Krishna K. Sinha

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

P. Basu, Biswanath Chattopadhyay, Prasanta K. Gangopadhaya et al. · Human Genetics · 2000 · 76 citations

Cag Repeats, Genetics, Eastern India +5

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India

Krishna K. Sinha · Journal of Neurology Neurosurgery & Psychiatry · 2004 · 72 citations · Full text

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India

Biswanath Chattopadhyay, Subho Ghosh, Prasanta Kumar Gangopadhyay et al. · Neuroscience Letters · 2003 · 65 citations

Alzheimer's Disease, Eastern India, Degenerative Disease +7

Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India

P. Basu, Prasanta K. Gangopadhaya, Krishna K. Sinha et al. · European Journal of Human Genetics · 2000 · 43 citations · Full text

Allelic Variant, Genetics, Huntingtin Gene +9

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

P. Basu, Biswanath Chattopadhyay, Prasanta K. Gangopadhaya et al. · Human Genetics · 2000 · 30 citations

Cag Repeats, Genetics, Eastern India +5