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Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia : Suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

Identifieur interne : 004126 ( PascalFrancis/Corpus ); précédent : 004125; suivant : 004127

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia : Suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

Auteurs : Brian K. Suarez ; Jubao Duan ; Alan R. Sanders ; Anthony L. Hinrichs ; Carol H. Jin ; CUIPING HOU ; Nancy G. Buccola ; Nancy Hale ; Ann N. Weilbaecher ; Deborah A. Nertney ; Ann Olincy ; Susan Green ; Arthur W. Schaffer ; Christopher J. Smith ; Dominique E. Hannah ; John P. Rice ; Nancy J. Cox ; Maria Martinez ; Bryan J. Mowry ; Farooq Amin ; Jeremy M. Silverman ; Donald W. Black ; William F. Byerley ; Raymond R. Crowe ; Robert Freedman ; C. Robert Cloninger ; Douglas F. Levinson ; Pablo V. Gejman

Source :

RBID : Pascal:06-0468036

Descripteurs français

English descriptors

Abstract

We report the clinical characteristics of a schizophrenia sample of 409 pedigrees-263 of European ancestry (EA) and 146 of African American ancestry (AA)-together with the results of a genome scan (with a simple tandem repeat polymorphism interval of 9 cM) and follow-up fine mapping. A family was required to have a proband with schizophrenia (SZ) and one or more siblings of the proband with SZ or schizoaffective disorder. Linkage analyses included 403 independent full-sibling affected sibling pairs (ASPs) (279 EA and 124 AA) and 100 all-possible half-sibling ASPs (15 EA and 85 AA). Nonparametric multipoint linkage analysis of all families detected two regions with suggestive evidence of linkage at 8p23.3-q12 and llpll.2-q22.3 (empirical Z likelihood-ratio score [Zlr] threshold ≥2.65) and, in exploratory analyses, two other regions at 4p16.1-p15.32 in AA families and at 5p14.3-q11.2 in EA families. The most significant linkage peak was in chromosome 8p; its signal was mainly driven by the EA families. Zlr scores >2.0 in 8p were observed from 30.7 cM to 61.7 cM (Center for Inherited Disease Research map locations). The maximum evidence in the full sample was a multipoint Zlr of 3.25 (equivalent Kong-Cox LOD of 2.30) near D8S1771 (at 52 cM); there appeared to be two peaks, both telomeric to neuregulin 1 (NRG1). There is a paracentric inversion common in EA individuals within this region, the effect of which on the linkage evidence remains unknown in this and in other previously analyzed samples. Fine mapping of 8p did not significantly alter the significance or length of the peak. We also performed fine mapping of 4p16.3-p15.2, 5p15.2-q13.3, 10p15.3-p14, 10q25.3-q26.3, and 11p13-q23.3. The highest increase in Zlr scores was observed for 5p14.1-q12.1, where the maximum Zlr increased from 2.77 initially to 3.80 after fine mapping in the EA families.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A08 01  1  ENG  @1 Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia : Suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample
A11 01  1    @1 SUAREZ (Brian K.)
A11 02  1    @1 DUAN (Jubao)
A11 03  1    @1 SANDERS (Alan R.)
A11 04  1    @1 HINRICHS (Anthony L.)
A11 05  1    @1 JIN (Carol H.)
A11 06  1    @1 CUIPING HOU
A11 07  1    @1 BUCCOLA (Nancy G.)
A11 08  1    @1 HALE (Nancy)
A11 09  1    @1 WEILBAECHER (Ann N.)
A11 10  1    @1 NERTNEY (Deborah A.)
A11 11  1    @1 OLINCY (Ann)
A11 12  1    @1 GREEN (Susan)
A11 13  1    @1 SCHAFFER (Arthur W.)
A11 14  1    @1 SMITH (Christopher J.)
A11 15  1    @1 HANNAH (Dominique E.)
A11 16  1    @1 RICE (John P.)
A11 17  1    @1 COX (Nancy J.)
A11 18  1    @1 MARTINEZ (Maria)
A11 19  1    @1 MOWRY (Bryan J.)
A11 20  1    @1 AMIN (Farooq)
A11 21  1    @1 SILVERMAN (Jeremy M.)
A11 22  1    @1 BLACK (Donald W.)
A11 23  1    @1 BYERLEY (William F.)
A11 24  1    @1 CROWE (Raymond R.)
A11 25  1    @1 FREEDMAN (Robert)
A11 26  1    @1 CLONINGER (C. Robert)
A11 27  1    @1 LEVINSON (Douglas F.)
