A citation-based method for searching scientific literature

Sidharth Tyagi, Angeles B Ribera, Roger A Bannister. Front Mol Neurosci 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


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
98
40

The ß subunit of voltage-gated Ca2+ channels.
Zafir Buraei, Jian Yang. Physiol Rev 2010
237
40

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

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
177
40

A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.
Romina Romaniello, Claudio Zucca, Alessandra Tonelli, Sara Bonato, Cinzia Baschirotto, Nicoletta Zanotta, Roberta Epifanio, Andrea Righini, Nereo Bresolin, Maria T Bassi,[...]. J Neurol Neurosurg Psychiatry 2010
34
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
34
40

Neurobiology of migraine.
Daniela Pietrobon, Jörg Striessnig. Nat Rev Neurosci 2003
382
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

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
40

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
156
40

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
40

Rare CACNA1A mutations leading to congenital ataxia.
Mercè Izquierdo-Serra, José M Fernández-Fernández, Mercedes Serrano. Pflugers Arch 2020
5
40

CRISPR base editors: genome editing without double-stranded breaks.
Ayman Eid, Sahar Alshareef, Magdy M Mahfouz. Biochem J 2018
87
20

Ion channels and transporters of the retinal pigment epithelium.
Nadine Reichhart, Olaf Strauss. Exp Eye Res 2014
38
20

Localization of inward rectifier potassium channel Kir7.1 in the basolateral membrane of distal nephron and collecting duct.
Kayoko Ookata, Akihiro Tojo, Yoshiro Suzuki, Nobuhiro Nakamura, Kenjiro Kimura, Christopher S Wilcox, Shigehisa Hirose. J Am Soc Nephrol 2000
55
20

Structure-function analysis of the bestrophin family of anion channels.
Takashi Tsunenari, Hui Sun, John Williams, Hugh Cahill, Philip Smallwood, King-Wai Yau, Jeremy Nathans. J Biol Chem 2003
164
20

PTC124 targets genetic disorders caused by nonsense mutations.
Ellen M Welch, Elisabeth R Barton, Jin Zhuo, Yuki Tomizawa, Westley J Friesen, Panayiota Trifillis, Sergey Paushkin, Meenal Patel, Christopher R Trotta, Seongwoo Hwang,[...]. Nature 2007
713
20

Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands.
Li Huang, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, Wenmin Sun, Yan Xu, Wei Xin, Xiangming Guo, Qingjiong Zhang. Exp Eye Res 2016
35
20

Release of ATP from retinal pigment epithelial cells involves both CFTR and vesicular transport.
David Reigada, Claire H Mitchell. Am J Physiol Cell Physiol 2005
82
20

Cyclic nucleotide-gated ion channels.
U Benjamin Kaupp, Reinhard Seifert. Physiol Rev 2002
784
20


AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia.
Ji-jing Pang, Wen-Tao Deng, Xufeng Dai, Bo Lei, Drew Everhart, Yumiko Umino, Jie Li, Keqing Zhang, Song Mao, Sanford L Boye,[...]. PLoS One 2012
85
20

Strategies against Nonsense: Oxadiazoles as Translational Readthrough-Inducing Drugs (TRIDs).
Ambra Campofelice, Laura Lentini, Aldo Di Leonardo, Raffaella Melfi, Marco Tutone, Andrea Pace, Ivana Pibiri. Int J Mol Sci 2019
13
20

Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genes.
Li Huang, Qingyan Zhang, Shiqiang Li, Liping Guan, Xueshan Xiao, Jianguo Zhang, Xiaoyun Jia, Wenmin Sun, Zhihong Zhu, Yang Gao,[...]. PLoS One 2013
38
20



Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
Sureka Thiagalingam, Terri L McGee, Richard G Weleber, Michael A Sandberg, Karmen M Trzupek, Eliot L Berson, Thaddeus P Dryja. Ophthalmic Genet 2007
35
20


TRPM channels: same ballpark, different players, and different rules in immunogenetics.
Ammad Ahmad Farooqi, Mohammed Khalid Javeed, Zeeshan Javed, Asma M Riaz, Shahzeray Mukhtar, Sehrish Minhaj, Sana Abbas, Shahzad Bhatti. Immunogenetics 2011
15
20

Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a Novel BEST1 Mutation.
Adiv A Johnson, Lori A Bachman, Benjamin J Gilles, Samuel D Cross, Kimberly E Stelzig, Zachary T Resch, Lihua Y Marmorstein, Jose S Pulido, Alan D Marmorstein. Invest Ophthalmol Vis Sci 2015
26
20

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
20

Progressive cone dystrophy associated with mutation in CNGB3.
Michel Michaelides, Irene A Aligianis, John R Ainsworth, Peter Good, John D Mollon, Eamonn R Maher, Anthony T Moore, David M Hunt. Invest Ophthalmol Vis Sci 2004
50
20

The gating mechanism in cyclic nucleotide-gated ion channels.
Monica Mazzolini, Manuel Arcangeletti, Arin Marchesi, Luisa M R Napolitano, Debora Grosa, Sourav Maity, Claudio Anselmi, Vincent Torre. Sci Rep 2018
13
20

Abnormalities of the photoreceptor-bipolar cell synapse in a substrain of C57BL/10 mice.
K Ruether, J Grosse, E Matthiessen, K Hoffmann, C Hartmann. Invest Ophthalmol Vis Sci 2000
26
20

Calcium channels at the photoreceptor synapse.
Steven Barnes, Melanie E M Kelly. Adv Exp Med Biol 2002
60
20

Unconstrained genome targeting with near-PAMless engineered CRISPR-Cas9 variants.
Russell T Walton, Kathleen A Christie, Madelynn N Whittaker, Benjamin P Kleinstiver. Science 2020
172
20


Chloride channel activity of bestrophin mutants associated with mild or late-onset macular degeneration.
Kuai Yu, Zhiqiang Qu, Yuanyuan Cui, H Criss Hartzell. Invest Ophthalmol Vis Sci 2007
41
20


Differential effects of Best disease causing missense mutations on bestrophin-1 trafficking.
Adiv A Johnson, Yong-Suk Lee, J Brett Stanton, Kuai Yu, Criss H Hartzell, Lihua Y Marmorstein, Alan D Marmorstein. Hum Mol Genet 2013
21
20

Single Cl- channels activated by Ca2+ in Drosophila S2 cells are mediated by bestrophins.
Li-Ting Chien, Zhi-Ren Zhang, H Criss Hartzell. J Gen Physiol 2006
52
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
53
20

"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
Anthony G Robson, Andrew R Webster, Michel Michaelides, Susan M Downes, Jill A Cowing, David M Hunt, Anthony T Moore, Graham E Holder. Retina 2010
44
20

Suppression of premature termination codons as a therapeutic approach.
Kim M Keeling, Dan Wang, Sara E Conard, David M Bedwell. Crit Rev Biochem Mol Biol 2012
62
20

Molecular chaperone functions in protein folding and proteostasis.
Yujin E Kim, Mark S Hipp, Andreas Bracher, Manajit Hayer-Hartl, F Ulrich Hartl. Annu Rev Biochem 2013
770
20

Calcium regulation in photoreceptors.
David Krizaj, David R Copenhagen. Front Biosci 2002
94
20


TRPM1 mutations are associated with the complete form of congenital stationary night blindness.
Makoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, Akishi Onishi, Koji M Nishiguchi, Chieko Koike, Mikiko Kadowaki, Mineo Kondo, Yozo Miyake, Takahisa Furukawa. Mol Vis 2010
72
20

Identification of Novel Mutation in CNGA3 gene by Whole-Exome Sequencing and In-Silico Analyses for Genotype-Phenotype Assessment with Autosomal Recessive Achromatopsia in Pakistani families.
Muhammad Waqar Arshad, Yujin Lee, Muhammad Arshad Malik, Jahangir Khan, Aslam Khan, Abdul Kareem, Changsoo Kang, Muhammad Imran Shabbir. J Pak Med Assoc 2019
1
100

Characterization of the R162W Kir7.1 mutation associated with snowflake vitreoretinopathy.
Wei Zhang, Xiaoming Zhang, Hui Wang, Anil K Sharma, Albert O Edwards, Bret A Hughes. Am J Physiol Cell Physiol 2013
15
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.