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Results: 1 to 20 of 21

1.

Genetic insight of schizophrenia: past and future perspectives.

Singh S, Kumar A, Agarwal S, Phadke SR, Jaiswal Y.

Gene. 2014 Feb 10;535(2):97-100. doi: 10.1016/j.gene.2013.09.110. Epub 2013 Oct 17. Review.

PMID:
24140491
[PubMed - indexed for MEDLINE]
2.

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
[PubMed - indexed for MEDLINE]
3.

Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.

Lopes AM, Aston KI, Thompson E, Carvalho F, Gonçalves J, Huang N, Matthiesen R, Noordam MJ, Quintela I, Ramu A, Seabra C, Wilfert AB, Dai J, Downie JM, Fernandes S, Guo X, Sha J, Amorim A, Barros A, Carracedo A, Hu Z, Hurles ME, Moskovtsev S, Ober C, Paduch DA, Schiffman JD, Schlegel PN, Sousa M, Carrell DT, Conrad DF.

PLoS Genet. 2013 Mar;9(3):e1003349. doi: 10.1371/journal.pgen.1003349. Epub 2013 Mar 21.

PMID:
23555275
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family.

Myles-Worsley M, Tiobech J, Browning SR, Korn J, Goodman S, Gentile K, Melhem N, Byerley W, Faraone SV, Middleton FA.

Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):87-95. doi: 10.1002/ajmg.b.32125. Epub 2013 Jan 22.

PMID:
23341099
[PubMed - indexed for MEDLINE]
5.

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.

Chapman J, Rees E, Harold D, Ivanov D, Gerrish A, Sims R, Hollingworth P, Stretton A; GERAD1 Consortium, Holmans P, Owen MJ, O'Donovan MC, Williams J, Kirov G.

Hum Mol Genet. 2013 Feb 15;22(4):816-24. doi: 10.1093/hmg/dds476. Epub 2012 Nov 11.

PMID:
23148125
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Implications of genetic findings for understanding schizophrenia.

Owen MJ.

Schizophr Bull. 2012 Sep;38(5):904-7. doi: 10.1093/schbul/sbs103. Review.

PMID:
22987847
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

[The etiology of schizophrenia].

Gejman PV, Sanders AR.

Medicina (B Aires). 2012;72(3):227-34. Review. Spanish.

PMID:
22763160
[PubMed - indexed for MEDLINE]
Free Article
8.

CNVs: harbingers of a rare variant revolution in psychiatric genetics.

Malhotra D, Sebat J.

Cell. 2012 Mar 16;148(6):1223-41. doi: 10.1016/j.cell.2012.02.039. Review.

PMID:
22424231
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

High frequencies of de novo CNVs in bipolar disorder and schizophrenia.

Malhotra D, McCarthy S, Michaelson JJ, Vacic V, Burdick KE, Yoon S, Cichon S, Corvin A, Gary S, Gershon ES, Gill M, Karayiorgou M, Kelsoe JR, Krastoshevsky O, Krause V, Leibenluft E, Levy DL, Makarov V, Bhandari A, Malhotra AK, McMahon FJ, Nöthen MM, Potash JB, Rietschel M, Schulze TG, Sebat J.

Neuron. 2011 Dec 22;72(6):951-63. doi: 10.1016/j.neuron.2011.11.007.

PMID:
22196331
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: what have we learnt?

Lee KW, Woon PS, Teo YY, Sim K.

Neurosci Biobehav Rev. 2012 Jan;36(1):556-71. doi: 10.1016/j.neubiorev.2011.09.001. Epub 2011 Sep 17. Review.

PMID:
21946175
[PubMed - indexed for MEDLINE]
11.

Recent genomic advances in schizophrenia.

Doherty JL, O'Donovan MC, Owen MJ.

Clin Genet. 2012 Feb;81(2):103-9. doi: 10.1111/j.1399-0004.2011.01773.x. Epub 2011 Oct 5. Review.

PMID:
21895634
[PubMed - indexed for MEDLINE]
12.

Common variants in the BCL9 gene conferring risk of schizophrenia.

Li J, Zhou G, Ji W, Feng G, Zhao Q, Liu J, Li T, Li Y, Chen P, Zeng Z, Wang T, Hu Z, Zheng L, Wang Y, Shen Y, He L, Shi Y.

