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Items: 1 to 20 of 119

1.

Leveraging electronic health records to study pleiotropic effects on bipolar disorder and medical comorbidities.

Prieto ML, Ryu E, Jenkins GD, Batzler A, Nassan MM, Cuellar-Barboza AB, Pathak J, McElroy SL, Frye MA, Biernacka JM.

Transl Psychiatry. 2016 Aug 16;6:e870. doi: 10.1038/tp.2016.138.

2.

A genome-wide association study of bipolar disorder and comorbid migraine.

Oedegaard KJ, Greenwood TA, Johansson S, Jacobsen KK, Halmoy A, Fasmer OB, Akiskal HS; Bipolar Genome Study (BiGS), Haavik J, Kelsoe JR.

Genes Brain Behav. 2010 Oct;9(7):673-80. doi: 10.1111/j.1601-183X.2010.00601.x. Epub 2010 Jun 29.

3.

CACNA1C rs1006737 genotype and bipolar disorder: Focus on intermediate phenotypes and cardiovascular comorbidity.

Ou X, Crane DE, MacIntosh BJ, Young LT, Arnold P, Ameis S, Goldstein BI.

Neurosci Biobehav Rev. 2015 Aug;55:198-210. doi: 10.1016/j.neubiorev.2015.04.022. Epub 2015 May 11. Review.

PMID:
25976633
4.

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample.

Green EK, Hamshere M, Forty L, Gordon-Smith K, Fraser C, Russell E, Grozeva D, Kirov G, Holmans P, Moran JL, Purcell S, Sklar P, Owen MJ, O'Donovan MC, Jones L; WTCCC, Jones IR, Craddock N.

Mol Psychiatry. 2013 Dec;18(12):1302-7. doi: 10.1038/mp.2012.142. Epub 2012 Oct 16.

5.

Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records.

Chen CY, Lee PH, Castro VM, Minnier J, Charney AW, Stahl EA, Ruderfer DM, Murphy SN, Gainer V, Cai T, Jones I, Pato CN, Pato MT, Landén M, Sklar P, Perlis RH, Smoller JW.

Transl Psychiatry. 2018 Apr 18;8(1):86. doi: 10.1038/s41398-018-0133-7.

6.

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
7.

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

Li M, Luo XJ, Rietschel M, Lewis CM, Mattheisen M, Müller-Myhsok B, Jamain S, Leboyer M, Landén M, Thompson PM, Cichon S, Nöthen MM, Schulze TG, Sullivan PF, Bergen SE, Donohoe G, Morris DW, Hargreaves A, Gill M, Corvin A, Hultman C, Toga AW, Shi L, Lin Q, Shi H, Gan L, Meyer-Lindenberg A, Czamara D, Henry C, Etain B, Bis JC, Ikram MA, Fornage M, Debette S, Launer LJ, Seshadri S, Erk S, Walter H, Heinz A, Bellivier F, Stein JL, Medland SE, Arias Vasquez A, Hibar DP, Franke B, Martin NG, Wright MJ; MooDS Bipolar Consortium; Swedish Bipolar Study Group; Alzheimer’s Disease Neuroimaging Initiative; ENIGMA Consortium; CHARGE Consortium, Su B.

Mol Psychiatry. 2014 Apr;19(4):452-61. doi: 10.1038/mp.2013.37. Epub 2013 Apr 9. Erratum in: Mol Psychiatry. 2014 Apr;19(4):527.

8.

CACNA1C SNP rs1006737 associates with bipolar I disorder independent of the Bcl-2 SNP rs956572 variant and its associated effect on intracellular calcium homeostasis.

Uemura T, Green M, Warsh JJ.

World J Biol Psychiatry. 2016 Oct;17(7):525-34. doi: 10.3109/15622975.2015.1019360. Epub 2015 Apr 5.

PMID:
25843436
9.

Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2.

Winham SJ, Cuellar-Barboza AB, Oliveros A, McElroy SL, Crow S, Colby C, Choi DS, Chauhan M, Frye M, Biernacka JM.

Mol Psychiatry. 2014 Sep;19(9):1010-6. doi: 10.1038/mp.2013.159. Epub 2013 Dec 10.

PMID:
24322204
10.

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.

