Further analyses of the NIMH bipolar dataset: Follow up on suggestive linkage results on 1p and 10p

J. Corbett, J. Rice, N. Saccone, A. Goate, T. Reich, Tatiana Foroud, John Nurnberger, Howard Edenberg, J. R. DePaulo, E. Gershon

Research output: Contribution to journalArticle

Abstract

Bipolar Affective Disorder (BP) is complex and familial. However, the genetics of BP is not consistent with a major locus inheritance. Linkage of BP has been reported in several chromosomal regions. Data from 540 subjects from 97 families in wave one of a four site collaborative study supported as part of the NIMH genetics initiative indicated possible linkage to a region on chromosome 1 near D1S224 (MOD 1.66, p

LanguageEnglish (US)
Pages469
Number of pages1
JournalAmerican Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
Volume96
Issue number4
StatePublished - Aug 7 2000
Externally publishedYes

Fingerprint

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 1
Mood Disorders
Bipolar Disorder
Datasets

ASJC Scopus subject areas

  • Genetics(clinical)
  • Neuropsychology and Physiological Psychology
  • Neuroscience(all)

Cite this

Further analyses of the NIMH bipolar dataset : Follow up on suggestive linkage results on 1p and 10p. / Corbett, J.; Rice, J.; Saccone, N.; Goate, A.; Reich, T.; Foroud, Tatiana; Nurnberger, John; Edenberg, Howard; DePaulo, J. R.; Gershon, E.

In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 96, No. 4, 07.08.2000, p. 469.

Research output: Contribution to journalArticle

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