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| Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral … S Ganesh, AV Delgado-Escueta, T Sakamoto, MR Avila, ... Human molecular genetics 11 (11), 1251-1262, 2002 | 259 | 2002 |
| Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes S Ganesh, KL Agarwala, K Ueda, T Akagi, K Shoda, T Usui, T Hashikawa, ... Human molecular genetics 9 (15), 2251-2261, 2000 | 178 | 2000 |
| Recent advances in the molecular basis of Lafora’s progressive myoclonus epilepsy S Ganesh, R Puri, S Singh, S Mittal, D Dubey Journal of human genetics 51 (1), 1-8, 2006 | 156 | 2006 |
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| Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis I Banerjee, V Gupta, S Ganesh Journal of human genetics 52 (3), 205-219, 2007 | 138 | 2007 |
| The malin–laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin–proteasome system P Garyali, P Siwach, PK Singh, R Puri, S Mittal, S Sengupta, R Parihar, ... Human molecular genetics 18 (4), 688-700, 2009 | 125 | 2009 |
| Inflammatory system gene polymorphism and the risk of stroke: a case–control study in an Indian population I Banerjee, V Gupta, T Ahmed, M Faizaan, P Agarwal, S Ganesh Brain research bulletin 75 (1), 158-165, 2008 | 112 | 2008 |
| Advances in the genetics of progressive myoclonus epilepsy AV Delgado‐Escueta, S Ganesh, K Yamakawa American journal of medical genetics 106 (2), 129-138, 2001 | 107 | 2001 |
| Genotype–phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive … S Ganesh, AV Delgado-Escueta, T Suzuki, S Francheschetti, C Riggio, ... Human molecular genetics 11 (11), 1263-1271, 2002 | 106 | 2002 |
| Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment S Mittal, D Dubey, K Yamakawa, S Ganesh Human molecular genetics 16 (7), 753-762, 2007 | 100 | 2007 |
| The SCN1A gene variants and epileptic encephalopathies R Parihar, S Ganesh Journal of human genetics 58 (9), 573-580, 2013 | 98 | 2013 |
| Dysfunctions in endosomal–lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora disease R Puri, T Suzuki, K Yamakawa, S Ganesh Human molecular genetics 21 (1), 175-184, 2012 | 96 | 2012 |
| Cloning and functional characterization of DSCAML1, a novel DSCAM-like cell adhesion molecule that mediates homophilic intercellular adhesion KL Agarwala, S Ganesh, Y Tsutsumi, T Suzuki, K Amano, K Yamakawa Biochemical and biophysical research communications 285 (3), 760-772, 2001 | 92 | 2001 |
| Association of ADAM33 gene polymorphisms with asthma in Indian children S Awasthi, P Tripathi, S Ganesh, N Husain Journal of human genetics 56 (3), 188-195, 2011 | 82 | 2011 |
| The carbohydrate-binding domain of Lafora disease protein targets Lafora polyglucosan bodies S Ganesh, N Tsurutani, T Suzuki, Y Hoshii, T Ishihara, ... Biochemical and biophysical research communications 313 (4), 1101-1109, 2004 | 80 | 2004 |
| Decreased O-linked GlcNAcylation protects from cytotoxicity mediated by huntingtin exon1 protein fragment A Kumar, PK Singh, R Parihar, V Dwivedi, SC Lakhotia, S Ganesh Journal of Biological chemistry 289 (19), 13543-13553, 2014 | 73 | 2014 |
| Association between inflammatory gene polymorphisms and coronary artery disease in an Indian population I Banerjee, U Pandey, OM Hasan, R Parihar, V Tripathi, S Ganesh Journal of thrombosis and thrombolysis 27, 88-94, 2009 | 71 | 2009 |
| Human satellite-III non-coding RNAs modulate heat-shock-induced transcriptional repression A Goenka, S Sengupta, R Pandey, R Parihar, GC Mohanta, M Mukerji, ... Journal of cell science 129 (19), 3541-3552, 2016 | 68 | 2016 |
