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Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population.
Bhaduri N, Das M, Sinha S, Chattopadhyay A, Gangopadhyay PK, Chaudhuri K, Singh M, Mukhopadhyay K. Bhaduri N, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):61-6. doi: 10.1002/ajmg.b.30225. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16331654
Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children.
Dutta S, Sinha S, Chattopadhyay A, Gangopadhyay PK, Mukhopadhyay J, Singh M, Mukhopadhyay K. Dutta S, et al. Behav Brain Funct. 2005 Dec 26;1:25. doi: 10.1186/1744-9081-1-25. Behav Brain Funct. 2005. PMID: 16375773 Free PMC article.
A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD).
Banerjee E, Sinha S, Chatterjee A, Gangopadhyay PK, Singh M, Nandagopal K. Banerjee E, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):361-6. doi: 10.1002/ajmg.b.30296. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16583436
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. Guhathakurta S, et al. Brain Res. 2006 May 30;1092(1):28-35. doi: 10.1016/j.brainres.2006.03.078. Epub 2006 May 3. Brain Res. 2006. PMID: 16674932
However, when a meta-analysis of all the available TDT data, inclusive of the present study is carried out, we observed a significant preferential transmission of S-allele from parents to the affected offspring (chi2 = 7.51, P = 0.006) indicating an association of 5-HTTLPR …
However, when a meta-analysis of all the available TDT data, inclusive of the present study is carried out, we observed a significant prefer …
MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children.
Das M, Bhowmik AD, Sinha S, Chattopadhyay A, Chaudhuri K, Singh M, Mukhopadhyay K. Das M, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):637-42. doi: 10.1002/ajmg.b.30385. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16856146
Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.
Dutta S, Guhathakurta S, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Gangopadhyay PK, Singh M, Usha R. Dutta S, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):106-12. doi: 10.1002/ajmg.b.30419. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 16941662
Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder.
Dutta S, Das S, Guhathakurta S, Sen B, Sinha S, Chatterjee A, Ghosh S, Ahmed S, Ghosh S, Usha R. Dutta S, et al. Cell Mol Neurobiol. 2007 Dec;27(8):1035-47. doi: 10.1007/s10571-007-9193-6. Epub 2007 Aug 22. Cell Mol Neurobiol. 2007. PMID: 17712621
Lack of association between down syndrome and polymorphisms in dopamine receptor D4 and serotonin transporter genes.
Das Bhowmik A, Dutta S, Sinha S, Chattopadhyay A, Mukhopadhyay K. Das Bhowmik A, et al. Neurochem Res. 2008 Jul;33(7):1286-91. doi: 10.1007/s11064-007-9581-9. Epub 2008 Feb 13. Neurochem Res. 2008. PMID: 18270821
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