A citation-based method for searching scientific literature

Mercè Izquierdo-Serra, José M Fernández-Fernández, Mercedes Serrano. Pflugers Arch 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
178
60

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
24
60

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
40

Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially.
Xi Luo, Jill A Rosenfeld, Shinya Yamamoto, Tamar Harel, Zhongyuan Zuo, Melissa Hall, Klaas J Wierenga, Matthew T Pastore, Dennis Bartholomew, Mauricio R Delgado,[...]. PLoS Genet 2017
32
40

Neurobiology of migraine.
Daniela Pietrobon, Jörg Striessnig. Nat Rev Neurosci 2003
383
40

Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
Lorena Travaglini, Marta Nardella, Emanuele Bellacchio, Adele D'Amico, Alessandro Capuano, Roberto Frusciante, Matteo Di Capua, Raffaella Cusmai, Sabina Barresi, Silvia Morlino,[...]. Eur J Paediatr Neurol 2017
27
40

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
359
40

Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.
Lubov Blumkin, Marina Michelson, Esther Leshinsky-Silver, Sara Kivity, Dorit Lev, Tally Lerman-Sagie. J Child Neurol 2010
34
40

Zebrafish as a Model System for the Study of Severe CaV2.1 (α1A) Channelopathies.
Sidharth Tyagi, Angeles B Ribera, Roger A Bannister. Front Mol Neurosci 2020
4
50

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics.
R L Kraus, M J Sinnegger, H Glossmann, S Hering, J Striessnig. J Biol Chem 1998
155
40


Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
Nuria García Segarra, Ivan Gautschi, Laureane Mittaz-Crettol, Christine Kallay Zetchi, Lama Al-Qusairi, Miguel Xavier Van Bemmelen, Philippe Maeder, Luisa Bonafé, Laurent Schild, Eliane Roulet-Perez. J Neurol Sci 2014
24
40

The neuropsychiatric phenotype in CACNA1A mutations: a retrospective single center study and review of the literature.
E Indelicato, W Nachbauer, E Karner, A Eigentler, M Wagner, I Unterberger, W Poewe, M Delazer, S Boesch. Eur J Neurol 2019
17
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
252
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

Neuronal Cav3 channelopathies: recent progress and perspectives.
Philippe Lory, Sophie Nicole, Arnaud Monteil. Pflugers Arch 2020
5
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
442
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
86
40

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
C F Fletcher, A Tottene, V A Lennon, S M Wilson, S J Dubel, R Paylor, D A Hosford, L Tessarollo, M W McEnery, D Pietrobon,[...]. FASEB J 2001
135
40

Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor.
Chengzu Long, Chad E Grueter, Kunhua Song, Song Qin, Xiaoxia Qi, Y Megan Kong, John M Shelton, James A Richardson, Chun-Li Zhang, Rhonda Bassel-Duby,[...]. Proc Natl Acad Sci U S A 2014
21
20

DeNovoGear: de novo indel and point mutation discovery and phasing.
Avinash Ramu, Michiel J Noordam, Rachel S Schwartz, Arthur Wuster, Matthew E Hurles, Reed A Cartwright, Donald F Conrad. Nat Methods 2013
102
20

Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
363
20

Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.
Fady M Mikhail, Edward J Lose, Nathaniel H Robin, Maria D Descartes, Katherine D Rutledge, S Lane Rutledge, Bruce R Korf, Andrew J Carroll. Am J Med Genet A 2011
118
20

Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Daniel Benjamin Callaghan, Sanja Rogic, Powell Patrick Cheng Tan, Kristina Calli, Ying Qiao, Robert Baldwin, Matthew Jacobson, Manuel Belmadani, Nathan Holmes, Chang Yu,[...]. Clin Genet 2019
8
20

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes.
Emanuele G Coci, Udo Koehler, Thomas Liehr, Armin Stelzner, Christian Fink, Hendrik Langen, Joachim Riedel. Mol Cytogenet 2016
6
20

AutDB: a gene reference resource for autism research.
Saumyendra N Basu, Ravi Kollu, Sharmila Banerjee-Basu. Nucleic Acids Res 2009
240
20

Novel Nonsense Calmodulin-Binding Transcription Activator 1 Mutation Presenting as a Tremor-Predominant Phenotype.
Shashank Agarwal, Rebecca Gilbert, Heather A Lau. Mov Disord Clin Pract 2016
2
50

De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability.
Iris G M Wijnen, Hermine E Veenstra-Knol, Fleur Vansenne, Erica H Gerkes, Tom de Koning, Yvonne J Vos, Marina A J Tijssen, Deborah Sival, Niklas Darin, Els K Vanhoutte,[...]. Eur J Hum Genet 2020
2
50

