Literature DB >> 12874606

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q.

E M Wijsman1, E A Rosenthal, D Hall, M L Blundell, C Sobin, S C Heath, R Williams, M J Brownstein, J A Gogos, M Karayiorgou.   

Abstract

It is widely accepted that founder populations hold promise for mapping loci for complex traits. However, the outcome of these mapping efforts will most likely depend on the individual demographic characteristics and historical circumstances surrounding the founding of a given genetic isolate. The 'ideal' features of a founder population are currently unknown. The Micronesian islandic population of Kosrae, one of the four islands comprising the Federated States of Micronesia (FSM), was founded by a small number of settlers and went through a secondary genetic 'bottleneck' in the mid-19th century. The potential for reduced etiological (genetic and environmental) heterogeneity, as well as the opportunity to ascertain extended and statistically powerful pedigrees makes the Kosraen population attractive for mapping schizophrenia susceptibility genes. Our exhaustive case ascertainment from this islandic population identified 32 patients who met DSM-IV criteria for schizophrenia or schizoaffective disorder. Three of these were siblings in one nuclear family, and 27 were from a single large and complex schizophrenia kindred that includes a total of 251 individuals. One of the most startling findings in our ascertained sample was the great difference in male and female disease rates. A genome-wide scan provided initial suggestive evidence for linkage to markers on chromosomes 1, 2, 3, 7, 13, 15, 19, and X. Follow-up multipoint analyses gave additional support for a region on 2q37 that includes a schizophrenia locus previously identified in another small genetic isolate, with a well-established recent genealogical history and a small number of founders, located on the eastern border of Finland. In addition to providing further support for a schizophrenia susceptibility locus at 2q37, our results highlight the analytic challenges associated with extremely large and complex pedigrees, as well as the limitations associated with genetic studies of complex traits in small islandic populations.

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Year:  2003        PMID: 12874606     DOI: 10.1038/sj.mp.4001356

Source DB:  PubMed          Journal:  Mol Psychiatry        ISSN: 1359-4184            Impact factor:   15.992


  19 in total

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Authors:  Duncan C Thomas; Robert W Haile; David Duggan
Journal:  Am J Hum Genet       Date:  2005-08-01       Impact factor: 11.025

2.  Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population.

Authors:  Tine Venken; Stephan Claes; Samuel Sluijs; Andrew D Paterson; Cornelia van Duijn; Rolf Adolfsson; Jurgen Del-Favero; Christine Van Broeckhoven
Journal:  Am J Hum Genet       Date:  2004-12-21       Impact factor: 11.025

3.  Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype.

Authors:  Michel Maziade; Yvon C Chagnon; Marc-André Roy; Alexandre Bureau; Alain Fournier; Chantal Mérette
Journal:  Eur J Hum Genet       Date:  2009-01-28       Impact factor: 4.246

4.  Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island.

Authors:  Stuart Macgregor; Claire Bellis; Rod A Lea; Hannah Cox; Tom Dyer; John Blangero; Peter M Visscher; Lyn R Griffiths
Journal:  Eur J Hum Genet       Date:  2010-01       Impact factor: 4.246

5.  Brief psychotic episode in a patient with chromosome 2q37 microdeletion syndrome.

Authors:  Kevin Lally; Nuraini Ibrahim; Mary Kelly; Gautam Gulati
Journal:  BMJ Case Rep       Date:  2017-11-27

Review 6.  The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries?

Authors:  Rami Abou Jamra; Christine Schmael; Sven Cichon; Marcella Rietschel; Johannes Schumacher; Markus M Nöthen
Journal:  Schizophr Bull       Date:  2006-08-16       Impact factor: 9.306

7.  A novel analytical framework for dissecting the genetic architecture of behavioral symptoms in neuropsychiatric disorders.

Authors:  Anthony J Deo; Ramiro Costa; Lynn E DeLisi; Rob DeSalle; Fatemeh Haghighi
Journal:  PLoS One       Date:  2010-03-16       Impact factor: 3.240

8.  Shared genomic segment analysis: the power to find rare disease variants.

Authors:  Stacey Knight; Ryan P Abo; Haley J Abel; Deborah W Neklason; Therese M Tuohy; Randall W Burt; Alun Thomas; Nicola J Camp
Journal:  Ann Hum Genet       Date:  2012-09-19       Impact factor: 1.670

9.  Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.

Authors:  Gonçalo R Abecasis; Rachel A Burt; Diana Hall; Sylvia Bochum; Kimberly F Doheny; S Laura Lundy; Marie Torrington; J Louw Roos; Joseph A Gogos; Maria Karayiorgou
Journal:  Am J Hum Genet       Date:  2004-01-28       Impact factor: 11.025

10.  Neuropsychological performance as endophenotypes in extended schizophrenia families from the Central Valley of Costa Rica.

Authors:  Hilary Bertisch; Andrea Mesen-Fainardi; Maureen V Martin; Vanessa Pérez-Vargas; Tatiana Vargas-Rodríguez; Gabriela Delgado; Camila Delgado; Michele Llach; Beatrice LaPrade; William Byerley; William E Bunney; Marquis P Vawter; Lynn E DeLisi
Journal:  Psychiatr Genet       Date:  2009-02       Impact factor: 2.458

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