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| Submitted by | Title | Working Group(s) | Name and Date of Professional Meeting | POST DATE |
|---|---|---|---|---|
| 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) | |
| 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 | |
| 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 | |
| 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) | |
| 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. | |
| 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) | |
| 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) | |
| 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) | |
| 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 | |
| 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 |
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