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Journal Abstract Search

114 related items for PubMed ID: 21182206

  • 1. Low CD38 expression in lymphoblastoid cells and haplotypes are both associated with autism in a family-based study.
    Lerer E, Levi S, Israel S, Yaari M, Nemanov L, Mankuta D, Nurit Y, Ebstein RP.
    Autism Res; 2010 Dec; 3(6):293-302. PubMed ID: 21182206
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  • 3. Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.
    Lerer E, Levi S, Salomon S, Darvasi A, Yirmiya N, Ebstein RP.
    Mol Psychiatry; 2008 Oct; 13(10):980-8. PubMed ID: 17893705
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  • 8. Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes.
    Guhathakurta S, Singh AS, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Usha R.
    Neurochem Int; 2009 Dec; 55(8):754-9. PubMed ID: 19647026
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  • 9. All-trans retinoic acid upregulates reduced CD38 transcription in lymphoblastoid cell lines from Autism spectrum disorder.
    Riebold M, Mankuta D, Lerer E, Israel S, Zhong S, Nemanov L, Monakhov MV, Levi S, Yirmiya N, Yaari M, Malavasi F, Ebstein RP.
    Mol Med; 2011 Dec; 17(7-8):799-806. PubMed ID: 21528155
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  • 10. Family-based association study between GRIK2 polymorphisms and autism spectrum disorders in the Korean trios.
    Kim SA, Kim JH, Park M, Cho IH, Yoo HJ.
    Neurosci Res; 2007 Jul; 58(3):332-5. PubMed ID: 17428563
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  • 11. Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study.
    Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, Sasaki T.
    Brain Dev; 2007 Sep; 29(8):510-3. PubMed ID: 17376622
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  • 12. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
    Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.
    Neurosci Lett; 2008 Aug 15; 441(1):56-60. PubMed ID: 18597938
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  • 14. Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios.
    Kim SA, Kim JH, Park M, Cho IH, Yoo HJ.
    Neuropsychobiology; 2006 Aug 15; 54(3):160-5. PubMed ID: 17230033
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  • 15. Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.
    Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH.
    Mol Psychiatry; 2004 May 15; 9(5):474-84. PubMed ID: 15024396
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  • 16. HTR1B and HTR2C in autism spectrum disorders in Brazilian families.
    Orabona GM, Griesi-Oliveira K, Vadasz E, Bulcão VL, Takahashi VN, Moreira ES, Furia-Silva M, Ros-Melo AM, Dourado F, Matioli SR, Otto P, Passos-Bueno MR.
    Brain Res; 2009 Jan 23; 1250():14-9. PubMed ID: 19038234
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  • 18. Associations between oxytocin-related genes and autistic-like traits.
    Hovey D, Zettergren A, Jonsson L, Melke J, Anckarsäter H, Lichtenstein P, Westberg L.
    Soc Neurosci; 2014 Jan 23; 9(4):378-86. PubMed ID: 24635660
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  • 19. Study of HOXD genes in autism particularly regarding the ratio of second to fourth digit length.
    Sugie Y, Sugie H, Fukuda T, Osawa J.
    Brain Dev; 2010 May 23; 32(5):356-61. PubMed ID: 19540081
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  • 20. Sensitive parenting is associated with plasma oxytocin and polymorphisms in the OXTR and CD38 genes.
    Feldman R, Zagoory-Sharon O, Weisman O, Schneiderman I, Gordon I, Maoz R, Shalev I, Ebstein RP.
    Biol Psychiatry; 2012 Aug 01; 72(3):175-81. PubMed ID: 22336563
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