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Items: 1 to 20 of 154

1.

Familial deletion within NLGN4 associated with autism and Tourette syndrome.

Lawson-Yuen A, Saldivar JS, Sommer S, Picker J.

Eur J Hum Genet. 2008 May;16(5):614-8. doi: 10.1038/sj.ejhg.5202006. Epub 2008 Jan 30.

2.

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
3.

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
4.

Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.

Macarov M, Zeigler M, Newman JP, Strich D, Sury V, Tennenbaum A, Meiner V.

J Intellect Disabil Res. 2007 May;51(Pt 5):329-33.

PMID:
17391250
5.

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.

Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A, Moizard MP, Raynaud M, Ronce N, Lemonnier E, Calvas P, Laudier B, Chelly J, Fryns JP, Ropers HH, Hamel BC, Andres C, Barthélémy C, Moraine C, Briault S.

Am J Hum Genet. 2004 Mar;74(3):552-7. Epub 2004 Feb 12.

6.

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.

7.

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
8.

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.

Talebizadeh Z, Lam DY, Theodoro MF, Bittel DC, Lushington GH, Butler MG.

J Med Genet. 2006 May;43(5):e21.

9.

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
10.

Disorder-associated mutations lead to functional inactivation of neuroligins.

Chih B, Afridi SK, Clark L, Scheiffele P.

Hum Mol Genet. 2004 Jul 15;13(14):1471-7. Epub 2004 May 18.

PMID:
15150161
11.

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
12.

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.

Yan J, Oliveira G, Coutinho A, Yang C, Feng J, Katz C, Sram J, Bockholt A, Jones IR, Craddock N, Cook EH Jr, Vicente A, Sommer SS.

Mol Psychiatry. 2005 Apr;10(4):329-32. No abstract available.

PMID:
15622415
13.

Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.

Chocholska S, Rossier E, Barbi G, Kehrer-Sawatzki H.

Am J Med Genet A. 2006 Mar 15;140(6):604-10.

PMID:
16470742
14.

A family with fragile-X syndrome.

Kerbeshian J, Burd L, Martsolf J.

J Nerv Ment Dis. 1984 Sep;172(9):549-51.

PMID:
6590782
15.

Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.

El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H.

Behav Brain Res. 2013 Aug 15;251:41-9. doi: 10.1016/j.bbr.2012.11.016. Epub 2012 Nov 23.

PMID:
23183221
16.

Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism.

Avdjieva-Tzavella DM, Todorov TP, Todorova AP, Kirov AV, Hadjidekova SP, Rukova BB, Litvinenko IO, Hristova-Naydenova DN, Tincheva RS, Toncheva DI.

Genet Couns. 2012;23(4):505-11.

PMID:
23431752
17.

Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation.

Kerbeshian J, Severud R, Burd L, Larson L.

Am J Med Genet. 2000 Feb 7;96(1):69-73.

PMID:
10686555
18.

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T; Paris Autism Research International Sibpair Study.

Nat Genet. 2003 May;34(1):27-9.

19.

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
20.

Tourette syndrome and autistic disorder: a significant relationship.

Sverd J.

Am J Med Genet. 1991 May 1;39(2):173-9.

PMID:
2063921

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