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Items: 1 to 20 of 61

1.

Polymorphism of CONNEXIN37 gene is a risk factor for ischemic stroke in Han Chinese population.

Li H, Yu S, Wang R, Sun Z, Zhou X, Zheng L, Yin Z, Sun Y.

Lipids Health Dis. 2018 Apr 10;17(1):72. doi: 10.1186/s12944-018-0727-3.

2.

The integrated landscape of causal genes and pathways in schizophrenia.

Ma C, Gu C, Huo Y, Li X, Luo XJ.

Transl Psychiatry. 2018 Mar 15;8(1):67. doi: 10.1038/s41398-018-0114-x.

3.

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T; GERAD1 Consortium:; CRESTAR Consortium:, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR; GERAD1 Consortium; CRESTAR Consortium; GERAD1 Consortium; CRESTAR Consortium.

Nat Genet. 2018 Mar;50(3):381-389. doi: 10.1038/s41588-018-0059-2. Epub 2018 Feb 26.

4.

Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.

Yang CP, Li X, Wu Y, Shen Q, Zeng Y, Xiong Q, Wei M, Chen C, Liu J, Huo Y, Li K, Xue G, Yao YG, Zhang C, Li M, Chen Y, Luo XJ.

Nat Commun. 2018 Feb 26;9(1):838. doi: 10.1038/s41467-018-03247-3.

5.

Further evidence for the genetic association between CACNA1I and schizophrenia.

Xie Y, Huang D, Wei L, Luo XJ.

Hereditas. 2018 Jan 2;155:16. doi: 10.1186/s41065-017-0054-0. eCollection 2018.

6.

Association between cerebral dopamine neurotrophic factor (CDNF) 2 polymorphisms and schizophrenia susceptibility and symptoms in the Han Chinese population.

Yang Y, Yu H, Li W, Liu B, Zhang H, Ding S, Lu Y, Jiang T, Lv L.

Behav Brain Funct. 2018 Jan 3;14(1):1. doi: 10.1186/s12993-017-0133-4.

7.

Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability.

Nakao A, Miyazaki N, Ohira K, Hagihara H, Takagi T, Usuda N, Ishii S, Murata K, Miyakawa T.

Mol Brain. 2017 Dec 12;10(1):60. doi: 10.1186/s13041-017-0339-2.

8.

Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach.

Falola O, Osamor VC, Adebiyi M, Adebiyi E.

Neuropsychiatr Dis Treat. 2017 Aug 23;13:2243-2250. doi: 10.2147/NDT.S111900. eCollection 2017.

9.

An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome.

Ng B, White CC, Klein HU, Sieberts SK, McCabe C, Patrick E, Xu J, Yu L, Gaiteri C, Bennett DA, Mostafavi S, De Jager PL.

Nat Neurosci. 2017 Oct;20(10):1418-1426. doi: 10.1038/nn.4632. Epub 2017 Sep 4.

10.

Progress in genome-wide association studies of schizophrenia in Han Chinese populations.

Yue W, Yu X, Zhang D.

NPJ Schizophr. 2017 Aug 10;3(1):24. doi: 10.1038/s41537-017-0029-1. Review.

11.

Genetic Variant of Kalirin Gene Is Associated with Ischemic Stroke in a Chinese Han Population.

Li H, Yu S, Wang R, Sun Z, Zhou X, Zheng L, Yin Z, Zhang X, Sun Y.

Biomed Res Int. 2017;2017:6594271. doi: 10.1155/2017/6594271. Epub 2017 Jun 19.

12.

Association of ARHGAP18 polymorphisms with schizophrenia in the Chinese-Han population.

Guo W, Cai Y, Zhang H, Yang Y, Yang G, Wang X, Zhao J, Lin J, Zhu J, Li W, Lv L.

PLoS One. 2017 Apr 6;12(4):e0175209. doi: 10.1371/journal.pone.0175209. eCollection 2017.

13.

Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits.

Wangler MF, Hu Y, Shulman JM.

Dis Model Mech. 2017 Feb 1;10(2):77-88. doi: 10.1242/dmm.027680. Review.

14.

Genetic association of rs1344706 in ZNF804A with bipolar disorder and schizophrenia susceptibility in Chinese populations.

Rao S, Yao Y, Ryan J, Jin C, Xu Y, Huang X, Guo J, Wen Y, Mao C, Meyre D, Zhang F.

Sci Rep. 2017 Jan 25;7:41140. doi: 10.1038/srep41140.

15.

Heritability of Neuropsychological Measures in Schizophrenia and Nonpsychiatric Populations: A Systematic Review and Meta-analysis.

Blokland GAM, Mesholam-Gately RI, Toulopoulou T, Del Re EC, Lam M, DeLisi LE, Donohoe G, Walters JTR; GENUS Consortium, Seidman LJ, Petryshen TL.

Schizophr Bull. 2017 Jul 1;43(4):788-800. doi: 10.1093/schbul/sbw146.

PMID:
27872257
16.

Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.

Gonzalez S, Gupta J, Villa E, Mallawaarachchi I, Rodriguez M, Ramirez M, Zavala J, Armas R, Dassori A, Contreras J, Flores D, Jerez A, Ontiveros A, Nicolini H, Escamilla M.

Bipolar Disord. 2016 Sep;18(6):520-527. doi: 10.1111/bdi.12438.

17.

MicroRNA-137 Inhibits EFNB2 Expression Affected by a Genetic Variant and Is Expressed Aberrantly in Peripheral Blood of Schizophrenia Patients.

Wu S, Zhang R, Nie F, Wang X, Jiang C, Liu M, Valenzuela RK, Liu W, Shi Y, Ma J.

EBioMedicine. 2016 Oct;12:133-142. doi: 10.1016/j.ebiom.2016.09.012. Epub 2016 Sep 15.

18.

SZDB: A Database for Schizophrenia Genetic Research.

Wu Y, Yao YG, Luo XJ.

Schizophr Bull. 2017 Mar 1;43(2):459-471. doi: 10.1093/schbul/sbw102.

19.

No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population.

Liu Y, Cheng Z, Wang J, Jin C, Yuan J, Wang G, Zhang F, Zhao X.

BMC Psychiatry. 2016 Jul 4;16:206. doi: 10.1186/s12888-016-0923-5.

20.

From Linkage Studies to Epigenetics: What We Know and What We Need to Know in the Neurobiology of Schizophrenia.

Cariaga-Martinez A, Saiz-Ruiz J, Alelú-Paz R.

Front Neurosci. 2016 May 11;10:202. doi: 10.3389/fnins.2016.00202. eCollection 2016. Review.

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