Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • A.P. Rajkumar, Denmark
  • Jane H. Christensen
  • Manuel Mattheisen
  • Iben Jacobsen, Translational Neuropsychiatry Unit, Department of Clinical Medicine, Aarhus University, Denmark., Denmark
  • Iben Bache, Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, Faculty of Health Science, University of Copenhagen, Denmark
  • Jonatan Pallesen
  • Jakob Grove
  • Per Qvist
  • Andrew Mcquillin, Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, United Kingdom
  • Hugh M. Gurling, Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, United Kingdom
  • Zeynep Tümer, Applied Molecular Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Denmark
  • Ole Mors
  • Anders D. Børglum
Original languageEnglish
JournalBipolar Disorders (English Edition, Online)
Volume17
Issue2
Pages (from-to)205-211
Number of pages7
ISSN1398-5647
DOIs
Publication statusPublished - 1 Jan 2015

    Research areas

  • Bipolar disorder, Genetic association studies, Genetic translocation, NPTX1, RPTOR

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