A citation-based method for searching scientific literature

Iori Ohmori, Mamoru Ouchida, Katsuhiro Kobayashi, Yoshimi Jitsumori, Akiko Mori, Hiroyuki Michiue, Teiichi Nishiki, Yoko Ohtsuka, Hideki Matsui. Neurobiol Dis 2013
Times Cited: 24



Christine S Cheah, Frank H Yu, Ruth E Westenbroek, Franck K Kalume, John C Oakley, Gregory B Potter, John L Rubenstein, William A Catterall. Proc Natl Acad Sci U S A 2012
Times Cited: 168




List of shared articles



Times cited

Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation.
Yunyao Xie, Nathan N Ng, Olga S Safrina, Carmen M Ramos, Kevin C Ess, Philip H Schwartz, Martin A Smith, Diane K O'Dowd. Neurobiol Dis 2020
7

The SCN1A gene variants and epileptic encephalopathies.
Rashmi Parihar, Subramaniam Ganesh. J Hum Genet 2013
43

Dravet Syndrome: Diagnosis and Long-Term Course.
Mary B Connolly. Can J Neurol Sci 2016
34

Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patients.
Hyun Woo Kim, Zhejiu Quan, Young-Beom Kim, Eunji Cheong, Heung Dong Kim, Minjung Cho, Jiho Jang, Young Rang Yoo, Joon Soo Lee, Ji Hun Kim,[...]. Brain Dev 2018
13

Genetics and gene therapy in Dravet syndrome.
Norimichi Higurashi, Vania Broccoli, Shinichi Hirose. Epilepsy Behav 2021
0