A citation-based method for searching scientific literature

N A Singh, C Charlier, D Stauffer, B R DuPont, R J Leach, R Melis, G M Ronen, I Bjerre, T Quattlebaum, J V Murphy, M L McHarg, D Gagnon, T O Rosales, A Peiffer, V E Anderson, M Leppert. Nat Genet 1998
Times Cited: 872



Affef Abidi, Jérôme J Devaux, Florence Molinari, Gisèle Alcaraz, François-Xavier Michon, Julie Sutera-Sardo, Hélène Becq, Caroline Lacoste, Cécilia Altuzarra, Alexandra Afenjar, Cyril Mignot, Diane Doummar, Bertrand Isidor, Sylvie N Guyen, Estelle Colin, Sabine De La Vaissière, Damien Haye, Adeline Trauffler, Catherine Badens, Fabienne Prieur, Gaetan Lesca, Laurent Villard, Mathieu Milh, Laurent Aniksztejn. Neurobiol Dis 2015
Times Cited: 40




List of shared articles



Times cited

Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy.
Laura Mary, Elsa Nourisson, Claire Feger, Vincent Laugel, Denys Chaigne, Boris Keren, Alexandra Afenjar, Thierry Billette, Detlef Trost, Cécile Cieuta-Walti,[...]. Am J Med Genet A 2021
0

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

Venom-derived modulators of epilepsy-related ion channels.
Chun Yuen Chow, Nathan Absalom, Kimberley Biggs, Glenn F King, Linlin Ma. Biochem Pharmacol 2020
1

Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction.
Piera Nappi, Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Vincenzo Barrese, Maurizio Taglialatela. Pflugers Arch 2020
9

Modulation of KV7 Channel Deactivation by PI(4,5)P2.
Carlos A Villalba-Galea. Front Pharmacol 2020
1


Two KCNQ2 Encephalopathy Variants in the Calmodulin-Binding Helix A Exhibit Dominant-Negative Effects and Altered PIP2 Interaction.
Baouyen Tran, Zhi-Gang Ji, Mingxuan Xu, Tammy N Tsuchida, Edward C Cooper. Front Physiol 2020
0

The Role of Kv7.2 in Neurodevelopment: Insights and Gaps in Our Understanding.
Nina Dirkx, Francesco Miceli, Maurizio Taglialatela, Sarah Weckhuysen. Front Physiol 2020
2

A de novo KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data.
Gianluigi Laccetta, Simona Fiori, Matteo Giampietri, Annarita Ferrari, Valentina Cetica, Manuela Bernardini, Francesca Chesi, Sara Mazzotti, Elena Parrini, Massimiliano Ciantelli,[...]. Front Pediatr 2019
0

KCNQ-Encoded Potassium Channels as Therapeutic Targets.
Vincenzo Barrese, Jennifer B Stott, Iain A Greenwood. Annu Rev Pharmacol Toxicol 2018
45