Bergen SE - Search Results

1

Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.

Bergen SE, Ploner A, Howrigan D; CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium; O'Donovan MC, Smoller JW, Sullivan PF, Sebat J, Neale B, Kendler KS. Bergen SE, et al. Am J Psychiatry. 2019 Jan 1;176(1):29-35. doi: 10.1176/appi.ajp.2018.17040467. Epub 2018 Nov 5. Am J Psychiatry. 2019. PMID: 30392412 Free PMC article.

2

Bergen SE, Gardner CO, Kendler KS. Bergen SE, et al. Twin Res Hum Genet. 2007 Jun;10(3):423-33. doi: 10.1375/twin.10.3.423. Twin Res Hum Genet. 2007. PMID: 17564500

3

Socioeconomic status and social support following illicit drug use: causal pathways or common liability?

Bergen SE, Gardner CO, Aggen SH, Kendler KS. Bergen SE, et al. Twin Res Hum Genet. 2008 Jun;11(3):266-74. doi: 10.1375/twin.11.3.266. Twin Res Hum Genet. 2008. PMID: 18498205 Free PMC article.

4

Polymorphisms in SLC6A4, PAH, GABRB3, and MAOB and modification of psychotic disorder features.

Bergen SE, Fanous AH, Walsh D, O'Neill FA, Kendler KS. Bergen SE, et al. Schizophr Res. 2009 Apr;109(1-3):94-7. doi: 10.1016/j.schres.2009.02.009. Epub 2009 Mar 5. Schizophr Res. 2009. PMID: 19268543 Free PMC article.

5

No association of dysbindin with symptom factors of schizophrenia in an Irish case-control sample.

Bergen SE, Fanous AH, Kuo PH, Wormley BK, O'Neill FA, Walsh D, Riley BP, Kendler KS. Bergen SE, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):700-705. doi: 10.1002/ajmg.b.31029. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19760674 Free PMC article.

6

Detection of susceptibility genes as modifiers due to subgroup differences in complex disease.

Bergen SE, Maher BS, Fanous AH, Kendler KS. Bergen SE, et al. Eur J Hum Genet. 2010 Aug;18(8):960-4. doi: 10.1038/ejhg.2010.39. Epub 2010 Mar 31. Eur J Hum Genet. 2010. PMID: 20354561 Free PMC article.

7

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.

Raychaudhuri S, Korn JM, McCarroll SA; International Schizophrenia Consortium; Altshuler D, Sklar P, Purcell S, Daly MJ. Raychaudhuri S, et al. PLoS Genet. 2010 Sep 9;6(9):e1001097. doi: 10.1371/journal.pgen.1001097. PLoS Genet. 2010. PMID: 20838587 Free PMC article.

8

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.

Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J, Zhang N, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Kendler KS, Freedman R, Dudbridge F, Pe'er I, Hakonarson H, Bergen SE, Fanous AH, Holmans PA, Gejman PV. Levinson DF, et al. Among authors: bergen se. Am J Psychiatry. 2011 Mar;168(3):302-16. doi: 10.1176/appi.ajp.2010.10060876. Epub 2011 Feb 1. Am J Psychiatry. 2011. PMID: 21285140 Free PMC article.

9

Modifiers and subtype-specific analyses in whole-genome association studies: a likelihood framework.

Lee PH, Bergen SE, Perlis RH, Sullivan PF, Sklar P, Smoller JW, Purcell SM. Lee PH, et al. Among authors: bergen se. Hum Hered. 2011;72(1):10-20. doi: 10.1159/000327158. Epub 2011 Aug 17. Hum Hered. 2011. PMID: 21849790 Free PMC article.

10

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.

Psychiatric GWAS Consortium Bipolar Disorder Working Group. Psychiatric GWAS Consortium Bipolar Disorder Working Group. Nat Genet. 2011 Sep 18;43(10):977-83. doi: 10.1038/ng.943. Nat Genet. 2011. PMID: 21926972 Free PMC article.

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