A citation-based method for searching scientific literature

Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna. F1000 Biol Rep 2010
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels.
Alexandre Mezghrani, Arnaud Monteil, Katrin Watschinger, Martina J Sinnegger-Brauns, Christian Barrère, Emmanuel Bourinet, Joël Nargeot, Jörg Striessnig, Philippe Lory. J Neurosci 2008
58
42

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.
Chung-Jiuan Jeng, Yu-Ting Chen, Yi-Wen Chen, Chih-Yung Tang. Am J Physiol Cell Physiol 2006
38
42

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
42

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.
S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams,[...]. Am J Hum Genet 2001
108
42

Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
198
42

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.
Elide Mantuano, Silvia Romano, Liana Veneziano, Cinzia Gellera, Barbara Castellotti, Sara Caimi, Daniela Testa, Margherita Estienne, Giovanna Zorzi, Marianna Bugiani,[...]. J Neurol Sci 2010
48
28

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
177
28

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
J Jen, J Wan, M Graves, H Yu, A F Mock, C J Coulin, G Kim, Q Yue, D M Papazian, R W Baloh. Neurology 2001
99
28

Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels.
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
450
28

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.
K Jun, E S Piedras-Rentería, S M Smith, D B Wheeler, S B Lee, T G Lee, H Chin, M E Adams, R H Scheller, R W Tsien,[...]. Proc Natl Acad Sci U S A 1999
352
28

Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.
E Mantuano, L Veneziano, M Spadaro, P Giunti, S Guida, M G Leggio, L Verriello, N Wood, C Jodice, M Frontali. J Med Genet 2004
33
28

Dominant-negative calcium channel suppression by truncated constructs involves a kinase implicated in the unfolded protein response.
Karen M Page, Fay Heblich, Anthony Davies, Adrian J Butcher, Jerôme Leroy, Federica Bertaso, Wendy S Pratt, Annette C Dolphin. J Neurosci 2004
69
28

N terminus is key to the dominant negative suppression of Ca(V)2 calcium channels: implications for episodic ataxia type 2.
Karen M Page, Fay Heblich, Wojciech Margas, Wendy S Pratt, Manuela Nieto-Rostro, Kanchan Chaggar, Kieran Sandhu, Anthony Davies, Annette C Dolphin. J Biol Chem 2010
41
28

Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia.
Edwin Wappl, Alexandra Koschak, Michael Poteser, Martina J Sinnegger, Doris Walter, Andreas Eberhart, Klaus Groschner, Hartmut Glossmann, Richard L Kraus, Manfred Grabner,[...]. J Biol Chem 2002
75
28

Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation.
D I Zafeiriou, F Lehmann-Horn, E Vargiami, E Teflioudi, A Ververi, K Jurkat-Rott. Eur J Paediatr Neurol 2009
11
28

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
456
28

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
V A Letts, R Felix, G H Biddlecome, J Arikkath, C L Mahaffey, A Valenzuela, F S Bartlett, Y Mori, K P Campbell, W N Frankel. Nat Genet 1998
447
28


CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
28

Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.
David Curtis, Anna E Vine, Andrew McQuillin, Nicholas James Bass, Ana Pereira, Radhika Kandaswamy, Jacob Lawrence, Adebayo Anjorin, Khalid Choudhury, Susmita R Datta,[...]. Psychiatr Genet 2011
53
28

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
28

The primary periodic paralyses: diagnosis, pathogenesis and treatment.
S L Venance, S C Cannon, D Fialho, B Fontaine, M G Hanna, L J Ptacek, M Tristani-Firouzi, R Tawil, R C Griggs. Brain 2006
180
28


Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
28

1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1.
M Dichgans, J Herzog, T Freilinger, M Wilke, D P Auer. Neurology 2005
59
28

Subunit structure of dihydropyridine-sensitive calcium channels from skeletal muscle.
M Takahashi, M J Seagar, J F Jones, B F Reber, W A Catterall. Proc Natl Acad Sci U S A 1987
368
28

Familial hemiplegic migraine.
Daniela Pietrobon. Neurotherapeutics 2007
135
28

Auxiliary subunits: essential components of the voltage-gated calcium channel complex.
Jyothi Arikkath, Kevin P Campbell. Curr Opin Neurobiol 2003
363
28

Calcium channel beta-subunit binds to a conserved motif in the I-II cytoplasmic linker of the alpha 1-subunit.
M Pragnell, M De Waard, Y Mori, T Tanabe, T P Snutch, K P Campbell. Nature 1994
535
28

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
144
28


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
222
28

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
179
28


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
28

The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons.
Laure Perrin-Vidoz, Olga M Sinilnikova, Dominique Stoppa-Lyonnet, Gilbert M Lenoir, Sylvie Mazoyer. Hum Mol Genet 2002
177
14

Nonsense-mediated decay approaches the clinic.
Jill A Holbrook, Gabriele Neu-Yilik, Matthias W Hentze, Andreas E Kulozik. Nat Genet 2004
458
14

Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant.
Isabel Alonso, Joana M Marques, Nuno Sousa, Jorge Sequeiros, I Anna S Olsson, Isabel Silveira. Neurobiol Aging 2008
22
14

Motor deficits in homozygous and heterozygous p/q-type calcium channel mutants.
Akira Katoh, Jenelle A Jindal, Jennifer L Raymond. J Neurophysiol 2007
28
14

Impairment of proteasome structure and function in aging.
Géraldine Carrard, Anne-Laure Bulteau, Isabelle Petropoulos, Bertrand Friguet. Int J Biochem Cell Biol 2002
208
14

Knockdown of Cav2.1 calcium channels is sufficient to induce neurological disorders observed in natural occurring Cacna1a mutants in mice.
Hiromitsu Saito, Motohiro Okada, Takafumi Miki, Minoru Wakamori, Akira Futatsugi, Yasuo Mori, Katsuhiko Mikoshiba, Noboru Suzuki. Biochem Biophys Res Commun 2009
15
14

Execution of nonsense-mediated mRNA decay: what defines a substrate?
Indrani Rebbapragada, Jens Lykke-Andersen. Curr Opin Cell Biol 2009
206
14

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
260
14


Reduced ACh release at neuromuscular synapses of heterozygous leaner Ca(v)2.1-mutant mice.
Simon Kaja, Rob C G Van De Ven, Rune R Frants, Michel D Ferrari, Arn M J M Van Den Maagdenberg, Jaap J Plomp. Synapse 2008
10
14

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
14

The expression of neuronal voltage-dependent calcium channels in human cerebellum.
S G Volsen, N C Day, A L McCormack, W Smith, P J Craig, R Beattie, P G Ince, P J Shaw, S B Ellis, A Gillespie. Brain Res Mol Brain Res 1995
92
14

Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.
Robert S Raike, Holly B Kordasiewicz, Randall M Thompson, Christopher M Gomez. Mol Cell Neurosci 2007
21
14


Oligosyndactylism, an early embryonic lethal in the mouse.
P Van Valen. J Embryol Exp Morphol 1966
29
14


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.