Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia


Autoria(s): Lewis, C. O.; Levinson, D.; Wise, L.; DeLisi, L.; Straub, R.; Mowry, B.
Contribuinte(s)

Stephen T Warren

Data(s)

01/01/2003

Resumo

Schizophrenia is a common disorder with high heritability and a 10-fold increase in risk to siblings of probands. Replication has been inconsistent for reports of significant genetic linkage. To assess evidence for linkage across studies, rank-based genome scan meta-analysis (GSMA) was applied to data from 20 schizophrenia genome scans. Each marker for each scan was assigned to 1 of 120 30-cM bins, with the bins ranked by linkage scores (1 = most significant) and the ranks averaged across studies (R-avg) and then weighted for sample size (rootN[affected cases]). A permutation test was used to compute the probability of observing, by chance, each bin's average rank (P-AvgRnk) or of observing it for a bin with the same place (first, second, etc.) in the order of average ranks in each permutation (P-ord). The GSMA produced significant genomewide evidence for linkage on chromosome 2q (P-AvgRnk

Identificador

http://espace.library.uq.edu.au/view/UQ:66835

Idioma(s)

eng

Publicador

University of Chicago Press

Palavras-Chave #Genetics & Heredity #Susceptibility Locus #Linkage Analysis #Wide Scan #Vulnerability Locus #Genetic-linkage #Sibling Pairs #Schizoaffective Disorder #Chromosome 6q #Follow-up #Families #C1 #321021 Psychiatry #730211 Mental health
Tipo

Journal Article