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The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration

期刊

NEUROPSYCHOPHARMACOLOGY
卷 40, 期 10, 页码 2287-2297

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2015.118

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资金

  1. One Mind
  2. Department of Veterans Affairs (DVA) [1I01CX000748-01A1, I01CX000120-01]
  3. Mid-Atlantic Mental Illness, Research, and Education Center
  4. NIH (NIMH)
  5. HHMI
  6. Burroughs Wellcome Fund
  7. Brain and Behavior Fund
  8. ProMedica Klarman Family Foundation ANGI Welcome Trust Strategic Awards Committee (London)
  9. US Department of Veterans Affairs
  10. NIH
  11. Thome Memorial Foundation
  12. American Foundation for Suicide Prevention
  13. Schering Plough Pharmaceuticals
  14. NARSAD [YI 19233]
  15. Conquer Cancer Foundation
  16. NIH [MH085806, MH088609, DK100392, MD009064]

向作者/读者索取更多资源

The development of posttraumatic stress disorder (PTSD) is influenced by genetic factors. Although there have been some replicated candidates, the identification of risk variants for PTSD has lagged behind genetic research of other psychiatric disorders such as schizophrenia, autism, and bipolar disorder. Psychiatric genetics has moved beyond examination of specific candidate genes in favor of the genome-wide association study (GWAS) strategy of very large numbers of samples, which allows for the discovery of previously unsuspected genes and molecular pathways. The successes of genetic studies of schizophrenia and bipolar disorder have been aided by the formation of a large-scale GWAS consortium: the Psychiatric Genomics Consortium (PGC). In contrast, only a handful of GWAS of PTSD have appeared in the literature to date. Here we describe the formation of a group dedicated to large-scale study of PTSD genetics: the PGC-PTSD. The PGC-PTSD faces challenges related to the contingency on trauma exposure and the large degree of ancestral genetic diversity within and across participating studies. Using the PGC analysis pipeline supplemented by analyses tailored to address these challenges, we anticipate that our first large-scale GWAS of PTSD will comprise over 10 000 cases and 30 000 trauma-exposed controls. Following in the footsteps of our PGC forerunners, this collaboration-of a scope that is unprecedented in the field of traumatic stress-will lead the search for replicable genetic associations and new insights into the biological underpinnings of PTSD.

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