A citation-based method for searching scientific literature

Qing-Long Miao, Stefan Herlitze, Melanie D Mark, Jeffrey L Noebels. Brain 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
49
66


Both gain-of-function and loss-of-function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox-Gastaut syndrome.
Xiao Jiang, Praveen K Raju, Nazzareno D'Avanzo, Mathieu Lachance, Julie Pepin, François Dubeau, Wendy G Mitchell, Luis E Bello-Espinosa, Tyler M Pierson, Berge A Minassian,[...]. Epilepsia 2019
34
66

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
154
66

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
A Jouvenceau, L H Eunson, A Spauschus, V Ramesh, S M Zuberi, D M Kullmann, M G Hanna. Lancet 2001
265
50

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.
Lena Damaj, Alexis Lupien-Meilleur, Anne Lortie, Émilie Riou, Luis H Ospina, Louise Gagnon, Catherine Vanasse, Elsa Rossignol. Eur J Hum Genet 2015
101
50

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
825
33


The genetic landscape of the epileptic encephalopathies of infancy and childhood.
Amy McTague, Katherine B Howell, J Helen Cross, Manju A Kurian, Ingrid E Scheffer. Lancet Neurol 2016
288
33

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
433
33

Dramatic Response After Lamotrigine in a Patient With Epileptic Encephalopathy and a De NovoCACNA1A Variant.
Heather M Byers, Christopher W Beatty, Si Houn Hahn, Sidney M Gospe. Pediatr Neurol 2016
13
33

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia.
Claudia Stendel, Maria Cristina D'Adamo, Manuela Wiessner, Marina Dusl, Marta Cenciarini, Silvia Belia, Ehsan Nematian-Ardestani, Peter Bauer, Jan Senderek, Thomas Klopstock,[...]. Int J Mol Sci 2020
9
33

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
154
33

Impaired motor skill learning and altered seizure susceptibility in mice with loss or gain of function of the Kcnt1 gene encoding Slack (KNa1.1) Na+-activated K+ channels.
Imran H Quraishi, Michael R Mercier, Heather McClure, Rachael L Couture, Michael L Schwartz, Robert Lukowski, Peter Ruth, Leonard K Kaczmarek. Sci Rep 2020
19
33

Isolated P/Q Calcium Channel Deletion in Layer VI Corticothalamic Neurons Generates Absence Epilepsy.
Valerie C Bomben, Isamu Aiba, Jing Qian, Melanie D Mark, Stefan Herlitze, Jeffrey L Noebels. J Neurosci 2016
31
33

Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.
P Prontera, P Sarchielli, S Caproni, C Bedetti, L M Cupini, P Calabresi, C Costa. Cephalalgia 2018
25
33

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
29
33


New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.
Katell Beauvais, Florence Cavé-Riant, Claire De Barace, Marc Tardieu, Elisabeth Tournier-Lasserve, Alain Furby. Eur Neurol 2004
36
33

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
33

Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
Sanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, Dimitrios Kotzadimitriou, Louise Eunson, Mary B Davis, Rosalyn Davies, Nicholas W Wood, Dimitri M Kullmann, Michael G Hanna,[...]. J Physiol 2010
57
33

Stepwise developmental regression associated with novel CACNA1A mutation.
Andrea A Guerin, Annette Feigenbaum, Elizabeth J Donner, Grace Yoon. Pediatr Neurol 2008
29
33

Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1A.
Alexander Balck, Henrike Hanssen, Yorck Hellenbroich, Katja Lohmann, Alexander Münchau. J Neurol 2017
9
33

Phenotypic variability of episodic ataxia type 2 mutations: a family study.
Julien Jung, Hervé Testard, Elisabeth Tournier-Lasserve, Florence Riant, Anne-Evelyne Vallet, Stéphane Berroir, Emmanuel Broussolle. Eur Neurol 2010
16
33

