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Krishna Sinha

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India

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Biswanath Chattopadhyay; S Gupta; Prasanta K Gangopadhyay; Shaymal K Das; Trishit Roy; Subhash C Mukherjee; Krishna K Sinha; Bhim S Singhal; Nitai P Bhattacharyya
Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.
Krishna K Sinha; Paul Worth; Dilip K Jha; S Sinha; VJ Stinton; Mary B Davis; Nicholas W Wood; Mary G Sweeney; Kailash P Bhatia
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
Biswanath Chattopadhyay; P Basu; Prasanta K Gangopadhyay; Subhash C Mukherjee; Krishna K Sinha; A Chakraborty; Trishit Roy; Susanta Roychoudhury; Partha P Majumder; Nitai P Bhattacharyya
Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India.

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All Publications

2004: Biswanath Chattopadhyay; S Gupta; Prasanta K Gangopadhyay; Shaymal K Das; Trishit Roy; Subhash C Mukherjee; Krishna K Sinha; Bhim S Singhal; Nitai P Bhattacharyya
Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.
Annals of human genetics 2004;68(Pt 3):189-95.
2004: Krishna K Sinha; Paul Worth; Dilip K Jha; S Sinha; VJ Stinton; Mary B Davis; Nicholas W Wood; Mary G Sweeney; Kailash P Bhatia
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
Journal of neurology, neurosurgery, and psychiatry 2004;75(3):448-52.
2003: Biswanath Chattopadhyay; P Basu; Prasanta K Gangopadhyay; Subhash C Mukherjee; Krishna K Sinha; A Chakraborty; Trishit Roy; Susanta Roychoudhury; Partha P Majumder; Nitai P Bhattacharyya
Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India.
Acta neurologica Scandinavica 2003;108(6):407-14.
2003: Biswanath Chattopadhyay; Subho Ghosh; Prasanta K Gangopadhyay; Shaymal K Das; Trishit Roy; Krishna K Sinha; Dilip K Jha; Subhash C Mukherjee; Ambar Chakraborty; Bhim S Singhal; Anup K Bhattacharya; Nitai P Bhattacharyya
Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India.
Neuroscience letters 2003;345(2):93-6.
2000: P Basu; PK Gangopadhaya; Subhash C Mukherjee; Shaymal K Das; Krishna K Sinha; Nitai P Bhattacharyya
Molecular anatomy of CTG expansion in myotonin protein kinase gene among myotonic dystrophy patients from eastern India.
Human mutation 2000;16(4):372.
2000: S Pramanik; P Basu; PK Gangopadhaya; Krishna K Sinha; Dilip K Jha; S Sinha; Shaymal K Das; B K Maity; Subhash C Mukherjee; S Roychoudhuri; Partha P Majumder; Nitai P Bhattacharyya
Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India.
European journal of human genetics : EJHG 2000;8(9):678-82.
2000: P Basu; Biswanath Chattopadhyay; PK Gangopadhaya; Subhash C Mukherjee; Krishna K Sinha; Shaymal K Das; Susanta Roychoudhury; Partha P Majumder; Nitai P Bhattacharyya
Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
Human genetics 2000;106(6):597-604.
1999: P Basu; PK Gangopadhaya; S C Murkherjee; Krishna K Sinha; Nitai P Bhattacharyya
Expansion of CTG repeat in myotonin protein kinase gene on Alu(ins)-HinfI-I background in a myotonic dystrophy patient from India. Mutations in brief no. 210. Online.
Human mutation 1999;13(1):84.