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Paper Details

Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
JAMA Netw Open
47
2019
AD, Alzheimer Disease, Alzheimer disease, Alzheimer's Disease, CADASIL, Dementias, NOTCH3, Nasu-Hakola disease, Participants, Q33X), Rare Coding Mutations, TREM2 rs104894002, bone cysts, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, dementia, dementia-associated genes, dementias, genetic variants, mild cognitive impairment, multifocal, p., participant, participants, rare variants, rs149307620, women
Author NameAffiliation
Badri N VardarajanColumbia University
Jae Yoon ChungBoston University School of Medicine
Jae Yoon ChungBoston University
Xiaoling ZhangBoston University School of Medicine
Xiaoling ZhangBoston University School of Public Health
John J FarrellBoston University School of Medicine
Oscar L LopezUniversity of Pittsburgh School of Medicine
Jonathan L HainesCase Western Reserve University School of Medicine
Jonathan L HainesCase Western Reserve University School of Medicine
Margaret A Pericak-VanceJohn P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami
Gerard D SchellenbergUniversity of Pennsylvania
John S K KauweBrigham Young University
Kathryn L LunettaBoston University School of Public Health
Lindsay A FarrerBoston University School of Medicine
Lindsay A FarrerBoston University
Lindsay A FarrerBoston University School of Medicine
Lindsay A FarrerBoston University School of Public Health
Lindsay A FarrerBoston University School of Medicine
Lindsay A FarrerBoston University School of Public Health
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Datasets

Release 1.2