A11 28  1    @1 GEJMAN (Pablo V.)
A14 01      @1 Departments of Psychiatry and Genetics, Washington University @2 St. Louis @3 USA @Z 1 aut. @Z 4 aut. @Z 5 aut. @Z 13 aut. @Z 16 aut. @Z 26 aut.
A14 02      @1 Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University @2 Evanston, IL @3 USA @Z 2 aut. @Z 3 aut. @Z 6 aut. @Z 18 aut. @Z 28 aut.
A14 03      @1 School of Nursing, Louisiana State University Health Sciences Center @2 New Orleans @3 USA @Z 7 aut.
A14 04      @1 Mental Health Clinical Research Center and Department of Psychiatry, University of Iowa College of Medicine @2 Iowa City @3 USA @Z 8 aut. @Z 22 aut. @Z 24 aut.
A14 05      @1 Department of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University @3 USA @Z 9 aut.
A14 06      @1 Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health @2 Wacol @3 AUS @Z 10 aut. @Z 15 aut. @Z 19 aut.
A14 07      @1 Department of Psychiatry, University of Queensland @2 Brisbane @3 AUS @Z 10 aut. @Z 15 aut. @Z 19 aut.
A14 08      @1 Department of Psychiatry and Colorado Psychiatric Health, University of Colorado School of Medicine @2 Denver @3 USA @Z 11 aut. @Z 25 aut.
A14 09      @1 Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University @2 Atlanta @3 USA @Z 12 aut. @Z 20 aut.
A14 10      @1 Department of Psychiatry, Mount Sinai School of Medicine @2 New York @3 USA @Z 14 aut. @Z 21 aut.
A14 11      @1 Department of Medicine, University of Chicago @2 Chicago @3 USA @Z 17 aut.
A14 12      @1 Méthodologie Statistique et Epidémiologie Génétique des Maladies Multifactorielles, Institut National de la Recherche et de la Santé Médicale @2 Evry @3 FRA @Z 18 aut.
A14 13      @1 Baylor College of Medicine @2 Houston @3 USA @Z 20 aut.
A14 14      @1 Department of Psychiatry, University of California at Irvine @2 Irvine @3 USA @Z 23 aut.
A14 15      @1 Department of Psychiatry, University of California-San Francisco @2 San Francisco @3 USA @Z 23 aut.
A14 16      @1 Department of Psychiatry, University of Pennsylvania @2 Philadelphia @3 USA @Z 27 aut.
A20       @1 315-333
A21       @1 2006
A23 01      @0 ENG
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A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
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A60       @1 P
A61       @0 A
A64 01  1    @0 American journal of human genetics
A66 01      @0 USA
C01 01    ENG  @0 We report the clinical characteristics of a schizophrenia sample of 409 pedigrees-263 of European ancestry (EA) and 146 of African American ancestry (AA)-together with the results of a genome scan (with a simple tandem repeat polymorphism interval of 9 cM) and follow-up fine mapping. A family was required to have a proband with schizophrenia (SZ) and one or more siblings of the proband with SZ or schizoaffective disorder. Linkage analyses included 403 independent full-sibling affected sibling pairs (ASPs) (279 EA and 124 AA) and 100 all-possible half-sibling ASPs (15 EA and 85 AA). Nonparametric multipoint linkage analysis of all families detected two regions with suggestive evidence of linkage at 8p23.3-q12 and llpll.2-q22.3 (empirical Z likelihood-ratio score [Zlr] threshold ≥2.65) and, in exploratory analyses, two other regions at 4p16.1-p15.32 in AA families and at 5p14.3-q11.2 in EA families. The most significant linkage peak was in chromosome 8p; its signal was mainly driven by the EA families. Zlr scores >2.0 in 8p were observed from 30.7 cM to 61.7 cM (Center for Inherited Disease Research map locations). The maximum evidence in the full sample was a multipoint Zlr of 3.25 (equivalent Kong-Cox LOD of 2.30) near D8S1771 (at 52 cM); there appeared to be two peaks, both telomeric to neuregulin 1 (NRG1). There is a paracentric inversion common in EA individuals within this region, the effect of which on the linkage evidence remains unknown in this and in other previously analyzed samples. Fine mapping of 8p did not significantly alter the significance or length of the peak. We also performed fine mapping of 4p16.3-p15.2, 5p15.2-q13.3, 10p15.3-p14, 10q25.3-q26.3, and 11p13-q23.3. The highest increase in Zlr scores was observed for 5p14.1-q12.1, where the maximum Zlr increased from 2.77 initially to 3.80 after fine mapping in the EA families.
