Achal K. Srivastava - Publications

Affiliations: 
Neuroscience Centre All India Institute of Medical Sciences, Badsa, Haryana, India 

14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Shakya S, Kumari R, Suroliya V, Tyagi N, Joshi A, Garg A, Singh I, Divya KP, Cherian A, Mukerji M, Srivastava AK, Faruq M. Whole exome and targeted gene sequencing to detect pathogenic recessive variants in early onset cerebellar ataxia. Clinical Genetics. PMID 31429931 DOI: 10.1111/Cge.13625  0.308
2018 Ramos A, Planchat M, Vieira Melo AR, Raposo M, Shamim U, Suroliya V, Srivastava AK, Faruq M, Morino H, Ohsawa R, Kawakami H, Jardim LB, Saraiva-Pereira ML, Vasconcelos J, Santos C, et al. Mitochondrial DNA haplogroups and age at onset of Machado-Joseph disease/Spinocerebellar ataxia type 3: a study in patients from multiple populations. European Journal of Neurology. PMID 30414314 DOI: 10.1111/Ene.13860  0.302
2018 Kumari R, Kumar D, Brahmachari SK, Srivastava AK, Faruq M, Mukerji M. Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias Journal of Genetics. 97: 589-609. DOI: 10.1007/S12041-018-0948-2  0.324
2016 Srivastava AK, Takkar A, Garg A, Faruq M. Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B. Brain : a Journal of Neurology. PMID 27864267 DOI: 10.1093/Brain/Aww269  0.335
2015 Faruq M, Srivastava AK, Singh S, Gupta R, Dada T, Garg A, Behari M, Mukerji M. Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population. The Indian Journal of Medical Research. 141: 187-98. PMID 25900954 DOI: 10.4103/0971-5916.155556  0.319
2014 Faruq M, Srivastava AK, Suroliya V, Kumar D, Garg A, Shukla G, Behari M. Identification of FXTAS presenting with SCA 12 like phenotype in India. Parkinsonism & Related Disorders. 20: 1089-93. PMID 25085749 DOI: 10.1016/J.Parkreldis.2014.07.001  0.346
2014 Shukla G, Gupta A, Pandey RM, Kalaivani M, Goyal V, Srivastava A, Behari M. What features differentiate unilateral from bilateral restless legs syndrome? A comparative observational study of 195 patients. Sleep Medicine. 15: 714-9. PMID 24813392 DOI: 10.1016/J.Sleep.2014.01.025  0.314
2012 Kaul B, Shukla G, Goyal V, Srivastava A, Behari M. Paroxysmal occipital discharges suppressed by eye opening: spectrum of clinical and imaging features at a tertiary care center in India. Neurology India. 60: 461. PMID 23135020 DOI: 10.4103/0028-3886.103183  0.319
2012 Gupta A, Shukla G, Goyal V, Srivastava A, Behari M. Clinical and polysomnographic characteristics in 20 North Indian patients with narcolepsy: a seven-year experience from a neurology service sleep clinic. Neurology India. 60: 75-78. PMID 22406785 DOI: 10.4103/0028-3886.93602  0.303
2012 Batla A, Goyal C, Shukla G, Goyal V, Srivastava A, Behari M. Hemifacial spasm: clinical characteristics of 321 Indian patients Journal of Neurology. 259: 1561-1565. PMID 22222858 DOI: 10.1007/S00415-011-6376-3  0.327
2011 Vibha D, Shukla G, Goyal V, Singh S, Srivastava AK, Behari M. RBD in Parkinson's disease: a clinical case control study from North India. Clinical Neurology and Neurosurgery. 113: 472-6. PMID 21414715 DOI: 10.1016/J.Clineuro.2011.02.007  0.327
2009 Faruq M, Scaria V, Singh I, Tyagi S, Srivastava AK, Mukerji M. SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias. Human Mutation. 30: 1037-1042. PMID 19370769 DOI: 10.1002/Humu.21006  0.314
2005 Padiath QS, Srivastava AK, Roy S, Jain S, Brahmachari SK. Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus American Journal of Medical Genetics. 133: 124-126. PMID 15457499 DOI: 10.1002/Ajmg.B.30088  0.322
2004 Pandey N, Mittal U, Srivastava AK, Mukerji M. SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies. Journal of Human Genetics. 49: 596-602. PMID 15368101 DOI: 10.1007/S10038-004-0194-8  0.302
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