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Items: 1 to 20 of 116

1.

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.

Martinez M, Goldin LR, Cao Q, Zhang J, Sanders AR, Nancarrow DJ, Taylor JM, Levinson DF, Kirby A, Crowe RR, Andreasen NC, Black DW, Silverman JM, Lennon DP, Nertney DA, Brown DM, Mowry BJ, Gershon ES, Gejman PV.

Am J Med Genet. 1999 Aug 20;88(4):337-43.

PMID:
10402499
2.

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.

Levinson DF, Holmans P, Straub RE, Owen MJ, Wildenauer DB, Gejman PV, Pulver AE, Laurent C, Kendler KS, Walsh D, Norton N, Williams NM, Schwab SG, Lerer B, Mowry BJ, Sanders AR, Antonarakis SE, Blouin JL, DeLeuze JF, Mallet J.

Am J Hum Genet. 2000 Sep;67(3):652-63. Epub 2000 Aug 2.

3.

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees.

Cao Q, Martinez M, Zhang J, Sanders AR, Badner JA, Cravchik A, Markey CJ, Beshah E, Guroff JJ, Maxwell ME, Kazuba DM, Whiten R, Goldin LR, Gershon ES, Gejman PV.

Genomics. 1997 Jul 1;43(1):1-8.

PMID:
9226366
4.

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.

5.

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees.

Schulze TG, Buervenich S, Badner JA, Steele CJ, Detera-Wadleigh SD, Dick D, Foroud T, Cox NJ, MacKinnon DF, Potash JB, Berrettini WH, Byerley W, Coryell W, DePaulo JR Jr, Gershon ES, Kelsoe JR, McInnis MG, Murphy DL, Reich T, Scheftner W, Nurnberger JI Jr, McMahon FJ.

Biol Psychiatry. 2004 Jul 1;56(1):18-23.

PMID:
15219468
6.

Investigation of susceptibility loci identified in the UK rheumatoid arthritis whole-genome scan in a further series of 217 UK affected sibling pairs.

Eyre S, Barton A, Shephard N, Hinks A, Brintnell W, MacKay K, Silman A, Ollier W, Wordsworth P, John S, Worthington J.

Arthritis Rheum. 2004 Mar;50(3):729-35.

7.

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.

8.

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
10.

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
11.

A genomic screen of autism: evidence for a multilocus etiology.

Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM.

Am J Hum Genet. 1999 Aug;65(2):493-507.

12.

Evidence for a novel rheumatoid arthritis susceptibility locus on chromosome 6p.

Brintnell W, Zeggini E, Barton A, Thomson W, Eyre S, Hinks A, Silman AJ, Worthington J.

Arthritis Rheum. 2004 Dec;50(12):3823-30.

13.

Genetic studies in familial ankylosing spondylitis susceptibility.

Zhang G, Luo J, Bruckel J, Weisman MA, Schumacher HR, Khan MA, Inman RD, Mahowald M, Maksymowych WP, Martin TM, Yu DT, Stone M, Rosenbaum JT, Newman P, Lee J, McClain JA, West OC, Jin L, Reveille JD.

Arthritis Rheum. 2004 Jul;50(7):2246-54.

14.

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia.

Petryshen TL, Kaplan BJ, Fu Liu M, de French NS, Tobias R, Hughes ML, Field LL.

Am J Med Genet. 2001 Aug 8;105(6):507-17.

PMID:
11496366
15.

Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.

Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, Kirov G, Lendon C, Jones L, Jones I, Holmans P, Gill M, Craddock N.

Mol Psychiatry. 2005 Sep;10(9):831-41. Erratum in: Mol Psychiatry. 2006 Dec;11(12):1140-3.

PMID:
15940300
16.

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
17.

Linkage of hypertension to chromosome 2q14-q23 in Chinese families.

Zhu DL, Wang HY, Xiong MM, He X, Chu SL, Jin L, Wang GL, Yuan WT, Zhao GS, Boerwinkle E, Huang W.

J Hypertens. 2001 Jan;19(1):55-61.

PMID:
11204305
18.

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

Alkelai A, Kohn Y, Olender T, Sarner-Kanyas K, Rigbi A, Hamdan A, Ben-Asher E, Lancet D, Lerer B.

Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):914-25. doi: 10.1002/ajmg.b.30918.

PMID:
19152384
19.

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
20.

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
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