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
20

A potential dimerization region of dCAMTA is critical for termination of fly visual response.
Ping Gong, Junhai Han, Keith Reddig, Hong-Sheng Li. J Biol Chem 2007
11
20

CAMTA1, a 1p36 tumor suppressor candidate, inhibits growth and activates differentiation programs in neuroblastoma cells.
Kai-Oliver Henrich, Tobias Bauer, Johannes Schulte, Volker Ehemann, Hedwig Deubzer, Sina Gogolin, Daniel Muth, Matthias Fischer, Axel Benner, Rainer König,[...]. Cancer Res 2011
57
20

CAMTA1 T polymorphism is associated with neuropsychological test performance in older adults with cardiovascular disease.
Lindsay A Miller, John Gunstad, Mary Beth Spitznagel, Jeanne McCaffery, John McGeary, Athena Poppas, Robert H Paul, Lawrence H Sweet, Ronald A Cohen. Psychogeriatrics 2011
9
20

Cell cycle-dependent transcriptional regulation of calmodulin-binding transcription activator 1 in neuroblastoma cells.
Kaname Nakatani, Junji Nishioka, Tatsuo Itakura, Yoshio Nakanishi, Jun-Ichi Horinouchi, Yasunori Abe, Hideo Wada, Tsutomu Nobori. Int J Oncol 2004
22
20

MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.
Julia Wang, Rami Al-Ouran, Yanhui Hu, Seon-Young Kim, Ying-Wooi Wan, Michael F Wangler, Shinya Yamamoto, Hsiao-Tuan Chao, Aram Comjean, Stephanie E Mohr,[...]. Am J Hum Genet 2017
80
20

Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia.
Jessica L Zambonin, Allison Bellomo, Hilla Ben-Pazi, David B Everman, Lee M Frazer, Michael T Geraghty, Amy D Harper, Julie R Jones, Benjamin Kamien, Kristin Kernohan,[...]. Orphanet J Rare Dis 2017
23
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
589
20

Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability.
Julien Thevenon, Estelle Lopez, Boris Keren, Delphine Heron, Cyril Mignot, Cecilia Altuzarra, Mylène Béri-Dexheimer, Céline Bonnet, Eloi Magnin, Lydie Burglen,[...]. J Med Genet 2012
30
20

A novel family of calmodulin-binding transcription activators in multicellular organisms.
Nicolas Bouché, Ariel Scharlat, Wayne Snedden, David Bouchez, Hillel Fromm. J Biol Chem 2002
156
20

Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.
Matthew J Huentelman, Andreas Papassotiropoulos, David W Craig, Frederic J Hoerndli, John V Pearson, Kim-Dung Huynh, Jason Corneveaux, Jürgen Hänggi, Christian R A Mondadori, Andreas Buchmann,[...]. Hum Mol Genet 2007
52
20

Recurrent genomic alterations with impact on survival in colorectal cancer identified by genome-wide array comparative genomic hybridization.
Mi-Young Kim, Seon-Hee Yim, Mi-Seon Kwon, Tae-Min Kim, Seung-Hun Shin, Hyun-Mi Kang, Charles Lee, Yeun-Jun Chung. Gastroenterology 2006
50
20

IBS: an illustrator for the presentation and visualization of biological sequences.
Wenzhong Liu, Yubin Xie, Jiyong Ma, Xiaotong Luo, Peng Nie, Zhixiang Zuo, Urs Lahrmann, Qi Zhao, Yueyuan Zheng, Yong Zhao,[...]. Bioinformatics 2015
369
20

The calmodulin-binding transcription activator CAMTA1 is required for long-term memory formation in mice.
Carlos Bas-Orth, Yan-Wei Tan, Ana M M Oliveira, C Peter Bengtson, Hilmar Bading. Learn Mem 2016
11
20


Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia.
Francesco Nicita, Marta Nardella, Emanuele Bellacchio, Paolo Alfieri, Gaetano Terrone, Giorgia Piccini, Federica Graziola, Claudio Pignata, Alessandro Capuano, Enrico Bertini,[...]. Clin Genet 2019
13
20

Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
M Shinawi, R Coorg, J S Shimony, D K Grange, H Al-Kateb. Clin Genet 2015
10
20

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Jennelle C Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M Seabra, Mary-Alice Abbott,[...]. Nat Genet 2017
126
20

Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
E Chérot, B Keren, C Dubourg, W Carré, M Fradin, A Lavillaureix, A Afenjar, L Burglen, S Whalen, P Charles,[...]. Clin Genet 2018
44
20

The transcriptional coactivator CAMTA2 stimulates cardiac growth by opposing class II histone deacetylases.
Kunhua Song, Johannes Backs, John McAnally, Xiaoxia Qi, Robert D Gerard, James A Richardson, Joseph A Hill, Rhonda Bassel-Duby, Eric N Olson. Cell 2006
112
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.