Bipolar disorder as a phenotype in genetic studies

Francis J. McMahon, Thomas G. Schulze

Research output: Contribution to journalArticle

Abstract

Human genetics has now advanced to the stage that technology is no longer the limiting step in mapping genes that contribute to disease. Instead we now must confront the problems inherent in our diagnostic definitions - what geneticists call phenotypes. This challenge is nowhere clearer than in the field of bipolar affective disorder, where genetic methods have given us a tantalizing glimpse at etiology, but where the imprecision and heterogeneity of the phenotype have slowed progress. It is now time to return to the phenotype as a chief focus of genetic investigation.

Original languageEnglish (US)
Pages (from-to)37-43
Number of pages7
JournalClinical Neuroscience Research
Volume5
Issue number1 SPEC. ISS.
DOIs
StatePublished - Sep 2005
Externally publishedYes

Fingerprint

Bipolar Disorder
Phenotype
Chromosome Mapping
Medical Genetics
Mood Disorders
Technology

Keywords

  • Bipolar disorder
  • Heterogeneous
  • Linkage
  • Nosology
  • Phenotype

ASJC Scopus subject areas

  • Clinical Neurology
  • Psychiatry and Mental health
  • Biological Psychiatry
  • Neurology
  • Neuropsychology and Physiological Psychology

Cite this

Bipolar disorder as a phenotype in genetic studies. / McMahon, Francis J.; Schulze, Thomas G.

In: Clinical Neuroscience Research, Vol. 5, No. 1 SPEC. ISS., 09.2005, p. 37-43.

Research output: Contribution to journalArticle

McMahon, Francis J. ; Schulze, Thomas G. / Bipolar disorder as a phenotype in genetic studies. In: Clinical Neuroscience Research. 2005 ; Vol. 5, No. 1 SPEC. ISS. pp. 37-43.
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