Format
Items per page
Sort by

Send to:

Choose Destination

Results: 20

1.

Research in China on the molecular genetics of schizophrenia.

Cui D, Jiang K.

Shanghai Arch Psychiatry. 2012 Aug;24(4):187-99. doi: 10.3969/j.issn.1002-0829.2012.04.001. Review.

PMID:
25324626
[PubMed]
Free PMC Article
2.

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.

PMID:
24474471
[PubMed - in process]
Free PMC Article
3.

An evaluation of association between a novel hippocampal biology related SNP (rs7294919) and schizophrenia.

Liu J, Numata S, Ikeda M, Watanabe Y, Zheng XB, Luo X, Kinoshita M, Nunokawa A, Someya T, Ohmori T, Bei JX, Chong SA, Lee J, Li Z, Liu J, Iwata N, Shi Y, Li M, Su B.

PLoS One. 2013 Nov 22;8(11):e80696. doi: 10.1371/journal.pone.0080696. eCollection 2013.

PMID:
24278305
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.

Lencz T, Guha S, Liu C, Rosenfeld J, Mukherjee S, DeRosse P, John M, Cheng L, Zhang C, Badner JA, Ikeda M, Iwata N, Cichon S, Rietschel M, Nöthen MM, Cheng AT, Hodgkinson C, Yuan Q, Kane JM, Lee AT, Pisanté A, Gregersen PK, Pe'er I, Malhotra AK, Goldman D, Darvasi A.

Nat Commun. 2013;4:2739. doi: 10.1038/ncomms3739.

PMID:
24253340
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

The genomics of schizophrenia: update and implications.

Giusti-Rodríguez P, Sullivan PF.

J Clin Invest. 2013 Nov 1;123(11):4557-63. doi: 10.1172/JCI66031. Epub 2013 Nov 1. Review.

PMID:
24177465
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naïve patients with schizophrenia.

Wang Q, Xiang B, Deng W, Wu J, Li M, Ma X, Wang Y, Jiang L, McAlonan G, Chua SE, Sham PC, Hu X, Li T.

PLoS One. 2013 Sep 24;8(9):e75083. doi: 10.1371/journal.pone.0075083. eCollection 2013.

PMID:
24086445
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Hiroi N, Takahashi T, Hishimoto A, Izumi T, Boku S, Hiramoto T.

Mol Psychiatry. 2013 Nov;18(11):1153-65. doi: 10.1038/mp.2013.92. Epub 2013 Aug 6. Review.

PMID:
23917946
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.

Psychosis Endophenotypes International Consortium; Wellcome Trust Case-Control Consortium 2, Bramon E, Pirinen M, Strange A, Lin K, Freeman C, Bellenguez C, Su Z, Band G, Pearson R, Vukcevic D, Langford C, Deloukas P, Hunt S, Gray E, Dronov S, Potter SC, Tashakkori-Ghanbaria A, Edkins S, Bumpstead SJ, Arranz MJ, Bakker S, Bender S, Bruggeman R, Cahn W, Chandler D, Collier DA, Crespo-Facorro B, Dazzan P, de Haan L, Di Forti M, Dragović M, Giegling I, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Kravariti E, Lawrie S, Linszen DH, Mata I, McDonald C, McIntosh A, Myin-Germeys I, Ophoff RA, Pariante CM, Paunio T, Picchioni M; Psychiatric Genomics Consortium, Ripke S, Rujescu D, Sauer H, Shaikh M, Sussmann J, Suvisaari J, Tosato S, Toulopoulou T, Van Os J, Walshe M, Weisbrod M, Whalley H, Wiersma D, Blackwell JM, Brown MA, Casas JP, Corvin A, Duncanson A, Jankowski JA, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Wood NW, Barroso I, Peltonen L, Lewis CM, Murray RM, Donnelly P, Powell J, Spencer CC.

Biol Psychiatry. 2014 Mar 1;75(5):386-97. doi: 10.1016/j.biopsych.2013.03.033. Epub 2013 Jul 17.

PMID:
23871474
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Immature dentate gyrus: an endophenotype of neuropsychiatric disorders.

