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Submitted by Title Working Group Name and Date of Professional Meeting Post date
Hui, Daniel Genetic and phenotypic association analyses of cardiometabolic traits in diverse African samples with whole-genome sequencing data
  • Anthropometry - Adiposity (includes Physical Activity)
  • Blood Pressure
  • Lipids
  • Population Genetics
  • Analysis
 American Society of Human Genetics, November 2023 10/30/23
Minster, Ryan L Genome-wide association studies of blood pressure phenotypes in 4,819 participants from Samoa and American Samoa
  • Blood Pressure
 ASHG (Nov 1-5, 2023) 10/22/23
Jang, Seonkyeong Cross-ancestry genetic architecture influences estimation of heritability and genetic correlation in diverse populations. ASHG 2023 10/18/23
Ruczinski, Ingo Whole genome sequencing interaction study identifies loci with sex-specific effects underlying platelet aggregation traits
  • Hematology and Hemostasis
 ASHG 2023 (November 2, 2023) 10/18/23
Stanislawski, Maggie Host genetics and gut microbiota in asthma among US Hispanics/Latinos: The Hispanic Community Study / Study of Latinos.
  • Asthma
 ASHG, Nov 1 2023 10/18/23
Kim, Kangjin Whole genome sequencing and proteomic analysis of mucus plugging in COPDGene
  • Lung
 ASHG 2023 Conference (Nov 3, 2023) 10/18/23
Wen, Jia Gene Expression and Splicing QTL Analysis of Blood Cells in African American Participants from the Jackson Heart Study
  • Multi-Omics
 2023 ASHG Annual Meeting, November 1-5, 2023 10/18/23
Rafique, Omar Longitudinal DNA methylation highlights genes for COPD progression.
  • Chronic Obstructive Pulmonary Disease
  • Epigenetics
  • Lung
 ASHG Annual Meeting 2023 ( Nov 1 -5) 10/15/23
Rocco, Alison Whole Genome Sequencing Analysis of Weight Loss in Chronic Obstructive Pulmonary Disease in Trans-Omics for Precision Medicine
  • Chronic Obstructive Pulmonary Disease
 ASHG (11/4/2023) 10/13/23
Orchard, Peter Cross-cohort eQTL analyses of 6,602 multi-ancestry TOPMed whole blood RNA-seq samples uncover regulatory relationships
  • Multi-Omics
 ASHG 2023 Annual Meeting (Nov. 1-5, 2023) 10/12/23
Lê, Brandon Characterizing epigenetic aging in an adult sickle cell disease cohort
  • Sickle Cell Disease
 American Society of Human Genetics 2023 Annual Meeting (November 1-5, 2023) 10/11/23
Palmer, Nicholette Multi-ancestry Whole Genome Sequencing (WGS) Meta-analysis to Identify Loci Associated with Non-alcoholic Fatty Liver Disease (NAFLD)
  • Anthropometry - Adiposity (includes Physical Activity)
 American Society of Human Genetics (ASHG); November 1-5, 2023 10/11/23
Palmer, Nicholette Multi-Ancestry Whole Genome Sequencing (WGS) AND Meta-Analysis to Identify Loci Associated with Non-Alcoholic Fatty Liver Disease (NAFLD)
  • Anthropometry - Adiposity (includes Physical Activity)
 American Association for the Study of Liver Diseases (AASLD), November 10-14, 2023 10/11/23
Yu, Bing Catalog and Genetic Architecture of Circulating Metabolites from Trans-Omics for Precision Medicine (TOPMed) Program
  • Metabolomics and Proteomics
 ASHG Nov 2023 10/10/23
Zhang, Xinruo Whole-genome Sequencing Analysis of Body Mass Index in the Trans-Omics for Precision Medicine (TOPMed) Program Identifies Novel African Ancestry-specific Risk Allele
  • Anthropometry - Adiposity (includes Physical Activity)
 ASHG (November 1, 2023) 10/10/23
Sun, Quan Genome-wide association studies for alloimmunization among patients with sickle cell disease
  • Sickle Cell Disease
 ASHG 2023 (Nov. 3, 2023) 10/10/23
Carlson, Jenna The extent to which augmenting extant reference panels with population-specific sequences improves imputation quality
  • Anthropometry - Adiposity (includes Physical Activity)
  • Population Genetics
 American Society of Human Genetics Annual Meeting (November 1-5, 2023) 10/09/23
Li, Xihao MultiSTAAR: A statistical framework for powerful rare variant multi-trait analysis in biobank-scale sequencing studies
  • Lipids
 American Society of Human Genetics Annual Meeting (November 1-5, 2023) 10/07/23
Van Buren, Eric cellSTAAR: Incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of non-coding regions
  • Lipids
 ASHG 2023 09/29/23
Keener, Rebecca Rare variants affecting telomere length and disease identified through multi-omic modeling
  • Multi-Omics
 ASHG Conference (November 5-9, 2023) 09/29/23
Wuichet, Kristin A Genotype Validated Bimodal Method for the Large-Scale Identification and Phenotyping of Persons with Sickle Cell Disease Using Electronic Health Record Data
  • Sickle Cell Disease
 ASH Annual Meeting 2023 08/10/23
Heard-Costa, Nancy Genetic return of results in a population-based cohort: Enrollment experience from the PopSeq Project
  • dbGaP
 ASHG Conference November 1-5, 2023 08/10/23
Zhou, Laura Use of Polygenic Risk Scores to Improve GFR Estimating Equation in CRIC and MESA
  • Kidney Function
 ASHG Conference (Nov 1-5 2023) 06/27/23
Debban, Catherine Multi-study pQTL analysis of Somascan proteomics in multi-ancestry TOPMed Cohorts
  • Multi-Omics
 ASHG Meeting (November 1-5 2023) 06/22/23
Hu, Xiaowei Multi-ancestry transcriptome predictions with functionally informed variants improve transcriptome-wide association studies in TOPMed MESA
  • Multi-Omics
 American Society of Human Genetics (November 1-5, 2023) 06/20/23
Yang, Chaojie Systematic integration of multi-omics data from TOPMed MESA for the study of coronary artery disease (CAD) and subclinical atherosclerosis
  • MESA Omics
 ASHG (November 1-5, 2023) 06/20/23
Sun, Quan MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric
  • Analysis
 IGES 2023 Annual Meeting (Nov.5-8, 2023) 06/08/23
Wheeler, Heather The genetically regulated transcriptome better predicts plasma protein levels than the observed transcriptome and reveals mechanisms underlying autoimmune diseases
  • MESA Omics
 ASHG November 1-5, 2023 06/07/23
Ockerman, Franklin Practical recommendations for TOPMed metabolomics data
  • Metabolomics and Proteomics
 American Society of Human Genetics Annual Meeting (November 1-5, 2023) 06/06/23
Keener, Rebecca Rare variants affecting telomere length and disease identified through multi-omic modeling
  • Hematology and Hemostasis
 ASHG Conference (November 5-9, 2023) 06/05/23
Sun, Quan Genome-wide association studies for alloimmunization among patients with sickle cell disease
