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Patterns of genic intolerance of rare copy number variation in 59,898 human exomes.

Ruderfer DM, Hamamsy T, Lek M, Karczewski KJ, Kavanagh D, Samocha KE; Exome Aggregation Consortium., Daly MJ, MacArthur DG, Fromer M, Purcell SM.

Nat Genet. 2016 Oct;48(10):1107-11. doi: 10.1038/ng.3638.


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. Review.


Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.

Johnstone M, Maclean A, Heyrman L, Lenaerts AS, Nordin A, Nilsson LG, De Rijk P, Goossens D, Adolfsson R, St Clair DM, Hall J, Lawrie SM, McIntosh AM, Del-Favero J, Blackwood DH, Pickard BS.

Mol Neuropsychiatry. 2015 Oct;1(3):175-190.


Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.

Kim KC, Gonzales EL, Lázaro MT, Choi CS, Bahn GH, Yoo HJ, Shin CY.

Biomol Ther (Seoul). 2016 May 1;24(3):207-43. doi: 10.4062/biomolther.2016.061. Review.


A comprehensive analysis of NDST3 for schizophrenia and bipolar disorder in Han Chinese.

Zhang C, Lu W, Wang Z, Ni J, Zhang J, Tang W, Fang Y.

Transl Psychiatry. 2016 Jan 5;6:e701. doi: 10.1038/tp.2015.199.


A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.

Low JS, Chin YM, Mushiroda T, Kubo M, Govindasamy GK, Pua KC, Yap YY, Yap LF, Subramaniam SK, Ong CA, Tan TY, Khoo AS; Malaysian NPC Study Group., Ng CC.

PLoS One. 2016 Jan 5;11(1):e0145774. doi: 10.1371/journal.pone.0145774.


Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia.

Zeledón M, Eckart N, Taub M, Vernon H, Szymanksi M, Wang R, Chen PL, Nestadt G, McGrath JA, Sawa A, Pulver AE, Avramopoulos D, Valle D.

Mol Neuropsychiatry. 2015 May;1(1):36-46.


Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case-control sample of schizophrenia.

Ingason A, Giegling I, Hartmann AM, Genius J, Konte B, Friedl M; Schizophrenia Working Group of the Psychiatric Genomics Consortium (PGC)., Ripke S, Sullivan PF, St Clair D, Collier DA, O'Donovan MC, Mirnics K, Rujescu D.

Transl Psychiatry. 2015 Oct 13;5:e656. doi: 10.1038/tp.2015.151.


Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.

Degenhardt F, Priebe L, Meier S, Lennertz L, Streit F, Witt SH, Hofmann A, Becker T, Mössner R, Maier W, Nenadic I, Sauer H, Mattheisen M, Buizer-Voskamp J, Ophoff RA; GROUP Consortium., Rujescu D, Giegling I, Ingason A, Wagner M, Delobel B, Andrieux J, Meyer-Lindenberg A, Heinz A, Walter H, Moebus S, Corvin A; Wellcome Trust Case Control Consortium 2, International Schizophrenia Consortium., Rietschel M, Nöthen MM, Cichon S.

Transl Psychiatry. 2013 Nov 26;3:e326. doi: 10.1038/tp.2013.101.


The deubiquitinating enzyme USP46 regulates AMPA receptor ubiquitination and trafficking.

Huo Y, Khatri N, Hou Q, Gilbert J, Wang G, Man HY.

J Neurochem. 2015 Sep;134(6):1067-80. doi: 10.1111/jnc.13194.


The genomic load of deleterious mutations: relevance to death in infancy and childhood.

Morris JA.

Front Immunol. 2015 Mar 16;6:105. doi: 10.3389/fimmu.2015.00105. Review.


A Likelihood-Based Framework for Association Analysis of Allele-Specific Copy Numbers.

Hu YJ, Lin DY, Sun W, Zeng D.

J Am Stat Assoc. 2014 Oct;109(508):1533-1545.


S-SCAM, a rare copy number variation gene, induces schizophrenia-related endophenotypes in transgenic mouse model.

Zhang N, Zhong P, Shin SM, Metallo J, Danielson E, Olsen CM, Liu QS, Lee SH.

J Neurosci. 2015 Feb 4;35(5):1892-904. doi: 10.1523/JNEUROSCI.3658-14.2015.


Candidate gene-environment interaction research: reflections and recommendations.

Dick DM, Agrawal A, Keller MC, Adkins A, Aliev F, Monroe S, Hewitt JK, Kendler KS, Sher KJ.

Perspect Psychol Sci. 2015 Jan;10(1):37-59. doi: 10.1177/1745691614556682. Review.


I-GSEA4GWAS v2: a web server for functional analysis of SNPs in trait-associated pathways identified from genome-wide association study.

Zhang K, Chang S, Guo L, Wang J.

Protein Cell. 2015 Mar;6(3):221-4. doi: 10.1007/s13238-014-0114-4. No abstract available.


Insertion-deletions burden in copy number polymorphisms of the Tibetan population.

Veerappa AM, Vishweswaraiah S, Lingaiah K, Murthy NM, Suresh RV, Belur K, Ramachandra NB, Tejaswini, Patel NB, Gowda PK.

Indian J Hum Genet. 2014 Apr;20(2):166-74. doi: 10.4103/0971-6866.142888.


Association study identifying a new susceptibility gene (AUTS2) for schizophrenia.

Zhang B, Xu YH, Wei SG, Zhang HB, Fu DK, Feng ZF, Guan FL, Zhu YS, Li SB.

Int J Mol Sci. 2014 Oct 24;15(11):19406-16. doi: 10.3390/ijms151119406.


CNVs in Epilepsy.

Mefford HC.

Curr Genet Med Rep. 2014 Jun 28;2:162-167. Review.


Chemical modulation of mutant mGlu1 receptors derived from deleterious GRM1 mutations found in schizophrenics.

Cho HP, Garcia-Barrantes PM, Brogan JT, Hopkins CR, Niswender CM, Rodriguez AL, Venable DF, Morrison RD, Bubser M, Daniels JS, Jones CK, Conn PJ, Lindsley CW.

ACS Chem Biol. 2014 Oct 17;9(10):2334-46. doi: 10.1021/cb500560h.


Copy number variation in bronchopulmonary dysplasia.

Hoffmann TJ, Shaw GM, Stevenson DK, Wang H, Quaintance CC, Oehlert J, Jelliffe-Pawlowski LL, Gould JB, Witte JS, O'Brodovich HM.

Am J Med Genet A. 2014 Oct;164A(10):2672-5. doi: 10.1002/ajmg.a.36659. No abstract available.

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