A citation-based method for searching scientific literature

Maria Cristina D'Adamo, Antonella Liantonio, Jean-Francois Rolland, Mauro Pessia, Paola Imbrici. Int J Mol Sci 2020
Times Cited: 17







List of co-cited articles
62 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature.
Orazio Brunetti, Paola Imbrici, Fabio Massimo Botti, Vito Enrico Pettorossi, Maria Cristina D'Adamo, Mario Valentino, Christian Zammit, Marina Mora, Sara Gibertini, Giuseppe Di Giovanni,[...]. Neurobiol Dis 2012
26
29

A mouse model of episodic ataxia type-1.
Paco S Herson, Michael Virk, Nathan R Rustay, Chris T Bond, John C Crabbe, John P Adelman, James Maylie. Nat Neurosci 2003
100
29

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
18
23

Action potential broadening in a presynaptic channelopathy.
Rahima Begum, Yamina Bakiri, Kirill E Volynski, Dimitri M Kullmann. Nat Commun 2016
37
23

Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation.
Tracey D Graves, Yoon-Hee Cha, Angelika F Hahn, Richard Barohn, Mohammed K Salajegheh, Robert C Griggs, Brian N Bundy, Joanna C Jen, Robert W Baloh, Michael G Hanna. Brain 2014
55
23

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia.
M Kinali, H Jungbluth, L H Eunson, C A Sewry, A Y Manzur, E Mercuri, M G Hanna, F Muntoni. Neuromuscul Disord 2004
42
23

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
Kelsey Paulhus, Lauren Ammerman, Edward Glasscock. Int J Mol Sci 2020
21
23

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
21

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions.
Paola Imbrici, Concetta Altamura, Francesca Gualandi, Giuseppe Felice Mangiatordi, Marcella Neri, Giovanni De Maria, Alessandra Ferlini, Alessandro Padovani, Maria Cristina D'Adamo, Orazio Nicolotti,[...]. Mol Cell Neurosci 2017
15
20


Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
581
17

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.
L H Eunson, R Rea, S M Zuberi, S Youroukos, C P Panayiotopoulos, R Liguori, P Avoni, R C McWilliam, J B Stephenson, M G Hanna,[...]. Ann Neurol 2000
169
17


Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.
S L Smart, V Lopantsev, C L Zhang, C A Robbins, H Wang, S Y Chiu, P A Schwartzkroin, A Messing, B L Tempel. Neuron 1998
430
11

Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1.
Paola Imbrici, Maria Cristina D'Adamo, Antonella Cusimano, Mauro Pessia. Am J Physiol Cell Physiol 2007
22
11

Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment.
Susumu Ito, Ikuo Ogiwara, Kazuyuki Yamada, Hiroyuki Miyamoto, Takao K Hensch, Makiko Osawa, Kazuhiro Yamakawa. Neurobiol Dis 2013
62
11

In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy.
Gaia Colasante, Yichen Qiu, Luca Massimino, Claudia Di Berardino, Jonathan H Cornford, Albert Snowball, Mikail Weston, Steffan P Jones, Serena Giannelli, Andreas Lieb,[...]. Brain 2020
24
11

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
11

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.
Arn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E Hoebeek, Curtis F Barrett, Lisa Gherardini, Rob C G van de Ven, Boyan Todorov,[...]. Ann Neurol 2010
147
11

Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy.
Chad R Frasier, Jacy L Wagnon, Yangyang Oliver Bao, Luke G McVeigh, Luis F Lopez-Santiago, Miriam H Meisler, Lori L Isom. Proc Natl Acad Sci U S A 2016
32
11

dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice.
Gaia Colasante, Gabriele Lignani, Simone Brusco, Claudia Di Berardino, Jenna Carpenter, Serena Giannelli, Nicholas Valassina, Simone Bido, Raffaele Ricci, Valerio Castoldi,[...]. Mol Ther 2020
53
11


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
11

Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery.
Paola Imbrici, Antonella Liantonio, Giulia M Camerino, Michela De Bellis, Claudia Camerino, Antonietta Mele, Arcangela Giustino, Sabata Pierno, Annamaria De Luca, Domenico Tricarico,[...]. Front Pharmacol 2016
62
11

Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I.
Zeynep S Karalok, Alfredo Megaro, Marta Cenciarini, Alev Guven, Sonia M Hasan, Birce D Taskin, Paola Imbrici, Serdar Ceylaner, Mauro Pessia, Maria C D'Adamo. Front Neurol 2018
6
33

Brainstem spreading depolarization and cortical dynamics during fatal seizures in Cacna1a S218L mice.
Inge C M Loonen, Nico A Jansen, Stuart M Cain, Maarten Schenke, Rob A Voskuyl, Andrew C Yung, Barry Bohnet, Piotr Kozlowski, Roland D Thijs, Michel D Ferrari,[...]. Brain 2019
36
11

