TY - JOUR
T1 - Further investigation of a chromosome 15 locus in Schizophrenia
T2 - Analysis of affected sibpairs from the NIMH genetics initiative
AU - Leonard, Sherry
AU - Gault, Judith
AU - Moore, Theodore
AU - Hopkins, Jan
AU - Robinson, Misi
AU - Olincy, Ann
AU - Adler, Lawrence E.
AU - Cloninger, C. Robert
AU - Kaufmann, Charles A.
AU - Tsuang, Ming T.
AU - Faraone, Stephen V.
AU - Malaspina, Dolores
AU - Svrakic, Dragan M.
AU - Freedman, Robert
PY - 1998/7/10
Y1 - 1998/7/10
N2 - Linkage of a neurophysiological deficit associated with schizophrenia, i.e., the failure to inhibit the auditory P50 response, was previously reported at chromosome 15q14. The marker with the highest pairwise lod score, D15S1360, was isolated from a yeast artificial chromosome containing a candidate gene, the α7-nicotinic acetylcholine receptor gene. In the present study, this linkage was further investigated in a subset of the NIMH Genetics Initiative schizophrenia families. These families have not been studied neurophysiologically, as were the families in the original report. Therefore, the DSMIII-R diagnosis of schizophrenia was used as the affected phenotype. Twenty families fulfilled the criteria of at least one sibpair concordant for schizophrenia, along with their two parents or another affected relative outside the nuclear family, available for genotyping. Sibpair analysis showed a significant proportion of D15S1360 alleles shared identical-by-descent (0.58; P < 0.0024). The results further support the involvement of this chromosomal locus in the genetic transmission of schizophrenia.
AB - Linkage of a neurophysiological deficit associated with schizophrenia, i.e., the failure to inhibit the auditory P50 response, was previously reported at chromosome 15q14. The marker with the highest pairwise lod score, D15S1360, was isolated from a yeast artificial chromosome containing a candidate gene, the α7-nicotinic acetylcholine receptor gene. In the present study, this linkage was further investigated in a subset of the NIMH Genetics Initiative schizophrenia families. These families have not been studied neurophysiologically, as were the families in the original report. Therefore, the DSMIII-R diagnosis of schizophrenia was used as the affected phenotype. Twenty families fulfilled the criteria of at least one sibpair concordant for schizophrenia, along with their two parents or another affected relative outside the nuclear family, available for genotyping. Sibpair analysis showed a significant proportion of D15S1360 alleles shared identical-by-descent (0.58; P < 0.0024). The results further support the involvement of this chromosomal locus in the genetic transmission of schizophrenia.
KW - Auditory evoked potential
KW - Genetic linkage
KW - Human chromosome pair 15
KW - Nicotinic receptor
KW - Polymorphism
UR - https://www.scopus.com/pages/publications/0032503911
U2 - 10.1002/(SICI)1096-8628(19980710)81:4<308::AID-AJMG6>3.0.CO;2-P
DO - 10.1002/(SICI)1096-8628(19980710)81:4<308::AID-AJMG6>3.0.CO;2-P
M3 - Article
C2 - 9674976
AN - SCOPUS:0032503911
SN - 1552-4841
VL - 81
SP - 308
EP - 312
JO - American Journal of Medical Genetics - Neuropsychiatric Genetics
JF - American Journal of Medical Genetics - Neuropsychiatric Genetics
IS - 4
ER -