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C03 01  X  ENG  @0 Schizophrenia @5 01
C03 01  X  SPA  @0 Esquizofrenia @5 01
C03 02  X  FRE  @0 Génome @5 09
C03 02  X  ENG  @0 Genome @5 09
C03 02  X  SPA  @0 Genoma @5 09
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C03 03  X  ENG  @0 Pathogenesis @5 10
C03 03  X  SPA  @0 Patogenia @5 10
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C03 05  X  FRE  @0 Liaison génétique @5 12
C03 05  X  ENG  @0 Genetic linkage @5 12
C03 05  X  SPA  @0 Ligamiento genético @5 12
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C03 06  X  ENG  @0 Genetic mapping @5 13
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C03 10  X  ENG  @0 Family study @5 17
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C03 11  X  FRE  @0 Gène CDKN1A @5 18
C03 11  X  ENG  @0 CDKN1A Gene @5 18
C03 11  X  SPA  @0 Gen CDKN1A @5 18
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C03 12  X  ENG  @0 Sample @5 19
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C03 13  X  ENG  @0 Genetics @5 20
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C07 01  X  SPA  @0 Psicosis @5 37
N21       @1 310
N44 01      @1 OTO
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Format Inist (serveur)

NO : PASCAL 06-0468036 INIST
ET : Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia : Suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample
AU : SUAREZ (Brian K.); DUAN (Jubao); SANDERS (Alan R.); HINRICHS (Anthony L.); JIN (Carol H.); CUIPING HOU; BUCCOLA (Nancy G.); HALE (Nancy); WEILBAECHER (Ann N.); NERTNEY (Deborah A.); OLINCY (Ann); GREEN (Susan); SCHAFFER (Arthur W.); SMITH (Christopher J.); HANNAH (Dominique E.); RICE (John P.); COX (Nancy J.); MARTINEZ (Maria); MOWRY (Bryan J.); AMIN (Farooq); SILVERMAN (Jeremy M.); BLACK (Donald W.); BYERLEY (William F.); CROWE (Raymond R.); FREEDMAN (Robert); CLONINGER (C. Robert); LEVINSON (Douglas F.); GEJMAN (Pablo V.)
AF : Departments of Psychiatry and Genetics, Washington University/St. Louis/Etats-Unis (1 aut., 4 aut., 5 aut., 13 aut., 16 aut., 26 aut.); Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University/Evanston, IL/Etats-Unis (2 aut., 3 aut., 6 aut., 18 aut., 28 aut.); School of Nursing, Louisiana State University Health Sciences Center/New Orleans/Etats-Unis (7 aut.); Mental Health Clinical Research Center and Department of Psychiatry, University of Iowa College of Medicine/Iowa City/Etats-Unis (8 aut., 22 aut., 24 aut.); Department of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University/Etats-Unis (9 aut.); Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health/Wacol/Australie (10 aut., 15 aut., 19 aut.); Department of Psychiatry, University of Queensland/Brisbane/Australie (10 aut., 15 aut., 19 aut.); Department of Psychiatry and Colorado Psychiatric Health, University of Colorado School of Medicine/Denver/Etats-Unis (11 aut., 25 aut.); Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University/Atlanta/Etats-Unis (12 aut., 20 aut.); Department of Psychiatry, Mount Sinai School of Medicine/New York/Etats-Unis (14 aut., 21 aut.); Department of Medicine, University of Chicago/Chicago/Etats-Unis (17 aut.); Méthodologie Statistique et Epidémiologie Génétique des Maladies Multifactorielles, Institut National de la Recherche et de la Santé Médicale/Evry/France (18 aut.); Baylor College of Medicine/Houston/Etats-Unis (20 aut.); Department of Psychiatry, University of California at Irvine/Irvine/Etats-Unis (23 aut.); Department of Psychiatry, University of California-San Francisco/San Francisco/Etats-Unis (23 aut.); Department of Psychiatry, University of Pennsylvania/Philadelphia/Etats-Unis (27 aut.)
