A citation-based method for searching scientific literature

Xiaoni Liu, Vasily Kerov, Françoise Haeseleer, Anurima Majumder, Nikolai Artemyev, Sheila A Baker, Amy Lee. Channels (Austin) 2013
Times Cited: 66







List of co-cited articles
1113 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
Fiona Mansergh, Noelle C Orton, John P Vessey, Melanie R Lalonde, William K Stell, Francois Tremblay, Steven Barnes, Derrick E Rancourt, N Torben Bech-Hansen. Hum Mol Genet 2005
191
59


Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott. Nat Genet 1998
372
43

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.
Bo Chang, John R Heckenlively, Philippa R Bayley, Nicholas C Brecha, Muriel T Davisson, Norm L Hawes, Arlene A Hirano, Ronald E Hurd, Akihiro Ikeda, Britt A Johnson,[...]. Vis Neurosci 2006
162
42

Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses.
Dana Specht, Shu-Biao Wu, Paul Turner, Peter Dearden, Frank Koentgen, Uwe Wolfrum, Marion Maw, Johann Helmut Brandstätter, Susanne tom Dieck. Invest Ophthalmol Vis Sci 2009
77
40

Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2.
Dagmar Knoflach, Vasily Kerov, Simone B Sartori, Gerald J Obermair, Claudia Schmuckermair, Xiaoni Liu, Vithiyanjali Sothilingam, Marina Garcia Garrido, Sheila A Baker, Martin Glösmann,[...]. Channels (Austin) 2013
39
69

Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
Hanna Regus-Leidig, Jenny Atorf, Andreas Feigenspan, Jan Kremers, Marion A Maw, Johann Helmut Brandstätter. PLoS One 2014
40
67

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.
Françoise Haeseleer, Yoshikazu Imanishi, Tadao Maeda, Daniel E Possin, Akiko Maeda, Amy Lee, Fred Rieke, Krzysztof Palczewski. Nat Neurosci 2004
218
39

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
T M Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, B H Weber, K Wutz, N Gutwillinger, K Rüther, B Drescher,[...]. Nat Genet 1998
350
37

Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology.
Mary A Raven, Noelle C Orton, Hadi Nassar, Gary A Williams, William K Stell, Gerald H Jacobs, N Torben Bech-Hansen, Benjamin E Reese. J Comp Neurol 2008
53
41

Characterization of Cav1.4 complexes (α11.4, β2, and α2δ4) in HEK293T cells and in the retina.
Amy Lee, Shiyi Wang, Brittany Williams, Jussara Hagen, Todd E Scheetz, Françoise Haeseleer. J Biol Chem 2015
37
56

Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.
Sherry L Ball, Patricia A Powers, Hee-Sup Shin, Catherine W Morgans, Neal S Peachey, Ronald G Gregg. Invest Ophthalmol Vis Sci 2002
146
30

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
Ariana Hemara-Wahanui, Stanislav Berjukow, Carolyn I Hope, Peter K Dearden, Shu-Biao Wu, Jane Wilson-Wheeler, Dianne M Sharp, Patricia Lundon-Treweek, Gillian M Clover, Jean-Charles Hoda,[...]. Proc Natl Acad Sci U S A 2005
99
28


The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution.
John E McRory, Jawed Hamid, Clinton J Doering, Esperanza Garcia, Robin Parker, Kevin Hamming, Lina Chen, Michael Hildebrand, Aaron M Beedle, Laura Feldcamp,[...]. J Neurosci 2004
148
28

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
Katharina Agnes Wycisk, Christina Zeitz, Silke Feil, Mariana Wittmer, Ursula Forster, John Neidhardt, Bernd Wissinger, Eberhart Zrenner, Robert Wilke, Susanne Kohl,[...]. Am J Hum Genet 2006
105
27

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
352
25

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
Katharina A Wycisk, Birgit Budde, Silke Feil, Sergej Skosyrski, Francesca Buzzi, John Neidhardt, Esther Glaus, Peter Nürnberg, Klaus Ruether, Wolfgang Berger. Invest Ophthalmol Vis Sci 2006
91
25


Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2.
Stylianos Michalakis, Lior Shaltiel, Vithiyanjali Sothilingam, Susanne Koch, Verena Schludi, Stefanie Krause, Christina Zeitz, Isabelle Audo, Marie-Elise Lancelot, Christian Hamel,[...]. Hum Mol Genet 2014
30
56

Photoreceptor calcium channels: insight from night blindness.
Catherine W Morgans, Philippa R Bayley, Nicholas W Oesch, Gaoying Ren, Lakshmi Akileswaran, W Rowland Taylor. Vis Neurosci 2005
89
24

C-terminal modulator controls Ca2+-dependent gating of Ca(v)1.4 L-type Ca2+ channels.
Anamika Singh, Daniel Hamedinger, Jean-Charles Hoda, Mathias Gebhart, Alexandra Koschak, Christoph Romanin, Jörg Striessnig. Nat Neurosci 2006
98
24


Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex.
Susanne tom Dieck, Wilko D Altrock, Michael M Kessels, Britta Qualmann, Hanna Regus, Dana Brauner, Anna Fejtová, Oliver Bracko, Eckart D Gundelfinger, Johann H Brandstätter. J Cell Biol 2005
300
22

