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Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.
Bhaduri N, Sinha S, Chattopadhyay A, Gangopadhyay PK, Singh M, Mukhopadhyay KK. Bhaduri N, et al. Among authors: gangopadhyay pk. Indian Pediatr. 2005 Feb;42(2):123-9. Indian Pediatr. 2005. PMID: 15767706
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients.
Gupta A, Aikath D, Neogi R, Datta S, Basu K, Maity B, Trivedi R, Ray J, Das SK, Gangopadhyay PK, Ray K. Gupta A, et al. Among authors: gangopadhyay pk. Hum Genet. 2005 Oct;118(1):49-57. doi: 10.1007/s00439-005-0007-y. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16133174
Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.
Chattopadhyay B, Gupta S, Gangopadhyay PK, Das SK, Roy T, Mukherjee SC, Sinha KK, Singhal BS, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: gangopadhyay pk. Ann Hum Genet. 2004 May;68(Pt 3):189-95. doi: 10.1046/j.1529-8817.2003.00087.x. Ann Hum Genet. 2004. PMID: 15180699
Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India.
Chattopadhyay B, Basu P, Gangopadhyay PK, Mukherjee SC, Sinha KK, Chakraborty A, Roy T, Roychoudhury S, Majumder PP, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: gangopadhyay pk. Acta Neurol Scand. 2003 Dec;108(6):407-14. doi: 10.1034/j.1600-0404.2003.00167.x. Acta Neurol Scand. 2003. PMID: 14616293
DNA linkage based diagnosis of Wilson disease in asymptomatic siblings.
Gupta A, Neogi R, Mukherjea M, Mukhopadhyay A, Roychoudhury S, Senapati A, Gangopadhyay PK, Ray K. Gupta A, et al. Among authors: gangopadhyay pk. Indian J Med Res. 2003 Nov;118:208-14. Indian J Med Res. 2003. PMID: 14723487
Albuminuria and neuropathy in newly detected diabetics: profile and correlation.
Karmakar RN, Khandakar MR, Gangopadhyay PK, Ghosh K, Babu AS. Karmakar RN, et al. Among authors: gangopadhyay pk. J Indian Med Assoc. 2011 Jun;109(6):396-9. J Indian Med Assoc. 2011. PMID: 22315767
Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.
Guhathakurta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Gangopadhyay PK, Usha R. Guhathakurta S, et al. Among authors: gangopadhyay pk. Brain Res. 2008 Nov 13;1240:12-21. doi: 10.1016/j.brainres.2008.08.063. Epub 2008 Sep 4. Brain Res. 2008. PMID: 18804097
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. Among authors: gangopadhyay pk. 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
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. Among authors: gangopadhyay pk. 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
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. Among authors: gangopadhyay pk. Behav Brain Funct. 2005 Dec 26;1:25. doi: 10.1186/1744-9081-1-25. Behav Brain Funct. 2005. PMID: 16375773 Free PMC article.
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