DT : Publication en série; Niveau analytique
SO : American journal of human genetics; ISSN 0002-9297; Coden AJHGAG; Etats-Unis; Da. 2006; Vol. 78; No. 2; Pp. 315-333; Bibl. 2 p.1/4
LA : Anglais
EA : We report the clinical characteristics of a schizophrenia sample of 409 pedigrees-263 of European ancestry (EA) and 146 of African American ancestry (AA)-together with the results of a genome scan (with a simple tandem repeat polymorphism interval of 9 cM) and follow-up fine mapping. A family was required to have a proband with schizophrenia (SZ) and one or more siblings of the proband with SZ or schizoaffective disorder. Linkage analyses included 403 independent full-sibling affected sibling pairs (ASPs) (279 EA and 124 AA) and 100 all-possible half-sibling ASPs (15 EA and 85 AA). Nonparametric multipoint linkage analysis of all families detected two regions with suggestive evidence of linkage at 8p23.3-q12 and llpll.2-q22.3 (empirical Z likelihood-ratio score [Zlr] threshold ≥2.65) and, in exploratory analyses, two other regions at 4p16.1-p15.32 in AA families and at 5p14.3-q11.2 in EA families. The most significant linkage peak was in chromosome 8p; its signal was mainly driven by the EA families. Zlr scores >2.0 in 8p were observed from 30.7 cM to 61.7 cM (Center for Inherited Disease Research map locations). The maximum evidence in the full sample was a multipoint Zlr of 3.25 (equivalent Kong-Cox LOD of 2.30) near D8S1771 (at 52 cM); there appeared to be two peaks, both telomeric to neuregulin 1 (NRG1). There is a paracentric inversion common in EA individuals within this region, the effect of which on the linkage evidence remains unknown in this and in other previously analyzed samples. Fine mapping of 8p did not significantly alter the significance or length of the peak. We also performed fine mapping of 4p16.3-p15.2, 5p15.2-q13.3, 10p15.3-p14, 10q25.3-q26.3, and 11p13-q23.3. The highest increase in Zlr scores was observed for 5p14.1-q12.1, where the maximum Zlr increased from 2.77 initially to 3.80 after fine mapping in the EA families.
CC : 002A04; 002A07C03; 002B23A; 002B18C06A
FD : Schizophrénie; Génome; Pathogénie; Déterminisme génétique; Liaison génétique; Carte génétique; Européen; Europe; Afro Américain; Etude familiale; Gène CDKN1A; Echantillon; Génétique; Homme
FG : Psychose
ED : Schizophrenia; Genome; Pathogenesis; Genetic determinism; Genetic linkage; Genetic mapping; European; Europe; African American; Family study; CDKN1A Gene; Sample; Genetics; Human
EG : Psychosis
SD : Esquizofrenia; Genoma; Patogenia; Determinismo genético; Ligamiento genético; Mapa genético; Europeo; Europa; Afroamericano; Estudio familiar; Gen CDKN1A; Muestra; Genética; Hombre
LO : INIST-2610.354000132911260120
ID : 06-0468036

Links to Exploration step

Pascal:06-0468036

Le document en format XML

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<s1>Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University</s1>
<s2>Atlanta</s2>
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<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
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<name sortKey="Smith, Christopher J" sort="Smith, Christopher J" uniqKey="Smith C" first="Christopher J." last="Smith">Christopher J. Smith</name>
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<s1>Department of Psychiatry, Mount Sinai School of Medicine</s1>
<s2>New York</s2>
<s3>USA</s3>
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<sZ>10 aut.</sZ>
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<sZ>10 aut.</sZ>
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<name sortKey="Rice, John P" sort="Rice, John P" uniqKey="Rice J" first="John P." last="Rice">John P. Rice</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
<s3>USA</s3>
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<name sortKey="Cox, Nancy J" sort="Cox, Nancy J" uniqKey="Cox N" first="Nancy J." last="Cox">Nancy J. Cox</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Department of Medicine, University of Chicago</s1>
<s2>Chicago</s2>
<s3>USA</s3>
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<name sortKey="Martinez, Maria" sort="Martinez, Maria" uniqKey="Martinez M" first="Maria" last="Martinez">Maria Martinez</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University</s1>
<s2>Evanston, IL</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
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<inist:fA14 i1="12">
<s1>Méthodologie Statistique et Epidémiologie Génétique des Maladies Multifactorielles, Institut National de la Recherche et de la Santé Médicale</s1>
<s2>Evry</s2>
<s3>FRA</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
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<name sortKey="Mowry, Bryan J" sort="Mowry, Bryan J" uniqKey="Mowry B" first="Bryan J." last="Mowry">Bryan J. Mowry</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health</s1>
<s2>Wacol</s2>
<s3>AUS</s3>
<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="07">
<s1>Department of Psychiatry, University of Queensland</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>19 aut.</sZ>
