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Paper Details

Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
JAMA Neurol
29
2015
A673, A673 allele, A673T, A673T variant, AD, APP, APP A673T variant, Alzheimer disease, HumanExome, Infinium HumanExome V1 Beadchip, PARTICIPANTS, Participants, alanine, alanine (A673) allele, alanine is replaced by threonine at position 673, amyloid precursor protein gene, mother, position 673, threonine
Author NameAffiliation
Li-San WangUniversity of Pennsylvania Perelman School of Medicine
Robert R Graham
Robert R Graham
Paul K CraneUniversity of Washington
Chiao-Feng LinUniversity of Pennsylvania Perelman School of Medicine
Otto ValladaresUniversity of Pennsylvania Perelman School of Medicine
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia
Peter St George-HyslopUniversity of Toronto, Canada25Cambridge Institute for Medical Research, University of Cambridge
Robert C GreenDepartment of Medicine and Partners Center for Personalized Genetic Medicine, Brigham and Women's Hospital/Harvard Medical School
Alison M GoateWashington University School of Medicine
Tatiana ForoudIndiana University
Eric B LarsonUniversity of Washington, Seattle28Group Health Research Institute
Timothy W Behrens
Timothy W Behrens
John S K KauweBrigham Young University
Jonathan L HainesCenter for Human Genetics and Research, Vanderbilt University
Jonathan L HainesCenter for Human Genetics and Research, Vanderbilt University
Lindsay A FarrerBrigham Young University, Boston University
Margaret A Pericak-VanceJohn P. Hussman Institute for Human Genomics, University of Miami, Florida34Dr John T. Macdonald Foundation Department of Human Genetics
Gerard D SchellenbergUniversity of Pennsylvania Perelman School of Medicine
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