Literature DB >> 1972325

The role of genetic factors in the etiology of the affective disorders.

S Hodgkinson1, M J Mullan, H M Gurling.   

Abstract

Recent application of genetic linkage analysis to the affective disorders has suggested that there are at least three genotypic forms. This is an important step toward defining the genetic etiology involved, as it had previously been suggested that the complex nature of the clinical phenotype would preclude any attempt to apply such a technique. However, to date no clinical evidence exists to discriminate these genotypes at the phenotypic level. Molecular geneticists now face a formidable task of identifying the aberrant gene and relating the gene product, a protein, to the observed psychopathology. Current molecular genetic research in the affective disorders is discussed and similar work applied to the study of nonpsychiatric disorders such as cystic fibrosis and Duchenne muscular dystrophy is reviewed. The clinical value of genetic risk analysis for individuals with a family history of the affective disorders is also considered.

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Year:  1990        PMID: 1972325     DOI: 10.1007/bf01067792

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  35 in total

1.  Ethics of predictive testing for Huntington's chorea: the need for more information.

Authors:  D I Craufurd; R Harris
Journal:  Br Med J (Clin Res Ed)       Date:  1986-07-26

Review 2.  Family history studies. I. Two types of affective disorders separated according to genetic and clinical factors.

Authors:  G Winokur; P Clayton
Journal:  Recent Adv Biol Psychiatry       Date:  1966

3.  Family history studies: V. The genetics of mania.

Authors:  T Reich; P J Clayton; G Winokur
Journal:  Am J Psychiatry       Date:  1969-04       Impact factor: 18.112

4.  A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.

Authors:  X Estivill; M Farrall; P J Scambler; G M Bell; K M Hawley; N J Lench; G P Bates; H C Kruyer; P A Frederick; P Stanier
Journal:  Nature       Date:  1987 Apr 30-May 6       Impact factor: 49.962

5.  Measurement and purification of human chromosomes by flow cytometry and sorting.

Authors:  A V Carrano; J W Gray; R G Langlois; K J Burkhart-Schultz; M A Van Dilla
Journal:  Proc Natl Acad Sci U S A       Date:  1979-03       Impact factor: 11.205

6.  Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

Authors:  C Ingle; R Williamson; A de la Chapelle; R R Herva; K Haapala; G Bates; H F Willard; P Pearson; K E Davies
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

7.  Birth-cohort changes in manic and depressive disorders in relatives of bipolar and schizoaffective patients.

Authors:  E S Gershon; J H Hamovit; J J Guroff; J I Nurnberger
Journal:  Arch Gen Psychiatry       Date:  1987-04

8.  A highly polymorphic locus very tightly linked to the Huntington's disease gene.

Authors:  J J Wasmuth; J Hewitt; B Smith; D Allard; J L Haines; D Skarecky; E Partlow; M R Hayden
Journal:  Nature       Date:  1988-04-21       Impact factor: 49.962

9.  Affective disorders in a US urban community: the use of research diagnostic criteria in an epidemiological survey.

Authors:  M M Weissman; J K Myers
Journal:  Arch Gen Psychiatry       Date:  1978-11

10.  Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Authors:  U Francke; H D Ochs; B de Martinville; J Giacalone; V Lindgren; C Distèche; R A Pagon; M H Hofker; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

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