1311 related articles for article (PubMed ID: 12669065)
1. 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;
Nat Genet; 2003 May; 34(1):27-9. PubMed ID: 12669065
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 23431752
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 16077734
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 19645625
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 16648374
[TBL] [Abstract][Full Text] [Related]
6. 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;
Am J Med Genet B Neuropsychiatr Genet; 2006 Apr; 141B(3):220-1. PubMed ID: 16508939
[TBL] [Abstract][Full Text] [Related]
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; 129B(1):82-4. PubMed ID: 15274046
[TBL] [Abstract][Full Text] [Related]
8. 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; 132B(1):74-5. PubMed ID: 15389766
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Durand CM; Betancur C; Boeckers TM; Bockmann J; Chaste P; Fauchereau F; Nygren G; Rastam M; Gillberg IC; Anckarsäter H; Sponheim E; Goubran-Botros H; Delorme R; Chabane N; Mouren-Simeoni MC; de Mas P; Bieth E; Rogé B; Héron D; Burglen L; Gillberg C; Leboyer M; Bourgeron T
Nat Genet; 2007 Jan; 39(1):25-7. PubMed ID: 17173049
[TBL] [Abstract][Full Text] [Related]
10. 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; Vicente A; Sommer SS
Mol Psychiatry; 2005 Apr; 10(4):329-32. PubMed ID: 15622415
[No Abstract] [Full Text] [Related]
11. Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
Talebizadeh Z; Bittel DC; Veatch OJ; Butler MG; Takahashi TN; Miles JH
J Autism Dev Disord; 2004 Dec; 34(6):735-6. PubMed ID: 15679194
[No Abstract] [Full Text] [Related]
12. Analysis of the neuroligin 4Y gene in patients with autism.
Yan J; Feng J; Schroer R; Li W; Skinner C; Schwartz CE; Cook EH; Sommer SS
Psychiatr Genet; 2008 Aug; 18(4):204-7. PubMed ID: 18628683
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 14963808
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 23851596
[TBL] [Abstract][Full Text] [Related]
15. Disorder-associated mutations lead to functional inactivation of neuroligins.
Chih B; Afridi SK; Clark L; Scheiffele P
Hum Mol Genet; 2004 Jul; 13(14):1471-7. PubMed ID: 15150161
[TBL] [Abstract][Full Text] [Related]
16. Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
Cheung J; Petek E; Nakabayashi K; Tsui LC; Vincent JB; Scherer SW
Genomics; 2001 Nov; 78(1-2):7-11. PubMed ID: 11707066
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 18231125
[TBL] [Abstract][Full Text] [Related]
18. 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; 147B(4):535-7. PubMed ID: 18189281
[TBL] [Abstract][Full Text] [Related]
19. Mutations in the gene encoding CADM1 are associated with autism spectrum disorder.
Zhiling Y; Fujita E; Tanabe Y; Yamagata T; Momoi T; Momoi MY
Biochem Biophys Res Commun; 2008 Dec; 377(3):926-9. PubMed ID: 18957284
[TBL] [Abstract][Full Text] [Related]
20. Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder.
Mikhailov A; Fennell A; Plong-on O; Sripo T; Hansakunachai T; Roongpraiwan R; Sombuntham T; Ruangdaraganon N; Vincent JB; Limprasert P
Psychiatr Genet; 2014 Feb; 24(1):42-3. PubMed ID: 24362370
[No Abstract] [Full Text] [Related]
[Next] [New Search]