A citation-based method for searching scientific literature

Jian Jiao, Manxue Zhang, Pingyuan Yang, Yan Huang, Xiao Hu, Jia Cai, Chan Yang, Mingjing Situ, Hui Zhang, Lei Fu, Kuifang Guo, Yi Huang. J Mol Neurosci 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Structure of the Cardiac Sodium Channel.
Daohua Jiang, Hui Shi, Lige Tonggu, Tamer M Gamal El-Din, Michael J Lenaeus, Yan Zhao, Craig Yoshioka, Ning Zheng, William A Catterall. Cell 2020
73
100

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
100

Modulation of voltage- and Ca2+-dependent gating of CaV1.3 L-type calcium channels by alternative splicing of a C-terminal regulatory domain.
Anamika Singh, Mathias Gebhart, Reinhard Fritsch, Martina J Sinnegger-Brauns, Chiara Poggiani, Jean-Charles Hoda, Jutta Engel, Christoph Romanin, Jörg Striessnig, Alexandra Koschak. J Biol Chem 2008
94
100

Genetic Causes of Functional Adrenocortical Adenomas.
Maria-Christina Zennaro, Sheerazed Boulkroun, Fabio Fernandes-Rosa. Endocr Rev 2017
45
100

Functional properties of a newly identified C-terminal splice variant of Cav1.3 L-type Ca2+ channels.
Gabriella Bock, Mathias Gebhart, Anja Scharinger, Wanchana Jangsangthong, Perrine Busquet, Chiara Poggiani, Simone Sartori, Matteo E Mangoni, Martina J Sinnegger-Brauns, Stefan Herzig,[...]. J Biol Chem 2011
84
100

New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy.
Alexandra Pinggera, Luisa Mackenroth, Andreas Rump, Jens Schallner, Filippo Beleggia, Bernd Wollnik, Jörg Striessnig. Hum Mol Genet 2017
51
100

Cav1.2 L-type Ca²⁺ channels mediate cocaine-induced GluA1 trafficking in the nucleus accumbens, a long-term adaptation dependent on ventral tegmental area Ca(v)1.3 channels.
Kathryn Schierberl, Jin Hao, Thomas F Tropea, Stephen Ra, Thomas P Giordano, Qinghao Xu, Sandra M Garraway, Franz Hofmann, Sven Moosmang, Joerg Striessnig,[...]. J Neurosci 2011
63
100

Role of voltage-gated calcium channels in the regulation of aldosterone production from zona glomerulosa cells of the adrenal cortex.
Paula Q Barrett, Nick A Guagliardo, Peter M Klein, Changlong Hu, David T Breault, Mark P Beenhakker. J Physiol 2016
23
100

SWISS-MODEL: homology modelling of protein structures and complexes.
Andrew Waterhouse, Martino Bertoni, Stefan Bienert, Gabriel Studer, Gerardo Tauriello, Rafal Gumienny, Florian T Heer, Tjaart A P de Beer, Christine Rempfer, Lorenza Bordoli,[...]. Nucleic Acids Res 2018
100

Pathophysiological role of omega pore current in channelopathies.
Karin Jurkat-Rott, James Groome, Frank Lehmann-Horn. Front Pharmacol 2012
41
100

Functional roles of Ca(v)1.3, Ca(v)3.1 and HCN channels in automaticity of mouse atrioventricular cells: insights into the atrioventricular pacemaker mechanism.
Laurine Marger, Pietro Mesirca, Jacqueline Alig, Angelo Torrente, Stefan Dubel, Birgit Engeland, Sandra Kanani, Pierre Fontanaud, Jörg Striessnig, Hee-Sup Shin,[...]. Channels (Austin) 2011
60
100

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
100


Molecular Heterogeneity in Aldosterone-Producing Adenomas.
Kazutaka Nanba, Andrew X Chen, Kei Omata, Michelle Vinco, Thomas J Giordano, Tobias Else, Gary D Hammer, Scott A Tomlins, William E Rainey. J Clin Endocrinol Metab 2016
56
100

21
100


De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
916
100


Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
J Platzer, J Engel, A Schrott-Fischer, K Stephan, S Bova, H Chen, H Zheng, J Striessnig. Cell 2000
616
100

