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Title Working Group(s) Name and Date of Professional Meeting POST DATE
Analysis of densely imputed UK Biobank genetic data reveals disease-associated rare loss of function variation Population Genetics ASHG Annual Meeting (October 2018)
An Omics Analysis, Search and Information System (OASIS) for Enabling Discovery in the TOPMed Diabetes Working Group Diabetes ASHG Conference (October 2018)
Novel structural variants originating in F8 non-coding regions explain previously unresolved cases of severe hemophilia A Hematology and Hemostasis ASHG
Large-scale characterization of CYP2D6 variation in African Americans using TOPMed whole genome sequencing data Structural Variation ASHG 2018 (TBD)
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
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)
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)
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)
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)
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
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