  • Sickle Cell Disease
 ASHG 2023 Annual Meeting (Nov. 1-5, 2023) 06/05/23
Wang, Nannan Catalog and Genetic Architecture of Circulating Metabolites from Trans-Omics for Precision Medicine (TOPMed) Program
  • Metabolomics and Proteomics
 ASHG Meeting (November 1-5, 2023) 06/04/23
Chen, Han StocSum: stochastic summary statistics for whole genome sequencing studies
  • Anthropometry - Adiposity (includes Physical Activity)
  • Blood Pressure
  • Lipids
  • Analysis
 ASHG Meeting (November 1-5, 2023) 06/01/23
Palmer, Nicholette Multi-ancestry Whole Genome Sequencing (WGS) and Meta-analysis to Identify Loci Associated with Non-alcoholic Fatty Liver Disease (NAFLD)
  • Anthropometry - Adiposity (includes Physical Activity)
 American Association for the Study of Liver Disease (AASLD; November 10-14, 2023) 05/26/23
Chen, Han StocSum: stochastic summary statistics for whole genome sequencing studies
  • Anthropometry - Adiposity (includes Physical Activity)
  • Blood Pressure
  • Lipids
  • Analysis
 Joint Statistical Meetings (August 5-10, 2023) 05/18/23
Xu, Weiling Mitochondrial DNA Copy Number Variation in Asthma Risk and Severity
  • Mitochondrial DNA
 CHARGE Boston (May 10, 2023) 05/02/23
Chami, Nathalie A multi-ancestry whole exome sequencing analyses of BMI and obesity identifies novel genes
  • Anthropometry - Adiposity (includes Physical Activity)
 Multi-omics in Metabolic Disease June 7-9, 2023 03/28/23
Zhang, Yixin TOPMed metabolomics association analysis of cardiovascular disease in participants with type 2 diabetes
  • Diabetes
 CHARGE Meeting (May 10th and 11th, 2023) 02/24/23
Nicholas, Jayna Multi-ancestry genome-wide analysis of circulating D-dimer
  • Hematology and Hemostasis
 Spring 2023 CHARGE Meeting (May 9-11) 02/17/23
Chen, Han StocSum: stochastic summary statistics for whole genome sequencing studies Joint Statistical Meetings 2023 (August 5-10, 2023) 01/31/23
Sarnowski, Chloé Effect of genetic clusters related to insulin resistance on neurological traits in diverse populations from the Trans-Omics for Precision Medicine (TOPMed) Program
  • Diabetes
  • Neurocognitive
 AAIC (July 16-20, Amsterdam) 01/23/23
Wang, Ningyuan Integrating Whole Genome Sequence Analysis and eQTL Data from the TOPMed Program Improves Understanding of Type 2 Diabetes Risk Loci in Diverse Populations
  • Diabetes
 American Diabetes Association's 83rd Scientific Sessions (June 23-26, 2023) 01/04/23
Wang, Heming Genetic variants for obstructive sleep apnea identified after modeling interactions with daytime sleepiness
  • Sleep Traits
 SLEEP (June 3, 2023) 12/15/22
Wang, Heming Whole genome sequence analyses for Excessive Daytime Sleepiness in the NHLBI TOPMed Program
  • Sleep Traits
 SLEEP (June 3, 2023) 12/15/22
Saunders, Gretchen The extent of allelic heterogeneity in a trans-ancestry GWAS meta-analysis of alcohol and tobacco addiction in 3.4 million individuals.
  • Smoking
 ASHG October 2022 10/21/22
Minster, Ryan L Genome-wide association studies of metabolic traits in Samoans
  • Diabetes
 ASHG Annual Meeting (Oct 25–29, 2022) 10/06/22
Wang, Yuxuan Whole genome sequence analysis of long non-coding RNAs for plasma lipid traits
  • Lipids
 CHARGE Seattle Conference (Oct 12-14, 2022) 10/06/22
Yang, Chaojie Systematic Integration of Multi-omics Data for Coronary Artery Disease and Subclinical Atherosclerosis
  • Atherosclerosis - Clinical and Subclinical
 ASHG Conference (Oct. 24-28, 2022) and CHARGE Seattle Conference (Oct. 13-14, 2022) 10/05/22
Dron, Jacqueline Rare protein-truncating DNA variants in APOB or PCSK9, low-density lipoprotein cholesterol, and risk of coronary artery disease
  • Lipids
 ASHG Meeting (October 2022) 10/04/22
Li, Xihao Whole Genome Sequencing Analyses of 87,652 Individuals Reveal Rare Variants in Promoter of HMGA1 Associated with Height
  • Anthropometry - Adiposity (includes Physical Activity)
 American Society of Human Genetics Annual Meeting (October 25-29, 2022) 10/04/22
Yun, Jeong Somatic mutations in chronic lung disease are associated with reduced lung function
  • Lung
 ASHG 10/26/2022 10/04/22
Wang, Yuxuan Whole genome sequence analysis of long non-coding RNAs for plasma lipid traits
  • Lipids
 ASHG (October 27, 2022) 09/28/22
Orchard, Peter Cross-cohort eQTL fine-mapping utilizing TOPMed whole genome sequencing identifies tens of thousands of independent eQTLs signals and thousands of eQTLs colocalizing with complex trait-associated variants
  • Multi-Omics
 ASHG 2022 Annual Meeting (Oct. 25 - 29, 2022) 09/26/22
Earley, Eric A Cox proportional hazards whole genome sequencing study of ischemic stroke risk in a Brazilian sickle cell population ASHG Oct 25-29, 2022 09/26/22
Li, Zilin Whole Genome Sequencing Analyses of 45,090 Individuals Reveal Rare Coding and Noncoding Variants Associated with Kidney Function
  • Kidney Function
 ASHG 2022 (Oct 25-Oct 29) 09/26/22
Johnson, Randi K. Predicted nasal epithelial transcriptome-wide association study in African-ancestry populations
  • Asthma
 ASHG October 2022 09/26/22
Carlson, Jenna Portability of a Multiethnic Polygenic Risk Score for Low-Density Lipoprotein Cholesterol in a Samoan Population
  • Lipids
 ASHG Annual Meeting 2022 (October 25-29, 2022) 08/29/22
Sarnowski, Chloé Leveraging multi-ancestry and whole genome sequence data to improve our understanding of the genetic architecture of neurological traits – applications from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program
  • Diabetes
  • Neurocognitive
 International Stoke Genetics Consortium (ISGC), 21-23 Sept 2022 08/17/22
Sarnowski, Chloé Polygenic scores for insulin resistance are associated with brain volumes in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program
  • Diabetes
  • Neurocognitive
 CHARGE Seattle Conference (Oct 12-14, 2022) 08/09/22
Wheeler, Heather Multiadaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations.
  • MESA Omics
 ASHG October 25-29, 2022 06/08/22
Wheeler, Heather Performing TWAS on proteomic data to understand cis and trans gene regulatory mechanisms underlying complex traits
  • MESA Omics
 ASHG October 25-29, 2022 06/08/22
Sarnowski, Chloé Polygenic scores for insulin resistance are associated with brain volumes in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program.