Functional Roles of Ca(v)1.3 (alpha(1D)) calcium channel in sinoatrial nodes: insight gained using gene-targeted null mutant mice.
Zhao Zhang, Yanfang Xu, Haitao Song, Jennifer Rodriguez, Dipika Tuteja, Yoon Namkung, Hee-Sup Shin, Nipavan Chiamvimonvat. Circ Res 2002
160
100

Gating defects of disease-causing de novo mutations in Cav1.3 Ca2+ channels.
Alexandra Pinggera, Giulia Negro, Petronel Tuluc, Morris J Brown, Andreas Lieb, Jörg Striessnig. Channels (Austin) 2018
15
100

Enhancing VTA Cav1.3 L-type Ca2+ channel activity promotes cocaine and mood-related behaviors via overlapping AMPA receptor mechanisms in the nucleus accumbens.
A Martínez-Rivera, J Hao, T F Tropea, T P Giordano, M Kosovsky, R C Rice, A Lee, R L Huganir, J Striessnig, N A Addy,[...]. Mol Psychiatry 2017
23
100

Cellular and Genetic Causes of Idiopathic Hyperaldosteronism.
Kei Omata, Fumitoshi Satoh, Ryo Morimoto, Sadayoshi Ito, Yuto Yamazaki, Yasuhiro Nakamura, Sharath K Anand, Zeng Guo, Michael Stowasser, Hironobu Sasano,[...]. Hypertension 2018
74
100

Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
Elena A B Azizan, Hanne Poulsen, Petronel Tuluc, Junhua Zhou, Michael V Clausen, Andreas Lieb, Carmela Maniero, Sumedha Garg, Elena G Bochukova, Wanfeng Zhao,[...]. Nat Genet 2013
311
100


Genomic diagnostics within a medically underserved population: efficacy and implications.
Kevin A Strauss, Claudia Gonzaga-Jauregui, Karlla W Brigatti, Katie B Williams, Alejandra K King, Cristopher Van Hout, Donna L Robinson, Millie Young, Kavita Praveen, Adam D Heaps,[...]. Genet Med 2018
27
100

Felodipine induces autophagy in mouse brains with pharmacokinetics amenable to repurposing.
Farah H Siddiqi, Fiona M Menzies, Ana Lopez, Eleanna Stamatakou, Cansu Karabiyik, Rodrigo Ureshino, Thomas Ricketts, Maria Jimenez-Sanchez, Miguel Angel Esteban, Liangxue Lai,[...]. Nat Commun 2019
41
100

A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia.
S E Flanagan, F Vairo, M B Johnson, R Caswell, T W Laver, H Lango Allen, K Hussain, S Ellard. Pediatr Diabetes 2017
37
100

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism.
Ute I Scholl, Gerald Goh, Gabriel Stölting, Regina Campos de Oliveira, Murim Choi, John D Overton, Annabelle L Fonseca, Reju Korah, Lee F Starker, John W Kunstman,[...]. Nat Genet 2013
343
100

Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists.
Marilyn M Li, Michael Datto, Eric J Duncavage, Shashikant Kulkarni, Neal I Lindeman, Somak Roy, Apostolia M Tsimberidou, Cindy L Vnencak-Jones, Daynna J Wolff, Anas Younes,[...]. J Mol Diagn 2017
590
100

Forebrain elimination of cacna1c mediates anxiety-like behavior in mice.
A S Lee, S Ra, Aditi M Rajadhyaksha, J K Britt, H De Jesus-Cortes, K L Gonzales, A Lee, S Moosmang, F Hofmann, A A Pieper,[...]. Mol Psychiatry 2012
55
100

Mechanisms Responsible for ω-Pore Currents in Cav Calcium Channel Voltage-Sensing Domains.
Stefania Monteleone, Andreas Lieb, Alexandra Pinggera, Giulia Negro, Julian E Fuchs, Florian Hofer, Jörg Striessnig, Petronel Tuluc, Klaus R Liedl. Biophys J 2017
9
100

Prevalence and characterization of somatic mutations in Chinese aldosterone-producing adenoma patients.
Baojun Wang, Xintao Li, Xu Zhang, Xin Ma, Luyao Chen, Yu Zhang, Xiangjun Lyu, Yuzhe Tang, Qingbo Huang, Yu Gao,[...]. Medicine (Baltimore) 2015
44
100

