A citation-based method for searching scientific literature

Philippe Lory, Sophie Nicole, Arnaud Monteil. Pflugers Arch 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism.
Ute I Scholl, Gabriel Stölting, Carol Nelson-Williams, Alfred A Vichot, Murim Choi, Erin Loring, Manju L Prasad, Gerald Goh, Tobias Carling, C Christofer Juhlin,[...]. Elife 2015
166
40

Somatic CACNA1H Mutation As a Cause of Aldosterone-Producing Adenoma.
Kazutaka Nanba, Amy R Blinder, Juilee Rege, Namita G Hattangady, Tobias Else, Chia-Jen Liu, Scott A Tomlins, Pankaj Vats, Chandan Kumar-Sinha, Thomas J Giordano,[...]. Hypertension 2020
35
40

De novo CACNA1D Ca2+ channelopathies: clinical phenotypes and molecular mechanism.
Nadine J Ortner, Teresa Kaserer, J Nathan Copeland, Jörg Striessnig. Pflugers Arch 2020
7
40

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
40

De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene.
Jean Chemin, Karine Siquier-Pernet, Michaël Nicouleau, Giulia Barcia, Ali Ahmad, Daniel Medina-Cano, Sylvain Hanein, Nami Altin, Laurence Hubert, Christine Bole-Feysot,[...]. Brain 2018
32
40

The Ca(V)3.3 calcium channel is the major sleep spindle pacemaker in thalamus.
Simone Astori, Ralf D Wimmer, Haydn M Prosser, Corrado Corti, Mauro Corsi, Nicolas Liaudet, Andrea Volterra, Paul Franken, John P Adelman, Anita Lüthi. Proc Natl Acad Sci U S A 2011
122
40

Expression of voltage-gated Ca2+ channel subtypes in cultured astrocytes.
Isabelle Latour, Jawed Hamid, Aaron M Beedle, Gerald W Zamponi, Brian A Macvicar. Glia 2003
98
40

Cryo-EM structures of apo and antagonist-bound human Cav3.1.
Yanyu Zhao, Gaoxingyu Huang, Qiurong Wu, Kun Wu, Ruiqi Li, Jianlin Lei, Xiaojing Pan, Nieng Yan. Nature 2019
36
40

Effects of a patient-derived de novo coding alteration of CACNA1I in mice connect a schizophrenia risk gene with sleep spindle deficits.
Ayan Ghoshal, David S Uygun, Lingling Yang, James M McNally, Violeta G Lopez-Huerta, Mario A Arias-Garcia, David Baez-Nieto, Andrew Allen, Megan Fitzgerald, Soonwook Choi,[...]. Transl Psychiatry 2020
8
40

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
91
40

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
29
40

Impaired chromaffin cell excitability and exocytosis in autistic Timothy syndrome TS2-neo mouse rescued by L-type calcium channel blockers.
Chiara Calorio, Daniela Gavello, Laura Guarina, Chiara Salio, Marco Sassoè-Pognetto, Chiara Riganti, Federico Tommaso Bianchi, Nadja T Hofer, Petronel Tuluc, Gerald J Obermair,[...]. J Physiol 2019
12
40

Structure and Pharmacology of Voltage-Gated Sodium and Calcium Channels.
William A Catterall, Michael J Lenaeus, Tamer M Gamal El-Din. Annu Rev Pharmacol Toxicol 2020
44
40

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism.
Georgios Daniil, Fabio L Fernandes-Rosa, Jean Chemin, Iulia Blesneac, Jacques Beltrand, Michel Polak, Xavier Jeunemaitre, Sheerazed Boulkroun, Laurence Amar, Tim M Strom,[...]. EBioMedicine 2016
73
40

CACNA1D de novo mutations in autism spectrum disorders activate Cav1.3 L-type calcium channels.
Alexandra Pinggera, Andreas Lieb, Bruno Benedetti, Michaela Lampert, Stefania Monteleone, Klaus R Liedl, Petronel Tuluc, Jörg Striessnig. Biol Psychiatry 2015
89
40

Biophysical classification of a CACNA1D de novo mutation as a high-risk mutation for a severe neurodevelopmental disorder.
Nadja T Hofer, Petronel Tuluc, Nadine J Ortner, Yuliia V Nikonishyna, Monica L Fernándes-Quintero, Klaus R Liedl, Bernhard E Flucher, Helen Cox, Jörg Striessnig. Mol Autism 2020
17
40

Loss of Cav1.3 channels reveals the critical role of L-type and BK channel coupling in pacemaking mouse adrenal chromaffin cells.
Andrea Marcantoni, David H F Vandael, Satyajit Mahapatra, Valentina Carabelli, Martina J Sinnegger-Brauns, Joerg Striessnig, Emilio Carbone. J Neurosci 2010
119
40

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Katherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, Ivana A Souza, Candace T Myers, Betül Uysal, Niklas Schwarz, Maria A Gandini, Sun Huang, Boris Keren,[...]. Am J Hum Genet 2018
38
40