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<name sortKey="Amin, Farooq" sort="Amin, Farooq" uniqKey="Amin F" first="Farooq" last="Amin">Farooq Amin</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University</s1>
<s2>Atlanta</s2>
<s3>USA</s3>
<sZ>12 aut.</sZ>
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<affiliation>
<inist:fA14 i1="13">
<s1>Baylor College of Medicine</s1>
<s2>Houston</s2>
<s3>USA</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
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<name sortKey="Silverman, Jeremy M" sort="Silverman, Jeremy M" uniqKey="Silverman J" first="Jeremy M." last="Silverman">Jeremy M. Silverman</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Department of Psychiatry, Mount Sinai School of Medicine</s1>
<s2>New York</s2>
<s3>USA</s3>
<sZ>14 aut.</sZ>
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<name sortKey="Black, Donald W" sort="Black, Donald W" uniqKey="Black D" first="Donald W." last="Black">Donald W. Black</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Mental Health Clinical Research Center and Department of Psychiatry, University of Iowa College of Medicine</s1>
<s2>Iowa City</s2>
<s3>USA</s3>
<sZ>8 aut.</sZ>
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<name sortKey="Byerley, William F" sort="Byerley, William F" uniqKey="Byerley W" first="William F." last="Byerley">William F. Byerley</name>
<affiliation>
<inist:fA14 i1="14">
<s1>Department of Psychiatry, University of California at Irvine</s1>
<s2>Irvine</s2>
<s3>USA</s3>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="15">
<s1>Department of Psychiatry, University of California-San Francisco</s1>
<s2>San Francisco</s2>
<s3>USA</s3>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
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<name sortKey="Crowe, Raymond R" sort="Crowe, Raymond R" uniqKey="Crowe R" first="Raymond R." last="Crowe">Raymond R. Crowe</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Mental Health Clinical Research Center and Department of Psychiatry, University of Iowa College of Medicine</s1>
<s2>Iowa City</s2>
<s3>USA</s3>
<sZ>8 aut.</sZ>
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<name sortKey="Freedman, Robert" sort="Freedman, Robert" uniqKey="Freedman R" first="Robert" last="Freedman">Robert Freedman</name>
<affiliation>
<inist:fA14 i1="08">
<s1>Department of Psychiatry and Colorado Psychiatric Health, University of Colorado School of Medicine</s1>
<s2>Denver</s2>
<s3>USA</s3>
<sZ>11 aut.</sZ>
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<name sortKey="Cloninger, C Robert" sort="Cloninger, C Robert" uniqKey="Cloninger C" first="C. Robert" last="Cloninger">C. Robert Cloninger</name>
<affiliation>
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<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
<s3>USA</s3>
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<name sortKey="Levinson, Douglas F" sort="Levinson, Douglas F" uniqKey="Levinson D" first="Douglas F." last="Levinson">Douglas F. Levinson</name>
<affiliation>
<inist:fA14 i1="16">
<s1>Department of Psychiatry, University of Pennsylvania</s1>
<s2>Philadelphia</s2>
<s3>USA</s3>
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</inist:fA14>
</affiliation>
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<author>
<name sortKey="Gejman, Pablo V" sort="Gejman, Pablo V" uniqKey="Gejman P" first="Pablo V." last="Gejman">Pablo V. Gejman</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University</s1>
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<s3>USA</s3>
<sZ>2 aut.</sZ>
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<idno type="wicri:Area/PascalFrancis/Corpus">004126</idno>
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<title xml:lang="en" level="a">Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia : Suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample</title>
<author>
<name sortKey="Suarez, Brian K" sort="Suarez, Brian K" uniqKey="Suarez B" first="Brian K." last="Suarez">Brian K. Suarez</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
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<author>
<name sortKey="Duan, Jubao" sort="Duan, Jubao" uniqKey="Duan J" first="Jubao" last="Duan">Jubao Duan</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University</s1>
<s2>Evanston, IL</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
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<name sortKey="Sanders, Alan R" sort="Sanders, Alan R" uniqKey="Sanders A" first="Alan R." last="Sanders">Alan R. Sanders</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University</s1>
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<author>
<name sortKey="Hinrichs, Anthony L" sort="Hinrichs, Anthony L" uniqKey="Hinrichs A" first="Anthony L." last="Hinrichs">Anthony L. Hinrichs</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Departments of Psychiatry and Genetics, Washington University</s1>
