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 |
|
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. |
|
ASHG, Nov 1 2023 |
10/18/23 |
Kim, Kangjin |
Whole genome sequencing and proteomic analysis of mucus plugging in COPDGene |
|
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 |
|
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 |
|
ASHG 2023 Annual Meeting (Nov. 1-5, 2023) |
10/12/23 |
Lê, Brandon |
Characterizing epigenetic aging in an adult sickle cell disease cohort |
|
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 |
|
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 |
|
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 |
|
ASHG 2023 |
09/29/23 |
Keener, Rebecca |
Rare variants affecting telomere length and disease identified through multi-omic modeling |
|
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 |
|
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 |
|
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 |
|
ASHG Conference (Nov 1-5 2023) |
06/27/23 |
Debban, Catherine |
Multi-study pQTL analysis of Somascan proteomics in multi-ancestry TOPMed Cohorts |
|
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 |
|
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 |
|
ASHG (November 1-5, 2023) |
06/20/23 |
Sun, Quan |
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 (June 3, 2023) |
12/15/22 |
Wang, Heming |
Whole genome sequence analyses for Excessive Daytime Sleepiness in the NHLBI TOPMed Program |
|
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. |
|
ASHG October 2022 |
10/21/22 |
Minster, Ryan L |
Genome-wide association studies of metabolic traits in Samoans |
|
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 |
|
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 |
|
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 |
|
ASHG 10/26/2022 |
10/04/22 |
Wang, Yuxuan |
Whole genome sequence analysis of long non-coding RNAs for plasma lipid traits |
|
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 |
|
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 |
|
ASHG 2022 (Oct 25-Oct 29) |
09/26/22 |
Johnson, Randi K. |
Predicted nasal epithelial transcriptome-wide association study in African-ancestry populations |
|
ASHG October 2022 |
09/26/22 |
Carlson, Jenna |
Portability of a Multiethnic Polygenic Risk Score for Low-Density Lipoprotein Cholesterol in a Samoan Population |
|
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 |
|
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 |
|
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. |
|
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 |
|
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. |
|
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 |
|
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 |
|
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 |
|
CHARGE Consortium Annual Meeting (April 28, 2022) |
02/21/22 |
Shade, Lincoln |
Whole Genome Sequence Association Analysis of Brain MRI Measures |
|
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) |
|
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 |
|
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. |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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. |
|
American Society of Human Genetics, October 18-21, 2021 |
06/09/21 |
Manichaikul, Ani |
Protein prediction for trait mapping in diverse populations |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
ASHG October 26, 2020 |
10/06/20 |
Saunders, Gretchen |
Alcohol and tobacco polygenic risk score prediction within and across diverse ancestries |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
American Society of Human Genetics (October 2019) |
10/10/19 |
Minster, Ryan L |
Identification of susceptibility loci for reproductive traits in Samoan women |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
ASHG (Oct 15-19, 2019) |
10/03/19 |
Ryan, Kathleen |
Effects of reference panel composition on genotype imputation quality in founder samples. |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
ASHG Annual Meeting (October 2019) |
06/05/19 |
Vrieze, Scott |
Trans-ethnic GWAS meta-analysis of tobacco and alcohol use |
|
ASHG October 2019 |
06/03/19 |
Sofer, Tamar |
Whole Genome Sequence Association Study of Sleep Duration in the TOPMed Program |
|
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 |
|
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 |
|
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) |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
ASHG Conference (October 16th - 20th, 2018) |
09/10/18 |
Russell, Emily |
Genomewide association study of type 2 diabetes phenotypes in Sāmoans |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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) |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 2018 (APSS, June 2-6,2018) |
12/19/17 |
Montasser, May E. |
B4GALT1: A Novel LDL-Associated Gene |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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) |
|
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 |
|
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. |
|
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. |
|
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. |
|
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 |
|
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. |
|
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. |
|
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. |
|
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 |
|
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 |
|
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) |
|
ASHG 2017 (October 17th-21st, 2017) |
09/01/17 |
Wessel, Jennifer |
TOPMed Whole Genome Sequence Association Analysis Of Type 2 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 |
|
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) |
|
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 |
|
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 |
|
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) |
|
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 |
|
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) |
|
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 |
|
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 |
|
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 |
|
American Heart Association (November 15, 2016) |
10/27/16 |
Rafaels, Nicholas |
Whole genome sequence analysis of asthma in families from Barbados |
|
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 |