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Results: 1 to 20 of 36

1.

Genetic modifiers and subtypes in schizophrenia: investigations of age at onset, severity, sex and family history.

Bergen SE, O'Dushlaine CT, Lee PH, Fanous AH, Ruderfer DM, Ripke S; International Schizophrenia Consortium, Swedish Schizophrenia Consortium, Sullivan PF, Smoller JW, Purcell SM, Corvin A.

Schizophr Res. 2014 Apr;154(1-3):48-53. doi: 10.1016/j.schres.2014.01.030. Epub 2014 Feb 26.

PMID:
24581549
[PubMed - in process]
2.

Rare Copy Number Variation in Treatment-Resistant Major Depressive Disorder.

O'Dushlaine C, Ripke S, Ruderfer DM, Hamilton SP, Fava M, Iosifescu DV, Kohane IS, Churchill SE, Castro VM, Clements CC, Blumenthal SR, Murphy SN, Smoller JW, Perlis RH.

Biol Psychiatry. 2014 Jan 19. pii: S0006-3223(14)00006-7. doi: 10.1016/j.biopsych.2013.10.028. [Epub ahead of print]

PMID:
24529801
[PubMed - as supplied by publisher]
3.

De novo mutations in schizophrenia implicate synaptic networks.

Fromer M, Pocklington AJ, Kavanagh DH, Williams HJ, Dwyer S, Gormley P, Georgieva L, Rees E, Palta P, Ruderfer DM, Carrera N, Humphreys I, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Grant SG, Hannon E, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Kirov G, Palotie A, McCarroll SA, Holmans P, Sklar P, Owen MJ, Purcell SM, O'Donovan MC.

Nature. 2014 Feb 13;506(7487):179-84. doi: 10.1038/nature12929. Epub 2014 Jan 22.

PMID:
24463507
[PubMed - indexed for MEDLINE]
4.

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.

Ruderfer DM, Fanous AH, Ripke S, McQuillin A, Amdur RL; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium; Cross-Disorder Working Group of the Psychiatric Genomics Consortium, Gejman PV, O'Donovan MC, Andreassen OA, Djurovic S, Hultman CM, Kelsoe JR, Jamain S, Landén M, Leboyer M, Nimgaonkar V, Nurnberger J, Smoller JW, Craddock N, Corvin A, Sullivan PF, Holmans P, Sklar P, Kendler KS.

Mol Psychiatry. 2013 Nov 26. doi: 10.1038/mp.2013.138. [Epub ahead of print]

PMID:
24280982
[PubMed - as supplied by publisher]
5.

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.

Chen Z, Tang H, Qayyum R, Schick UM, Nalls MA, Handsaker R, Li J, Lu Y, Yanek LR, Keating B, Meng Y, van Rooij FJ, Okada Y, Kubo M, Rasmussen-Torvik L, Keller MF, Lange L, Evans M, Bottinger EP, Linderman MD, Ruderfer DM, Hakonarson H, Papanicolaou G, Zonderman AB, Gottesman O; BioBank Japan Project; CHARGE Consortium, Thomson C, Ziv E, Singleton AB, Loos RJ, Sleiman PM, Ganesh S, McCarroll S, Becker DM, Wilson JG, Lettre G, Reiner AP.

Hum Mol Genet. 2013 Jun 15;22(12):2529-38. doi: 10.1093/hmg/ddt087. Epub 2013 Feb 26.

PMID:
23446634
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.

Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, Muzny D, Reid JG, Hawes A, Newsham I, Wu Y, Lewis L, Dinh H, Gross S, Wang LS, Lin CF, Valladares O, Gabriel SB, dePristo M, Altshuler DM, Purcell SM; NHLBI Exome Sequencing Project, State MW, Boerwinkle E, Buxbaum JD, Cook EH, Gibbs RA, Schellenberg GD, Sutcliffe JS, Devlin B, Roeder K, Daly MJ.

Neuron. 2013 Jan 23;77(2):235-42. doi: 10.1016/j.neuron.2012.12.029.

PMID:
23352160
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Implication of a rare deletion at distal 16p11.2 in schizophrenia.

Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, Malhotra AK, Rietschel M, Nöthen MM, Degenhardt F, Priebe L, Breuer R, Strohmaier J, Ruderfer DM, Moran JL, Chambert KD, Sanders AR, Shi J, Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S, Sklar P, Iwata N, Hultman CM, Sullivan PF, Sebat J, McCarthy S, Gejman PV, Levinson DF, Owen MJ, O'Donovan MC, Lencz T, Kirov G; Molecular Genetics of Schizophrenia Consortium; Wellcome Trust Case Control Consortium 2.

JAMA Psychiatry. 2013 Mar;70(3):253-60. doi: 10.1001/2013.jamapsychiatry.71.

PMID:
23325106
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Mosaic copy number variation in schizophrenia.

Ruderfer DM, Chambert K, Moran J, Talkowski M, Chen ES, Gigek C, Gusella JF, Blackwood DH, Corvin A, Gurling HM, Hultman CM, Kirov G, Magnusson P, O'Donovan MC, Owen MJ, Pato C, St Clair D, Sullivan PF, Purcell SM, Sklar P, Ernst C.

