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A genome‐wide search for risk genes using homozygosity mapping and microarrays with 1,494 single‐nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder
Author(s) -
Ewald H.,
Wikman F.P.,
Teruel B.M.,
Buttenschön H.N.,
Torralba M.,
Als T.D.,
El Daoud A.,
Flint T.J.,
Jorgensen T.H.,
Blanco L.,
Kruse T.A.,
Orntoft T.F.,
Mors O.
Publication year - 2004
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.30106
Subject(s) - genetics , disease gene identification , biology , single nucleotide polymorphism , microsatellite , genetic linkage , candidate gene , gene mapping , gene , chromosome , genotype , phenotype , allele , exome sequencing
Homozygosity mapping is a very powerful method for finding rare recessive disease genes in monogenic disorders and may also be useful for locating risk genes in complex disorders, late onset disorders where parents often are not available, and for rare phenotypic subgroups. In the present study, homozygosity mapping was applied to 24 persons with bipolar disorder from 22 inbred families. The families were selected irrespective of whether other affected family members were present or not. A genome wide screen using genotypes from only a single affected person in each family was performed using the AFFYMETRIX GeneChip HuSNP Mapping Assay, which contains 1,494 single nucleotide polymorphisms. At chromosome 17q24‐q25 a parametric multipoint LOD score of 1.96 was found at WIAF‐2407 and WIAF‐2405. When analyzing 19 additional microsatellite markers on chromosome 17q the maximum parametric multipoint LOD score was 2.08, 1.5 cM proximal to D17S668. The present study replicates a recent significant linkage finding. © 2004 Wiley‐Liss, Inc.