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O3–01–04: The identification of rare variants in late‐onset Alzheimer's disease using extended families
Author(s) -
Kohli Martin,
Kunkle Brian,
Naj Adam,
Carney Regina M.,
HamiltonNelson Kara,
Rolati Sophie,
Whitehead Patrice L.,
Gilbert John,
Martin Eden,
Beecham Gary,
Wang LiSan,
Mayeux Richard,
Haines Jonathan,
Farrer Lindsay,
Schellenberg Gerard,
Zuchner Stephan,
PericakVance Margaret
Publication year - 2013
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2013.04.239
Subject(s) - genetics , biology , exome sequencing , psen1 , pedigree chart , allele , trem2 , identity by descent , genome wide association study , genetic association , allele frequency , disease , single nucleotide polymorphism , alzheimer's disease , gene , haplotype , mutation , genotype , presenilin , medicine , receptor , myeloid cells , pathology
Imaging of Neurodegenerative Diseases; VAMedical Center andUCSF, San Francisco, California, United States; Boston University School of Medicine, Boston, Massachusetts, United States; Boston University, Boston, Massachusetts, United States; King’s College London, London,, United Kingdom; University of Perugia, Italy, Perugia, Italy; Clinic of Internal Medicine and Gerontology, Toulouse, France; Aristotle University of Thessaloniki, Thessaloniki, Greece; Medical University of Lodz, Lodz, Poland; Kuopio University and University Hospital, Kuopio, Finland. Contact e-mail: knho@iupui.edu