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
28
11

High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.
Tara L Klassen, Valerie C Bomben, Ankita Patel, Janice Drabek, Tim T Chen, Wenli Gu, Feng Zhang, Kevin Chapman, James R Lupski, Jeffrey L Noebels,[...]. Epilepsia 2014
58
11

Nerve excitability studies characterize Kv1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1.
Susan E Tomlinson, S Veronica Tan, Dimitri M Kullmann, Robert C Griggs, David Burke, Michael G Hanna, Hugh Bostock. Brain 2010
70
11


A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.
Sonia Hasan, Cecilia Bove, Gabriella Silvestri, Elide Mantuano, Anna Modoni, Liana Veneziano, Lara Macchioni, Therese Hunter, Gary Hunter, Mauro Pessia,[...]. Sci Rep 2017
8
25

Voltage-Gated Potassium Channel Kv1.3 as a Target in Therapy of Cancer.
Andrzej Teisseyre, Anna Palko-Labuz, Kamila Sroda-Pomianek, Krystyna Michalak. Front Oncol 2019
20
11

Voltage-Gated Sodium Channel β Subunits and Their Related Diseases.
Alexandra A Bouza, Lori L Isom. Handb Exp Pharmacol 2018
29
11

Mitochondrial Kv1.3: a New Target in Cancer Biology?
Vanessa Checchetto, Elena Prosdocimi, Luigi Leanza. Cell Physiol Biochem 2019
6
33

Targeting the Potassium Channel Kv1.3 Kills Glioblastoma Cells.
Elisa Venturini, Luigi Leanza, Michele Azzolini, Stephanie Kadow, Andrea Mattarei, Michael Weller, Ghazaleh Tabatabai, Michael J Edwards, Mario Zoratti, Cristina Paradisi,[...]. Neurosignals 2017
18
11

Direct Pharmacological Targeting of a Mitochondrial Ion Channel Selectively Kills Tumor Cells In Vivo.
Luigi Leanza, Matteo Romio, Katrin Anne Becker, Michele Azzolini, Livio Trentin, Antonella Managò, Elisa Venturini, Angela Zaccagnino, Andrea Mattarei, Luca Carraretto,[...]. Cancer Cell 2017
84
11

New insights into the pathogenesis and therapeutics of episodic ataxia type 1.
Maria Cristina D'Adamo, Sonia Hasan, Luca Guglielmi, Ilenio Servettini, Marta Cenciarini, Luigi Catacuzzeno, Fabio Franciolini. Front Cell Neurosci 2015
40
11

Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1.
Susan Elizabeth Tomlinson, Sanjeev Rajakulendran, Stella Veronica Tan, Tracey Dawn Graves, Doris-Eva Bamiou, Robyn W Labrum, David Burke, Carolyn M Sue, Paola Giunti, Stephanie Schorge,[...]. J Neurol Neurosurg Psychiatry 2013
31
11

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Xiao-Meng Yin, Jing-Han Lin, Li Cao, Tong-Mei Zhang, Sheng Zeng, Kai-Lin Zhang, Wo-Tu Tian, Zheng-Mao Hu, Nan Li, Jun-Ling Wang,[...]. Hum Mol Genet 2018
26
11


A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1.
P Imbrici, F Gualandi, M C D'Adamo, M Taddei Masieri, P Cudia, D De Grandis, R Mannucci, I Nicoletti, S J Tucker, A Ferlini,[...]. Neuroscience 2008
29
11




The Clinical Spectrum of Autosomal-Dominant Episodic Ataxias.
Stefan Kipfer, Michael Strupp. Mov Disord Clin Pract 2014
10
20


Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.
Haijun Chen, Christian von Hehn, Leonard K Kaczmarek, Laura R Ment, Barbara R Pober, Fuki M Hisama. Neurogenetics 2007
23
11

Review of the Diagnosis and Treatment of Periodic Paralysis.
Jeffrey M Statland, Bertrand Fontaine, Michael G Hanna, Nicholas E Johnson, John T Kissel, Valeria A Sansone, Perry B Shieh, Rabi N Tawil, Jaya Trivedi, Stephen C Cannon,[...]. Muscle Nerve 2018
63
11

Skeletal muscle ClC-1 chloride channels in health and diseases.
Concetta Altamura, Jean-Francois Desaphy, Diana Conte, Annamaria De Luca, Paola Imbrici. Pflugers Arch 2020
8
25

Sodium Channelopathies of Skeletal Muscle.
Stephen C Cannon. Handb Exp Pharmacol 2018
62
11


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.