Increasing the Clinical Psychiatric Knowledge Base About Pathogenic Copy Number Variation.

Journal: The American journal of psychiatry
Published Date:

Abstract

Specific copy number variants (CNVs) have been robustly associated with intellectual disability, autism, and schizophrenia. Most of the literature focus has been on documenting the existence of these phenomena. There are few data to guide therapeutic choices for these “orphan” diseases. We call for systematic and longitudinal case reports which, if carefully conducted, may provide crucial initial knowledge to guide therapeutics. We provide a step-by-step overview, a tailored set of consensus criteria for high-quality case reports, and a specific set of learning resources.

Authors

  • Patrick F Sullivan
    Departments of Genetics and Psychiatry, University of North Carolina at Chapel Hill, and Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm (Sullivan); Medical Research Center for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Wales, United Kingdom (Owen).
  • Michael J Owen
    Departments of Genetics and Psychiatry, University of North Carolina at Chapel Hill, and Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm (Sullivan); Medical Research Center for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Wales, United Kingdom (Owen).