  • Diabetes
  • Neurocognitive
 American Society of Human Genetics, ASHG (Oct 25-29, 2022) 06/07/22
Kim, John Association of rheumatoid arthritis-related antibodies, HLA-DRB1, and MUC5B (rs35705950) with high attenuation area, forced vital capacity, and interstitial lung abnormalities
  • Lung
 International Colloquium on Lung and Airway Fibrosis (October 1-5 2022) 05/24/22
Karasik, David Sequence variants associated with variation in lean mass: Replication and Epigenomic follow-up
  • Bone Mineralization
 The 2022 Annual Meeting will be held at the Austin Convention Center in Austin, TX, USA, September 9-12. 05/09/22
Shade, Lincoln Whole Genome Sequence Association Analysis of Brain MRI Measures
  • Neurocognitive
 CHARGE Consortium Annual Meeting (April 28, 2022) 02/21/22
Shade, Lincoln Whole Genome Sequence Association Analysis of Brain MRI Measures
  • Neurocognitive
 Alzheimer's Association International Conference, AAIC (July 29th, 2022) 02/21/22
Xiao, Shujie Ancestry-specific markers for asthma exacerbation among African American individuals in the Trans-Omics for Precision Medicine (TOPMed) Program’s Asthma Translational Genomics Collaborative (ATGC)
  • Asthma
 ATS 2022 (May 13-18, 2022) 11/02/21
Liu, Dajiang Trans-Ethnic Fine-Mapping using 3.4 Million Individuals from diverse ancestries elucidates the genetic architecture for Smoking Addiction Phenotypes
  • Smoking
 ASHG 2021 (Oct.18-Oct.22) 10/07/21
Liu, Dajiang A Statistical framework to assess replicability of signals from trans-ethnic genome-wide association meta-analysis: Applications to smoking/drinking addiction traits using 3.4 million individuals.
  • Smoking
 ASHG Annual Meeting (October 18-22, 2021) 10/06/21
Liu, Dajiang Trans-ethnic Transcriptome-wide Association Study and fine-mapping analysis in 3.4 million individuals shed lights on the genetic architecture of alcohol and smoking addiction
  • Smoking
 ASHG 2021 (October 18-22, 2021) 10/06/21
Hasbani, Natalie The genetics of coronary artery calcification in individuals with type 2 diabetes.
  • Atherosclerosis - Clinical and Subclinical
  • Diabetes
 CHARGE Consortium October 7-8, 2021 10/05/21
Hasbani, Natalie The genetics of coronary artery calcification in individuals with type 2 diabetes.
  • Atherosclerosis - Clinical and Subclinical
  • Diabetes
 CHARGE Consortium October 7-8, 2021 10/05/21
Hasbani, Natalie The genetics of coronary artery calcification in individuals with type 2 diabetes.
  • Atherosclerosis - Clinical and Subclinical
  • Diabetes
 ASHG Conference October 18-22, 2021 10/05/21
Gilhool, Steven Rare variant GWAS of African American and Hispanic patients using WGS data from the TOPMed program on the NHLBI BioData Catalyst
  • Asthma
 ASHG Virtual Meeting 2021 (October 18-22, 2021) 10/01/21
Mak, Angel CY Genome-wide gene expression analyses reveals ancestry-specific genetic architecture in Latino and African American children
  • Asthma
 ASHG 2021 (Oct 18-22) 09/28/21
Jun, Goo Multi-tool discovery and joint genotyping of structural variations in 138,134 multi-ethnic TOPMed WGS samples
  • Structural Variation
 ASHG Virtual Meeting 2021 (Oct. 18-22, 2021) 09/28/21
Qiao, Dandi Association of Clonal Hematopoiesis with Chronic Obstructive Pulmonary Disease
  • Chronic Obstructive Pulmonary Disease
 American Society of Human Genetics Annual Meeting (October 18, 2021) 09/27/21
Johnson, Randi K. Prediction of genetically regulated expression of asthma target tissues for African-ancestry populations
  • Asthma
 ASHG October 2021 09/27/21
Chiles, III, Joe Whole Genome Sequence Analysis of Dyspnea in Current and Former Smokers in COPDGene ASHG Conference, October 18, 2021 09/27/21
Smith, Jennifer Whole genome sequencing association analysis of general cognitive function in a multi-ethnic sample from the Trans-Omics for Precision Medicine (TOPMed) Program
  • Neurocognitive
 American Society of Human Genetics, October 18-22, 2021 09/24/21
Hu, Xiaowei Polygenic transcriptome risk scores improve cross-ethnic portability for COPD and lung function in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program
  • Chronic Obstructive Pulmonary Disease
  • Lung
  • PFT Lung Population Cohorts
 American Society of Human Genetics (October 18, 2021) 09/24/21
Manichaikul, Ani Systemic Biomarkers of Lung Function and FEV1 Decline Across Multiple Cohorts
  • PFT Lung Population Cohorts
 American Thoracic Society Virtual Meeting - June 24, 2020 08/19/21
Pino-Yanes, Maria Epigenome-wide association study of bronchodilator response in African Americans
  • Asthma
 European Respiratory Society (ERS) International Congress 2021 (5–8 September, 2021) 08/19/21
Pino-Yanes, Maria Identification of DNA methylation markers associated with lung function in Latino youth with asthma
  • Asthma
 EAACI Pediatric Allergy and Asthma Meeting (PAAM), 12–13 November 2021 08/19/21
Katz, Daniel H Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults
  • Metabolomics and Proteomics
  • Population Genetics
 AHA Scientific Sessions (Nov 13-15, 2021) 06/17/21
Musharoff, Shaila Causal variant effect sizes of complex traits differ between populations
  • Analysis
 American Society of Human Genetics Annual Meeting (October 19, 2021) 06/10/21
Chami, Nathalie Whole exome sequencing analyses of BMI and obesity in a multi-ancestry cohort of > 300,000 individuals
  • Anthropometry - Adiposity (includes Physical Activity)
 ASHG (October 18, 2021) 06/10/21
Manichaikul, Ani Mitochondrial and sex chromosome genetically regulated gene expression implicates new genes in complex traits across multiple human populations.
