Germer, Soren |
Discovery and typing of polymorphic non-deletions of ancestral hominid sequence in the human genome |
Population Genetics |
AGBT (February 12-15th, 2018) |
|
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) |
|
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) |
|
Wessel, Jennifer |
TOPMed Whole Genome Sequence Association Analysis Of Type 2 Diabetes |
Diabetes |
American Society of Human Genetics (October 17-21) |
|
Wessel, Jennifer |
TOPMed Whole Genome Sequence Association Analysis Of Type 2 Diabetes |
Diabetes |
American Society of Human Genetics (October 17-21) |
|
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 |
|
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) |
|
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 |
|
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) |
|
Zhu, Xiaofeng |
Low frequency and rare variants of RBFOX1 are associated with blood pressure |
Blood Pressure |
ASHG 2017 annual meeting |
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