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O1‐09‐03: Whole Genome Sequencing in Familial Late‐Onset Alzheimer’s Disease Identifies Variations in TTC3 and FSIP2
Author(s) -
Beecham Gary W.,
Vardarajan Badri N.,
Blue Elizabeth,
Barral Sandra,
Haines Jonathan L.,
Bush William S.,
Duijn Cornelia M.,
Martin Eden R.,
Schellenberg Gerard D.,
Mayeux Richard,
Wijsman Ellen,
Pericak-Vance Margaret A.
Publication year - 2016
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.2016.06.343
Subject(s) - genetics , 1000 genomes project , biology , missense mutation , genome , whole genome sequencing , disease , genetic linkage , genomics , genotype , computational biology , gene , mutation , medicine , single nucleotide polymorphism , pathology
O1-09-03 WHOLE GENOME SEQUENCING IN FAMILIAL LATE-ONSETALZHEIMER’S DISEASE IDENTIFIES VARIATIONS IN TTC3 AND FSIP2 GaryW. Beecham, Badri N. Vardarajan, Elizabeth Blue, Sandra Barral, Jonathan L. Haines, William S. Bush, Cornelia M. van Duijn, Eden R. Martin, Gerard D. Schellenberg, Richard Mayeux, Ellen Wijsman, Margaret A. Pericak-Vance and the Alzheimer Disease Sequencing Project, University of Miami Miller School of Medicine, Miami, FL, USA; Columbia University, New York, NY, USA; University of Washington, Seattle, WA, USA; Case Western Reserve University School of Medicine, Cleveland, OH, USA; 5 Case Western Reserve University, Cleveland, OH, USA; 6 Erasmus University Medical Center, Rotterdam, Netherlands; University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA. Contact e-mail: gbeecham@med.miami.edu