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Results: 1 to 20 of 73

1.

Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.

Yanagi K, Kaname T, Wakui K, Hashimoto O, Fukushima Y, Naritomi K.

Autism Res Treat. 2012;2012:724072. doi: 10.1155/2012/724072. Epub 2012 Jul 16.

PMID:
22934180
[PubMed]
Free PMC Article
2.

No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level.

Wermter AK, Kamp-Becker I, Strauch K, Schulte-Körne G, Remschmidt H.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):535-7. doi: 10.1002/ajmg.b.30618.

PMID:
18189281
[PubMed - indexed for MEDLINE]
3.

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection.

Blasi F, Bacchelli E, Pesaresi G, Carone S, Bailey AJ, Maestrini E; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):220-1.

PMID:
16508939
[PubMed - indexed for MEDLINE]
4.

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.

Steinberg KM, Ramachandran D, Patel VC, Shetty AC, Cutler DJ, Zwick ME.

Mol Autism. 2012 Sep 28;3(1):8. doi: 10.1186/2040-2392-3-8.

PMID:
23020841
[PubMed]
Free PMC Article
5.

Analysis of four neuroligin genes as candidates for autism.

Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I.

Eur J Hum Genet. 2005 Dec;13(12):1285-92.

PMID:
16077734
[PubMed - indexed for MEDLINE]
Free Article
6.

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):82-4.

PMID:
15274046
[PubMed - indexed for MEDLINE]
7.

Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level.

Daoud H, Bonnet-Brilhault F, Védrine S, Demattéi MV, Vourc'h P, Bayou N, Andres CR, Barthélémy C, Laumonnier F, Briault S.

Biol Psychiatry. 2009 Nov 15;66(10):906-10. doi: 10.1016/j.biopsych.2009.05.008. Epub 2009 Jul 9.

PMID:
19545860
[PubMed - indexed for MEDLINE]
8.

Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.

Xu X, Xiong Z, Zhang L, Liu Y, Lu L, Peng Y, Guo H, Zhao J, Xia K, Hu Z.

Mol Biol Rep. 2014 Jun;41(6):4133-40. doi: 10.1007/s11033-014-3284-5. Epub 2014 Feb 26.

PMID:
24570023
[PubMed - in process]
9.

Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE.

Nava C, Lamari F, Héron D, Mignot C, Rastetter A, Keren B, Cohen D, Faudet A, Bouteiller D, Gilleron M, Jacquette A, Whalen S, Afenjar A, Périsse D, Laurent C, Dupuits C, Gautier C, Gérard M, Huguet G, Caillet S, Leheup B, Leboyer M, Gillberg C, Delorme R, Bourgeron T, Brice A, Depienne C.

Transl Psychiatry. 2012 Oct 23;2:e179. doi: 10.1038/tp.2012.102.

PMID:
23092983
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism.

Volaki K, Pampanos A, Kitsiou-Tzeli S, Vrettou C, Oikonomakis V, Sofocleous C, Kanavakis E.

Psychiatr Genet. 2013 Oct;23(5):198-203. doi: 10.1097/YPG.0b013e3283643644.

PMID:
23851596
[PubMed - indexed for MEDLINE]
11.

Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder.

Yasuda Y, Hashimoto R, Yamamori H, Ohi K, Fukumoto M, Umeda-Yano S, Mohri I, Ito A, Taniike M, Takeda M.

Mol Autism. 2011 May 26;2(1):9. doi: 10.1186/2040-2392-2-9.

PMID:
21615902
[PubMed]
Free PMC Article
12.

A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.

Pampanos A, Volaki K, Kanavakis E, Papandreou O, Youroukos S, Thomaidis L, Karkelis S, Tzetis M, Kitsiou-Tzeli S.

Genet Test Mol Biomarkers. 2009 Oct;13(5):611-5. doi: 10.1089/gtmb.2009.0005.

PMID:
19645625
[PubMed - indexed for MEDLINE]
13.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
[PubMed - indexed for MEDLINE]
14.

Analysis of X chromosome inactivation in autism spectrum disorders.

Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Gillberg C, Moreno-De-Luca D, Carone S, Nummela I, Rossi M, Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC), Jarvela I, Maestrini E, Bourgeron T.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):830-5. doi: 10.1002/ajmg.b.30688.

PMID:
18361425
[PubMed - indexed for MEDLINE]
15.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
[PubMed - indexed for MEDLINE]
16.

Analysis of the neuroligin 4Y gene in patients with autism.

Yan J, Feng J, Schroer R, Li W, Skinner C, Schwartz CE, Cook EH Jr, Sommer SS.

Psychiatr Genet. 2008 Aug;18(4):204-7. doi: 10.1097/YPG.0b013e3282fb7fe6.

PMID:
18628683
[PubMed - indexed for MEDLINE]
17.

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.

Gauthier J, Bonnel A, St-Onge J, Karemera L, Laurent S, Mottron L, Fombonne E, Joober R, Rouleau GA.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):74-5.

PMID:
15389766
[PubMed - indexed for MEDLINE]
18.

Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case-control study in a Japanese population and functional analysis.

Ma WJ, Hashii M, Munesue T, Hayashi K, Yagi K, Yamagishi M, Higashida H, Yokoyama S.

Mol Autism. 2013 Jul 1;4(1):22. doi: 10.1186/2040-2392-4-22.

PMID:
23815867
[PubMed]
Free PMC Article
19.

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.

Cai G, Edelmann L, Goldsmith JE, Cohen N, Nakamine A, Reichert JG, Hoffman EJ, Zurawiecki DM, Silverman JM, Hollander E, Soorya L, Anagnostou E, Betancur C, Buxbaum JD.

BMC Med Genomics. 2008 Oct 16;1:50. doi: 10.1186/1755-8794-1-50.

PMID:
18925931
[PubMed]
Free PMC Article
20.

Fmr1 and Nlgn3 knockout rats: novel tools for investigating autism spectrum disorders.

Hamilton SM, Green JR, Veeraragavan S, Yuva L, McCoy A, Wu Y, Warren J, Little L, Ji D, Cui X, Weinstein E, Paylor R.

Behav Neurosci. 2014 Apr;128(2):103-9. doi: 10.1037/a0035988.

PMID:
24773431
[PubMed - in process]

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