Shameer K, Denny JC, Ding K, Jouni H, Crosslin DR, de Andrade M, Chute CG, Peissig P, Pacheco JA, Li R, Bastarache L, Kho AN, Ritchie MD, Masys DR, Chisholm RL, Larson EB, McCarty CA, Roden DM, Jarvik GP, Kullo IJ.

Hum Genet. 2014 Jan;133(1):95-109. doi: 10.1007/s00439-013-1355-7. Epub 2013 Sep 12.

11.

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
12.

Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder.

Jacobsen KK, Nievergelt CM, Zayats T, Greenwood TA, Anttila V, Akiskal HS; BiGS Consortium; IHG Consortium, Haavik J, Bernt Fasmer O, Kelsoe JR, Johansson S, Oedegaard KJ.

J Affect Disord. 2015 Feb 1;172:453-61. doi: 10.1016/j.jad.2014.10.004. Epub 2014 Oct 12.

13.

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill FA, Kendler KS, Sklar P, Purcell S, Kranz J; Schizophrenia Psychiatric Genome-wide Association Study Consortium; Wellcome Trust Case Control Consortium+; Wellcome Trust Case Control Consortium 2, Morris D, Gill M, Holmans P, Craddock N, Corvin A, Owen MJ, O'Donovan MC.

Mol Psychiatry. 2013 Jun;18(6):708-12. doi: 10.1038/mp.2012.67. Epub 2012 May 22. Erratum in: Mol Psychiatry. 2013 Jun;18(6):738. O'Neill, T [corrected to O'Neill, F A].

14.

Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.

Kondo K, Ikeda M, Kajio Y, Saito T, Iwayama Y, Aleksic B, Yamada K, Toyota T, Hattori E, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, Iwata N.

PLoS One. 2013 Aug 13;8(8):e70964. doi: 10.1371/journal.pone.0070964. eCollection 2013.

15.

A genome wide association study suggests the association of muskelin with early onset bipolar disorder: Implications for a GABAergic epileptogenic neurogenesis model.

Nassan M, Li Q, Croarkin PE, Chen W, Colby CL, Veldic M, McElroy SL, Jenkins GD, Ryu E, Cunningham JM, Leboyer M, Frye MA, Biernacka JM.

J Affect Disord. 2017 Jan 15;208:120-129. doi: 10.1016/j.jad.2016.09.049. Epub 2016 Sep 30.

PMID:
27769005
16.

Bipolar disorder risk alleles in adult ADHD patients.

Landaas ET, Johansson S, Halmøy A, Oedegaard KJ, Fasmer OB, Haavik J.

Genes Brain Behav. 2011 Jun;10(4):418-23. doi: 10.1111/j.1601-183X.2011.00680.x. Epub 2011 Feb 18.

17.

Modeling complex genetic and environmental influences on comorbid bipolar disorder with tobacco use disorder.

McEachin RC, Saccone NL, Saccone SF, Kleyman-Smith YD, Kar T, Kare RK, Ade AS, Sartor MA, Cavalcoli JD, McInnis MG.

BMC Med Genet. 2010 Jan 26;11:14. doi: 10.1186/1471-2350-11-14.

18.

Glutamatergic and HPA-axis pathway genes in bipolar disorder comorbid with alcohol- and substance use disorders.

Dalvie S, Fabbri C, Ramesar R, Serretti A, Stein DJ.

Metab Brain Dis. 2016 Feb;31(1):183-9. doi: 10.1007/s11011-015-9762-1. Epub 2015 Nov 12.

PMID:
26563126
19.

ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples.

Kloiber S, Czamara D, Karbalai N, Müller-Myhsok B, Hennings J, Holsboer F, Lucae S.

J Psychiatr Res. 2012 Aug;46(8):973-9. doi: 10.1016/j.jpsychires.2012.04.017. Epub 2012 May 29.

PMID:
22647524
20.

Bipolar disorder risk alleles in children with ADHD.

Schimmelmann BG, Hinney A, Scherag A, Pütter C, Pechlivanis S, Cichon S, Jöckel KH, Schreiber S, Wichmann HE, Albayrak Ö, Dauvermann M, Konrad K, Wilhelm C, Herpertz-Dahlmann B, Lehmkuhl G, Sinzig J, Renner TJ, Romanos M, Warnke A, Lesch KP, Reif A, Hebebrand J.

J Neural Transm (Vienna). 2013 Nov;120(11):1611-7. doi: 10.1007/s00702-013-1035-8. Epub 2013 May 28.

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