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Items: 9

1.

Imaging genetics in neurodevelopmental psychopathology.

Klein M, van Donkelaar M, Verhoef E, Franke B.

Am J Med Genet B Neuropsychiatr Genet. 2017 Jul;174(5):485-537. doi: 10.1002/ajmg.b.32542. Review.

PMID:
29984470
2.

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.

3.

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.

4.

Epilepsy associated with autism and attention deficit hyperactivity disorder: is there a genetic link?

Lo-Castro A, Curatolo P.

Brain Dev. 2014 Mar;36(3):185-93. doi: 10.1016/j.braindev.2013.04.013. Epub 2013 May 29. Review.

PMID:
23726375
5.

NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series - further understanding of the relevance of NRXN1 to neurodevelopmental disorders.

Curran S, Ahn JW, Grayton H, Collier DA, Ogilvie CM.

J Mol Psychiatry. 2013 Apr 23;1(1):4. doi: 10.1186/2049-9256-1-4. eCollection 2013.

6.

A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.

Wang KS, Liu XF, Aragam N.

Schizophr Res. 2010 Dec;124(1-3):192-9. doi: 10.1016/j.schres.2010.09.002.

PMID:
20889312
7.

Do candidate genes discriminate patients with an autism spectrum disorder from those with attention deficit/hyperactivity disorder and is there an effect of lifetime substance use disorders?

Sizoo B, van den Brink W, Franke B, Vasquez AA, van Wijngaarden-Cremers P, van der Gaag RJ.

World J Biol Psychiatry. 2010 Aug;11(5):699-708. doi: 10.3109/15622975.2010.480985.

PMID:
20446882
8.

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.

Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, Grant SF, Berrettini W, Devoto M, Shaikh TH, Hakonarson H, White PS.

Mol Psychiatry. 2010 Jun;15(6):637-46. doi: 10.1038/mp.2009.57. Epub 2009 Jun 23. Erratum in: Mol Psychiatry. 2010 Nov;15(11):1122.

9.

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.

Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA; Tourette Syndrome Association International Consortium for Genetics.

Genomics. 2003 Jul;82(1):1-9.

PMID:
12809671

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