Format
Sort by
Items per page

Send to

Choose Destination

Best matches for CNTNAP2 schizophrenia:

Search results

Items: 1 to 20 of 36

1.

CNTNAP2 stabilizes interneuron dendritic arbors through CASK.

Gao R, Piguel NH, Melendez-Zaidi AE, Martin-de-Saavedra MD, Yoon S, Forrest MP, Myczek K, Zhang G, Russell TA, Csernansky JG, Surmeier DJ, Penzes P.

Mol Psychiatry. 2018 Apr 2. doi: 10.1038/s41380-018-0027-3. [Epub ahead of print]

PMID:
29610457
2.

Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elements.

Piluso G, Monteleone P, Galderisi S, Giugliano T, Bertolino A, Rocca P, Rossi A, Mucci A, Aguglia E, Andriola I, Bellomo A, Comparelli A, Gambi F, Fagiolini A, Marchesi C, Roncone R, Sacchetti E, Santonastaso P, Siracusano A, Stratta P, Tortorella A, Steardo L Jr, Bucci P, Nigro V, Maj M; Italian Network for Research on Psychoses.

World J Biol Psychiatry. 2017 Nov 20:1-11. doi: 10.1080/15622975.2017.1395072. [Epub ahead of print]

PMID:
29069978
3.

Patient-derived hiPSC neurons with heterozygous CNTNAP2 deletions display altered neuronal gene expression and network activity.

Flaherty E, Deranieh RM, Artimovich E, Lee IS, Siegel AJ, Levy DL, Nestor MW, Brennand KJ.

NPJ Schizophr. 2017 Oct 2;3:35. doi: 10.1038/s41537-017-0033-5. eCollection 2017.

PMID:
28975140
4.

Patient-derived hiPSC neurons with heterozygous CNTNAP2 deletions display altered neuronal gene expression and network activity.

Flaherty E, Deranieh RM, Artimovich E, Lee IS, Siegel AJ, Levy DL, Nestor MW, Brennand KJ.

NPJ Schizophr. 2017 Oct 2;3(1):35. doi: 10.1038/s41537-017-0033-5.

5.

Intragenic CNTNAP2 Deletions: A Bridge Too Far?

Poot M.

Mol Syndromol. 2017 May;8(3):118-130. doi: 10.1159/000456021. Epub 2017 Feb 10. Review.

6.

Rodent models of genetic and chromosomal variations in psychiatric disorders.

Nomura J, Kannan G, Takumi T.

Psychiatry Clin Neurosci. 2017 Aug;71(8):508-517. doi: 10.1111/pcn.12524. Epub 2017 Apr 23. Review.

7.

Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2).

Lu Z, Reddy MV, Liu J, Kalichava A, Liu J, Zhang L, Chen F, Wang Y, Holthauzen LM, White MA, Seshadrinathan S, Zhong X, Ren G, Rudenko G.

J Biol Chem. 2016 Nov 11;291(46):24133-24147. Epub 2016 Sep 12.

8.

Prevalence of serum anti-neuronal autoantibodies in patients admitted to acute psychiatric care.

Schou M, Sæther SG, Borowski K, Teegen B, Kondziella D, Stoecker W, Vaaler A, Reitan SK.

Psychol Med. 2016 Dec;46(16):3303-3313. Epub 2016 Sep 9.

PMID:
27609625
9.

Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells.

Lee IS, Carvalho CM, Douvaras P, Ho SM, Hartley BJ, Zuccherato LW, Ladran IG, Siegel AJ, McCarthy S, Malhotra D, Sebat J, Rapoport J, Fossati V, Lupski JR, Levy DL, Brennand KJ.

NPJ Schizophr. 2015 Jun 24;1. pii: 15019.

10.

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.

Nascimento PP, Bossolani-Martins AL, Rosan DB, Mattos LC, Brandão-Mattos C, Fett-Conte AC.

Genet Mol Res. 2016 Feb 5;15(1). doi: 10.4238/gmr.15017422.

11.

Characterisation of CASPR2 deficiency disorder--a syndrome involving autism, epilepsy and language impairment.

