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Journal Abstract Search

248 related items for PubMed ID: 16648374

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  • 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
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  • 4. 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 05; 132B(1):74-5. PubMed ID: 15389766
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  • 5. 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 Jan 05; 23(4):505-11. PubMed ID: 23431752
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  • 7. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
    Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X.
    PLoS One; 2013 Jan 05; 8(2):e56639. PubMed ID: 23468870
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  • 8. 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 05; 34(6):735-6. PubMed ID: 15679194
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  • 10. 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 05; 147B(4):535-7. PubMed ID: 18189281
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  • 11. 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. PubMed ID: 15274046
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  • 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 15; 18(4):204-7. PubMed ID: 18628683
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  • 13. 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 15; 23(5):198-203. PubMed ID: 23851596
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  • 14. 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 15; 16(5):614-8. PubMed ID: 18231125
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  • 15. Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
    Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G, Thiruvahindrapuram B, Merico D, Prasad A, Anagnostou E, Fombonne E, Zwaigenbaum L, Roberts W, Szatmari P, Fernandez BA, Georgieva L, Brzustowicz LM, Roetzer K, Kaschnitz W, Vincent JB, Windpassinger C, Marshall CR, Trifiletti RR, Kirmani S, Kirov G, Petek E, Hodge JC, Bassett AS, Scherer SW.
    Hum Mol Genet; 2013 May 15; 22(10):2055-66. PubMed ID: 23393157
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  • 16. 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 15; 74(3):552-7. PubMed ID: 14963808
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  • 17. A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export.
    Zhang C, Milunsky JM, Newton S, Ko J, Zhao G, Maher TA, Tager-Flusberg H, Bolliger MF, Carter AS, Boucard AA, Powell CM, Südhof TC.
    J Neurosci; 2009 Sep 02; 29(35):10843-54. PubMed ID: 19726642
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  • 18. Trafficking of cholinesterases and neuroligins mutant proteins. An association with autism.
    De Jaco A, Comoletti D, King CC, Taylor P.
    Chem Biol Interact; 2008 Sep 25; 175(1-3):349-51. PubMed ID: 18555979
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  • 20. Novel interactive partners of neuroligin 3: new aspects for pathogenesis of autism.
    Shen C, Huo LR, Zhao XL, Wang PR, Zhong N.
    J Mol Neurosci; 2015 May 25; 56(1):89-101. PubMed ID: 25464930
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