A citation-based method for searching scientific literature

B Rudy, C J McBain. Trends Neurosci 2001
Times Cited: 501



Karine Poirier, Géraldine Viot, Laura Lombardi, Clémence Jauny, Pierre Billuart, Thierry Bienvenu. Eur J Hum Genet 2017
Times Cited: 14




List of shared articles



Times cited

Progressive myoclonus epilepsy KCNC1 variant causes a developmental dendritopathy.
Jenna C Carpenter, Roope Männikkö, Catherine Heffner, Jana Heneine, Marisol Sampedro-Castañeda, Gabriele Lignani, Stephanie Schorge. Epilepsia 2021
2

Kv3.1 channels regulate the rate of critical period plasticity.
Yoshi-Taka Matsuda, Hiroyuki Miyamoto, Rolf H Joho, Takao K Hensch. Neurosci Res 2021
1

Kv3.1 channelopathy: a novel loss-of-function variant and the mechanistic basis of its clinical phenotypes.
Xiaoyang Li, Yongsheng Zheng, Shaoyuan Li, Umesh Nair, Chong Sun, Chongbo Zhao, Jiahong Lu, Victor Wei Zhang, Snezana Maljevic, Steven Petrou,[...]. Ann Transl Med 2021
0

Age-related hearing loss pertaining to potassium ion channels in the cochlea and auditory pathway.
Barbara Peixoto Pinheiro, Barbara Vona, Hubert Löwenheim, Lukas Rüttiger, Marlies Knipper, Youssef Adel. Pflugers Arch 2021
8

Genetic potassium channel-associated epilepsies: Clinical review of the Kv family.
Nicholas M Allen, Sarah Weckhuysen, Kathleen Gorman, Mary D King, Holger Lerche. Eur J Paediatr Neurol 2020
19

Intellectual Disability and Potassium Channelopathies: A Systematic Review.
Miriam Kessi, Baiyu Chen, Jing Peng, Yulin Tang, Eleonore Olatoutou, Fang He, Lifen Yang, Fei Yin. Front Genet 2020
7

Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations.
Jillian M Cameron, Snezana Maljevic, Umesh Nair, Ye Htet Aung, Benjamin Cogné, Stéphane Bézieau, Edward Blair, Bertrand Isidor, Christiane Zweier, André Reis,[...]. Ann Clin Transl Neurol 2019
10

KCNC1-related disorders: new de novo variants expand the phenotypic spectrum.
Joohyun Park, Mahmoud Koko, Ulrike B S Hedrich, Andreas Hermann, Kirsten Cremer, Edda Haberlandt, Mona Grimmel, Bader Alhaddad, Stefanie Beck-Woedl, Merle Harrer,[...]. Ann Clin Transl Neurol 2019
11

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
79