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Items: 1 to 20 of 152

1.

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.

Rosenfeld JA, Patel A.

J Pediatr Genet. 2017 Mar;6(1):42-50. doi: 10.1055/s-0036-1584306. Epub 2016 May 30. Review.

PMID:
28180026
2.

Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.

Rutkowski TP, Schroeder JP, Gafford GM, Warren ST, Weinshenker D, Caspary T, Mulle JG.

J Neurosci Res. 2017 May;95(5):1144-1160. doi: 10.1002/jnr.23970. Epub 2016 Nov 8. Review.

PMID:
27859486
3.

Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub.

Blizinsky KD, Diaz-Castro B, Forrest MP, Schürmann B, Bach AP, Martin-de-Saavedra MD, Wang L, Csernansky JG, Duan J, Penzes P.

Proc Natl Acad Sci U S A. 2016 Jul 26;113(30):8520-5. doi: 10.1073/pnas.1607014113. Epub 2016 Jul 11.

4.

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. Epub 2015 Oct 7.

5.

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.

Fry AE, Rees E, Thompson R, Mantripragada K, Blake P, Jones G, Morgan S, Jose S, Mugalaasi H, Archer H, McCann E, Clarke A, Taylor C, Davies S, Gibbon F, Te Water Naude J, Hartley L, Thomas G, White C, Natarajan J, Thomas RH, Drew C, Chung SK, Rees MI, Holmans P, Owen MJ, Kirov G, Pilz DT, Kerr MP.

BMC Med Genet. 2016 Apr 26;17(1):34. doi: 10.1186/s12881-016-0294-2.

6.

Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons.

D'Rozario M, Zhang T, Waddell EA, Zhang Y, Sahin C, Sharoni M, Hu T, Nayal M, Kutty K, Liebl F, Hu W, Marenda DR.

Cell Rep. 2016 Apr 12;15(2):386-97. doi: 10.1016/j.celrep.2016.03.034. Epub 2016 Mar 31.

7.

Advances in schizophrenia genetics bring new challenges for clinicians and researchers.

Deshpande SN, Rao GP, Nimgaonkar VL.

Indian J Psychiatry. 2016 Jan-Mar;58(1):4-5. doi: 10.4103/0019-5545.174353. No abstract available.

8.

Cyfip1 Regulates Presynaptic Activity during Development.

Hsiao K, Harony-Nicolas H, Buxbaum JD, Bozdagi-Gunal O, Benson DL.

J Neurosci. 2016 Feb 3;36(5):1564-76. doi: 10.1523/JNEUROSCI.0511-15.2016.

9.

Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register Study.

Vangkilde A, Olsen L, Hoeffding LK, Pedersen CB, Mortensen PB, Werge T, Trabjerg B.

Schizophr Bull. 2016 May;42(3):824-31. doi: 10.1093/schbul/sbv195. Epub 2016 Jan 5.

PMID:
26738530
10.

Using hiPSCs to model neuropsychiatric copy number variations (CNVs) has potential to reveal underlying disease mechanisms.

Flaherty EK, Brennand KJ.

Brain Res. 2017 Jan 15;1655:283-293. doi: 10.1016/j.brainres.2015.11.009. Epub 2015 Nov 12. Review.

PMID:
26581337
11.

Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation.

Carroll LS, Woolf R, Ibrahim Y, Williams HJ, Dwyer S, Walters J, Kirov G, O'Donovan MC, Owen MJ.

Psychiatr Genet. 2016 Apr;26(2):60-5. doi: 10.1097/YPG.0000000000000110.

12.

Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia.

Merner ND, Chandler MR, Bourassa C, Liang B, Khanna AR, Dion P, Rouleau GA, Kahle KT.

Front Cell Neurosci. 2015 Oct 12;9:386. doi: 10.3389/fncel.2015.00386. eCollection 2015.

13.

New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings.

Kotlar AV, Mercer KB, Zwick ME, Mulle JG.

Eur J Med Genet. 2015 Dec;58(12):704-14. doi: 10.1016/j.ejmg.2015.10.008. Epub 2015 Oct 19. Review.

14.

A New Method for Detecting Associations with Rare Copy-Number Variants.

Tzeng JY, Magnusson PK, Sullivan PF; Swedish Schizophrenia Consortium., Szatkiewicz JP.

PLoS Genet. 2015 Oct 2;11(10):e1005403. doi: 10.1371/journal.pgen.1005403. eCollection 2015 Oct.

15.

Evidence for the multiple hits genetic theory for inherited language impairment: a case study.

Centanni TM, Green JR, Iuzzini-Seigel J, Bartlett CW, Hogan TP.

Front Genet. 2015 Aug 24;6:272. doi: 10.3389/fgene.2015.00272. eCollection 2015.

16.

NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation.

Gennarino VA, Alcott CE, Chen CA, Chaudhury A, Gillentine MA, Rosenfeld JA, Parikh S, Wheless JW, Roeder ER, Horovitz DD, Roney EK, Smith JL, Cheung SW, Li W, Neilson JR, Schaaf CP, Zoghbi HY.

Elife. 2015 Aug 27;4. doi: 10.7554/eLife.10782.

17.

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.

18.

Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.

Duan J, Sanders AR, Moy W, Drigalenko EI, Brown EC, Freda J, Leites C, Göring HH; MGS., Gejman PV.

Hum Mol Genet. 2015 Aug 15;24(16):4674-85. doi: 10.1093/hmg/ddv199. Epub 2015 May 28.

19.

The clustering of functionally related genes contributes to CNV-mediated disease.

Andrews T, Honti F, Pfundt R, de Leeuw N, Hehir-Kwa J, Vulto-van Silfhout A, de Vries B, Webber C.

Genome Res. 2015 Jun;25(6):802-13. doi: 10.1101/gr.184325.114. Epub 2015 Apr 17.

20.

Can genomics help usher schizophrenia into the age of RDoC and DSM-6?

Fanous AH.

Schizophr Bull. 2015 May;41(3):535-41. doi: 10.1093/schbul/sbv029. No abstract available.

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