  • Analysis
 American Society of Human Genetics, October 18-21, 2021 06/09/21
Manichaikul, Ani Protein prediction for trait mapping in diverse populations
  • Analysis
 American Society of Human Genetics, October 18-21, 2021 06/09/21
Moll, Matt Integration of a MUC5B Promoter Variant and a Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities
  • Chronic Obstructive Pulmonary Disease
  • Interstitial Lung Disease
 American Society of Human Genetics October 18-22,2021 06/01/21
Leiser, Claire Associations between ambient air pollutants and clonal hematopoiesis of indeterminate potential (CHIP)
  • Hematology and Hemostasis
 International Society for Environmental Epidemiology Annual Meeting (August 23-26, 2021) 03/29/21
Wang, Heming Upregulation in the heme biosynthesis pathway increases obstructive sleep apnea severity: a mendelian randomization study
  • Hematology and Hemostasis
  • Multi-Omics
  • Sleep Traits
 Joint meeting of the American Academy of Sleep Medicine and the Sleep Research Society (June10,2021) 03/15/21
Manichaikul, Ani Multi-omic association studies identify novel genes and proteins regulating cellular sensitivity to chemotherapy in diverse populations
  • Analysis
 Great Lakes Bioinformatics Meeting; May 10-13, 2021 02/22/21
Nakao, Tetsushi Bidirectional Mendelian Randomization Revealed Bidirectional Causality Between Telomere Length and Clonal Hematopoiesis of Intermediate Potential
  • Hematology and Hemostasis
 CHARGE Consortium Meeting (May 6 and 7, 2021) 02/09/21
Westerman, Kenneth Identification of gene-diet interactions impacting glycemic biomarkers in the multi-ethnic TOPMed cohorts
  • Diabetes
 American Society for Nutrition Conference (June 7-10, 2021) 02/08/21
Satizabal , Claudia Association of mitochondrial DNA copy number with brain MRI and cognitive function in the TOPMed Program
  • Mitochondrial DNA
  • Neurocognitive
 Alzheimer's Association International Conference (AAIC), July 26-30, 2021 02/03/21
Karasik, David A whole genome sequencing study to identify novel genetic variants associated with lean mass: Multi-ethnic meta-analysis
  • Bone Mineralization
 ECTS, May 19-22 2021 01/11/21
Kelly, Rachel S. Metabo-Endotypes of Asthma Reveal Clinically Important Differences in Lung Function
  • Asthma
  • Metabolomics and Proteomics
  • Multi-Omics
 ATS 2021; May 14-19, 2021 12/21/20
Urbut, Sarah Understanding the Genetic E!ects on Multivariate Lipid Phenotypes: An exploration of the Million Veterans Project Resource
  • Lipids
 ASHG 12/11/20
Jiang, Min-Zhi Multi-Omics Data Integration with Sparse Multiple Canonical Correlation Analysis in the Multi-Ethnic Study of Atherosclerosis (MESA) Study
  • Hematology and Hemostasis
 ASHG Virtual Meeting 2020 (October 27-30) 11/05/20
Khan, Alyna Guidelines on the Use and Reporting of Race, Ethnicity, and Ancestry in the NHLBI Trans-Omics Precision Medicine Initiative (TOPMed) Program
  • Ancillary Working Group
 American Society for Human Genetics, October 27-30, 2020 11/05/20
Prizment, Anna Functional CFTR mutations may predispose to increasing risk of colorectal cancer
  • Ancillary Working Group
 ASHG virtual meetig (October 27-30, 2020) 10/17/20
Weinstock, Joshua A compendium of recurrent somatic variation in 46,080 TOPMed whole genomes
  • Hematology and Hemostasis
 ASHG 2020 10/16/20
Otto, Jacqueline Colocalization of GWAS-associated loci for alcohol and tobacco use phenotypes with expression quantitative trait loci in 49 tissues
  • Smoking
 ASHG (October 2020) 10/16/20
Krishnan, Mohanraj Genome-wide association study of telomere length in individuals of Samoan ancestry
  • Hematology and Hemostasis
  • Structural Variation
 ASHG Conference (October 27, 2020) 10/07/20
Li, Xihao MultiSTAAR: Powerful rare variant multi-trait analysis incorporating functional annotations for large-scale whole genome sequencing studies, with application to TOPMed lipid data
  • Lipids
 ASHG 2020 Annual Meeting (October 27-31, 2020) 10/07/20
Erdoğan-Yıldırım, Zeynep Genome-wide association study of high vs low risk of polycystic ovarian syndrome in Samoan women
  • Reproductive Health
 American Society of Human Genetics (October 27-30,2020) 10/07/20
Minster, Ryan L Genome-wide association study of height in Samoan individuals
  • Anthropometry - Adiposity (includes Physical Activity)
 2020 Annual Meeting of ASHG 10/07/20
Hsu, Yi-Hsiang Novel osteoporosis loci identified by whole genome sequencing and CRISPR editing screening in zebrafish
  • Bone Mineralization
 ASHG October 26, 2020 10/06/20
Saunders, Gretchen Alcohol and tobacco polygenic risk score prediction within and across diverse ancestries
  • Smoking
 ASHG (October, 2020) 10/06/20
Qiao, Dandi Shorter telomere associates with moderate-to-severe COPD and demonstrates shortening by GOLD grade
  • Chronic Obstructive Pulmonary Disease
  • Lung
 ASHG Virtual Meeting 2020 (October 27, 2020) 10/06/20
Himes, Blanca Genetics of Bronchodilator Response in Diverse Populations
  • Asthma
  • Lung
 ASHG 2020 10/05/20
Kim, Wonji Whole Genome Sequence Analysis of Pulmonary Function and COPD using ~40,000 Multi-ethnic Samples in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program
  • PFT Lung Population Cohorts
 ASHG 2020 Virtual Meeting (October 27-30, 2020) 10/04/20
Selvaraj, Margaret Sunitha Whole genome sequence analysis of plasma lipids in a multi-ethnic cohort of 66,329 individuals
  • Lipids
 ASHG (Oct,2020) 10/02/20
Mathur, Ravi A generalizable protocol for leveraging whole genome sequenced cohorts as population controls for new genome wide association studies
  • Analysis
 ASHG Annual Meeting (October 27-30, 2020) 10/02/20
Keener, Rebecca Trans-ethnic meta-analysis reveals novel loci, genes, and pathways regulating adult telomere length.
  • Hematology and Hemostasis
  • Structural Variation
 American Society of Human Genetics (October, 2020) 10/02/20
Carlson, Jenna Samoan genome-wide association studies identify novel associations with blood pressure phenotypes
  • Blood Pressure
 ASHG Virtual Meeting 2020 (October 27-30, 2020) 10/02/20
Kasela, Silva Genetic and non-genetic factors affecting the expression of COVID-19-related genes in bronchial epithelium
  • Lung
 ASHG (October 27-30, 2020) 10/02/20
Stilp, Adrienne M. Whole genome sequencing association analyses of red blood cell traits in a large, multi-ethnic sample from the Trans-Omics for Precision Medicine (TOPMed) Program
  • Hematology and Hemostasis
 American Society of Human Genetics (October 2020) 09/29/20
Kelly, Rachel S. Metabo-Endotypes of Asthma Reveal Clinically Important Differences in Lung Function
  • Lung
 October 27-29 2020, Metabolomics Society Annual Conference 09/17/20
Wen, Fayuan Genome Wide Association Analysis of Iron Overload in the Trans-Omics for Precision Medicine (TOPMed) sickle cell disease cohorts
  • Sickle Cell Disease
 62nd Annual Meeting of the American Society of Hematology (ASH) (Saturday, December 5 to Tuesday, December 8, 2020) 08/11/20
Daya, Michelle An HLA association study of total serum IgE levels using whole-genome sequence data from TOPMed
  • Asthma
  • Lung
 ASHG (Oct 2020) 07/13/20
Hsu, Yi-Hsiang GDF10, A Novel BMD Locus Identified by Whole Genome Sequencing Showed Reduced Vertebral Bone Mass & Mineralization in CRISPR KO Zebrafish: The NHLBI Trans-Omics for Precision Medicine (TOPMED) Study
  • Bone Mineralization
 ASBMR Sep 2020 07/01/20
Hsu, Yi-Hsiang Novel osteoporosis loci identified by whole genome sequencing and CRISPR editing screening in zebrafish: The NHLBI Trans-Omics for Precision Medicine (TOPMED) Study
  • Bone Mineralization
 American Society of Human Genetics (October 2020) 07/01/20
Li, Xihao Powerful and resource-efficient rare variant meta-analysis for large-scale whole genome sequencing studies using summary statistics and functional annotations, with application to TOPMed lipid data
  • Lipids
 ASHG 2020 Annual Meeting (October 27-31, 2020) 06/18/20
Kasela, Silva Mapping of mQTLs in TOPMed/MESA and implications in lung disease risk and GxE interactions
  • Lung
 ASHG (October 27-31, 2020) 06/16/20
Manichaikul, Ani Phenome-wide and molecular consequences of inbreeding
  • Anthropometry - Adiposity (includes Physical Activity)
  • Diabetes
  • Lipids
  • Multi-Omics
  • PFT Lung Population Cohorts
  • Population Genetics
 American Society of Human Genetics (Oct 27-31, 2020) 06/15/20
Li, Zilin A framework for detecting non-coding rare variant associations in large whole genome sequencing studies at scale, with application to 30,138 TOPMed participants for lipid traits
  • Lipids
 ASHG Conference (October 27-31) 06/14/20
McHugh, Caitlin A mixed model approach to testing multiple correlated traits in large samples: An application to the Trans-Omics for Precision Medicine (TOPMed) program hematology phenotypes.
