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Paper Details

Rare and low-frequency coding variants alter human adult height.
Nature
376
2017
ADAMTS3, AR, CRISPLD2, IGFBP-4, IHH, IL11RA, NOX4, PAPP, STC2, allele, coding variants, height-associated coding variants, human, insulin-like growth factors, low, monogenic growth disorders
Author NameAffiliation
Eirini MarouliWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London
Mariaelisa GraffUniversity of North Carolina
Ken Sin LoMontreal Heart Institute
Andrew R WoodUniversity of Exeter Medical School, University of Exeter
Rebecca S FineBroad Institute of MIT and Harvard
Rebecca S FineDivision of Endocrinology and Center for Basic and Translational Obesity Research, Boston Children's Hospital
Rebecca S FineHarvard Medical School
Yingchang LuVanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine
Yingchang LuIchan School of Medicine at Mount Sinai
Yingchang LuThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Claudia SchurmannThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Claudia SchurmannIchan School of Medicine at Mount Sinai
Heather M HighlandUniversity of North Carolina
Heather M HighlandThe University of Texas School of Public Health, The University of Texas Graduate School of Biomedical Sciences at Houston, The University of Texas Health Science Center at Houston
Gudmar ThorleifssondeCODE Genetics/Amgen inc.
Gudmar ThorleifssondeCODE Genetics/Amgen inc.
Anne E JusticeUniversity of North Carolina
Kathleen StirrupsWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London
Kathleen StirrupsUniversity of Cambridge
Kathleen StirrupsWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London
Kathleen StirrupsUniversity of Cambridge
Kristin L YoungUniversity of North Carolina
Thomas W WinklerUniversity of Regensburg
Tõnu EskoBroad Institute of MIT and Harvard
Tõnu EskoUniversity of Tartu
Tõnu EskoDivision of Endocrinology and Center for Basic and Translational Obesity Research, Boston Children's Hospital
Adam E LockeDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Adam E LockeMcDonnell Genome Institute, Washington University School of Medicine
Maggie C Y NgCenter for Diabetes Research, Wake Forest School of Medicine
Maggie C Y NgCenter for Genomics and Personalized Medicine Research, Wake Forest School of Medicine
Manuel A RivasBroad Institute of MIT and Harvard
Manuel A Rivas
Manuel A RivasBroad Institute of MIT and Harvard
Manuel A Rivas
Sailaja VedantamBroad Institute of MIT and Harvard
Sailaja VedantamDivision of Endocrinology and Center for Basic and Translational Obesity Research, Boston Children's Hospital
Sailaja VedantamHarvard Medical School
Anubha MahajanUniversity of Oxford
Xiuqing GuoInstitute for Translational Genomics and Population Sciences, LABioMed at Harbor-university of california los angeles Medical Center
Gon??alo R AbecasisDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Gon??alo R AbecasisDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Katja K H Aben
Katja K H AbenRadboud University Medical Center
Linda S AdairUniversity of North Carolina
Eva AlbrechtInstitute of Genetic Epidemiology, Helmholtz Zentrum Munchen - German Research Center for Environmental Health
Matthew A AllisonUniversity of California
Matthew A AllisonUniversity of California
Philippe AmouyelINSERM U1167
Philippe AmouyelUniversite de Lille
Philippe AmouyelInstitut Pasteur de Lille
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