Items where Author is "Srivastava, Achal K."

Kumari, Renu ; Kumar, Deepak ; Brahmachari, Samir K. ; Srivastava, Achal K. ; Faruq, Mohammed ; Mukerji, Mitali (2018) Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias Journal of Genetics, 97 (3). pp. 589-609. ISSN 0022-1333

Singh, Inder ; Faruq, Mohammed ; Padma, Madakasira Vasantha ; Goyal, Vinay ; Behari, Madhuri ; Grover, Ashoo ; Mukerji, Mitali ; Srivastava, Achal K. (2015) Investigation of mitochondrial DNA variations among Indian Friedreich's ataxia (FRDA) patients Mitochondrion, 25 . pp. 1-5. ISSN 1567-7249

Singh, Inder ; Faruq, Mohammed ; Mukherjee, Odity ; Jain, Sanjeev ; Pal, Pramod Kumar ; Padma Srivastav, M. V. ; Behari, Madhuri ; Srivastava, Achal K. ; Mukerji, Mitali (2010) North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion Annals of Human Genetics, 74 (3). pp. 202-210. ISSN 0003-4800

Faruq, Mohammed ; Scaria, Vinod ; Singh, Inder ; Tyagi, Shivani ; Srivastava, Achal K. ; Mukerji, Mitali (2009) SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias Human Mutation, 30 (7). pp. 1037-1042. ISSN 1059-7794

Bhardwaj, Anshu ; Mukerji, Mitali ; Sharma, Shipra ; Paul, Jinny ; Gokhale, Chaitanya S. ; Srivastava, Achal K. ; Tiwari, Shrish (2009) MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease BMC Bioinformatics, 10 (8). S7. ISSN 1471-2105

Mittal, Uma ; Srivastava, Achal K. ; Jain, Satish ; Jain, Sanjeev ; Mukerji, Mitali (2005) Founder haplotype for Machado-Joseph disease in the Indian population Archives of Neurology, 62 (4). pp. 637-640. ISSN 0003-9942

Mittal, Uma ; Sharma, Sangeeta ; Chopra, Rupali ; Dheeraj, Kalladka ; Pal, Pramod Kr. ; Srivastava, Achal K. ; Mukerji, Mitali (2005) Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms Human Genetics, 118 (1). Article ID 107. ISSN 0340-6717

Mittal, Uma ; Roy, Sanghamitra ; Jain, Satish ; Srivastava, Achal K. ; Mukerji, Mitali (2005) Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family Journal of Human Genetics, 50 (3). pp. 155-157. ISSN 1434-5161

Pandey, Neeraj ; Mittal, Uma ; Srivastava, Achal K. ; Mukerji, Mitali (2004) SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies Journal of Human Genetics, 49 (11). pp. 596-602. ISSN 1434-5161

Srivastava, Achal K. ; Choudhry, Shweta ; Gopinath, Musuwadi S. ; Roy, Sanghamitra ; Tripathi, Manjari ; Brahmachari, Samir K. ; Jain, Satish (2001) Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12 Annals of Neurology, 50 (6). pp. 769-800. ISSN 0364-5134

Choudhry, Shweta ; Mukerji, Mitali ; Srivastava, Achal K. ; Jain, Satish ; Brahmachari, Samir K. (2001) CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms Human Molecular Genetics, 10 (21). pp. 2437-2446. ISSN 0964-6906