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Items: 1 to 20 of 67

1.

Singleton deletions throughout the genome increase risk of bipolar disorder.

Zhang D, Cheng L, Qian Y, Alliey-Rodriguez N, Kelsoe JR, Greenwood T, Nievergelt C, Barrett TB, McKinney R, Schork N, Smith EN, Bloss C, Nurnberger J, Edenberg HJ, Foroud T, Sheftner W, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon F, Schulze TG, Berrettini W, Potash JB, Belmonte PL, Zandi PP, McInnis MG, Zöllner S, Craig D, Szelinger S, Koller D, Christian SL, Liu C, Gershon ES.

Mol Psychiatry. 2009 Apr;14(4):376-80. doi: 10.1038/mp.2008.144. Epub 2008 Dec 30.

2.

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Nöthen MM, Cichon S, Mühleisen TW.

Mol Psychiatry. 2012 Apr;17(4):421-32. doi: 10.1038/mp.2011.8. Epub 2011 Mar 1.

PMID:
21358712
3.

Reduced burden of very large and rare CNVs in bipolar affective disorder.

Grozeva D, Kirov G, Conrad DF, Barnes CP, Hurles M, Owen MJ, O'Donovan MC, Craddock N.

Bipolar Disord. 2013 Dec;15(8):893-8. doi: 10.1111/bdi.12125. Epub 2013 Oct 16.

PMID:
24127788
4.

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.

Bergen SE, O'Dushlaine CT, Ripke S, Lee PH, Ruderfer DM, Akterin S, Moran JL, Chambert KD, Handsaker RE, Backlund L, Ösby U, McCarroll S, Landen M, Scolnick EM, Magnusson PK, Lichtenstein P, Hultman CM, Purcell SM, Sklar P, Sullivan PF.

Mol Psychiatry. 2012 Sep;17(9):880-6. doi: 10.1038/mp.2012.73. Epub 2012 Jun 12.

5.

Rare chromosomal deletions and duplications increase risk of schizophrenia.

International Schizophrenia Consortium.

Nature. 2008 Sep 11;455(7210):237-41. doi: 10.1038/nature07239. Epub 2008 Jul 30.

6.

TRPM2 variants and bipolar disorder risk: confirmation in a family-based association study.

Xu C, Li PP, Cooke RG, Parikh SV, Wang K, Kennedy JL, Warsh JJ.

Bipolar Disord. 2009 Feb;11(1):1-10. doi: 10.1111/j.1399-5618.2008.00655.x.

PMID:
19133961
7.

Polymorphisms in seizure 6-like gene are associated with bipolar disorder I: evidence of gene × gender interaction.

Xu C, Mullersman JE, Wang L, Bin Su B, Mao C, Posada Y, Camarillo C, Mao Y, Escamilla MA, Wang KS.

J Affect Disord. 2013 Feb 15;145(1):95-9. doi: 10.1016/j.jad.2012.07.017. Epub 2012 Aug 22.

PMID:
22920719
8.

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

Kim JH, Jung SH, Bae JS, Lee HS, Yim SH, Park SY, Bang SY, Hu HJ, Shin HD, Bae SC, Chung YJ.

Arthritis Rheum. 2013 Apr;65(4):1055-63. doi: 10.1002/art.37854.

9.

A genome-wide association study of suicide severity scores in bipolar disorder.

Zai CC, Gonçalves VF, Tiwari AK, Gagliano SA, Hosang G, de Luca V, Shaikh SA, King N, Chen Q, Xu W, Strauss J, Breen G, Lewis CM, Farmer AE, McGuffin P, Knight J, Vincent JB, Kennedy JL.

J Psychiatr Res. 2015 Jun;65:23-9. doi: 10.1016/j.jpsychires.2014.11.002. Epub 2014 Nov 20.

PMID:
25917933
10.

Association of genetic variation in CACNA1C with bipolar disorder in Han Chinese.

Zhang X, Zhang C, Wu Z, Wang Z, Peng D, Chen J, Hong W, Yuan C, Li Z, Yu S, Fang Y.

J Affect Disord. 2013 Sep 5;150(2):261-5. doi: 10.1016/j.jad.2013.04.004. Epub 2013 May 13.

PMID:
23680436
11.

A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.

Wang KS, Liu XF, Aragam N.

Schizophr Res. 2010 Dec;124(1-3):192-9. doi: 10.1016/j.schres.2010.09.002.

PMID:
20889312
12.

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.

Saadati HR, Wittig M, Helbig I, Häsler R, Anderson CA, Mathew CG, Kupcinskas L, Parkes M, Karlsen TH, Rosenstiel P, Schreiber S, Franke A.

BMC Med Genet. 2016 Apr 1;17:26. doi: 10.1186/s12881-016-0289-z.

13.

Association at SYNE1 in both bipolar disorder and recurrent major depression.

Green EK, Grozeva D, Forty L, Gordon-Smith K, Russell E, Farmer A, Hamshere M, Jones IR, Jones L, McGuffin P, Moran JL, Purcell S, Sklar P, Owen MJ, O'Donovan MC, Craddock N.

Mol Psychiatry. 2013 May;18(5):614-7. doi: 10.1038/mp.2012.48. Epub 2012 May 8.

PMID:
22565781
14.

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder.

Kember RL, Georgi B, Bailey-Wilson JE, Stambolian D, Paul SM, Bućan M.

BMC Genet. 2015 Mar 15;16:27. doi: 10.1186/s12863-015-0184-1.

15.

Design of tag SNP whole genome genotyping arrays.

Peiffer DA, Gunderson KL.

Methods Mol Biol. 2009;529:51-61. doi: 10.1007/978-1-59745-538-1_4.

PMID:
19381970
16.

MAGI1 copy number variation in bipolar affective disorder and schizophrenia.

Karlsson R, Graae L, Lekman M, Wang D, Favis R, Axelsson T, Galter D, Belin AC, Paddock S.

Biol Psychiatry. 2012 May 15;71(10):922-30. doi: 10.1016/j.biopsych.2012.01.020. Epub 2012 Feb 28.

PMID:
22381734
17.

Genome-wide association study on bipolar disorder in the Bulgarian population.

Yosifova A, Mushiroda T, Kubo M, Takahashi A, Kamatani Y, Kamatani N, Stoianov D, Vazharova R, Karachanak S, Zaharieva I, Dimova I, Hadjidekova S, Milanova V, Madjirova N, Gerdjikov I, Tolev T, Poryazova N, O'Donovan MC, Owen MJ, Kirov G, Toncheva D, Nakamura Y.

Genes Brain Behav. 2011 Oct;10(7):789-97. doi: 10.1111/j.1601-183X.2011.00721.x. Epub 2011 Aug 18.

18.

Increase in GSK3beta gene copy number variation in bipolar disorder.

Lachman HM, Pedrosa E, Petruolo OA, Cockerham M, Papolos A, Novak T, Papolos DF, Stopkova P.

Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):259-65.

PMID:
17357145
19.

Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder.

Kandaswamy R, McQuillin A, Curtis D, Gurling H.

Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):365-72. doi: 10.1002/ajmg.b.32239. Epub 2014 May 8.

20.

Glycogen synthase kinase 3 beta gene structural variants as possible risk factors of bipolar depression.

Ronai Z, Kovacs-Nagy R, Szantai E, Elek Z, Sasvari-Szekely M, Faludi G, Benkovits J, Rethelyi JM, Szekely A.

Am J Med Genet B Neuropsychiatr Genet. 2014 Apr;165B(3):217-22. doi: 10.1002/ajmg.b.32223. Epub 2014 Feb 21.

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