Toolkit and Pipeline for Genetic Analyses of Admixed Populations.bioRxiv2023
36960714Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.Circ Genom Precis Med2023
34855941Association of clonal hematopoiesis with chronic obstructive pulmonary disease.Blood2022
35647563Accounting for population structure in genetic studies of cystic fibrosis.HGG Adv2022
36268164Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.HGG Adv2022
36119389Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program.Cell Genom2022
36055210Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.Am J Hum Genet2022
35399580Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.HGG Adv2022
34337551BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion.HGG Adv2021
34165540Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.Hum Mol Genet2021
34214102Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program.PLoS One2021
34035245Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.Nat Commun2021
32439900Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.Nat Commun2020
31883642Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.Am J Hum Genet2020
31329242Genetic association testing using the GENESIS R/Bioconductor package.2019
29917119Novel Common Genetic Susceptibility Loci for Colorectal Cancer.J Natl Cancer Inst2019
30653739A fully adjusted two-stage procedure for rank-normalization in genetic association studies.Genet Epidemiol2019
27958378Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.Pharmacogenomics J2018
28719597Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.Pharmacogenomics J2018
28520984Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).Nicotine Tob Res2018
30535219Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.JAMA2018
29859855Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma.EBioMedicine2018
29618737Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.Sci Rep2018
29127183Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at <i>ID2</i>.Heart2018
29505938Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos.J Psychiatr Res2018
28039329A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.J Med Genet2017
28767105Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Nat Commun2017
28334390SeqArray-a storage-efficient high-performance data format for WGS variant calls.Bioinformatics2017
28613276Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Nat Commun2017
28610988Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.Heart Rhythm2017
29213071GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.Sci Rep2017
29074945Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.Nat Genet2017
27159506Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos.Am J Med Genet B Neuropsychiatr Genet2017
27663718Genetic variation near IRS1 is associated with adiposity and a favorable metabolic profile in U.S. Hispanics/Latinos.2016
26805783Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.Am J Hum Genet2016
26748518Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.Am J Hum Genet2016
27172203Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL).G3: Genes, Genomes, Genetics2016
27038408GENOME-WIDE ASSOCIATION STUDY (GWAS) AND GENOME-WIDE BY ENVIRONMENT INTERACTION STUDY (GWEIS) OF DEPRESSIVE SYMPTOMS IN AFRICAN AMERICAN AND HISPANIC/LATINA WOMEN.Depress Anxiety2016
26718567Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.Neurology2016
27256683Meta-Analysis of Genome-Wide Association Studies with Correlated Individuals: Application to the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).Genetic Epidemiology2016
26239294Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans.Mol Psychiatry2016
26151821Genome-wide association study of colorectal cancer identifies six new susceptibility loci.Nat Commun2015
26498495Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci.Nat Commun2015
26377959Exact Inference for Hardy-Weinberg Proportions with Missing Genotypes: Single and Multiple Imputation.G3 (Bethesda)2015
24651765Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke.PLoS Genet2014
24681907VariantAnnotation: a Bioconductor package for exploration and annotation of genetic variants.Bioinformatics2014
25147783Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial.Front Public Health2014
23266556Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.Gastroenterology2013
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