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<name sortKey="Jin, Carol H" sort="Jin, Carol H" uniqKey="Jin C" first="Carol H." last="Jin">Carol H. Jin</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
<s3>USA</s3>
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<name sortKey="Cuiping Hou" sort="Cuiping Hou" uniqKey="Cuiping Hou" last="Cuiping Hou">CUIPING HOU</name>
<affiliation>
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<s1>Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University</s1>
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<sZ>2 aut.</sZ>
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<name sortKey="Buccola, Nancy G" sort="Buccola, Nancy G" uniqKey="Buccola N" first="Nancy G." last="Buccola">Nancy G. Buccola</name>
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<inist:fA14 i1="03">
<s1>School of Nursing, Louisiana State University Health Sciences Center</s1>
<s2>New Orleans</s2>
<s3>USA</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hale, Nancy" sort="Hale, Nancy" uniqKey="Hale N" first="Nancy" last="Hale">Nancy Hale</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Mental Health Clinical Research Center and Department of Psychiatry, University of Iowa College of Medicine</s1>
<s2>Iowa City</s2>
<s3>USA</s3>
<sZ>8 aut.</sZ>
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<name sortKey="Weilbaecher, Ann N" sort="Weilbaecher, Ann N" uniqKey="Weilbaecher A" first="Ann N." last="Weilbaecher">Ann N. Weilbaecher</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Department of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University</s1>
<s3>USA</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
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<name sortKey="Nertney, Deborah A" sort="Nertney, Deborah A" uniqKey="Nertney D" first="Deborah A." last="Nertney">Deborah A. Nertney</name>
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<inist:fA14 i1="06">
<s1>Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health</s1>
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<s3>AUS</s3>
<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
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</inist:fA14>
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<affiliation>
<inist:fA14 i1="07">
<s1>Department of Psychiatry, University of Queensland</s1>
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<sZ>10 aut.</sZ>
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<name sortKey="Olincy, Ann" sort="Olincy, Ann" uniqKey="Olincy A" first="Ann" last="Olincy">Ann Olincy</name>
<affiliation>
<inist:fA14 i1="08">
<s1>Department of Psychiatry and Colorado Psychiatric Health, University of Colorado School of Medicine</s1>
<s2>Denver</s2>
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<sZ>11 aut.</sZ>
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<name sortKey="Green, Susan" sort="Green, Susan" uniqKey="Green S" first="Susan" last="Green">Susan Green</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University</s1>
<s2>Atlanta</s2>
<s3>USA</s3>
<sZ>12 aut.</sZ>
<sZ>20 aut.</sZ>
</inist:fA14>
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<name sortKey="Schaffer, Arthur W" sort="Schaffer, Arthur W" uniqKey="Schaffer A" first="Arthur W." last="Schaffer">Arthur W. Schaffer</name>
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<inist:fA14 i1="01">
<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
<s3>USA</s3>
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<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
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<name sortKey="Smith, Christopher J" sort="Smith, Christopher J" uniqKey="Smith C" first="Christopher J." last="Smith">Christopher J. Smith</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Department of Psychiatry, Mount Sinai School of Medicine</s1>
<s2>New York</s2>
<s3>USA</s3>
<sZ>14 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
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<name sortKey="Hannah, Dominique E" sort="Hannah, Dominique E" uniqKey="Hannah D" first="Dominique E." last="Hannah">Dominique E. Hannah</name>
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<inist:fA14 i1="06">
<s1>Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health</s1>
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<s3>AUS</s3>
<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="07">
<s1>Department of Psychiatry, University of Queensland</s1>
<s2>Brisbane</s2>
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<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
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</inist:fA14>
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<author>
<name sortKey="Rice, John P" sort="Rice, John P" uniqKey="Rice J" first="John P." last="Rice">John P. Rice</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Departments of Psychiatry and Genetics, Washington University</s1>
<s2>St. Louis</s2>
<s3>USA</s3>
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<sZ>4 aut.</sZ>
