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Linkage analysis of schizophrenia to chromosome 15.
Gejman, P V; Sanders, A R; Badner, J A; Cao, Q; Zhang, J.
Affiliation
  • Gejman PV; Unit on Molecular Clinical Investigation, Clinical Neurogenetics Branch, National Institute of Mental Health, Natinaol Institutes of Health, Bethesda, Maryland, USA. pgejman@uchicago.edu
Am J Med Genet ; 105(8): 789-93, 2001 Dec 08.
Article de En | MEDLINE | ID: mdl-11803532
ABSTRACT
We have mapped a sample of 68 families consisting of one or more affected sibling pairs with schizophrenia or schizoaffective disorder with 20 markers spanning all of chromosome 15 to investigate whether there is a locus on chromosome 15 that confers an increased susceptibility to schizophrenia using parametric and nonparametric linkage analyses. Allele sharing identical by descent and multipoint maximum likelihood score (MLS) statistics were employed. Results show excess allele sharing for multiple markers in 15q11.2-q25, a chromosomal region previously found linked to a decrease in the normal inhibition of the P50 auditory-evoked response to the second of paired stimuli, a decrease associated with schizophrenia. Excess allele sharing was found for markers spanning about 48 cM in 15q11.2-q25 (D15S1002-D15S1023). The greatest single point allele sharing was found at D15S659 (62.6%). The multipoint MLS scores were greater than 1.0 in the 30-52 cM interval delimited by ACTC and D15S150, with a maximum value of 2.0 with GENEHUNTER PLUS near D15S1039.
Sujet(s)
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Schizophrénie / Chromosomes humains de la paire 15 Limites: Humans Langue: En Journal: Am J Med Genet Année: 2001 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Schizophrénie / Chromosomes humains de la paire 15 Limites: Humans Langue: En Journal: Am J Med Genet Année: 2001 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
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