Rodenas-Cuadrado P, Pietrafusa N, Francavilla T, La Neve A, Striano P, Vernes SC.

BMC Med Genet. 2016 Feb 3;17:8. doi: 10.1186/s12881-016-0272-8.

12.

A novel relationship for schizophrenia, bipolar and major depressive disorder Part 7: A hint from chromosome 7 high density association screen.

Chen X, Long F, Cai B, Chen X, Chen G.

Behav Brain Res. 2015 Oct 15;293:241-51. doi: 10.1016/j.bbr.2015.06.043. Epub 2015 Jul 17.

PMID:
26192912
13.

Interaction effect between handedness and CNTNAP2 polymorphism (rs7794745 genotype) on voice-specific frontotemporal activity in healthy individuals: an fMRI study.

Koeda M, Watanabe A, Tsuda K, Matsumoto M, Ikeda Y, Kim W, Tateno A, Naing BT, Karibe H, Shimada T, Suzuki H, Matsuura M, Okubo Y.

Front Behav Neurosci. 2015 Apr 20;9:87. doi: 10.3389/fnbeh.2015.00087. eCollection 2015.

14.

Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons.

Varea O, Martin-de-Saavedra MD, Kopeikina KJ, Schürmann B, Fleming HJ, Fawcett-Patel JM, Bach A, Jang S, Peles E, Kim E, Penzes P.

Proc Natl Acad Sci U S A. 2015 May 12;112(19):6176-81. doi: 10.1073/pnas.1423205112. Epub 2015 Apr 27.

15.

Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders.

Poot M.

Mol Syndromol. 2015 Feb;6(1):7-22. doi: 10.1159/000371594. Epub 2015 Feb 3. Review.

16.

Genetic markers of white matter integrity in schizophrenia revealed by parallel ICA.

Gupta CN, Chen J, Liu J, Damaraju E, Wright C, Perrone-Bizzozero NI, Pearlson G, Luo L, Michael AM, Turner JA, Calhoun VD.

Front Hum Neurosci. 2015 Mar 3;9:100. doi: 10.3389/fnhum.2015.00100. eCollection 2015.

17.

Utility of Scalp Hair Follicles as a Novel Source of Biomarker Genes for Psychiatric Illnesses.

Maekawa M, Yamada K, Toyoshima M, Ohnishi T, Iwayama Y, Shimamoto C, Toyota T, Nozaki Y, Balan S, Matsuzaki H, Iwata Y, Suzuki K, Miyashita M, Kikuchi M, Kato M, Okada Y, Akamatsu W, Mori N, Owada Y, Itokawa M, Okano H, Yoshikawa T.

Biol Psychiatry. 2015 Jul 15;78(2):116-25. doi: 10.1016/j.biopsych.2014.07.025. Epub 2014 Sep 11.

18.

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission.

Karayannis T, Au E, Patel JC, Kruglikov I, Markx S, Delorme R, Héron D, Salomon D, Glessner J, Restituito S, Gordon A, Rodriguez-Murillo L, Roy NC, Gogos JA, Rudy B, Rice ME, Karayiorgou M, Hakonarson H, Keren B, Huguet G, Bourgeron T, Hoeffer C, Tsien RW, Peles E, Fishell G.

Nature. 2014 Jul 10;511(7508):236-40.

19.

CNTNAP2 polymorphisms and structural brain connectivity: a diffusion-tensor imaging study.

Clemm von Hohenberg C, Wigand MC, Kubicki M, Leicht G, Giegling I, Karch S, Hartmann AM, Konte B, Friedl M, Ballinger T, Eckbo R, Bouix S, Jäger L, Shenton ME, Rujescu D, Mulert C.

J Psychiatr Res. 2013 Oct;47(10):1349-56. doi: 10.1016/j.jpsychires.2013.07.002. Epub 2013 Jul 17.

20.

Shining a light on CNTNAP2: complex functions to complex disorders.

Rodenas-Cuadrado P, Ho J, Vernes SC.

Eur J Hum Genet. 2014 Feb;22(2):171-8. doi: 10.1038/ejhg.2013.100. Epub 2013 May 29. Review.

Supplemental Content

Loading ...
Support Center