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<name sortKey="Cox, Nancy J" sort="Cox, Nancy J" uniqKey="Cox N" first="Nancy J." last="Cox">Nancy J. Cox</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Department of Medicine, University of Chicago</s1>
<s2>Chicago</s2>
<s3>USA</s3>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Martinez, Maria" sort="Martinez, Maria" uniqKey="Martinez M" first="Maria" last="Martinez">Maria Martinez</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University</s1>
<s2>Evanston, IL</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>6 aut.</sZ>
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</inist:fA14>
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<affiliation>
<inist:fA14 i1="12">
<s1>Méthodologie Statistique et Epidémiologie Génétique des Maladies Multifactorielles, Institut National de la Recherche et de la Santé Médicale</s1>
<s2>Evry</s2>
<s3>FRA</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
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<author>
<name sortKey="Mowry, Bryan J" sort="Mowry, Bryan J" uniqKey="Mowry B" first="Bryan J." last="Mowry">Bryan J. Mowry</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health</s1>
<s2>Wacol</s2>
<s3>AUS</s3>
<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="07">
<s1>Department of Psychiatry, University of Queensland</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>10 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
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<author>
<name sortKey="Amin, Farooq" sort="Amin, Farooq" uniqKey="Amin F" first="Farooq" last="Amin">Farooq Amin</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University</s1>
<s2>Atlanta</s2>
<s3>USA</s3>
<sZ>12 aut.</sZ>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="13">
<s1>Baylor College of Medicine</s1>
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<title level="j" type="main">American journal of human genetics</title>
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<term>Genetic determinism</term>
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<div type="abstract" xml:lang="en">We report the clinical characteristics of a schizophrenia sample of 409 pedigrees-263 of European ancestry (EA) and 146 of African American ancestry (AA)-together with the results of a genome scan (with a simple tandem repeat polymorphism interval of 9 cM) and follow-up fine mapping. A family was required to have a proband with schizophrenia (SZ) and one or more siblings of the proband with SZ or schizoaffective disorder. Linkage analyses included 403 independent full-sibling affected sibling pairs (ASPs) (279 EA and 124 AA) and 100 all-possible half-sibling ASPs (15 EA and 85 AA). Nonparametric multipoint linkage analysis of all families detected two regions with suggestive evidence of linkage at 8p23.3-q12 and llpll.2-q22.3 (empirical Z likelihood-ratio score [Z
<sub>lr</sub>
] threshold ≥2.65) and, in exploratory analyses, two other regions at 4p16.1-p15.32 in AA families and at 5p14.3-q11.2 in EA families. The most significant linkage peak was in chromosome 8p; its signal was mainly driven by the EA families. Z
<sub>lr</sub>
scores >2.0 in 8p were observed from 30.7 cM to 61.7 cM (Center for Inherited Disease Research map locations). The maximum evidence in the full sample was a multipoint Z
<sub>lr</sub>
of 3.25 (equivalent Kong-Cox LOD of 2.30) near D8S1771 (at 52 cM); there appeared to be two peaks, both telomeric to neuregulin 1 (NRG1). There is a paracentric inversion common in EA individuals within this region, the effect of which on the linkage evidence remains unknown in this and in other previously analyzed samples. Fine mapping of 8p did not significantly alter the significance or length of the peak. We also performed fine mapping of 4p16.3-p15.2, 5p15.2-q13.3, 10p15.3-p14, 10q25.3-q26.3, and 11p13-q23.3. The highest increase in Z
<sub>lr</sub>
scores was observed for 5p14.1-q12.1, where the maximum Z
<sub>lr</sub>
increased from 2.77 initially to 3.80 after fine mapping in the EA families.</div>
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<s5>20</s5>
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<s5>21</s5>
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<s0>Hombre</s0>
<s5>21</s5>
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<s0>Psychose</s0>
<s5>37</s5>
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<s0>Psychosis</s0>
<s5>37</s5>
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<s0>Psicosis</s0>
<s5>37</s5>
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<s1>310</s1>
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<s1>OTO</s1>
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<NO>PASCAL 06-0468036 INIST</NO>
<ET>Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia : Suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample</ET>
