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Paper Details

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.
Nat Commun
7
2022
S1PR3, S1PR3 monocyte enhancer, blood cell, blood or hematopoietic disorders, monocyte, participants, platelet, red cell, single nucleotide variants, structural variants
Author NameAffiliation
Adrienne M StilpUniversity of Washington
Laura M RaffieldUniversity of North Carolina
Goo JunSchool of Public Health, The University of Texas Health Science Center at Houston
Goo JunSchool of Public Health, The University of Texas Health Science Center at Houston
Fritz J SedlazeckBaylor College of Medicine
Ginger A MetcalfBaylor College of Medicine
Paul S de VriesSchool of Public Health, The University of Texas Health Science Center at Houston
Paul S de VriesSchool of Public Health, The University of Texas Health Science Center at Houston
James S FloydCardiovascular Health Research Unit, University of Washington
James S FloydCardiovascular Health Research Unit, University of Washington
Wonji KimBrigham and Women's Hospital
Aakrosh RatanCenter for Public Health Genomics, University of Virginia
Lisa R YanekJohns Hopkins University School of Medicine
John BlangeroDepartment of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine
Michael H ChoBrigham and Women's Hospital
Michael H ChoBrigham and Women's Hospital
Joanne E CurranDepartment of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine
Myriam FornageBrown Foundation Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston
Robert C KaplanAlbert Einstein College of Medicine
Joshua P LewisUniversity of Maryland School of Medicine
Ruth J F LoosThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Ruth J F LoosNovo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen
Ruth J F LoosThe Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Ruth J F LoosIcahn School of Medicine at Mount Sinai
Braxton D MitchellUniversity of Maryland School of Medicine
Alanna C MorrisonSchool of Public Health, The University of Texas Health Science Center at Houston
Michael PreussThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Bruce M PsatyCardiovascular Health Research Unit, University of Washington
Stephen S RichCenter for Public Health Genomics, University of Virginia
Jerome I RotterThe Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation at Harbor-university of california los angeles Medical Center
Russell P TracyLarner College of Medicine at the University of Vermont
Eric BoerwinkleSchool of Public Health, The University of Texas Health Science Center at Houston
Eric BoerwinkleSchool of Public Health, The University of Texas Health Science Center at Houston
Gon??alo R AbecasisTOPMed Informatics Research Center, University of Michigan ann arbor
Gon??alo R AbecasisTOPMed Informatics Research Center, University of Michigan ann arbor
Thomas W BlackwellTOPMed Informatics Research Center, University of Michigan ann arbor
Albert V SmithTOPMed Informatics Research Center, University of Michigan ann arbor
Albert V SmithTOPMed Informatics Research Center, University of Michigan ann arbor
Andrew D JohnsonLung and Blood Institute
Andrew D JohnsonLung and Blood Institute
Deborah A NickersonUniversity of Washington
Deborah A NickersonUniversity of Washington
Matthew P ConomosUniversity of Washington
Yongjun LiUniversity of North Carolina at Chapel Hill
Unnur ThorsteinsdottirdeCODE genetics/Amgen Inc.
Unnur ThorsteinsdottirUniversity of Iceland
Unnur ThorsteinsdottirdeCODE genetics/Amgen Inc.
Unnur ThorsteinsdottirUniversity of Iceland
Kari StefanssondeCODE genetics/Amgen Inc.
Kari StefanssonUniversity of Iceland
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