Aldosterone-Producing Adenomas: Histopathology-Genotype Correlation and Identification of a Novel CACNA1D Mutation.
Geok Chin Tan, Giulia Negro, Alexandra Pinggera, Nur Maya Sabrina Tizen Laim, Isa Mohamed Rose, Jiri Ceral, Ales Ryska, Long Kha Chin, Nor Azmi Kamaruddin, Norfilza Mohd Mokhtar,[...]. Hypertension 2017
26
100

Structure of the voltage-gated calcium channel Ca(v)1.1 at 3.6 Å resolution.
Jianping Wu, Zhen Yan, Zhangqiang Li, Xingyang Qian, Shan Lu, Mengqiu Dong, Qiang Zhou, Nieng Yan. Nature 2016
231
100

Structural basis for gating pore current in periodic paralysis.
Daohua Jiang, Tamer M Gamal El-Din, Christopher Ing, Peilong Lu, Régis Pomès, Ning Zheng, William A Catterall. Nature 2018
23
100

Isoform-specific regulation of mood behavior and pancreatic beta cell and cardiovascular function by L-type Ca 2+ channels.
Martina J Sinnegger-Brauns, Alfred Hetzenauer, Irene G Huber, Erik Renström, Georg Wietzorrek, Stanislav Berjukov, Maurizio Cavalli, Doris Walter, Alexandra Koschak, Ralph Waldschütz,[...]. J Clin Invest 2004
152
100

CaV1.3 L-type Ca2+ channels modulate depression-like behaviour in mice independent of deaf phenotype.
Perrine Busquet, Ngoc Khoi Nguyen, Eduard Schmid, Naoyuki Tanimoto, Mathias W Seeliger, Tamar Ben-Yosef, Fengxia Mizuno, Abram Akopian, Jörg Striessnig, Nicolas Singewald. Int J Neuropsychopharmacol 2010
75
100

Structures of closed and open states of a voltage-gated sodium channel.
Michael J Lenaeus, Tamer M Gamal El-Din, Christopher Ing, Karthik Ramanadane, Régis Pomès, Ning Zheng, William A Catterall. Proc Natl Acad Sci U S A 2017
61
100

Lower Affinity of Isradipine for L-Type Ca2+ Channels during Substantia Nigra Dopamine Neuron-Like Activity: Implications for Neuroprotection in Parkinson's Disease.
Nadine J Ortner, Gabriella Bock, Antonios Dougalis, Maria Kharitonova, Johanna Duda, Simon Hess, Petronel Tuluc, Thomas Pomberger, Nadia Stefanova, Florian Pitterl,[...]. J Neurosci 2017
38
100

Calcium Channel Mutations in Cardiac Arrhythmia Syndromes.
Matthew J Betzenhauser, Geoffrey S Pitt, Charles Antzelevitch. Curr Mol Pharmacol 2015
28
100

Old and new genes in primary aldosteronism.
Sheerazed Boulkroun, Fabio Luiz Fernandes-Rosa, Maria-Christina Zennaro. Best Pract Res Clin Endocrinol Metab 2020
5
100

Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness.
Shahid M Baig, Alexandra Koschak, Andreas Lieb, Mathias Gebhart, Claudia Dafinger, Gudrun Nürnberg, Amjad Ali, Ilyas Ahmad, Martina J Sinnegger-Brauns, Niels Brandt,[...]. Nat Neurosci 2011
174
100

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.
Jörg Striessnig, Hanno Jörn Bolz, Alexandra Koschak. Pflugers Arch 2010
92
100


Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
419
100

Voltage-gated calcium channels in the human adrenal and primary aldosteronism.
Saulo J A Felizola, Takashi Maekawa, Yasuhiro Nakamura, Fumitoshi Satoh, Yoshikiyo Ono, Kumi Kikuchi, Shizuka Aritomi, Keiichi Ikeda, Michihiro Yoshimura, Katsuyoshi Tojo,[...]. J Steroid Biochem Mol Biol 2014
26
100


The L-type calcium channel Cav1.3 is required for proper hippocampal neurogenesis and cognitive functions.
Julia Marschallinger, Anupam Sah, Claudia Schmuckermair, Michael Unger, Peter Rotheneichner, Maria Kharitonova, Alexander Waclawiczek, Philipp Gerner, Heidi Jaksch-Bogensperger, Stefan Berger,[...]. Cell Calcium 2015
34
100

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
100


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.