<AU>SUAREZ (Brian K.); DUAN (Jubao); SANDERS (Alan R.); HINRICHS (Anthony L.); JIN (Carol H.); CUIPING HOU; BUCCOLA (Nancy G.); HALE (Nancy); WEILBAECHER (Ann N.); NERTNEY (Deborah A.); OLINCY (Ann); GREEN (Susan); SCHAFFER (Arthur W.); SMITH (Christopher J.); HANNAH (Dominique E.); RICE (John P.); COX (Nancy J.); MARTINEZ (Maria); MOWRY (Bryan J.); AMIN (Farooq); SILVERMAN (Jeremy M.); BLACK (Donald W.); BYERLEY (William F.); CROWE (Raymond R.); FREEDMAN (Robert); CLONINGER (C. Robert); LEVINSON (Douglas F.); GEJMAN (Pablo V.)</AU>
<AF>Departments of Psychiatry and Genetics, Washington University/St. Louis/Etats-Unis (1 aut., 4 aut., 5 aut., 13 aut., 16 aut., 26 aut.); Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, Evanston Northwestern Healthcare and Feinberg School of Medicine, Northwestern University/Evanston, IL/Etats-Unis (2 aut., 3 aut., 6 aut., 18 aut., 28 aut.); School of Nursing, Louisiana State University Health Sciences Center/New Orleans/Etats-Unis (7 aut.); Mental Health Clinical Research Center and Department of Psychiatry, University of Iowa College of Medicine/Iowa City/Etats-Unis (8 aut., 22 aut., 24 aut.); Department of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University/Etats-Unis (9 aut.); Queensland Centre for Schizophrenia Mental Health Research, The Park, Centre for Mental Health/Wacol/Australie (10 aut., 15 aut., 19 aut.); Department of Psychiatry, University of Queensland/Brisbane/Australie (10 aut., 15 aut., 19 aut.); Department of Psychiatry and Colorado Psychiatric Health, University of Colorado School of Medicine/Denver/Etats-Unis (11 aut., 25 aut.); Atlanta VA Medical Center and Department of Psychiatry and Behavioral Sciences, Emory University/Atlanta/Etats-Unis (12 aut., 20 aut.); Department of Psychiatry, Mount Sinai School of Medicine/New York/Etats-Unis (14 aut., 21 aut.); Department of Medicine, University of Chicago/Chicago/Etats-Unis (17 aut.); Méthodologie Statistique et Epidémiologie Génétique des Maladies Multifactorielles, Institut National de la Recherche et de la Santé Médicale/Evry/France (18 aut.); Baylor College of Medicine/Houston/Etats-Unis (20 aut.); Department of Psychiatry, University of California at Irvine/Irvine/Etats-Unis (23 aut.); Department of Psychiatry, University of California-San Francisco/San Francisco/Etats-Unis (23 aut.); Department of Psychiatry, University of Pennsylvania/Philadelphia/Etats-Unis (27 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>American journal of human genetics; ISSN 0002-9297; Coden AJHGAG; Etats-Unis; Da. 2006; Vol. 78; No. 2; Pp. 315-333; Bibl. 2 p.1/4</SO>
<LA>Anglais</LA>
<EA>We report the clinical characteristics of a schizophrenia sample of 409 pedigrees-263 of European ancestry (EA) and 146 of African American ancestry (AA)-together with the results of a genome scan (with a simple tandem repeat polymorphism interval of 9 cM) and follow-up fine mapping. A family was required to have a proband with schizophrenia (SZ) and one or more siblings of the proband with SZ or schizoaffective disorder. Linkage analyses included 403 independent full-sibling affected sibling pairs (ASPs) (279 EA and 124 AA) and 100 all-possible half-sibling ASPs (15 EA and 85 AA). Nonparametric multipoint linkage analysis of all families detected two regions with suggestive evidence of linkage at 8p23.3-q12 and llpll.2-q22.3 (empirical Z likelihood-ratio score [Z
<sub>lr</sub>
] threshold ≥2.65) and, in exploratory analyses, two other regions at 4p16.1-p15.32 in AA families and at 5p14.3-q11.2 in EA families. The most significant linkage peak was in chromosome 8p; its signal was mainly driven by the EA families. Z
<sub>lr</sub>
scores >2.0 in 8p were observed from 30.7 cM to 61.7 cM (Center for Inherited Disease Research map locations). The maximum evidence in the full sample was a multipoint Z
<sub>lr</sub>
of 3.25 (equivalent Kong-Cox LOD of 2.30) near D8S1771 (at 52 cM); there appeared to be two peaks, both telomeric to neuregulin 1 (NRG1). There is a paracentric inversion common in EA individuals within this region, the effect of which on the linkage evidence remains unknown in this and in other previously analyzed samples. Fine mapping of 8p did not significantly alter the significance or length of the peak. We also performed fine mapping of 4p16.3-p15.2, 5p15.2-q13.3, 10p15.3-p14, 10q25.3-q26.3, and 11p13-q23.3. The highest increase in Z
<sub>lr</sub>
scores was observed for 5p14.1-q12.1, where the maximum Z
<sub>lr</sub>
increased from 2.77 initially to 3.80 after fine mapping in the EA families.</EA>
<CC>002A04; 002A07C03; 002B23A; 002B18C06A</CC>
<FD>Schizophrénie; Génome; Pathogénie; Déterminisme génétique; Liaison génétique; Carte génétique; Européen; Europe; Afro Américain; Etude familiale; Gène CDKN1A; Echantillon; Génétique; Homme</FD>
<FG>Psychose</FG>
<ED>Schizophrenia; Genome; Pathogenesis; Genetic determinism; Genetic linkage; Genetic mapping; European; Europe; African American; Family study; CDKN1A Gene; Sample; Genetics; Human</ED>
<EG>Psychosis</EG>
<SD>Esquizofrenia; Genoma; Patogenia; Determinismo genético; Ligamiento genético; Mapa genético; Europeo; Europa; Afroamericano; Estudio familiar; Gen CDKN1A; Muestra; Genética; Hombre</SD>
<LO>INIST-2610.354000132911260120</LO>
<ID>06-0468036</ID>
</server>
</inist>
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