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Journal Abstract Search
191 related items for PubMed ID: 37019319
1. Association of GABRG3, GABRB3, HTR2A gene variants with autism spectrum disorder. Coskunpinar EM, Tur S, Cevher Binici N, Yazan Songür C. Gene; 2023 Jun 20; 870():147399. PubMed ID: 37019319 [Abstract] [Full Text] [Related]
2. Gamma-Aminobutyric Acid Type A Receptor Variants are Associated with Autism Spectrum Disorders. Adak P, Banerjee N, Sinha S, Bandyopadhyay AK. J Mol Neurosci; 2023 May 20; 73(4-5):237-249. PubMed ID: 36943547 [Abstract] [Full Text] [Related]
3. 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 20; 55(8):754-9. PubMed ID: 19647026 [Abstract] [Full Text] [Related]
4. [Relationship between gene polymorphism of GABAA receptors gene and childhood autism]. Lu GB, Ou P, Xu LP, Huang HL, Cheng L, Yang SW, Qian QF, Huang Y, Xie YQ, Yu QJ, Wang ZQ, Lin Y. Zhonghua Yu Fang Yi Xue Za Zhi; 2012 May 20; 46(5):460-4. PubMed ID: 22883737 [Abstract] [Full Text] [Related]
5. GABAA receptor subunit gene polymorphisms predict symptom-based and developmental deficits in Chinese Han children and adolescents with autistic spectrum disorders. Yang S, Guo X, Dong X, Han Y, Gao L, Su Y, Dai W, Zhang X. Sci Rep; 2017 Jun 12; 7(1):3290. PubMed ID: 28607477 [Abstract] [Full Text] [Related]
11. Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population. Wang L, Li J, Shuang M, Lu T, Wang Z, Zhang T, Yue W, Jia M, Ruan Y, Liu J, Wu Z, Zhang D, Wang L. Transl Psychiatry; 2018 Aug 14; 8(1):152. PubMed ID: 30108208 [Abstract] [Full Text] [Related]
12. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. Cho IH, Yoo HJ, Park M, Lee YS, Kim SA. Brain Res; 2007 Mar 30; 1139():34-41. PubMed ID: 17280648 [Abstract] [Full Text] [Related]
13. An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. Ann Hum Genet; 2006 May 30; 70(Pt 3):281-92. PubMed ID: 16674551 [Abstract] [Full Text] [Related]
14. An Association Study of Gamma-Aminobutyric Acid Type A Receptor Variants and Susceptibility to Autism Spectrum Disorders. Adak P, Sinha S, Banerjee N. J Autism Dev Disord; 2021 Nov 30; 51(11):4043-4053. PubMed ID: 33442857 [Abstract] [Full Text] [Related]
16. Hypomethylation of the serotonin receptor type-2A Gene (HTR2A) at T102C polymorphic site in DNA derived from the saliva of patients with schizophrenia and bipolar disorder. Ghadirivasfi M, Nohesara S, Ahmadkhaniha HR, Eskandari MR, Mostafavi S, Thiagalingam S, Abdolmaleky HM. Am J Med Genet B Neuropsychiatr Genet; 2011 Jul 30; 156B(5):536-45. PubMed ID: 21598376 [Abstract] [Full Text] [Related]
17. Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA. Am J Hum Genet; 2005 Sep 30; 77(3):377-88. PubMed ID: 16080114 [Abstract] [Full Text] [Related]
18. Serotonin receptor gene (HTR2A) T102C polymorphism modulates individuals' perspective taking ability and autistic-like traits. Gong P, Liu J, Blue PR, Li S, Zhou X. Front Hum Neurosci; 2015 Sep 30; 9():575. PubMed ID: 26557070 [Abstract] [Full Text] [Related]
20. Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD). Mahdavi M, Kheirollahi M, Riahi R, Khorvash F, Khorrami M, Mirsafaie M. J Mol Neurosci; 2018 May 30; 65(1):1-9. PubMed ID: 29725984 [Abstract] [Full Text] [Related] Page: [Next] [New Search]