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Reviews | 1 January 2006
Recent advances in the molecular basis of Lafora’s progressive myoclonus epilepsy
- Subramaniam Ganesh
- , Rajat Puri
- , Shweta Singh
- , Shuchi Mittal
- & Deepti Dubey
Journal of Human Genetics 51 , 1–8

Rights & permissionsfor article Recent advances in the molecular basis of Lafora’s progressive myoclonus epilepsy . Opens in a new window.
29 March 2012
Phenotype variations in Lafora progressive myoclonus epilepsy: possible involvement of genetic modifiers?
- Shweta Singh
- & Subramaniam Ganesh
Journal of Human Genetics 57 , 283–285

Rights & permissionsfor article Phenotype variations in Lafora progressive myoclonus epilepsy: possible involvement of genetic modifiers? . Opens in a new window.
Research | 1 July 2005
Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population
- Shweta Singh
- , Toshimitsu Suzuki
- , Akira Uchiyama
- , Satoko Kumada
- , Nobuko Moriyama
- , Shinichi Hirose
- , Yukitoshi Takahashi
- , Hideo Sugie
- , Koichi Mizoguchi
- , Yushi Inoue
- , Kazue Kimura
- , Yukio Sawaishi
- , Kazuhiro Yamakawa
- & Subramaniam Ganesh
Journal of Human Genetics 50 , 347–352

Rights & permissionsfor article Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population . Opens in a new window.
Research | 23 December 2010
Association of ADAM33 gene polymorphisms with asthma in Indian children
Journal of Human Genetics 56 , 188–195

Rights & permissionsfor article Association of ADAM33 gene polymorphisms with asthma in Indian children . Opens in a new window.
Research | 8 February 2018 | Open
Glycogen synthase protects neurons from cytotoxicity of mutant huntingtin by enhancing the autophagy flux
Cell Death & Disease 9 , 1–15

Rights & permissionsfor article Glycogen synthase protects neurons from cytotoxicity of mutant huntingtin by enhancing the autophagy flux . Opens in a new window.
25 July 2013
The SCN1A gene variants and epileptic encephalopathies
- Rashmi Parihar
- & Subramaniam Ganesh
Journal of Human Genetics 58 , 573–580

Rights & permissionsfor article The SCN1A gene variants and epileptic encephalopathies . Opens in a new window.
Research | 14 December 2006
Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis
Journal of Human Genetics 52 , 205–219

Rights & permissionsfor article Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis . Opens in a new window.
Research | 18 July 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsy
- Toshimitsu Suzuki
- , Antonio V Delgado-Escueta
- , Kripamoy Aguan
- , Maria E Alonso
- , Jun Shi
- , Yuji Hara
- , Motohiro Nishida
- , Tomohiro Numata
- , Marco T Medina
- , Tamaki Takeuchi
- , Ryoji Morita
- , Dongsheng Bai
- , Subramaniam Ganesh
- , Yoshihisa Sugimoto
- , Johji Inazawa
- , Julia N Bailey
- , Adriana Ochoa
- , Aurelio Jara-Prado
- , Astrid Rasmussen
- , Jaime Ramos-Peek
- , Sergio Cordova
- , Francisco Rubio-Donnadieu
- , Yushi Inoue
- , Makiko Osawa
- , Sunao Kaneko
- , Hirokazu Oguni
- , Yasuo Mori
- & Kazuhiro Yamakawa
Nature Genetics 36 , 842–849

Rights & permissionsfor article Mutations in EFHC1 cause juvenile myoclonic epilepsy . Opens in a new window.

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