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Items: 1 to 20 of 146

1.

Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis.

Schwab SG, Hallmayer J, Lerer B, Albus M, Borrmann M, Hönig S, Strauss M, Segman R, Lichtermann D, Knapp M, Trixler M, Maier W, Wildenauer DB.

Am J Hum Genet. 1998 Oct;63(4):1139-52.

2.

Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis.

Schwab SG, Eckstein GN, Hallmayer J, Lerer B, Albus M, Borrmann M, Lichtermann D, Ertl MA, Maier W, Wildenauer DB.

Mol Psychiatry. 1997 Mar;2(2):156-60.

PMID:
9106241
3.

Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.

Schwab SG, Hallmayer J, Albus M, Lerer B, Hanses C, Kanyas K, Segman R, Borrman M, Dreikorn B, Lichtermann D, Rietschel M, Trixler M, Maier W, Wildenauer DB.

Am J Med Genet. 1998 Jul 10;81(4):302-7.

PMID:
9674975
4.

A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6.

Schwab SG, Hallmayer J, Albus M, Lerer B, Eckstein GN, Borrmann M, Segman RH, Hanses C, Freymann J, Yakir A, Trixler M, Falkai P, Rietschel M, Maier W, Wildenauer DB.

Mol Psychiatry. 2000 Nov;5(6):638-49.

PMID:
11126394
5.

Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.

Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B.

Eur J Hum Genet. 2005 Jun;13(6):763-71.

6.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
7.

Evidence of linkage and association on 18p11.2 for psychosis.

Mukherjee O, Meera P, Ghosh S, Kubendran S, Kiran K, Manjunath KR, Subhash MN, Benegal V, Brahmachari SK, Majumder PP, Jain S.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):868-73.

PMID:
16941653
8.

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.

Lerer B, Segman RH, Hamdan A, Kanyas K, Karni O, Kohn Y, Korner M, Lanktree M, Kaadan M, Turetsky N, Yakir A, Kerem B, Macciardi F.

Mol Psychiatry. 2003 May;8(5):488-98.

PMID:
12808429
9.

Evidence for two schizophrenia susceptibility genes on chromosome 22q13.

Condra JA, Neibergs H, Wei W, Brennan MD.

Psychiatr Genet. 2007 Oct;17(5):292-8.

PMID:
17728668
10.

Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.

Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, Vanden Eng JL, Boehnke M, Tsuang MT, Schellenberg GD.

Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):91-100.

PMID:
16152571
11.

Linkage disequilibrium analysis of G-olf alpha (GNAL) in bipolar affective disorder.

Tsiouris SJ, Breschel TS, Xu J, McInnis MG, McMahon FJ.

Am J Med Genet. 1996 Sep 20;67(5):491-4.

PMID:
8886169
12.

Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder.

DeLisi LE, Shaw S, Sherrington R, Nanthakumar B, Shields G, Smith AB, Wellman N, Larach VW, Loftus J, Razi K, Stewart J, Comazzi M, Vita A, De Hert M, Crow TJ.

Am J Med Genet. 2000 Jun 12;96(3):335-41.

PMID:
10898911
13.

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.

Stöber G, Saar K, Rüschendorf F, Meyer J, Nürnberg G, Jatzke S, Franzek E, Reis A, Lesch KP, Wienker TF, Beckmann H.

Am J Hum Genet. 2000 Nov;67(5):1201-7. Epub 2000 Sep 19.

14.

Association and linkage of allelic variants of the dopamine transporter gene in ADHD.

Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J.

Mol Psychiatry. 2007 Oct;12(10):923-33. Epub 2007 Apr 10.

PMID:
17579611
15.

Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families.

Riley BP, Makoff A, Mogudi-Carter M, Jenkins T, Williamson R, Collier D, Murray R.

Am J Med Genet. 2000 Apr 3;96(2):196-201.

PMID:
10893497
16.

Linkage analysis of 153 prostate cancer families over a 30-cM region containing the putative susceptibility locus HPCX.

Lange EM, Chen H, Brierley K, Perrone EE, Bock CH, Gillanders E, Ray ME, Cooney KA.

Clin Cancer Res. 1999 Dec;5(12):4013-20.

17.

6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP.

Maziade M, Bissonnette L, Rouillard E, Martinez M, Turgeon M, Charron L, Pouliot V, Boutin P, Cliche D, Dion C, Fournier JP, Garneau Y, Lavallée JC, Montgrain N, Nicole L, Pirès A, Ponton AM, Potvin A, Wallot H, Roy MA, Mérette C.

Am J Med Genet. 1997 May 31;74(3):311-8.

PMID:
9184316
18.

ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies.

Faul T, Gawlik M, Bauer M, Jung S, Pfuhlmann B, Jabs B, Knapp M, Stöber G.

BMC Psychiatry. 2005 Oct 14;5:35.

19.

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15.

PMID:
17823922
20.

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.

Arch Gen Psychiatry. 2009 Oct;66(10):1058-67. doi: 10.1001/archgenpsychiatry.2009.136.

PMID:
19805696

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