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Items: 14


Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.

Song J, Bergen SE, Di Florio A, Karlsson R, Charney A, Ruderfer DM, Stahl EA; Members of the International Cohort Collection for Bipolar Disorder (ICCBD), Chambert KD, Moran JL, Gordon-Smith K, Forty L, Green EK, Jones I, Jones L, Scolnick EM, Sklar P, Smoller JW, Lichtenstein P, Hultman C, Craddock N, Landén M, Smoller JW, Perlis RH, Lee PH, Castro VM, Hoffnagle AG, Sklar P, Stahl EA, Purcell SM, Ruderfer DM, Charney AW, Roussos P, Michele Pato CP, Medeiros H, Sobel J, Craddock N, Jones I, Forty L, Florio AD, Green E, Jones L, Gordon-Smith K, Landen M, Hultman C, Jureus A, Bergen S, McCarroll S, Moran J, Smoller JW, Chambert K, Belliveau RA.

Mol Psychiatry. 2016 Sep;21(9):1290-7. doi: 10.1038/mp.2015.165. Epub 2015 Oct 27. Erratum in: Mol Psychiatry. 2017 Aug;22(8):1223.


Validation of electronic health record phenotyping of bipolar disorder cases and controls.

Castro VM, Minnier J, Murphy SN, Kohane I, Churchill SE, Gainer V, Cai T, Hoffnagle AG, Dai Y, Block S, Weill SR, Nadal-Vicens M, Pollastri AR, Rosenquist JN, Goryachev S, Ongur D, Sklar P, Perlis RH, Smoller JW; International Cohort Collection for Bipolar Disorder Consortium.

Am J Psychiatry. 2015 Apr;172(4):363-72. doi: 10.1176/appi.ajp.2014.14030423. Epub 2014 Dec 12.


Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.

Cross-Disorder Group of the Psychiatric Genomics Consortium.

Lancet. 2013 Apr 20;381(9875):1371-9. doi: 10.1016/S0140-6736(12)62129-1. Epub 2013 Feb 28. Erratum in: Lancet. 2013 Apr 20;381(9875):1360.


Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors.

Andreassen OA, Djurovic S, Thompson WK, Schork AJ, Kendler KS, O'Donovan MC, Rujescu D, Werge T, van de Bunt M, Morris AP, McCarthy MI; International Consortium for Blood Pressure GWAS; Diabetes Genetics Replication and Meta-analysis Consortium; Psychiatric Genomics Consortium Schizophrenia Working Group, Roddey JC, McEvoy LK, Desikan RS, Dale AM.

Am J Hum Genet. 2013 Feb 7;92(2):197-209. doi: 10.1016/j.ajhg.2013.01.001. Epub 2013 Jan 31.


Patterns of deficits in brain function in bipolar disorder and schizophrenia: a cluster analytic study.

Hall MH, Smoller JW, Cook NR, Schulze K, Hyoun Lee P, Taylor G, Bramon E, Coleman MJ, Murray RM, Salisbury DF, Levy DL.

Psychiatry Res. 2012 Dec 30;200(2-3):272-80. doi: 10.1016/j.psychres.2012.07.052. Epub 2012 Aug 24.


The association between a polygenic Alzheimer score and cortical thickness in clinically normal subjects.

Sabuncu MR, Buckner RL, Smoller JW, Lee PH, Fischl B, Sperling RA; Alzheimer's Disease Neuroimaging Initiative.

Cereb Cortex. 2012 Nov;22(11):2653-61. doi: 10.1093/cercor/bhr348. Epub 2011 Dec 13.


Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.

Belmonte Mahon P, Pirooznia M, Goes FS, Seifuddin F, Steele J, Lee PH, Huang J, Hamshere ML; Bipolar Genome Study (BiGS) Consortium, The Wellcome Trust Case Control Consortium Bipolar Disorder Group, Depaulo JR Jr, Kelsoe JR, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, Smoller JW, Craddock N, Schulze TG, McMahon FJ, Potash JB, Zandi PP.

Am J Med Genet B Neuropsychiatr Genet. 2011 Apr;156B(3):370-8. doi: 10.1002/ajmg.b.31172. Epub 2011 Feb 8. Erratum in: Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):749-50.


Functionally informative tag SNP selection using a Pareto-optimal approach.

Lee PH, Jung JY, Shatkay H.

Adv Exp Med Biol. 2010;680:173-80. doi: 10.1007/978-1-4419-5913-3_20.


An integrative scoring system for ranking SNPs by their potential deleterious effects.

Lee PH, Shatkay H.

Bioinformatics. 2009 Apr 15;25(8):1048-55. doi: 10.1093/bioinformatics/btp103. Epub 2009 Feb 19.


Ranking single nucleotide polymorphisms by potential deleterious effects.

Lee PH, Shatkay H.

AMIA Annu Symp Proc. 2008 Nov 6:667-71.


Using cluster ensemble and validation to identify subtypes of pervasive developmental disorders.

Shen JJ, Lee PH, Holden JJ, Shatkay H.

AMIA Annu Symp Proc. 2007 Oct 11:666-70.


F-SNP: computationally predicted functional SNPs for disease association studies.

Lee PH, Shatkay H.

Nucleic Acids Res. 2008 Jan;36(Database issue):D820-4. Epub 2007 Nov 5.


BNTagger: improved tagging SNP selection using Bayesian networks.

Lee PH, Shatkay H.

Bioinformatics. 2006 Jul 15;22(14):e211-9.


Modularized learning of genetic interaction networks from biological annotations and mRNA expression data.

Lee PH, Lee D.

Bioinformatics. 2005 Jun 1;21(11):2739-47. Epub 2005 Mar 29.


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