24493018 15162027 16791389 16419095 19246517 16823807 16773131 15575414 23776346 15517821 17967920 24995986 18197051 21129364 16418599 17004120 - Search Results

Year	Number of Results
2004	3
2006	5
2007	2
2008	1
2009	2
2010	1
2011	1
2014	2
2022	0

1

Glutamatergic candidate genes in autism spectrum disorder: an overview.

Chiocchetti AG, Bour HS, Freitag CM. Chiocchetti AG, et al. J Neural Transm (Vienna). 2014 Sep;121(9):1081-106. doi: 10.1007/s00702-014-1161-y. Epub 2014 Feb 4. J Neural Transm (Vienna). 2014. PMID: 24493018 Review.

2

Cytological indications of the complex subtelomeric structure.

Drets ME. Drets ME. Cytogenet Genome Res. 2004;104(1-4):137-41. doi: 10.1159/000077478. Cytogenet Genome Res. 2004. PMID: 15162027 Review.

3

[Autism: genetics].

Gupta AR, State MW. Gupta AR, et al. Braz J Psychiatry. 2006 May;28 Suppl 1:S29-38. doi: 10.1590/s1516-44462006000500005. Epub 2006 Jun 12. Braz J Psychiatry. 2006. PMID: 16791389 Review. Portuguese.

4

The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders.

Battaglia A, Bonaglia MC. Battaglia A, et al. Am J Med Genet C Semin Med Genet. 2006 Feb 15;142C(1):8-12. doi: 10.1002/ajmg.c.30077. Am J Med Genet C Semin Med Genet. 2006. PMID: 16419095

5

Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder.

Cuscó I, Medrano A, Gener B, Vilardell M, Gallastegui F, Villa O, González E, Rodríguez-Santiago B, Vilella E, Del Campo M, Pérez-Jurado LA. Cuscó I, et al. Hum Mol Genet. 2009 May 15;18(10):1795-804. doi: 10.1093/hmg/ddp092. Epub 2009 Feb 26. Hum Mol Genet. 2009. PMID: 19246517 Free PMC article.

6

Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation.

Di Bella MA, Calì F, Seidita G, Mirisola M, Ragusa A, Ragalmuto A, Galesi O, Elia M, Greco D, Zingale M, Gambino G, D'Anna RP, Regan R, Carbone MC, Gallo A, Romano V. Di Bella MA, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):584-90. doi: 10.1002/ajmg.b.30328. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823807

7

Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.

Saugier-Veber P, Goldenberg A, Drouin-Garraud V, de La Rochebrochard C, Layet V, Drouot N, Le Meur N, Gilbert-Du-Ssardier B, Joly-Hélas G, Moirot H, Rossi A, Tosi M, Frébourg T. Saugier-Veber P, et al. Eur J Hum Genet. 2006 Sep;14(9):1009-17. doi: 10.1038/sj.ejhg.5201661. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773131

8

The genetics of autism.

Spence SJ. Spence SJ. Semin Pediatr Neurol. 2004 Sep;11(3):196-204. doi: 10.1016/j.spen.2004.07.003. Semin Pediatr Neurol. 2004. PMID: 15575414 Free article. Review.

9

The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder.

Stam AJ, Schothorst PF, Vorstman JA, Staal WG. Stam AJ, et al. Appl Clin Genet. 2009 Mar 10;2:7-13. doi: 10.2147/tacg.s4683. Print 2009. Appl Clin Genet. 2009. PMID: 23776346 Free PMC article.

10

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.

Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K. Lukusa T, et al. Genet Couns. 2004;15(3):293-301. Genet Couns. 2004. PMID: 15517821

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