Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 189

1.

Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families.

Kendler KS, MacLean CJ, O'Neill FA, Burke J, Murphy B, Duke F, Shinkwin R, Easter SM, Webb BT, Zhang J, Walsh D, Straub RE.

Am J Psychiatry. 1996 Dec;153(12):1534-40.

PMID:
8942448
2.

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families.

Straub RE, MacLean CJ, O'Neill FA, Walsh D, Kendler KS.

Mol Psychiatry. 1997 Mar;2(2):148-55.

PMID:
9106240
3.

A schizophrenia locus may be located in region 10p15-p11.

Straub RE, MacLean CJ, Martin RB, Ma Y, Myakishev MV, Harris-Kerr C, Webb BT, O'Neill FA, Walsh D, Kendler KS.

Am J Med Genet. 1998 Jul 10;81(4):296-301.

PMID:
9674974
4.

Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families.

Kendler KS, Myers JM, O'Neill FA, Martin R, Murphy B, MacLean CJ, Walsh D, Straub RE.

Am J Psychiatry. 2000 Mar;157(3):402-8.

PMID:
10698816
5.

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

Straub RE, MacLean CJ, O'Neill FA, Burke J, Murphy B, Duke F, Shinkwin R, Webb BT, Zhang J, Walsh D, et al.

Nat Genet. 1995 Nov;11(3):287-93.

PMID:
7581452
6.

Linkage of familial schizophrenia to chromosome 13q32.

Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS.

Am J Hum Genet. 1999 Oct;65(4):1096-103.

7.

Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22.

Wang S, Sun CE, Walczak CA, Ziegle JS, Kipps BR, Goldin LR, Diehl SR.

Nat Genet. 1995 May;10(1):41-6.

PMID:
7647789
8.

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D.

Am J Hum Genet. 2001 Mar;68(3):661-73.

9.

A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder.

Asherson P, Mant R, Williams N, Cardno A, Jones L, Murphy K, Collier DA, Nanko S, Craddock N, Morris S, Muir W, Blackwood B, McGuffin P, Owen MJ.

Mol Psychiatry. 1998 Jul;3(4):310-20.

PMID:
9702739
10.

Evaluation of linkage of markers on chromosome 6p with schizophrenia in Taiwanese families.

Hwu HG, Lin MW, Lee PC, Lee SF, Ou-Yang WC, Liu CM.

Am J Med Genet. 2000 Feb 7;96(1):74-8.

PMID:
10686556
11.

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.

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

Am J Psychiatry. 2002 May;159(5):803-12.

PMID:
11986135
12.

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.

13.

Linkage analysis of chromosome 22q12-13 in a United Kingdom/Icelandic sample of 23 multiplex schizophrenia families.

Kalsi G, Brynjolfsson J, Butler R, Sherrington R, Curtis D, Sigmundsson T, Read T, Murphy P, Sharma T, Petursson H, et al.

Am J Med Genet. 1995 Aug 14;60(4):298-301.

PMID:
7485264
14.

Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method.

Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M.

Am J Hum Genet. 2001 Dec;69(6):1278-89. Epub 2001 Oct 19.

15.

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.

Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV.

Am J Hum Genet. 2006 Feb;78(2):315-33. Epub 2006 Jan 3.

16.

Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis.

Schwab SG, Albus M, Hallmayer J, Hönig S, Borrmann M, Lichtermann D, Ebstein RP, Ackenheil M, Lerer B, Risch N, et al.

Nat Genet. 1995 Nov;11(3):325-7.

PMID:
7581458
17.

Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.

Straub RE, MacLean CJ, Ma Y, Webb BT, Myakishev MV, Harris-Kerr C, Wormley B, Sadek H, Kadambi B, O'Neill FA, Walsh D, Kendler KS.

Mol Psychiatry. 2002;7(6):542-59.

18.

Potential linkage for schizophrenia on chromosome 22q12-q13: a replication study.

Schwab SG, Lerer B, Albus M, Maier W, Hallmayer J, Fimmers R, Lichtermann D, Minges J, Bondy B, Ackenheil M, et al.

Am J Med Genet. 1995 Oct 9;60(5):436-43.

PMID:
8546158
19.

Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.

Gazda H, Lipton JM, Willig TN, Ball S, Niemeyer CM, Tchernia G, Mohandas N, Daly MJ, Ploszynska A, Orfali KA, Vlachos A, Glader BE, Rokicka-Milewska R, Ohara A, Baker D, Pospisilova D, Webber A, Viskochil DH, Nathan DG, Beggs AH, Sieff CA.

Blood. 2001 Apr 1;97(7):2145-50.

20.

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

Supplemental Content

Support Center