Hagihara H, Takao K, Walton NM, Matsumoto M, Miyakawa T.

Neural Plast. 2013;2013:318596. doi: 10.1155/2013/318596. Epub 2013 Jun 12. Review.

PMID:
23840971
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Meta-analysis indicates that the European GWAS-identified risk SNP rs1344706 within ZNF804A is not associated with schizophrenia in Han Chinese population.

Li M, Zhang H, Luo XJ, Gao L, Qi XB, Gourraud PA, Su B.

PLoS One. 2013 Jun 12;8(6):e65780. doi: 10.1371/journal.pone.0065780. Print 2013.

PMID:
23776546
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

"Selfish spermatogonial selection": a novel mechanism for the association between advanced paternal age and neurodevelopmental disorders.

Goriely A, McGrath JJ, Hultman CM, Wilkie AO, Malaspina D.

Am J Psychiatry. 2013 Jun;170(6):599-608. doi: 10.1176/appi.ajp.2013.12101352. Review.

PMID:
23639989
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Replication study confirms link between TSPAN18 mutation and schizophrenia in Han Chinese.

Yuan J, Jin C, Qin HD, Wang J, Sha W, Wang M, Zhang Y, Zhang F, Li J, Li J, Yu S, Qi S, Shugart YY.

PLoS One. 2013;8(3):e58785. doi: 10.1371/journal.pone.0058785. Epub 2013 Mar 7.

PMID:
23505562
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Deficiency of schnurri-2, an MHC enhancer binding protein, induces mild chronic inflammation in the brain and confers molecular, neuronal, and behavioral phenotypes related to schizophrenia.

Takao K, Kobayashi K, Hagihara H, Ohira K, Shoji H, Hattori S, Koshimizu H, Umemori J, Toyama K, Nakamura HK, Kuroiwa M, Maeda J, Atsuzawa K, Esaki K, Yamaguchi S, Furuya S, Takagi T, Walton NM, Hayashi N, Suzuki H, Higuchi M, Usuda N, Suhara T, Nishi A, Matsumoto M, Ishii S, Miyakawa T.

Neuropsychopharmacology. 2013 Jul;38(8):1409-25. doi: 10.1038/npp.2013.38. Epub 2013 Feb 6.

PMID:
23389689
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Association study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample.

Kukshal P, Bhatia T, Bhagwat AM, Gur RE, Gur RC, Deshpande SN, Nimgaonkar VL, Thelma BK.

Schizophr Res. 2013 Mar;144(1-3):24-30. doi: 10.1016/j.schres.2012.12.017. Epub 2013 Jan 26.

PMID:
23360725
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Common variant at 16p11.2 conferring risk of psychosis.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E; GROUP, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B; Wellcome Trust Case Control Consortium 2, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K.

Mol Psychiatry. 2014 Jan;19(1):108-14. doi: 10.1038/mp.2012.157. Epub 2012 Nov 20.

PMID:
23164818
[PubMed - indexed for MEDLINE]
Free PMC Article
16.
17.

Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.

Irish Schizophrenia Genomics Consortium and the Wellcome Trust Case Control Consortium 2.

Biol Psychiatry. 2012 Oct 15;72(8):620-8. doi: 10.1016/j.biopsych.2012.05.035. Epub 2012 Aug 9.

PMID:
22883433
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetic architectures of psychiatric disorders: the emerging picture and its implications.

Sullivan PF, Daly MJ, O'Donovan M.

Nat Rev Genet. 2012 Jul 10;13(8):537-51. doi: 10.1038/nrg3240. Review.

PMID:
22777127
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

The genetic variability and commonality of neurodevelopmental disease.

Coe BP, Girirajan S, Eichler EE.

Am J Med Genet C Semin Med Genet. 2012 May 15;160C(2):118-29. doi: 10.1002/ajmg.c.31327. Epub 2012 Apr 12. Review.

PMID:
22499536
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease.

Goriely A, Wilkie AO.

Am J Hum Genet. 2012 Feb 10;90(2):175-200. doi: 10.1016/j.ajhg.2011.12.017. Review.

PMID:
22325359
[PubMed - indexed for MEDLINE]
Free PMC Article
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk