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380 related items for PubMed ID: 16674932
1. Serotonin transporter promoter variants: Analysis in Indian autistic and control population. Guhathakurta S, Ghosh S, Sinha S, Chatterjee A, Ahmed S, Chowdhury SR, Gangopadhyay PK, Ghosh S, Singh M, Usha R. Brain Res; 2006 May 30; 1092(1):28-35. PubMed ID: 16674932 [Abstract] [Full Text] [Related]
2. Serotonin transporter gene promoter polymorphism and autism: a family-based genetic association study in Japanese population. Koishi S, Yamamoto K, Matsumoto H, Koishi S, Enseki Y, Oya A, Asakura A, Aoki Y, Atsumi M, Iga T, Inomata J, Inoko H, Sasaki T, Nanba E, Kato N, Ishii T, Yamazaki K. Brain Dev; 2006 May 30; 28(4):257-60. PubMed ID: 16481140 [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 30; 55(8):754-9. PubMed ID: 19647026 [Abstract] [Full Text] [Related]
4. Novel allelic variants in the human serotonin transporter gene linked polymorphism (5-HTTLPR) among depressed patients with suicide attempt. Segal J, Schenkel LC, Oliveira MH, Salum GA, Bau CH, Manfro GG, Leistner-Segal S. Neurosci Lett; 2009 Feb 13; 451(1):79-82. PubMed ID: 19103261 [Abstract] [Full Text] [Related]
5. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M, Damiani V, Baldi A, Keller F. Am J Med Genet; 2000 Feb 07; 96(1):123-7. PubMed ID: 10686565 [Abstract] [Full Text] [Related]
6. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH. Mol Psychiatry; 2002 Feb 07; 7(3):278-88. PubMed ID: 11920155 [Abstract] [Full Text] [Related]
7. Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children. Persico AM, Pascucci T, Puglisi-Allegra S, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Rabinowitz D, Reichelt KL, Conciatori M, Marino R, Keller F. Mol Psychiatry; 2002 Feb 07; 7(7):795-800. PubMed ID: 12192626 [Abstract] [Full Text] [Related]
8. Family-based studies indicate association of Engrailed 2 gene with autism in an Indian population. Sen B, Singh AS, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Usha R. Genes Brain Behav; 2010 Mar 01; 9(2):248-55. PubMed ID: 20050924 [Abstract] [Full Text] [Related]
9. Serotonin transporter gene promoter (5-HTTLPR) and intron 2 (VNTR) polymorphisms: a study on Slovenian population of suicide victims. Pungercic G, Videtic A, Pestotnik A, Pajnic IZ, Zupanc T, Balazic J, Tomori M, Komel R. Psychiatr Genet; 2006 Oct 01; 16(5):187-91. PubMed ID: 16969272 [Abstract] [Full Text] [Related]
10. Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura. Todt U, Freudenberg J, Goebel I, Heinze A, Heinze-Kuhn K, Rietschel M, Göbel H, Kubisch C. Neurology; 2006 Nov 14; 67(9):1707-9. PubMed ID: 17101915 [Abstract] [Full Text] [Related]
11. Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism. Ramoz N, Reichert JG, Corwin TE, Smith CJ, Silverman JM, Hollander E, Buxbaum JD. Biol Psychiatry; 2006 Jul 15; 60(2):186-91. PubMed ID: 16616719 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
13. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder. Betancur C, Corbex M, Spielewoy C, Philippe A, Laplanche JL, Launay JM, Gillberg C, Mouren-Siméoni MC, Hamon M, Giros B, Nosten-Bertrand M, Leboyer M. Mol Psychiatry; 2002 Aug 15; 7(1):67-71. PubMed ID: 11803447 [Abstract] [Full Text] [Related]
14. Single nucleotide polymorphisms of the serotonin transporter gene in migraine--an association study. Bayerer B, Engelbergs J, Savidou I, Boes T, Küper M, Schorn CF, Wissmann A, Knop D, Diener HC, Limmroth V. Headache; 2010 Feb 15; 50(2):319-22. PubMed ID: 19845785 [Abstract] [Full Text] [Related]
15. Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population. Conroy J, Meally E, Kearney G, Fitzgerald M, Gill M, Gallagher L. Mol Psychiatry; 2004 Jun 15; 9(6):587-93. PubMed ID: 14708029 [Abstract] [Full Text] [Related]
16. Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism. Coutinho AM, Oliveira G, Morgadinho T, Fesel C, Macedo TR, Bento C, Marques C, Ataíde A, Miguel T, Borges L, Vicente AM. Mol Psychiatry; 2004 Mar 15; 9(3):264-71. PubMed ID: 15094787 [Abstract] [Full Text] [Related]
17. Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism. Wassink TH, Hazlett HC, Epping EA, Arndt S, Dager SR, Schellenberg GD, Dawson G, Piven J. Arch Gen Psychiatry; 2007 Jun 15; 64(6):709-17. PubMed ID: 17548752 [Abstract] [Full Text] [Related]
18. Response of risperidone treatment may be associated with polymorphisms of HTT gene in Chinese schizophrenia patients. Wang L, Yu L, He G, Zhang J, Zhang AP, Du J, Tang RQ, Zhao XZ, Ma J, Xuan JK, Xiao Y, Gu NF, Feng GY, Xu MQ, Xing QH, He L. Neurosci Lett; 2007 Feb 27; 414(1):1-4. PubMed ID: 17287080 [Abstract] [Full Text] [Related]
19. No influence of 5-HTTLPR gene polymorphism on migraine symptomatology, comorbid depression, and chronification. Wieser T, Dresler K, Evers S, Gaul C, König D, Hölzl D, Berger K, Nyholt D, Deufel T. Headache; 2010 Mar 27; 50(3):420-30. PubMed ID: 19438736 [Abstract] [Full Text] [Related]
20. Association between 5-hydroxytryptamine transporter gene-linked polymorphic region and smoking behavior in Chinese males. Chu SL, Xiao D, Wang C, Jing H. Chin Med J (Engl); 2009 Jun 20; 122(12):1365-8. PubMed ID: 19567154 [Abstract] [Full Text] [Related] Page: [Next] [New Search]