A citation-based method for searching scientific literature

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
Times Cited: 190







List of co-cited articles
1662 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
53

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
45

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
346
40

Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2.
Xiaoni Liu, Vasily Kerov, Françoise Haeseleer, Anurima Majumder, Nikolai Artemyev, Sheila A Baker, Amy Lee. Channels (Austin) 2013
66
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
369
37


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
27

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
308
26

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
49

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
27

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
24

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
60

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
76
30

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
56

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

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
34



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
146
19

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
54

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
18

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
351
18


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
32

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
87
19

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
Christina Zeitz, Barbara Kloeckener-Gruissem, Ursula Forster, Susanne Kohl, István Magyar, Bernd Wissinger, Gábor Mátyás, François-Xavier Borruat, Daniel F Schorderet, Eberhart Zrenner,[...]. Am J Hum Genet 2006
122
17

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
96
17

Synaptogenesis in the photoreceptor terminal of the mouse retina.
J C Blanks, A M Adinolfi, R N Lolley. J Comp Neurol 1974
182
16

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
299
16

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
62
25

The diverse roles of ribbon synapses in sensory neurotransmission.
Gary Matthews, Paul Fuchs. Nat Rev Neurosci 2010
191
16

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
17

Synaptic transmission at retinal ribbon synapses.
Ruth Heidelberger, Wallace B Thoreson, Paul Witkovsky. Prog Retin Eye Res 2005
163
15

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
15

Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.
M Masu, H Iwakabe, Y Tagawa, T Miyoshi, M Yamashita, Y Fukuda, H Sasaki, K Hiroi, Y Nakamura, R Shigemoto. Cell 1995
369
15

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
50

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
26


Deletion of the presynaptic scaffold CAST reduces active zone size in rod photoreceptors and impairs visual processing.
Susanne tom Dieck, Dana Specht, Nicola Strenzke, Yamato Hida, Vidhyasankar Krishnamoorthy, Karl-Friedrich Schmidt, Eiji Inoue, Hiroyoshi Ishizaki, Miki Tanaka-Okamoto, Jun Miyoshi,[...]. J Neurosci 2012
59
23

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
21

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani,[...]. Proc Natl Acad Sci U S A 2010
199
14

Mechanism for Selective Synaptic Wiring of Rod Photoreceptors into the Retinal Circuitry and Its Role in Vision.
Yan Cao, Ignacio Sarria, Katherine E Fehlhaber, Naomi Kamasawa, Cesare Orlandi, Kiely N James, Jennifer L Hazen, Matthew R Gardner, Michael Farzan, Amy Lee,[...]. Neuron 2015
64
21

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
16


Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.
Shigeru Sato, Yoshihiro Omori, Kimiko Katoh, Mineo Kondo, Motoi Kanagawa, Kentaro Miyata, Kazuo Funabiki, Toshiyuki Koyasu, Naoko Kajimura, Tomomitsu Miyoshi,[...]. Nat Neurosci 2008
191
12

Early steps in the assembly of photoreceptor ribbon synapses in the mouse retina: the involvement of precursor spheres.
Hanna Regus-Leidig, Susanne Tom Dieck, Dana Specht, Lars Meyer, Johann Helmut Brandstätter. J Comp Neurol 2009
80
15

A novel CACNA1F gene mutation causes Aland Island eye disease.
Reetta Jalkanen, N Torben Bech-Hansen, Rose Tobias, Eeva-Marja Sankila, Maija Mäntyjärvi, Henrik Forsius, Albert de la Chapelle, Tiina Alitalo. Invest Ophthalmol Vis Sci 2007
38
31

TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells.
Catherine W Morgans, Jianmei Zhang, Brett G Jeffrey, Steve M Nelson, Neal S Burke, Robert M Duvoisin, R Lane Brown. Proc Natl Acad Sci U S A 2009
203
12

A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
Karin W Littink, Maria M van Genderen, Rob W J Collin, Susanne Roosing, Arjan P M de Brouwer, Frans C C Riemslag, Hanka Venselaar, Alberta A H J Thiadens, Carel B Hoyng, Klaus Rohrschneider,[...]. Invest Ophthalmol Vis Sci 2009
57
21

The ß subunit of voltage-gated Ca2+ channels.
Zafir Buraei, Jian Yang. Physiol Rev 2010
249
12


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.