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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