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The collaborative study on the genetics of alcoholism: Sample and clinical data
Authors:Danielle M. Dick  Emily Balcke  Vivia McCutcheon  Meredith Francis  Sally Kuo  Jessica Salvatore  Jacquelyn Meyers  Laura J. Bierut  Marc Schuckit  Victor Hesselbrock  Howard J. Edenberg  Bernice Porjesz  COGA Collaborators  Samuel Kuperman  John Kramer  Kathleen Bucholz
Affiliation:1. Department of Psychiatry, Rutgers Robert Wood Johnson Medical School, Piscataway, New Jersey, USA;2. Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA;3. School of Social Work, Virginia Commonwealth University, Richmond, Virginia, USA;4. Department of Psychiatry and Behavioral Sciences, SUNY Downstate Health Sciences University, Brooklyn, New York, USA;5. Department of Psychiatry, University of California San Diego School of Medicine, La Jolla, California, USA;6. Department of Psychiatry, University of Connecticut School of Medicine, Farmington, Connecticut, USA;7. Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA

Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana, USA;8. Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA

Abstract:The collaborative study on the genetics of alcoholism (COGA) is a multi-site, multidisciplinary project with the goal of identifying how genes are involved in alcohol use disorder and related outcomes, and characterizing how genetic risk unfolds across development and in conjunction with the environment and brain function. COGA is a multi-generational family-based study in which probands were recruited through alcohol treatment centers, along with a set of community comparison families. Nearly 18,000 individuals from >2200 families have been assessed over a period of over 30 years with a rich phenotypic battery that includes semi-structured psychiatric interviews and questionnaire measures, along with DNA collection and electrophysiological data on a large subset. Participants range in age from 7 to 97, with many having longitudinal assessments, providing a valuable opportunity to study alcohol use and problems across the lifespan. Here we provide an overview of data collection methods for the COGA sample, and details about sample characteristics and comorbidity. We also review key research findings that have emerged from analyses of the COGA data. COGA data are available broadly to researchers, and we hope this overview will encourage further collaboration and use of these data to advance the field.
Keywords:alcohol  comorbidity  development  drug  environment  genetics  lifespan
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