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



Eija Gaily, Anna-Kaisa Anttonen, Leena Valanne, Elina Liukkonen, Ann-Liz Träskelin, Anne Polvi, Markus Lommi, Mikko Muona, Kai Eriksson, Anna-Elina Lehesjoki. Epilepsia 2013
Times Cited: 29




List of shared articles



Times cited

Scn1a and Cacna1a mutations mutually alter their original phenotypes in rats.
Iori Ohmori, Kiyoka Kobayashi, Mamoru Ouchida. Neurochem Int 2020
1

Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.
Michael F Hammer, Atsushi Ishii, Laurel Johnstone, Alexander Tchourbanov, Branden Lau, Ryan Sprissler, Brian Hallmark, Miao Zhang, Jin Zhou, Joseph Watkins,[...]. PLoS One 2017
11

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

Ion Channels Involvement in Neurodevelopmental Disorders.
Maria Cristina D'Adamo, Antonella Liantonio, Elena Conte, Mauro Pessia, Paola Imbrici. Neuroscience 2020
7

Modifier genes in SCN1A-related epilepsy syndromes.
Iris M de Lange, Flip Mulder, Ruben van 't Slot, Anja C M Sonsma, Marjan J A van Kempen, Isaac J Nijman, Robert F Ernst, Nine V A M Knoers, Eva H Brilstra, Bobby P C Koeleman. Mol Genet Genomic Med 2020
4