  • Hematology and Hemostasis
 ASHG Conference October 27, 2020 06/11/20
Raffield, Laura eSCAN: Scan regulatory regions for aggregate association testing using whole genome sequencing data
  • Hematology and Hemostasis
 American Society of Human Genetics, October 27-31, 2020 06/10/20
Yu, Bing Multi-Ethnic Whole-Genome Sequencing Analysis of Human Metabolome Identifies 93 Novel Genetic Loci
  • Metabolomics and Proteomics
 ASHG (Oct 27, 2020) 06/09/20
Manichaikul, Ani Multi-ethnic fine mapping optimizes proteome association studies
  • Analysis
 American Society of Human Genetics (October 27-31, 2020) 06/01/20
Karasik, David A whole genome sequencing to identify genetic variants associated with lean mass: The NHLBI Trans-Omics for Precision Medicine (TOPMED) Program
  • Bone Mineralization
 ASBMR 2020 Annual Meeting (Sept 2020) 05/26/20
Huffman, Jennifer Multi-ethnic whole genome sequence analysis of plasma fibrinogen in over 150,000 samples
  • Hematology and Hemostasis
 ISTH 2020 Congress (July 11-15, 2020) 02/11/20
de Vries, Paul Whole genome sequencing study of coagulation factor VIII and von Willebrand factor reveals new genetic associations
  • Hematology and Hemostasis
 ISTH (July 11-15, 2020) 02/04/20
Sarnowski, Chloé Whole Genome Sequence Association Analyses of Brain Volumes in the TOPMed Program
  • Neurocognitive
 Alzheimer's Association International Conference, AAIC (July 26-30, 2020) 01/27/20
Raffield, Laura Causal gene candidates for type 2 diabetes based on protein-coding variants in 127,676 individuals
  • Diabetes
 American Diabetes Association, June 12-16 01/14/20
El Boueiz, Adel Whole genome sequencing and integrative genomics analyses to identify genetic determinants of pulmonary vascular remodeling in COPD
  • Lung
 Pulmonary Vascular Research Institute (PVRI) (January 2020) 12/05/19
Sarnowski, Chloé Leveraging multi-ethnic populations along with multiple handgrip measurements in association analyses with sequence data: the Trans-Omics for Precision Medicine (TOPMed) Program
  • Longevity and Healthy Aging
 CHARGE meeting (January 30-31, 2020) 11/18/19
Yu, Bing Metabolomic Associations with Pulmonary Function: Findings from the TOPMed Program
  • Metabolomics and Proteomics
 ATS 2020 (May 15, 2020) 10/28/19
Liu, Dajiang Near-optimal trans-ethnic association and fine mapping of smoking associated genes integrating GWAS and TOPMed sequence data of 1.3 million individuals
  • Smoking
 the American Society of Human Genetics annual meeting 10/16/19
Reiner, Alex Prospective Association of TET2 Mediated Clonal Hematopoiesis and Heart Failure and tis subtypes in Post Menopausal Women
  • Heart Failure - Cardiac Function - Morphology
  • Hematology and Hemostasis
 AHA Epi Council March 6, 2020 10/10/19
Hsu, Yi-Hsiang A large-scale whole genome sequencing to identify less common and rare variants associated with osteoporosis and fracture: The NHLBI TopMed Study
  • Bone Mineralization
 American Society of Human Genetics (October 2019) 10/10/19
Minster, Ryan L Identification of susceptibility loci for reproductive traits in Samoan women
  • Reproductive Health
 ASHG (Oct 18, 2019) 10/08/19
Minster, Ryan L A novel variant in CETP is associated with higher HDL-cholesterol in people of Polynesian ancestry
  • Lipids
 ASHG (Oct 16, 2019) 10/08/19
Jaiswal, Sidd Clonal hematopoiesis of indeterminate potential and epigenetic age acceleration
  • Atherosclerosis - Clinical and Subclinical
  • Epigenetics
  • Hematology and Hemostasis
  • Longevity and Healthy Aging
 ASHG Conference October 14-19, 2019 10/07/19
Manning, Alisa Understanding the genetic basis of type 2 diabetes risk: whole genome sequence analysis of glycemic traits from the NHBLI’s TOPMed Program
  • Diabetes
 American Society of Human Genetics Conference (October 18, 2019) 10/04/19
Russell, Emily Evidence of natural selection in Samoans is associated with BMI and the immune system
  • Population Genetics
 ASHG Conference (October 18, 2019) 10/04/19
Zhu, Xiaofeng Targeted genome sequencing identifies multiple rare variants in Caveolin-1 (CAV1) associated with obstructive sleep apnea trait
  • Sleep Traits
 ASHG 2019 10/04/19
Zoellner, Sebastian Estimating the ages of rare variants using long ­range identity by ­descent (IBD) ASHG Poster number 2405F 10/04/19
Mathias, Rasika Integrating eQTLs to Identify SNP Associations in Whole-Genome Sequencing Association Studies: A Genetic Study of Platelet Aggregation.
  • Hematology and Hemostasis
 ASHG 2019 10/03/19
Hecker, Julian A unifying framework for region-based association testing in family-based designs without the need for asymptotic assumptions or approximations, including higher criticism approaches, SKATs, multivariate and burden tests
  • Asthma
 ASHG (Oct 15-19, 2019) 10/03/19
Ryan, Kathleen Effects of reference panel composition on genotype imputation quality in founder samples.
