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Items: 1 to 20 of 27

1.

Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders.

Hoeffding LK, Duong LT, Ingason A, Rosengren A, Sorbanski E, Witt SH, Djurovic S, Andreassen OA, Hansen T, Werge T, Rasmussen HB.

Nord J Psychiatry. 2016 May;70(4):276-9. doi: 10.3109/08039488.2015.1095944. Epub 2015 Nov 11.

PMID:
26559242
2.

A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease.

Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E.

PLoS One. 2014 Nov 7;9(11):e111462. doi: 10.1371/journal.pone.0111462. eCollection 2014.

3.

Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: a systematic review of literature and meta-analysis.

Giaroli G, Bass N, Strydom A, Rantell K, McQuillin A.

Schizophr Res. 2014 Nov;159(2-3):340-6. doi: 10.1016/j.schres.2014.09.025. Epub 2014 Oct 11. Review.

4.

Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder.

Cardno AG, Owen MJ.

Schizophr Bull. 2014 May;40(3):504-15. doi: 10.1093/schbul/sbu016. Epub 2014 Feb 24. Review.

5.

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.

Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, Strange A, Freeman C, Thiselton DL, Elves RL, Regan R, Ennis S, Dinan TG, McDonald C, Murphy KC, O'Callaghan E, Waddington JL, Walsh D, O'Donovan M, Grozeva D, Craddock N, Stone J, Scolnick E, Purcell S, Sklar P, Coe B, Eichler EE, Ophoff R, Buizer J, Szatkiewicz J, Hultman C, Sullivan P, Gurling H, Mcquillin A, St Clair D, Rees E, Kirov G, Walters J, Blackwood D, Johnstone M, Donohoe G; International Schizophrenia Consortium, SGENE+ Consortium, O'Neill FA; Wellcome Trust Case Control Consortium 2, Kendler KS, Gill M, Riley BP, Spencer CC, Corvin A.

Hum Mol Genet. 2014 Jun 15;23(12):3316-26. doi: 10.1093/hmg/ddu025. Epub 2014 Jan 28.

6.

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
7.

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
8.

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.

9.

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
10.

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.

11.

Implications of genetic findings for understanding schizophrenia.

Owen MJ.

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

12.

[The etiology of schizophrenia].

Gejman PV, Sanders AR.

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

13.

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.

14.

Susceptibility genes for schizophrenia: mutant models, endophenotypes and psychobiology.

O'Tuathaigh CM, Desbonnet L, Moran PM, Waddington JL.

Curr Top Behav Neurosci. 2012;12:209-50. doi: 10.1007/7854_2011_194. Review.

PMID:
22367925
15.

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.

16.

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
17.

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
18.

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
19.

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
20.
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