SEQUENTIAL STRATEGY TO IDENTIFY A SUSCEPTIBILITY GENE FOR SCHIZOPHRENIA - REPORT OF POTENTIAL LINKAGE ON CHROMOSOME 22Q12-Q13.1 .1.

被引:295
作者
PULVER, AE
KARAYIORGOU, M
WOLYNIEC, PS
LASSETER, VK
KASCH, L
NESTADT, G
ANTONARAKIS, S
HOUSMAN, D
KAZAZIAN, HH
MEYERS, D
OTT, J
LAMACZ, M
LIANG, KY
HANFELT, J
ULLRICH, G
DEMARCHI, N
RAMU, E
MCHUGH, PR
ADLER, L
THOMAS, M
CARPENTER, WT
MANSCHRECK, T
GORDON, CT
KIMBERLAND, M
BABB, R
PUCK, J
CHILDS, B
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,DEPT BIOSTAT,BALTIMORE,MD
[3] UNIV MARYLAND,NIMH,DEPT PSYCHIAT,BETHESDA,MD
[4] COLUMBIA UNIV,DEPT GENET & DEV,NEW YORK,NY
[5] COLUMBIA UNIV,DEPT PSYCHIAT,NEW YORK,NY
[6] MIT,CTR CANC RES,CAMBRIDGE,MA 02139
[7] DARTMOUTH COLL,DEPT PSYCHIAT,HANOVER,NH 03755
[8] CHILDRENS HOSP,PHILADELPHIA,PA 19104
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 54卷 / 01期
关键词
GENETIC LINKAGE ANALYSIS; SCHIZOPHRENIA; HUMAN CHROMOSOME 22; HETEROGENEITY; RANDOM SEARCH;
D O I
10.1002/ajmg.1320540108
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To identify genes responsible for the susceptibility for schizophrenia, and to test the hypothesis that schizophrenia is etiologically heterogeneous, we have studied 39 multiplex families from a systematic sample of schizophrenic patients. Using a complex autosomal dominant model, which considers only those with a diagnosis of schizophrenia or schizoaffective disorder as affected, a random search of the genome for detection of Linkage was undertaken. Pairwise linkage analyses suggest a potential linkage (LRH = 34.7 or maximum lod score = 1.54) for one region (22q12-q13.1). Reanalyses, varying parameters in the dominant model, maximized the LRH at 660.7 (maximum lod score 2.82). This finding is of sufficient interest to warrant further investigation through collaborative studies. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:36 / 43
页数:8
相关论文
共 72 条
[1]  
ANDERSON MA, 1984, IN VITRO CELL DEV B, V20, P856
[2]   NO EVIDENCE FOR LINKAGE BETWEEN CHROMOSOME-5 MARKERS AND SCHIZOPHRENIA [J].
ASCHAUER, HN ;
ASCHAUERTREIBER, G ;
ISENBERG, KE ;
TODD, RD ;
KNESEVICH, MA ;
GARVER, DL ;
REICH, T ;
CLONINGER, CR .
HUMAN HEREDITY, 1990, 40 (02) :109-115
[3]   NO EVIDENCE FOR A PSEUDOAUTOSOMAL LOCUS FOR SCHIZOPHRENIA - LINKAGE ANALYSIS OF MULTIPLY AFFECTED FAMILIES [J].
ASHERSON, P ;
PARFITT, E ;
SARGEANT, M ;
TIDMARSH, S ;
BUCKLAND, P ;
TAYLOR, C ;
CLEMENTS, A ;
GILL, M ;
MCGUFFIN, P ;
OWEN, M .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 161 :63-68
[4]   THE SCHEDULE FOR SCHIZOTYPAL PERSONALITIES (SSP) - A DIAGNOSTIC INTERVIEW FOR SCHIZOTYPAL FEATURES [J].
BARON, M ;
ASNIS, L ;
GRUEN, R .
PSYCHIATRY RESEARCH, 1981, 4 (02) :213-228
[5]   MORTALITY IN DSM-IIIR SCHIZOPHRENIA [J].
BLACK, DW ;
FISHER, R .
SCHIZOPHRENIA RESEARCH, 1992, 7 (02) :109-116
[6]   SEARCH FOR MUTATIONS IN THE BETA-1 GABA(A) RECEPTOR SUBUNIT GENE IN PATIENTS WITH SCHIZOPHRENIA [J].
COON, H ;
SOBELL, J ;
HESTON, L ;
SOMMER, S ;
HOFF, M ;
HOLIK, J ;
UMAR, F ;
ROBERTSON, M ;
REIMHERR, F ;
WENDER, P ;
VEST, K ;
MYLESWORSLEY, M ;
GERSHON, ES ;
DELISI, LE ;
SHIELDS, G ;
DALE, PW ;
POLLOI, A ;
WALDO, M ;
LEONARD, S ;
SIKELA, J ;
FREEDMAN, R ;
BYERLEY, W .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 54 (01) :12-20
[7]   EVIDENCE FOR A PSEUDOAUTOSOMAL LOCUS FOR SCHIZOPHRENIA .2. REPLICATION OF A NONRANDOM SEGREGATION OF ALLELES AT THE DXYS14 LOCUS [J].
DAMATO, T ;
CAMPION, D ;
GORWOOD, P ;
JAY, M ;
SABATE, O ;
PETIT, C ;
ABBAR, M ;
MALAFOSSE, A ;
LEBOYER, M ;
HILLAIRE, D ;
CLERGETDARPOUX, F ;
FEINGOLD, J ;
WAKSMAN, G ;
MALLET, J .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 161 :59-62
[8]   EXCLUSION OF LINKAGE TO 5Q11-13 IN FAMILIES WITH SCHIZOPHRENIA AND OTHER PSYCHIATRIC-DISORDERS [J].
DETERAWADLEIGH, SD ;
GOLDIN, LR ;
SHERRINGTON, R ;
ENCIO, I ;
DEMIGUEL, C ;
BERRETTINI, W ;
GURLING, H ;
GERSHON, ES .
NATURE, 1989, 340 (6232) :391-393
[9]  
DRACOPOLI NC, 1987, CANCER RES, V47, P3995
[10]   UPDATE ON THE EPIDEMIOLOGY OF SCHIZOPHRENIA [J].
EATON, WW .
EPIDEMIOLOGIC REVIEWS, 1991, 13 :320-328