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Author Details

Gina M Peloso
2007
142
52
PMIDPaper TitleJournal TitlePublished Year
37961373Frequency of Variants in Mendelian Alzheimer's Disease Genes within the Alzheimer's Disease Sequencing Project (ADSP).medRxiv2024
37492105Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of atherogenic lipoproteins.Cell Genom2023
37766997Bayesian multivariate genetic analysis improves translational insights.2023
37662416Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies.bioRxiv2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37961553Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course.2023
37961350A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.bioRxiv2023
37693521Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.medRxiv2023
37693453Key variants via Alzheimer's Disease Sequencing Project whole genome sequence data.medRxiv2023
37405741Novel Association of the NOTCH Pathway Regulator MIB1 Gene With the Development of Bicuspid Aortic Valve.JAMA Cardiol2023
37011137Genetic and clinical factors underlying a self-reported family history of heart disease.2023
36802703Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program.Circulation2023
37186683Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease.Circulation2023
37429843Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure.Nat Commun2023
37425786Integrative metabolomics differentiate coronary artery disease, peripheral artery disease, and venous thromboembolism risks.2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
36723951Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.JAMA Cardiol2023
37498674Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk.J Clin Invest2023
34690355Exploiting family history in aggregation unit-based genetic association tests.European Journal of Human Genetics2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36220816Whole genome sequence analysis of blood lipid levels in >66,000 individuals.Nat Commun2022
35379992New insights into the genetic etiology of Alzheimer's disease and related dementias.Nat Genet2022
35995843Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations.Commun Biol2022
35871328Association of Carotid Intima Media Thickening with Future Brain Region Specific Amyloid-β Burden.J Alzheimers Dis2022
36269708Genome-wide discovery for diabetes-dependent triglycerides-associated loci.PLoS ONE2022
35547845Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.medRxiv2022
35664994Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.Res Sq2022
36424512Whole genome DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases.Sci Rep2022
36515558Bayesian Genetic Colocalization Test of Two Traits Using coloc.2022
36774119Sugar-Sweetened Beverage Consumption and Plasma Lipoprotein Cholesterol, Apolipoprotein, and Lipoprotein Particle Size Concentrations in US Adults.J Nutr2022
35316615Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study.American Journal of Human Genetics2022
35027740Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.Nat Genet2022
35222515Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program.Front Genet2022
34936225Two-Sample Multivariable Mendelian Randomization Analysis Using R.Current Protocols2021
33631942Lipoprotein(a) and Coronary Artery Disease Risk Without a Family History of Heart Disease.Journal of the American Heart Association2021
33846329Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.Nat Commun2021
33791713Alternative splicing of OAS1 alters the risk for severe COVID-19.medRxiv2021
34270325Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations.Circ Genom Precis Med2021
33720349Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.Genetics2021
35128521History of Suicide Attempts and COVID-19 Infection in Veterans with Schizophrenia or Schizoaffective Disorder: Moderating Effects of Age and Body Mass Index.2021
32608112Evaluation of population stratification adjustment using genome-wide or exonic variants.Genetic Epidemiology2020
32098600Beverage Consumption and Longitudinal Changes in Lipoprotein Concentrations and Incident Dyslipidemia in US Adults: The Framingham Heart Study.Journal of the American Heart Association2020
32213464EDEM3 Modulates Plasma Triglyceride Level through Its Regulation of LRP1 Expression.iScience2020
32862661Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery Disease.Circ Genom Precis Med2020
32804569Genetic Variation in Cardiometabolic Traits and Medication Targets and the Risk of Hypertensive Disorders of Pregnancy.Circulation2020
32690788Cardiovascular health, genetic risk, and risk of dementia in the Framingham Heart Study.Neurology2020
31160809Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2019
31727424Long-Term Cardiovascular Risk in Women With Hypertension During Pregnancy.J Am Coll Cardiol2019
29273807Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2018
28719597Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.Pharmacogenomics J2018
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