Literature DB >> 9184312

Selection of homogeneous populations for genetic study: the Portugal genetics of psychosis project.

C N Pato1, M H Azevedo, M T Pato, J L Kennedy, I Coelho, A Dourado, A Macedo, J Valente, C P Ferreira, J Madeira, J Gago da Camara, M Moniz, C Correia.   

Abstract

Molecular genetic studies of psychiatric disorders must face the possibility that despite the significant contribution of genetic factors to the expression of syndromes like schizophrenia, these syndromes may be a heterogeneous collection of genetic and non-genetic illnesses. These illnesses may be etiologically distinct from each other and still share many clinical features in common. Linkage studies of families with multiple affected members tend to favor the selection of genetic forms of a syndrome but can still represent a heterogeneous set of different genetic illnesses. To limit the potential genetic heterogeneity of a study sample, we selected a population that was geographically isolated and was historically relatively genetically homogeneous. We then assessed the relative level of homogeneity utilizing a surname analysis of the population of the Azores, mainland Portugal, rural USA, and urban USA. The average number of families with the same last name corrected for population size in the Azores is 30.88, in Coimbra it is 21.42, compared to 1.13 in a rural American population and 0.38 in an urban American population. The results of this analysis indicate that the Azores have the highest degree of homogeneity, and mainland Portugal has a high degree of homogeneity.

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Year:  1997        PMID: 9184312

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

Review 1.  Genetic analyses of schizophrenia.

Authors:  C N Pato; K M Schindler; M T Pato
Journal:  Curr Psychiatry Rep       Date:  2000-04       Impact factor: 5.285

2.  Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

Authors:  M Daniele Fallin; Virginia K Lasseter; Paula S Wolyniec; John A McGrath; Gerald Nestadt; David Valle; Kung-Yee Liang; Ann E Pulver
Journal:  Am J Hum Genet       Date:  2003-08-15       Impact factor: 11.025

3.  Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

Authors:  F A Middleton; M T Pato; K L Gentile; C P Morley; X Zhao; A F Eisener; A Brown; T L Petryshen; A N Kirby; H Medeiros; C Carvalho; A Macedo; A Dourado; I Coelho; J Valente; M J Soares; C P Ferreira; M Lei; M H Azevedo; J L Kennedy; M J Daly; P Sklar; C N Pato
Journal:  Am J Hum Genet       Date:  2004-04-01       Impact factor: 11.025

  3 in total

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