  • Analysis
 ASHG 2019 Meeting (October 17, 2019) 10/03/19
Weinstock, Joshua Inherited causes and clinical consequences of clonal hematopoiesis from 100,002 whole genomes
  • Hematology and Hemostasis
 ASHG 2019 09/19/19
Hersh, Craig Characterization of CFTR mutations in chronic obstructive pulmonary disease
  • Chronic Obstructive Pulmonary Disease
 ASHG 2019 09/12/19
Johnson, Andrew Genome-wide association study of on-aspirin platelet aggregation identifies ACYP2 and other loci as novel pharmacogenetic candidates
  • Hematology and Hemostasis
 ASHG 2019 09/11/19
Blangero, John Spinocerebellar ataxia STRs identified in Mexican Americans families show association with decreased cerebellum volume and decreased working memory ASHG October 16, 2019 08/05/19
Carlson, Jenna A large effect, Polynesian-specific, stop-gained variant in BTNL9 is associated with atherogenic lipid profiles
  • Lipids
 ASHG 2019 (October 15-19, 2019) 07/25/19
Cox, Corey Utilizing whole genome sequence data to elucidate the genetics of total serum IgE concentrations
  • Asthma
 ASHG 2019 06/26/19
Elise Lim TOPMed Whole Genome Sequence Analysis of Waist-to-Hip Ratio and Waist Circumference
  • Anthropometry - Adiposity (includes Physical Activity)
 CHARGe 6/26/2019 06/18/19
Vrieze, Scott Near-Optimal Trans-ethnic Association and Fine Mapping of Smoking Associated Genes Integrating GWAS and TOPMed sequence Data of 1.3 million individuals
  • Smoking
 ASHG October 2019 06/12/19
Carlson, Jenna Creating population-specific reference panels for improved genotype imputation American Society of Human Genetics 2018 Annual Meeting (October 16-20, 2018) 06/11/19
Willer, Cristen Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease
  • Lipids
 ASHG 2019 (October 15-19, 2019) 06/11/19
Hindy, George Association of Exome Sequence Variation with Blood Lipids in 170,000 Individuals Across Multiple Ancestries
  • Lipids
 ASHG (Oct 2019() 06/10/19
Sarnowski, Chloé Association analysis of handgrip strength in targeted loci from GWAS using longitudinal measures and whole-genome sequence data from the Trans-Omics for Precision Medicine (TOPMed) Program
  • Longevity and Healthy Aging
 American Society of Human Genetics (Oct 15-19, 2019) 06/10/19
de Vries, Paul Multi-ancestry whole genome sequencing analysis of coronary artery calcification
  • Atherosclerosis - Clinical and Subclinical
 AHA Scientific Sessions (November 16-18, 2019) 06/07/19
de Vries, Paul Whole genome sequencing and associations with coagulation factors VII and VIII and von Willebrand factor: the TOPMed program
  • Hematology and Hemostasis
 ASHG (October 15-19, 2019) 06/07/19
Huffman, Jennifer Multi-ethnic whole genome sequence analysis of fibrinogen, fibrin D-dimer, tissue plasminogen activator & plasminogen activator inhibitor 1 within the TOPMed program
  • Hematology and Hemostasis
 ASHG 2019 Annual Meeting (Oct 15-19, 2019) 06/07/19
Li, Xihao Dynamic incorporation of multiple in-silico functional annotations empowers rare variant association analysis in large-scale whole genome sequencing studies
  • Lipids
 ASHG 2019 Annual Meeting (October 15-19, 2019) 06/06/19
Taub, Margaret Thirteen novel genetic loci identified for telomere length leveraging 75K whole genome sequences in the Trans-Omics for Precision Medicine (TOPMed) Program
  • Hematology and Hemostasis
  • Structural Variation
 American Society of Human Genetics, Oct 15-19, 2019 06/06/19
Hasbani, Natalie Multi-ancestry whole genome sequencing study of carotid intima media thickness and carotid plaque
  • Atherosclerosis - Clinical and Subclinical
 ASHG 2019 Annual Meeting (October 15-19 2019) 06/06/19
Natarajan, Pradeep An X Chromosome Genetic Association Analysis Identifies Variants in ChrXq23 with Lower Atherogenic Lipids and Lower Risk for Coronary Heart Disease
  • Lipids
 American Heart Association (AHA) Scientific Sessions (November 16-18 2019) 06/06/19
Conomos, Matthew Sparse Empirical Kinship Matrices Enable Computationally Efficient and Accurate Association Tests in Large Samples
  • Hematology and Hemostasis
  • Analysis
 ASHG October 15-19, 2019 06/06/19
Zilin Li Whole Genome Sequence Association Analysis of Body Mass Index in 45,159 TOPMed Participants
  • Anthropometry - Adiposity (includes Physical Activity)
 ASHG (October 15-19, 2019) 06/06/19
Gagliano Taliun, Sarah High-specificity variant filter enables joint analysis of whole genome sequence data from multiple studies and sequencing centers
  • Ancillary Working Group
 ASHG Annual Meeting (October 2019) 06/05/19
Vrieze, Scott Trans-ethnic GWAS meta-analysis of tobacco and alcohol use
  • Smoking
 ASHG October 2019 06/03/19
Sofer, Tamar Whole Genome Sequence Association Study of Sleep Duration in the TOPMed Program
  • Sleep Traits
 ASHG, October 2019 06/03/19
Li, Yun Calling and Imputation of the Common a-globin Copy Number Variant with Whole Genome Sequencing Data in TOPMed and Association with Hematologic and Other Clinical Phenotypes
  • Hematology and Hemostasis
 American Society of Human Genetics, October 15-19, 2019 05/31/19
Gui, Hongsheng Fine mapping of human leukocyte antigen complex to study asthma in African Americans
  • Lung
 American Society of Human Genetics Annual Meeting (Oct 15-19, 2019) 05/30/19
Sofer, Tamar Carriers-only tests of association of a rare genetic variant with a binary outcome
  • Sleep Traits
  • Analysis
 ASHG, October 15, 2019. 05/28/19
Sarnowski, Chloé Association analyses of handgrip strength leveraging longitudinal and sequence data from the Trans-Omics for Precision Medicine (TOPMed) Program
  • Longevity and Healthy Aging
 International Genetic Epidemiology Society (IGES), 12-14 Oct 2019 05/27/19
Hu, Yao Whole Genome Sequencing Association Analysis of Stroke and Its Subtypes in a Multi-Ethnic Population from Trans-Omics for Precision Medicine (TOPMed)
  • Stroke
 American Society of Human Genetics 2019 Annual Meeting (October 15-19,2019) 05/20/19
Highland, Heather M Whole Genome Sequence Analysis of Type 2 Diabetes Risk in 44,713 Humans of Diverse Ancestry in the TOPMed Study
  • Diabetes
 American Diabetes Association Scientific Sessions, June 7-11, 2019 01/14/19
Sarnowski, Chloé Chromosome X association analysis of Hemoglobin A1c (HbA1c) in African Americans using sequence data from TOPMed
  • Diabetes
 TOPMed Meeting (05-06 Dec 2018) 11/14/18
Laurie, Cathy Overview of the NHLBI Trans-Omics for Precision Medicine (TOPMed) program: whole-genome sequencing of >100,000 deeply phenotyped individuals
  • Ancillary Working Group
 American Society of Human Genetics, October 18, 2018 10/12/18
Parker, Margaret Integrating whole genome sequencing and RNA sequencing through allele specific expression analysis in the COPDGene study
  • Lung
 American Society of Human Genetics, 10/19 10/10/18
Raffield, Laura Multiple signals at known loci revealed by analysis of C-reactive protein levels in the Trans-Omics for Precision Medicine (TOPMed) whole genome sequencing data
  • Inflammation Biomarkers
 American Society of Human Genetics, October 19, 2018 09/28/18
Raffield, Laura (on behalf of Kowalski, Madeline) TOPMed based Imputation in Minority Samples
  • Hematology and Hemostasis
 American Society of Human Genetics, October 18, 2018 09/28/18
Seplyarskiy, Vladimir Approach to determine germline epigenetic state and mutators alleles based on local mutation rate
  • Population Genetics
 ASHG 09/10/18
Russell, Emily Rare variation in and near CREBRF and association with fasting glucose in non-Polynesian participants in the TOPMed Program
  • Diabetes
 ASHG Conference (October 16th - 20th, 2018) 09/10/18
Russell, Emily Genome­wide association study of type 2 diabetes phenotypes in Sāmoans
  • Diabetes
 ASHG Conference (October 16th - 20th, 2018) 09/10/18
Luo, Yang Using ~20,000 public whole genomes to build reference panels for fine-mapping HLA effects in multi-ethnic cohorts
  • Population Genetics
 ASHG (Oct 16-20, 2018) 09/09/18