Eur J Hum Genet. 2013 Sep;21(9):1007-11. doi: 10.1038/ejhg.2012.287. Epub 2013 Jan 16.

PMID:
23321615
[PubMed - indexed for MEDLINE]
9.

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.

Fromer M, Moran JL, Chambert K, Banks E, Bergen SE, Ruderfer DM, Handsaker RE, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, Sullivan PF, Hultman CM, Sklar P, Purcell SM.

Am J Hum Genet. 2012 Oct 5;91(4):597-607. doi: 10.1016/j.ajhg.2012.08.005.

PMID:
23040492
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genetic schizophrenia risk variants jointly modulate total brain and white matter volume.

Terwisscha van Scheltinga AF, Bakker SC, van Haren NE, Derks EM, Buizer-Voskamp JE, Boos HB, Cahn W, Hulshoff Pol HE, Ripke S, Ophoff RA, Kahn RS; Psychiatric Genome-wide Association Study Consortium.

Biol Psychiatry. 2013 Mar 15;73(6):525-31. doi: 10.1016/j.biopsych.2012.08.017. Epub 2012 Oct 3.

PMID:
23039932
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia.

Jia P, Wang L, Fanous AH, Pato CN, Edwards TL; International Schizophrenia Consortium, Zhao Z.

PLoS Comput Biol. 2012;8(7):e1002587. doi: 10.1371/journal.pcbi.1002587. Epub 2012 Jul 5.

PMID:
22792057
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.

Derks EM, Vorstman JA, Ripke S, Kahn RS; Schizophrenia Psychiatric Genomic Consortium, Ophoff RA.

PLoS One. 2012;7(6):e37852. doi: 10.1371/journal.pone.0037852. Epub 2012 Jun 22. Erratum in: PLoS One. 2013;8(3). doi:10.1371/annotation/6ff0353a-cc91-4d12-896a-d1de0dcb0fe0.

PMID:
22761660
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
22688191
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia.

Jia P, Wang L, Fanous AH, Chen X, Kendler KS; International Schizophrenia Consortium, Zhao Z.

J Med Genet. 2012 Feb;49(2):96-103. doi: 10.1136/jmedgenet-2011-100397. Epub 2011 Dec 20.

PMID:
22187495
[PubMed - indexed for MEDLINE]
15.

Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.

Talkowski ME, Mullegama SV, Rosenfeld JA, van Bon BW, Shen Y, Repnikova EA, Gastier-Foster J, Thrush DL, Kathiresan S, Ruderfer DM, Chiang C, Hanscom C, Ernst C, Lindgren AM, Morton CC, An Y, Astbury C, Brueton LA, Lichtenbelt KD, Ades LC, Fichera M, Romano C, Innis JW, Williams CA, Bartholomew D, Van Allen MI, Parikh A, Zhang L, Wu BL, Pyatt RE, Schwartz S, Shaffer LG, de Vries BB, Gusella JF, Elsea SH.

Am J Hum Genet. 2011 Oct 7;89(4):551-63. doi: 10.1016/j.ajhg.2011.09.011.

PMID:
21981781
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Genome-wide association study identifies five new schizophrenia loci.

Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium.

Nat Genet. 2011 Sep 18;43(10):969-76. doi: 10.1038/ng.940.

PMID:
21926974
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia.

Chen J, Lee G, Fanous AH, Zhao Z, Jia P, O'Neill A, Walsh D, Kendler KS, Chen X; International Schizophrenia Consortium.

Schizophr Res. 2011 Sep;131(1-3):43-51. doi: 10.1016/j.schres.2011.06.023. Epub 2011 Jul 14.

PMID:
21752600
[PubMed - indexed for MEDLINE]
18.

Genetic classification of populations using supervised learning.

Bridges M, Heron EA, O'Dushlaine C, Segurado R; International Schizophrenia Consortium (ISC), Morris D, Corvin A, Gill M, Pinto C.

PLoS One. 2011 May 12;6(5):e14802. doi: 10.1371/journal.pone.0014802.

PMID:
21589856
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

A family-based study of common polygenic variation and risk of schizophrenia.

Ruderfer DM, Kirov G, Chambert K, Moran JL, Owen MJ, O'Donovan MC, Sklar P, Purcell SM.

Mol Psychiatry. 2011 Sep;16(9):887-8. doi: 10.1038/mp.2011.34. Epub 2011 Apr 12. No abstract available.

PMID:
21483432
[PubMed - indexed for MEDLINE]
20.

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain.

Richards AL, Jones L, Moskvina V, Kirov G, Gejman PV, Levinson DF, Sanders AR; Molecular Genetics of Schizophrenia Collaboration (MGS); International Schizophrenia Consortium (ISC), Purcell S, Visscher PM, Craddock N, Owen MJ, Holmans P, O'Donovan MC.

Mol Psychiatry. 2012 Feb;17(2):193-201. doi: 10.1038/mp.2011.11. Epub 2011 Feb 22.

PMID:
21339752
[PubMed - indexed for MEDLINE]

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