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
373
33

Cognitive impairment in children with CACNA1A mutations.
Veronique Humbertclaude, Florence Riant, Benjamin Krams, Valerie Zimmermann, Nicolas Nagot, Daniel Annequin, Bernard Echenne, Elisabeth Tournier-Lasserve, Agathe Roubertie. Dev Med Child Neurol 2020
17
33

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
33


A mutation in GABRB3 associated with Dravet syndrome.
Sy Vinh Le, Phan Hoang Truc Le, Thi Khanh Van Le, Thi Thuy Kieu Huynh, Thi Thu Hang Do. Am J Med Genet A 2017
16
16

Novel SCN1A and GABRA1 Gene Mutations With Diverse Phenotypic Features and the Question on the Existence of a Broader Spectrum of Dravet Syndrome.
Maria P Gontika, Christopher Konialis, Constantine Pangalos, Antigone Papavasiliou. Child Neurol Open 2017
6
16

Isolation, characterization, and localization of human genomic DNA encoding the beta 1 subunit of the GABAA receptor (GABRB1).
E F Kirkness, J W Kusiak, J T Fleming, J Menninger, J D Gocayne, D C Ward, J C Venter. Genomics 1991
54
16




A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.
Colette Kananura, Karsten Haug, Thomas Sander, Uwe Runge, Wenli Gu, Kerstin Hallmann, Johannes Rebstock, Armin Heils, Ortrud K Steinlein. Arch Neurol 2002
209
16

Neonatal Onset of Epilepsy of Infancy with Migrating Focal Seizures Associated with a Novel GABRB3 Variant in Monozygotic Twins.
Katalin Štěrbová, Markéta Vlčková, Petr Klement, Jana Neupauerová, David Staněk, Hana Zůnová, Pavel Seeman, Petra Laššuthová. Neuropediatrics 2018
7
16

Sequence and functional expression of the GABA A receptor shows a ligand-gated receptor super-family.
P R Schofield, M G Darlison, N Fujita, D R Burt, F A Stephenson, H Rodriguez, L M Rhee, J Ramachandran, V Reale, T A Glencorse. Nature 1987
16


A novel variant in GABRB2 associated with intellectual disability and epilepsy.
Siddharth Srivastava, Julie Cohen, Jonathan Pevsner, Swaroop Aradhya, Dianalee McKnight, Elizabeth Butler, Michael Johnston, Ali Fatemi. Am J Med Genet A 2014
48
16

Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2+/Q390X Dravet syndrome mice.
Xuan Huang, Chengwen Zhou, Mengnan Tian, Jing-Qiong Kang, Wangzhen Shen, Kelienne Verdier, Aurea Pimenta, Robert L MacDonald. Epilepsia 2017
14
16

A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity.
Lydia Urak, Martha Feucht, Nahid Fathi, Kurt Hornik, Karoline Fuchs. Hum Mol Genet 2006
69
16

A novel GABRG2 mutation associated with febrile seizures.
D Audenaert, E Schwartz, K G Claeys, L Claes, L Deprez, A Suls, T Van Dyck, L Lagae, C Van Broeckhoven, R L Macdonald,[...]. Neurology 2006
107
16

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.
Rikke S Møller, Thomas V Wuttke, Ingo Helbig, Carla Marini, Katrine M Johannesen, Eva H Brilstra, Ulvi Vaher, Ingo Borggraefe, Inga Talvik, Tiina Talvik,[...]. Neurology 2017
59
16


Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
16



Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.
Miyabi Tanaka, Richard W Olsen, Marco T Medina, Emily Schwartz, Maria Elisa Alonso, Reyna M Duron, Ramon Castro-Ortega, Iris E Martinez-Juarez, Ignacio Pascual-Castroviejo, Jesus Machado-Salas,[...]. Am J Hum Genet 2008
106
16


A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.
S Baulac, I Gourfinkel-An, F Picard, M Rosenberg-Bourgin, J F Prud'homme, M Baulac, A Brice, E LeGuern. Am J Hum Genet 1999
150
16


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.