Johnson, Andrew Leveraging whole genome sequencing to identify novel determinants of platelet function
  • Hematology and Hemostasis
 ASHG (October 2018) 07/26/18
Majarian, Timothy Leveraging T2D specific omics data in rare variant association analysis in TOPMed
  • Diabetes
 American Society of Human Genetics 07/25/18
Franceschini, Nora Discovery of novel genetic loci for kidney traits using whole genome sequencing: the Trans-Omics for Precision Medicine (TOPMed) Project
  • Kidney Function
 ASHG, Oct 16-20, 2018 & IGES, Oct 14-15, 2018 07/20/18
de Vries, Paul Trans-ancestry whole genome sequencing analysis of coronary artery calcification
  • Atherosclerosis - Clinical and Subclinical
 CHARGE Investigator Meeting (October 10-12 2018) 07/18/18
Sarnowski, Chloé Chromosome X association analysis of Hemoglobin A1c (HbA1c) in African Americans using TOPMed whole genome sequence (WGS) data
  • Diabetes
 CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium) meeting, Baltimore, 11-12 Oct 2018 07/17/18
Manning, Alisa Fine-mapping of type 2 diabetes and glycemic traits with whole genome sequence data using 49,022 individuals from the NHBLI’s TOPMed WGS Program
  • Diabetes
 ASHG Conference (October 2018) 07/09/18
Jang, Seon-Kyeong Rare variant associations with cigarette smoking in the Trans-Omics for Precision Medicine Whole Genome Sequencing Program (TOPMed)
  • Smoking
 American Society of Human Genetics (October 16-20, 2018) 06/14/18
Taub, Margaret Novel genetic loci identified for telomere length leveraging 50,000 whole genome sequences in the Trans-Omics for Precision Medicine (TOPMed) project
  • Hematology and Hemostasis
  • Structural Variation
 ASHG (Oct 16-20) 06/14/18
Laurie, Cecelia Genetic association study of venous thromboembolism based on whole-genome sequencing in the Trans-Omics for Precision Medicine (TOPMed) program
  • Venous Thromboembolism
 ASHG 2018 (October 16-20, 2018) 06/12/18
Manichaikul, Ani Whole Genome Sequence Analysis of Pulmonary Function and COPD in >16,000 Multi-ethnic Participants of the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program Identifies New Associated Loci
  • Chronic Obstructive Pulmonary Disease
  • Lung
  • PFT Lung Population Cohorts
 American Society of Human Genetics (October 16-20, 2018) 06/07/18
He, Karen Linkage evidence and TOPMed whole genome sequencing identify multiple genes on chromosome 1 with rare variants associated with blood pressure
  • Blood Pressure
 ASHG (October, 2018) 06/07/18
Brody, Jennifer Whole-Genome Sequence Analysis of Body Mass Index in the Trans-Omics for Precision Medicine (TOPMed) Program
  • Anthropometry - Adiposity (includes Physical Activity)
 ASHG (October 2018) 06/06/18
Peloso, Gina Monogenic and polygenic predictors of plasma lipid extremes from whole genome sequencing in diverse ancestries: The NHLBI TOPMed program
  • Lipids
 ASHG (October 2018) 06/05/18
Hu, Yao Whole genome sequencing association analysis of red blood cell traits in a multi-ethnic population sample from the Trans-Omics for Precision Medicine (TOPMed) Project
  • Hematology and Hemostasis
 October 17, 2018 06/05/18
Natarajan, Pradeep Whole genome sequence association with plasma lipids in 28,541 individuals
  • Lipids
 American Heart Association Scientific Sessions (November 10-12, 2018) 06/05/18
Gagliano, Sarah Analysis of densely imputed UK Biobank genetic data reveals disease-associated rare loss of function variation
  • Population Genetics
 ASHG Annual Meeting (October 2018) 06/05/18
Perry, James An Omics Analysis, Search and Information System (OASIS) for Enabling Discovery in the TOPMed Diabetes Working Group
  • Diabetes
 ASHG Conference (October 2018) 06/04/18
Wheeler, Marsha Novel structural variants originating in F8 non-coding regions explain previously unresolved cases of severe hemophilia A
  • Hematology and Hemostasis
 ASHG 06/04/18
Lee, Seung-been Large-scale characterization of CYP2D6 variation in African Americans using TOPMed whole genome sequencing data
  • Structural Variation
 ASHG 2018 (TBD) 06/01/18
Sarnowski, Chloé Chromosome X association analysis of Hemoglobin A1c (HbA1c) in African Americans using TOPMed whole genome sequence (WGS) data
  • Diabetes
 IGES meeting, October 14-16, 2018, San Diego 06/01/18
Auer, Paul Whole genome sequences association with E-selectin levels reveals Loss-of-function variant in African Americans
  • Inflammation Biomarkers
 American Society of Human Genetics (October 16-20, 2018) 05/29/18
Auer, Paul Multiple signals at known loci revealed by analysis of C-reactive protein levels in the Trans-Omics for Precision Medicine (TOPMed) whole genome sequencing data
  • Inflammation Biomarkers
 American Society of Human Genetics (October 16-20, 2018) 05/29/18
Mak, Angel CY Whole Genome Sequencing To Identify Novel Genetic Variation And Gene-By-Air Pollution Interactions That Influence Lung Function In Minority Children
  • Asthma
  • Lung
 American Thoracic Society International Converence (May18-23, 2018) 05/16/18
Young, Hannah Discovering rare variants associated with substance use in 65,000 deep whole genome sequences in the Trans-Omics for Precision Medicine (TOPMed) Program
  • Smoking
 Behavior Genetics Association (Boston, June 20-23, 2018) 04/02/18
Sarnowski, Chloé NHLBI Trans-Omics for Precision Medicine (TOPMed) trans-ethnic association analysis of Hemoglobin A1c (A1C) in erythrocyte genes using Whole Genome Sequence (WGS) data
  • Diabetes
 CHARGE meeting, Rotterdam, April 18-19 2018 01/10/18
Sarnowski, Chloé Ancestral differences in Hemoglobin A1c (A1C) associations of erythrocyte genes using NHLBI Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequence (WGS) data
  • Diabetes
 American Diabetes Association (ADA), Orlando, June 22-26 2018 01/09/18
Cade, Brian Whole Genomic Associations of Transcription Factor Networks With Sleep Disordered Breathing Traits in Trans-Omics for Precision Medicine (TOPMed)
  • Sleep Traits
 Sleep 2018 (APSS, June 2-6,2018) 12/19/17
Montasser, May E. B4GALT1: A Novel LDL-Associated Gene
  • Lipids
 Genomics of Common Diseases (GCD) meeting. Hinxton, Cambridge, UK. Sep 2017. Oral. American Society for Human Genetics (ASHG) meeting. Orlando, FL, USA. Oct 2017. Poster. African Society for Human Genetics (AfSHG) meeting. Cairo, Egypt, Nov 2017. Oral. 11/22/17
Zekavat, Maryam Analyzing the full spectrum of genomic variation with Lp(a) cholesterol: novel insights from deep, whole genome sequence data in 5,192 Estonians and African Americans
  • Lipids
 Harvard Program in Quantitative Genomics (PQG) meeting (November 2016) 11/21/17
Zekavat, Maryam Multi-ethnic whole genome sequence analysis of Lp(a) and phenome-wide scan
  • Lipids
 Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) meeting (Sep 2017) 11/21/17
Natarajan, Pradeep Impact of whole genome sequence variation on plasma lipids in 8,368 TOPMed Program participants
  • Lipids
 MGH Center for Human Genetics (CHGR) retreat. Cambridge, MA, USA. Sept 2016 11/15/17
Natarajan, Pradeep Rare variant association in non-coding sequence: an analysis of deep coverage whole genome sequences and blood lipids in 16,324 individuals
  • Lipids
 Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) meeting. Boston, MA, USA. Sep 2017 11/15/17
Natarajan, Pradeep Rare variant association in non-coding sequence: an analysis of deep coverage whole genome sequences and blood lipids in 16,324 individuals
  • Lipids
 American Society for Human Genetics (ASHG) meeting. Orlando, FL, USA. Oct 2017 11/15/17
Manning, Alisa Accounting for Obesity in Whole Genome Sequence Analyses of Type 2 Diabetes (T2D)
  • Diabetes
 Annual Biomedical Research Conference For Minority Students (November 1-4, 2017) 11/11/17
Sarnowski, Chloe TOPMed Whole Genome Sequence (WGS) Associations with Brain MRI Measures in the Framingham Study
  • Neurocognitive
 Alzheimer's Association International Conference (AAIC), 16-20 July 2017, London (UK) 11/01/17
Sarnowski, Chloe Whole genome sequence analysis of brain MRI measures in the Framingham Study.