Arch Gen Psychiatry. 2011 Mar;68(3):232-40. doi: 10.1001/archgenpsychiatry.2011.1.

PMID:
21383261
[PubMed - indexed for MEDLINE]
13.

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

Gershon ES, Alliey-Rodriguez N, Liu C.

Am J Psychiatry. 2011 Mar;168(3):253-6. doi: 10.1176/appi.ajp.2010.10091340. Epub 2011 Feb 1. Review.

PMID:
21285144
[PubMed - indexed for MEDLINE]
14.

New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.

Rudan I.

Psychiatr Danub. 2010 Jun;22(2):190-2. Review.

PMID:
20562745
[PubMed - indexed for MEDLINE]
Free Article
15.

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK, St Clair DM, Young AH, Ferrier N, Farmer AE, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N; Wellcome Trust Case Control Consortium.

Arch Gen Psychiatry. 2010 Apr;67(4):318-27. doi: 10.1001/archgenpsychiatry.2010.25.

PMID:
20368508
[PubMed - indexed for MEDLINE]
16.

Expanding the range of ZNF804A variants conferring risk of psychosis.

Steinberg S, Mors O, Børglum AD, Gustafsson O, Werge T, Mortensen PB, Andreassen OA, Sigurdsson E, Thorgeirsson TE, Böttcher Y, Olason P, Ophoff RA, Cichon S, Gudjonsdottir IH, Pietiläinen OP, Nyegaard M, Tuulio-Henriksson A, Ingason A, Hansen T, Athanasiu L, Suvisaari J, Lonnqvist J, Paunio T, Hartmann A, Jürgens G, Nordentoft M, Hougaard D, Norgaard-Pedersen B, Breuer R, Möller HJ, Giegling I, Glenthøj B, Rasmussen HB, Mattheisen M, Bitter I, Réthelyi JM, Sigmundsson T, Fossdal R, Thorsteinsdottir U, Ruggeri M, Tosato S, Strengman E; Genetic Risk and Outcome in Psychosis, Kiemeney LA, Melle I, Djurovic S, Abramova L, Kaleda V, Walshe M, Bramon E, Vassos E, Li T, Fraser G, Walker N, Toulopoulou T, Yoon J, Freimer NB, Cantor RM, Murray R, Kong A, Golimbet V, Jönsson EG, Terenius L, Agartz I, Petursson H, Nöthen MM, Rietschel M, Peltonen L, Rujescu D, Collier DA, Stefansson H, St Clair D, Stefansson K.

Mol Psychiatry. 2011 Jan;16(1):59-66. doi: 10.1038/mp.2009.149. Epub 2010 Jan 5.

PMID:
20048749
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression.

Knight HM, Pickard BS, Maclean A, Malloy MP, Soares DC, McRae AF, Condie A, White A, Hawkins W, McGhee K, van Beck M, MacIntyre DJ, Starr JM, Deary IJ, Visscher PM, Porteous DJ, Cannon RE, St Clair D, Muir WJ, Blackwood DH.

Am J Hum Genet. 2009 Dec;85(6):833-46. doi: 10.1016/j.ajhg.2009.11.003. Epub .

PMID:
19944402
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetic overlap between autism, schizophrenia and bipolar disorder.

Carroll LS, Owen MJ.

Genome Med. 2009 Oct 30;1(10):102. doi: 10.1186/gm102.

PMID:
19886976
[PubMed]
Free PMC Article
19.

Schizophrenia genetics: new insights from new approaches.

Williams HJ, Owen MJ, O'Donovan MC.

Br Med Bull. 2009;91:61-74. doi: 10.1093/bmb/ldp017. Epub 2009 May 14. Review.

PMID:
19443537
[PubMed - indexed for MEDLINE]
20.

Genomewide association studies: history, rationale, and prospects for psychiatric disorders.

Psychiatric GWAS Consortium Coordinating Committee, Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF.

Am J Psychiatry. 2009 May;166(5):540-56. doi: 10.1176/appi.ajp.2008.08091354. Epub 2009 Apr 1. Review.

PMID:
19339359
[PubMed - indexed for MEDLINE]
Free PMC Article

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