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Paper Details

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Am J Hum Genet
49
2016
ALAS2, CD36, HCT, HGB, HNF4A, MAP1A, Mendelian non-spherocytic hemolytic anemia, PKLR, Pleiotropic Variants, RBC, RBC distribution, RBC phenotypes, RBC variants, Red Blood Cell, Red blood cell, coding genetic variants, common, corpuscular hemoglobin, differentiated human erythroblasts, erythropoietic protoporphyria, ex, exome array, hemoglobin, human, nonsense variant, platelet, rs1800961, rs201062903, rs3211938, rs55707100, sideroblastic anemia, white blood cell
Author NameAffiliation
John D Eicherand Blood Institute
Evangelos EvangelouSchool of Public Health, Imperial College London, University of Ioannina Medical School
Evangelos EvangelouSchool of Public Health, Imperial College London, University of Ioannina Medical School
Salman M TajuddinNational Institute on Aging
Jennifer A BrodyUniversity of Washington
Claudia SchurmannThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Nathan PankratzUniversity of Minnesota
Nathan PankratzUniversity of Minnesota
Lisa R YanekJohns Hopkins University
Ani ManichaikulCenter for Public Health Genomics, University of Virginia
Evelin MihailovUniversity of Tartu
Laura M RaffieldUniversity of North Carolina
Diane M BeckerJohns Hopkins University
Eric BoerwinkleSchool of Public Health, University of Texas Health Science Center at Houston, Baylor College of Medicine
Eric BoerwinkleSchool of Public Health, University of Texas Health Science Center at Houston, Baylor College of Medicine
Jette Bork-JensenThe Novo Nordisk Foundation, Center for Basic Metabolic Research, University of Copenhagen
Erwin P BottingerThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Erwin P BottingerThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
David R CrosslinUniversity of Washington
David R CrosslinUniversity of Washington
Paul ElliottSchool of Public Health, Imperial College London
Michele K EvansNational Institute on Aging
James S FloydUniversity of Washington
James S FloydUniversity of Washington
Myriam FornageInstitute of Molecular Medicine, The University of Texas Health Science Center at Houston
Vilmundur GudnasonUniversity of Iceland
Torben HansenThe Novo Nordisk Foundation, Center for Basic Metabolic Research, University of Copenhagen
Tamara B HarrisNational Institute on Aging
Tamara B HarrisNational Institute on Aging
Caroline HaywardInstitute of Genetics and Molecular Medicine, University of Edinburgh
Heather M HighlandSchool of Public Health, University of Texas Health Science Center at Houston, University of North Carolina at Chapel Hill
Joel N HirschhornBroad Institute, Boston Children's Hospital
Joel N HirschhornBroad Institute, Boston Children's Hospital
Albert HofmanHarvard TH Chan School of Public Health
Albert HofmanHarvard TH Chan School of Public Health
Marguerite R IrvinSchool of Public Health, University of Alabama at Birmingham
Mika K??h??nenTampere University Hospital, University of Tampere School of Medicine
Mika K??h??nenTampere University Hospital, University of Tampere School of Medicine
Ethan M LangeUniversity of North Carolina at Chapel Hill
Lenore J LaunerNational Institute on Aging
Terho Lehtim??kiUniversity of Tampere School of Medicine
Terho Lehtim??kiUniversity of Tampere School of Medicine
Jin LiStanford University
Allan LinnebergResearch Centre for Prevention and Health, Rigshospitalet, University of Copenhagen
Yongmei LiuCenter for Human Genetics, Wake Forest School of Medicine
Yingchang LuThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Leo-Pekka Lyytik??inenUniversity of Tampere School of Medicine
Leo-Pekka Lyytik??inenUniversity of Tampere School of Medicine
Reedik MägiUniversity of Tartu
Olle MelanderLund University, Sweden Skane University Hospital
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