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
989
40


BKCa-Cav channel complexes mediate rapid and localized Ca2+-activated K+ signaling.
Henrike Berkefeld, Claudia A Sailer, Wolfgang Bildl, Volker Rohde, Jörg-Oliver Thumfart, Silke Eble, Norbert Klugbauer, Ellen Reisinger, Josef Bischofberger, Dominik Oliver,[...]. Science 2006
259
40

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
40

The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential.
Gerald W Zamponi, Joerg Striessnig, Alexandra Koschak, Annette C Dolphin. Pharmacol Rev 2015
470
40

Rare CACNA1A mutations leading to congenital ataxia.
Mercè Izquierdo-Serra, José M Fernández-Fernández, Mercedes Serrano. Pflugers Arch 2020
7
40


Specific properties of T-type calcium channels generated by the human alpha 1I subunit.
A Monteil, J Chemin, V Leuranguer, C Altier, G Mennessier, E Bourinet, P Lory, J Nargeot. J Biol Chem 2000
101
20

Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibility.
Veit-Simon Eckle, Aleksandr Shcheglovitov, Iuliia Vitko, Deblina Dey, Chan Choo Yap, Bettina Winckler, Edward Perez-Reyes. J Physiol 2014
53
20

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
353
20

Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population.
Wei Xu, Yahui Liu, Jianhua Chen, Qingli Guo, Ke Liu, Zujia Wen, Zhaowei Zhou, Zhijian Song, Juan Zhou, Lin He,[...]. Hereditas 2017
6
20

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
11
20

The NEURON simulation environment.
M L Hines, N T Carnevale. Neural Comput 1997
20

Resting-State Structure and Gating Mechanism of a Voltage-Gated Sodium Channel.
Goragot Wisedchaisri, Lige Tonggu, Eedann McCord, Tamer M Gamal El-Din, Liguo Wang, Ning Zheng, William A Catterall. Cell 2019
62
20

Support for calcium channel gene defects in autism spectrum disorders.
Ake Tzu-Hui Lu, Xiaoxian Dai, Julian A Martinez-Agosto, Rita M Cantor. Mol Autism 2012
44
20

L-type calcium channels in adrenal chromaffin cells: role in pace-making and secretion.
A Marcantoni, P Baldelli, J M Hernandez-Guijo, V Comunanza, V Carabelli, E Carbone. Cell Calcium 2007
56
20

MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains.
Laurens Wiel, Coos Baakman, Daan Gilissen, Joris A Veltman, Gerrit Vriend, Christian Gilissen. Hum Mutat 2019
55
20

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
612
20

Role of voltage-gated calcium channels in epilepsy.
Gerald W Zamponi, Philippe Lory, Edward Perez-Reyes. Pflugers Arch 2010
116
20

Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy.
E Tsakiridou, L Bertollini, M de Curtis, G Avanzini, H C Pape. J Neurosci 1995
283
20

Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.
Christina Zeitz, Christelle Michiels, Marion Neuillé, Christoph Friedburg, Christel Condroyer, Fiona Boyard, Aline Antonio, Nassima Bouzidi, Diana Milicevic, Robin Veaux,[...]. Hum Mutat 2019
11
20


Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online.
Baljinder Singh, Arnaud Monteil, Isabelle Bidaud, Yoshihisa Sugimoto, Toshimitsu Suzuki, Shin-ichiro Hamano, Hirokazu Oguni, Makiko Osawa, Maria E Alonso, Antonio V Delgado-Escueta,[...]. Hum Mutat 2007
54
20

A rare schizophrenia risk variant of CACNA1I disrupts CaV3.3 channel activity.
A Andrade, J Hope, A Allen, V Yorgan, D Lipscombe, J Q Pan. Sci Rep 2016
33
20

Calcium signaling and epilepsy.
Ortrud K Steinlein. Cell Tissue Res 2014
29
20

Calcium channel types contributing to chromaffin cell excitability, exocytosis and endocytosis.
S Mahapatra, C Calorio, D H F Vandael, A Marcantoni, V Carabelli, E Carbone. Cell Calcium 2012
45
20

Reduced Sleep Spindles in Schizophrenia: A Treatable Endophenotype That Links Risk Genes to Impaired Cognition?
Dara S Manoach, Jen Q Pan, Shaun M Purcell, Robert Stickgold. Biol Psychiatry 2016
98
20

Specific contribution of human T-type calcium channel isotypes (alpha(1G), alpha(1H) and alpha(1I)) to neuronal excitability.
Jean Chemin, Arnaud Monteil, Edward Perez-Reyes, Emmanuel Bourinet, Joël Nargeot, Philippe Lory. J Physiol 2002
168
20

In vivo, in vitro, and computational analysis of dendritic calcium currents in thalamic reticular neurons.
A Destexhe, D Contreras, M Steriade, T J Sejnowski, J R Huguenard. J Neurosci 1996
174
20

Further evidence for the genetic association between CACNA1I and schizophrenia.
Yijun Xie, Di Huang, Li Wei, Xiong-Jian Luo. Hereditas 2018
7
20


Sorting of the neuroendocrine secretory protein Secretogranin II into the regulated secretory pathway: role of N- and C-terminal alpha-helical domains.
Maïté Courel, Michael S Vasquez, Vivian Y Hook, Sushil K Mahata, Laurent Taupenot. J Biol Chem 2008
41
20


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.