  • Neurocognitive
 International Stroke Genetics Consortium (ISGC). Milan (Italy), 03-04 Nov 2016 11/01/17
Sarnowski, Chloe Whole genome sequence analysis of brain MRI measures in the Framingham Study.
  • Neurocognitive
 Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) meeting, Charlottesville (USA), 28-29 Sept 2016 11/01/17
Sarnowski, Chloe Whole genome sequence analysis of brain MRI measures in the Framingham Study.
  • Neurocognitive
 American Society of Human Genetics (ASHG). Vancouver (Canada), 18-22 Oct 2016 11/01/17
Wu Peitao Whole Genome Sequence Association Analysis of Fasting Glucose in the Trans-Omics for Precision Medicine (TOPMed) program
  • Diabetes
 Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) meeting, Boston (USA), 27-28 Sept 2017. 11/01/17
Sarnowski, Chloe Whole Genome Sequence (WGS) Associations with Hemoglobin A1c (A1C) in White and Black Populations.
  • Diabetes
 American Diabetes Association (ADA) meeting, San Diego (USA), 9-13 June 2017. 11/01/17
Sarnowski, Chloe Rare variant analysis of fasting glucose and fasting insulin using TOPMed-Framingham Heart Study whole genome sequence data.
  • Diabetes
 Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) meeting, Charlottesville (USA), 28-29 Sept 2016 11/01/17
Taub, Margaret Telomere length estimation and analysis on large scale whole-genome sequencing data
  • Hematology and Hemostasis
 ASHG Conference (Oct 18, 2017) 10/26/17
Rice, Ken We didn't see this in GWAS: Understanding and fixing unfamiliar problems in association analyses, when pooling whole genome sequence data from multiple studies.
  • Analysis
 ASHG (October, 2017) 10/17/17
Raffield, Laura Analysis of platelet related traits in the Trans-Omics for Precision Medicine (TOPMed) whole genome sequencing project
  • Hematology and Hemostasis
 American Heart Association Epi/Lifestyle Session, March 20-23 10/08/17
Germer, Soren Discovery and typing of polymorphic non-deletions of ancestral hominid sequence in the human genome
  • Population Genetics
 AGBT (February 12-15th, 2018) 10/02/17
Peloso, Gina Monogenic and polygenic predictors of extreme dyslipidemia from whole genome sequencing in 8,394 white and black NHLBI TOPMed participants
  • Lipids
 Genomics of Common Disease (Sep 6-8, 2017) 09/19/17
Datta, Gargi Whole genome sequence association analysis of tobacco use in the Trans-Omics for Precision Medicine Whole Genome Sequencing Program (TOPMed)
  • Smoking
 ASHG 2017 (October 17th-21st, 2017) 09/01/17
Wessel, Jennifer TOPMed Whole Genome Sequence Association Analysis Of Type 2 Diabetes
  • Diabetes
 American Society of Human Genetics (October 17-21) 07/07/17
Manning, Alisa Fine­mapping fasting glucose and fasting insulin loci with whole genome sequence data from the Trans­Omics for Precision Medicine (TOPMed) Program
  • Diabetes
 American Society of Human Genetics 07/07/17
Cade, Brian Whole Genome Sequence Association Analysis of Sleep Disordered Breathing Traits in Trans-Omics for Precision Medicine (TOPMed)
  • Sleep Traits
 World Sleep (October 7-11, 2017) 06/30/17
Wheeler, Marsha Genomic characterization of F8 and F9 copy number variants in the My Life, Our Future TOPMed hemophilia cohort
  • Hematology and Hemostasis
 ASHG Annual Meeting October 17th 06/22/17
Zheng, Xiuwen Whole genome sequencing association analysis of red blood cell traits in a multi-ethnic population from the Trans-Omics for Precision Medicine (TOPMed) Project
  • Hematology and Hemostasis
 American Society of Human Genetics 2017 Annual Meeting (Oct, 2017) 06/11/17
Zhu, Xiaofeng Low frequency and rare variants of RBFOX1 are associated with blood pressure
  • Blood Pressure
 ASHG 2017 annual meeting 06/09/17
Zhu, Xiaofeng Low frequency and rare variants in multiple genes are associated with sleep related traits using whole genome sequencing data
  • Sleep Traits
 ASHG 2017 Annual Meetng 06/09/17
Levine, David High-Performance Whole Genome Sequence Variant Analysis in the TOPMed Project Using Cloud Environments 67th Annual Meeting of the American Society of Human Genetics (October 17-21, 2017) 05/25/17
Wessel, Jennifer Whole Genome Sequence Association Analysis Of Type 2 Diabetes And Glycemic Traits In Trans-omics For Precision Medicine (TOPMed)
  • Diabetes
 International Genetic Epidemiology Society (September 9-11, 2017) 05/17/17
Lunetta, Kathryn Adjusting family aggregation and population stratification via genetic relationship matrix in association analysis of genetic variants and a binary trait
  • EKG - Arrhythmia
 International Genetic Epidemiology Society meeting, (September 9-11, 2017) 05/16/17
Manning, Alisa Whole Genome Sequence Association Analysis Of Fasting Glucose And Fasting Insulin From 7,121 Non-diabetic Individuals In Trans-omics For Precision Medicine (TOPMed)
  • Diabetes
 American Diabetes Association 77th Scientific Sessions (June 9 - 13, 2017) 01/04/17
Leong, Aaron TOPMed Whole Genome Sequence (WGS) Associations with Hemoglobin A1c (A1C) in White and Black Populations
  • Diabetes
 American Diabetes Association Scientific Sessions (June 9-13, 2017) 12/28/16
Sarnowski, Chloe Trans-ethnic association analysis of Hemoglobin A1c (A1C) using TOPMed Whole Genome Sequence (WGS) data
  • Diabetes
 CHARGE meeting in New York (March 23-24, 2016) 12/28/16
Cho, Michael Whole Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease
  • Chronic Obstructive Pulmonary Disease
 American Thoracic Society May 19, 2017 11/02/16
Ellinor, Patrick Feasibility of Whole Genome Sequencing for Atrial Fibrillation
  • EKG - Arrhythmia
 American Heart Association (November 15, 2016) 10/27/16
Rafaels, Nicholas Whole genome sequence analysis of asthma in families from Barbados
  • Asthma
 ASHG Conference, October 19, 2016 10/25/16
Cho, Michael Whole Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease
  • Chronic Obstructive Pulmonary Disease
 ATS 2015 10/24/16
Abecasis, Goncalo TOPMed: Early Insights from Sequencing and Analysis of 45,934 Deep Human Genomes
  • Anthropometry - Adiposity (includes Physical Activity)
  • Lipids
 ASHG 2016 10/24/16
Brody, Jennifer Analysis Commons: Team Science in a Big-Data Environment for Genetic Epidemiology
  • Hematology and Hemostasis
 AHA EPI 2016 10/24/16
258 Abstracts