Synaptic transmission at retinal ribbon synapses.
Ruth Heidelberger, Wallace B Thoreson, Paul Witkovsky. Prog Retin Eye Res 2005
167
22


Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Mieke M C Bijveld, Ralph J Florijn, Arthur A B Bergen, L Ingeborgh van den Born, Maarten Kamermans, Liesbeth Prick, Frans C C Riemslag, Mary J van Schooneveld, Astrid M L Kappers, Maria M van Genderen. Ophthalmology 2013
57
26

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
R Jalkanen, M Mäntyjärvi, R Tobias, J Isosomppi, E-M Sankila, T Alitalo, N T Bech-Hansen. J Med Genet 2006
58
24

The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina.
Oliver Dick, Susanne tom Dieck, Wilko Detlef Altrock, Josef Ammermüller, Reto Weiler, Craig Curtis Garner, Eckart Dieter Gundelfinger, Johann Helmut Brandstätter. Neuron 2003
312
21

The diverse roles of ribbon synapses in sensory neurotransmission.
Gary Matthews, Paul Fuchs. Nat Rev Neurosci 2010
194
21

Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.
Carolyn I Hope, Dianne M Sharp, Ariana Hemara-Wahanui, Jennifer I Sissingh, Patricia Lundon, Ed A Mitchell, Marion A Maw, Gillian M Clover. Clin Exp Ophthalmol 2005
58
22


Complex regulation of voltage-dependent activation and inactivation properties of retinal voltage-gated Cav1.4 L-type Ca2+ channels by Ca2+-binding protein 4 (CaBP4).
Lior Shaltiel, Christos Paparizos, Stefanie Fenske, Sami Hassan, Christian Gruner, Katrin Rötzer, Martin Biel, Christian A Wahl-Schott. J Biol Chem 2012
33
39

Switching off calcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain.
Christian Wahl-Schott, Ludwig Baumann, Hartmut Cuny, Christian Eckert, Kristina Griessmeier, Martin Biel. Proc Natl Acad Sci U S A 2006
63
20

Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina.
Krisztina Wutz, Christian Sauer, Eberhart Zrenner, Birgit Lorenz, Tiina Alitalo, Martina Broghammer, Martin Hergersberg, Albert de la Chapelle, Bernhard H F Weber, Bernd Wissinger,[...]. Eur J Hum Genet 2002
56
23

Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina.
Ludwig Baumann, Andrea Gerstner, Xiangang Zong, Martin Biel, Christian Wahl-Schott. Invest Ophthalmol Vis Sci 2004
88
19

The Auxiliary Calcium Channel Subunit α2δ4 Is Required for Axonal Elaboration, Synaptic Transmission, and Wiring of Rod Photoreceptors.
Yuchen Wang, Katherine E Fehlhaber, Ignacio Sarria, Yan Cao, Norianne T Ingram, Debbie Guerrero-Given, Ben Throesch, Kristin Baldwin, Naomi Kamasawa, Toshihisa Ohtsuka,[...]. Neuron 2017
55
23

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
77
18

Zebrafish Cacna1fa is required for cone photoreceptor function and synaptic ribbon formation.
Sujuan Jia, Akira Muto, Wilda Orisme, Hannah E Henson, Chaithanyarani Parupalli, Bensheng Ju, Herwig Baier, Michael R Taylor. Hum Mol Genet 2014
26
46

Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation.
Alexandra Koschak, Daniel Reimer, Doris Walter, Jean-Charles Hoda, Thomas Heinzle, Manfred Grabner, Jörg Striessnig. J Neurosci 2003
97
18

Gain-of-function nature of Cav1.4 L-type calcium channels alters firing properties of mouse retinal ganglion cells.
Dagmar Knoflach, Klaus Schicker, Martin Glösmann, Alexandra Koschak. Channels (Austin) 2015
16
75

Characterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina.
Françoise Haeseleer, Brittany Williams, Amy Lee. J Biol Chem 2016
20
60

α2δ-4 Is Required for the Molecular and Structural Organization of Rod and Cone Photoreceptor Synapses.
Vasily Kerov, Joseph G Laird, Mei-Ling Joiner, Sharmon Knecht, Daniel Soh, Jussara Hagen, Sarah H Gardner, Wade Gutierrez, Takeshi Yoshimatsu, Sajag Bhattarai,[...]. J Neurosci 2018
35
34

Voltage-gated calcium channels.
William A Catterall. Cold Spring Harb Perspect Biol 2011
821
16



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
625
16

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.
K M Boycott, T A Maybaum, M J Naylor, R G Weleber, J Robitaille, Y Miyake, A A Bergen, M E Pierpont, W G Pearce, N T Bech-Hansen. Hum Genet 2001
66
16

International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels.
William A Catterall, Edward Perez-Reyes, Terrance P Snutch, Joerg Striessnig. Pharmacol Rev 2005
857
15

Bassoon and the synaptic ribbon organize Ca²+ channels and vesicles to add release sites and promote refilling.
Thomas Frank, Mark A Rutherford, Nicola Strenzke, Andreas Neef, Tina Pangršič, Darina Khimich, Anna Fejtova, Eckart D Gundelfinger, M Charles Liberman, Benjamin Harke,[...]. Neuron 2010
188
15


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.