A citation-based method for searching scientific literature

D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
Times Cited: 577



S M Zuberi, L H Eunson, A Spauschus, R De Silva, J Tolmie, N W Wood, R C McWilliam, J B Stephenson, D M Kullmann, M G Hanna. Brain 1999
Times Cited: 253




List of shared articles



Times cited

Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel.
Paola Imbrici, Andrea Accogli, Rikard Blunck, Concetta Altamura, Michele Iacomino, Maria Cristina D'adamo, Anna Allegri, Marina Pedemonte, Noemi Brolatti, Stella Vari,[...]. Biomedicines 2021
1

Paroxysmal Genetic Movement Disorders and Epilepsy.
Claudio M de Gusmão, Lucas Garcia, Mohamad A Mikati, Samantha Su, Laura Silveira-Moriyama. Front Neurol 2021
2

Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature.
Stephan Lauxmann, Lukas Sonnenberg, Nils A Koch, Christian Bosselmann, Natalie Winter, Niklas Schwarz, Thomas V Wuttke, Ulrike B S Hedrich, Yuanyuan Liu, Holger Lerche,[...]. Front Neurol 2021
0

Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia.
Edgard Verdura, Carme Fons, Agatha Schlüter, Montserrat Ruiz, Stéphane Fourcade, Carlos Casasnovas, Antonio Castellano, Aurora Pujol. J Med Genet 2020
14

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
Kelsey Paulhus, Lauren Ammerman, Edward Glasscock. Int J Mol Sci 2020
15

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches.
Maria Cristina D'Adamo, Antonella Liantonio, Jean-Francois Rolland, Mauro Pessia, Paola Imbrici. Int J Mol Sci 2020
13

A Common Kinetic Property of Mutations Linked to Episodic Ataxia Type 1 Studied in the Shaker Kv Channel.
Juan Zhao, Dimitri Petitjean, Georges A Haddad, Zarah Batulan, Rikard Blunck. Int J Mol Sci 2020
2

Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice.
Man Si, Krystle Trosclair, Kathryn A Hamilton, Edward Glasscock. Am J Physiol Cell Physiol 2019
8



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
75

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
4


Regulation of Ion Channels by MicroRNAs and the Implication for Epilepsy.
Christina Gross, Durgesh Tiwari. Curr Neurol Neurosci Rep 2018
12

De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants.
Amanda Rogers, Paul Golumbek, Elena Cellini, Viola Doccini, Renzo Guerrini, Carina Wallgren-Pettersson, Ann-Charlotte Thuresson, Christina A Gurnett. Am J Med Genet A 2018
17

Paroxysmal motor disorders: expanding phenotypes lead to coalescing genotypes.
Laura Zima, Sophia Ceulemans, Gail Reiner, Serena Galosi, Dillon Chen, Michelle Sahagian, Richard H Haas, Keith Hyland, Jennifer Friedman. Ann Clin Transl Neurol 2018
7

Kv1.1 channelopathy abolishes presynaptic spike width modulation by subthreshold somatic depolarization.
Umesh Vivekananda, Pavel Novak, Oscar D Bello, Yuri E Korchev, Shyam S Krishnakumar, Kirill E Volynski, Dimitri M Kullmann. Proc Natl Acad Sci U S A 2017
14

Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP).
Vikas Mishra, Bharat K Karumuri, Nicole M Gautier, Rui Liu, Timothy N Hutson, Stephanie L Vanhoof-Villalba, Ioannis Vlachos, Leonidas Iasemidis, Edward Glasscock. Hum Mol Genet 2017
27

Rearrangement of potassium ions and Kv1.1/Kv1.2 potassium channels in regenerating axons following end-to-end neurorrhaphy: ionic images from TOF-SIMS.
Chiung-Hui Liu, Hung-Ming Chang, Tsung-Huan Wu, Li-You Chen, Yin-Shuo Yang, To-Jung Tseng, Wen-Chieh Liao. Histochem Cell Biol 2017
2

Venom-derived peptide inhibitors of voltage-gated potassium channels.
Raymond S Norton, K George Chandy. Neuropharmacology 2017
45

Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentations.
Catherine A Brownstein, Alan H Beggs, Lance Rodan, Jiahai Shi, Meghan C Towne, Renee Pelletier, Siqi Cao, Paul A Rosenberg, David K Urion, Jonathan Picker,[...]. Neurogenetics 2016
21

Distinctive role of KV1.1 subunit in the biology and functions of low threshold K(+) channels with implications for neurological disease.
Saak V Ovsepian, Marie LeBerre, Volker Steuber, Valerie B O'Leary, Christian Leibold, J Oliver Dolly. Pharmacol Ther 2016
29

Potassium Channels and Human Epileptic Phenotypes: An Updated Overview.
Chiara Villa, Romina Combi. Front Cell Neurosci 2016
57

Action potential broadening in a presynaptic channelopathy.
Rahima Begum, Yamina Bakiri, Kirill E Volynski, Dimitri M Kullmann. Nat Commun 2016
35

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.
Namik Kaya, Maysoon Alsagob, Maria Cristina D'Adamo, Albandary Al-Bakheet, Sonia Hasan, Maria Muccioli, Faten B Almutairi, Rawan Almass, Mazhor Aldosary, Dorota Monies,[...]. J Med Genet 2016
11

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.
Mark A Corbett, Susannah T Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L Carvill, Candace T Myers, Katherine B Howell, Snezana Maljevic, Holger Lerche,[...]. Neurology 2016
41

Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
J Spillane, D M Kullmann, M G Hanna. J Neurol Neurosurg Psychiatry 2016
54

A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermia.
Tiago A Mestre, Andreea Manole, Heather MacDonald, Sheila Riazi, Natalia Kraeva, Michael G Hanna, Anthony E Lang, Roope Männikkö, Grace Yoon. Neurogenetics 2016
17



Auditory deficits of Kcna1 deletion are similar to those of a monaural hearing impairment.
Anita Karcz, Paul D Allen, Joseph Walton, James R Ison, Cornelia Kopp-Scheinpflug. Hear Res 2015
8

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene.
Maria C D'Adamo, Constanze Gallenmüller, Ilenio Servettini, Elisabeth Hartl, Stephen J Tucker, Larissa Arning, Saskia Biskup, Alessandro Grottesi, Luca Guglielmi, Paola Imbrici,[...]. Front Physiol 2015
27