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Discovering Schizophrenia Endophenotypes in Randomly Ascertained Pedigrees

Year: 2014
Type: article
Study design: Observational Study
DOI: 10.1016/j.biopsych.2014.06.027
Authors: David C. Glahn, Jeff T. Williams, D. Reese McKay, Emma E. Knowles, Emma Sprooten, Samuel R. Mathias, Joanne E. Curran, Jack W. Kent, Melanie A. Carless, Harald H.H. Göring, Thomas D. Dyer, Mary D. Woolsey, Anderson M. Winkler, Rene L. Olvera, Peter Kochunov, Peter T. Fox, Ravi Duggirala, Laura Almasy, John Blangero
Institutions: Hartford Hospital, Yale University, Texas Biomedical Research Institute, The University of Texas at San Antonio Health Science Center, University of Oxford, Wellcome Centre for Integrative Neuroimaging, University of Maryland, Baltimore, University of Hong Kong
Language: English
Field: Medicine
Open Access status: bronze
Awards: G140538419, 1/2 Genetics of Brain Structure and Function, Quantitative Trait Locus Mapping in Human Pedigrees, G2169778925, G2946664248, G3257426095, G332954602, EXTRAMULAR RESEARCH FACILITIES CONSTRUCTION, G3907386461, G4204893666, 2/2 Genetics of Brain Structure and Function, High Performance Computing System for Human Genomics, G518778165, Genetics of Brain Structure and Function: Genome-Wide Association, Solar-Eclipse Computational Tools for Imaging Genetics, MOLECULAR AND BIOCHEMICAL GENETICS LABORATORY RENOVATION, G7239431997, G7852197243, G879628117, QUANTITATIVE TRAIT LOCUS MAPPING IN HUMAN PEDIGREES, G9000054199, Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD Risk
OpenAlex ID: W1978970994
FWCI: 3.563
Cites: 74
Cited by: 29
Related to: 10