A citation-based method for searching scientific literature

Ana Quelle-Regaldie, Daniel Sobrido-Cameán, Antón Barreiro-Iglesias, María Jesús Sobrido, Laura Sánchez. Cells 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.
Robert A Kozol, Alexander J Abrams, David M James, Elena Buglo, Qing Yan, Julia E Dallman. Front Mol Neurosci 2016
38
66

Cerebellar ataxias.
Mario Manto, Daniele Marmolino. Curr Opin Neurol 2009
107
66

Characterization of the zebrafish atxn1/axh gene family.
Kerri M Carlson, Laura Melcher, Shaojuan Lai, Huda Y Zoghbi, H Brent Clark, Harry T Orr. J Neurogenet 2009
14
66

Zebrafish: Housing and husbandry recommendations.
Peter Aleström, Livia D'Angelo, Paul J Midtlyng, Daniel F Schorderet, Stefan Schulte-Merker, Frederic Sohm, Susan Warner. Lab Anim 2020
127
66


The zebrafish reference genome sequence and its relationship to the human genome.
Kerstin Howe, Matthew D Clark, Carlos F Torroja, James Torrance, Camille Berthelot, Matthieu Muffato, John E Collins, Sean Humphray, Karen McLaren, Lucy Matthews,[...]. Nature 2013
33


Genome engineering using the CRISPR-Cas9 system.
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
33

Differential requirement for ptf1a in endocrine and exocrine lineages of developing zebrafish pancreas.
John W Lin, Andrew V Biankin, Marko E Horb, Bidyut Ghosh, Nijaguna B Prasad, Nelson S Yee, Michael A Pack, Steven D Leach. Dev Biol 2004
59
33

Zebrafish cancer: the state of the art and the path forward.
Richard White, Kristin Rose, Leonard Zon. Nat Rev Cancer 2013
231
33

Graded levels of Ptf1a differentially regulate endocrine and exocrine fates in the developing pancreas.
P Duc Si Dong, Elayne Provost, Steven D Leach, Didier Y R Stainier. Genes Dev 2008
61
33

Cell senescence contributes to tissue regeneration in zebrafish.
Sabela Da Silva-Álvarez, Jorge Guerra-Varela, Daniel Sobrido-Cameán, Ana Quelle, Antón Barreiro-Iglesias, Laura Sánchez, Manuel Collado. Aging Cell 2020
29
33

PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.
Matthis Synofzik, Michael A Gonzalez, Charles Marques Lourenco, Marie Coutelier, Tobias B Haack, Adriana Rebelo, Didier Hannequin, Tim M Strom, Holger Prokisch, Christoph Kernstock,[...]. Brain 2014
131
33

Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse.
Jamee M Bomar, Paul J Benke, Eric L Slattery, Radhika Puttagunta, Larry P Taylor, Eunju Seong, Arne Nystuen, Weidong Chen, Roger L Albin, Paresh D Patel,[...]. Nat Genet 2003
99
33

Hereditary ataxias.
V G Evidente, K A Gwinn-Hardy, J N Caviness, S Gilman. Mayo Clin Proc 2000
52
33

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
Hemant Khanna, Erica E Davis, Carlos A Murga-Zamalloa, Alejandro Estrada-Cuzcano, Irma Lopez, Anneke I den Hollander, Marijke N Zonneveld, Mohammad I Othman, Naushin Waseem, Christina F Chakarova,[...]. Nat Genet 2009
215
33

Loss of wwox expression in zebrafish embryos causes edema and alters Ca(2+) dynamics.
Yusuke Tsuruwaka, Masataka Konishi, Eriko Shimada. PeerJ 2015
13
33

The Ciliopathy Gene ahi1 Is Required for Zebrafish Cone Photoreceptor Outer Segment Morphogenesis and Survival.
Emma M Lessieur, Joseph Fogerty, Robert J Gaivin, Ping Song, Brian D Perkins. Invest Ophthalmol Vis Sci 2017
23
33



Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome.
Tawfeg Ben-Omran, Somayyeh Fahiminiya, Natalie Sorfazlian, Mariam Almuriekhi, Zafar Nawaz, Javad Nadaf, Kitam Abu Khadija, Samiha Zaineddin, Hussein Kamel, Jacek Majewski,[...]. J Med Genet 2015
20
33

The ciliopathy protein TALPID3/KIAA0586 acts upstream of Rab8 activation in zebrafish photoreceptor outer segment formation and maintenance.
Irene Ojeda Naharros, Flavia B Cristian, Jingjing Zang, Matthias Gesemann, Philip W Ingham, Stephan C F Neuhauss, Ruxandra Bachmann-Gagescu. Sci Rep 2018
10
33

laminin alpha 1 gene is essential for normal lens development in zebrafish.
Natalya S Zinkevich, Dmitry V Bosenko, Brian A Link, Elena V Semina. BMC Dev Biol 2006
38
33

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Alexander J Abrams, Robert B Hufnagel, Adriana Rebelo, Claudia Zanna, Neville Patel, Michael A Gonzalez, Ion J Campeanu, Laurie B Griffin, Saskia Groenewald, Alleene V Strickland,[...]. Nat Genet 2015
114
33

Arl13b Interacts With Vangl2 to Regulate Cilia and Photoreceptor Outer Segment Length in Zebrafish.
Ping Song, Lynn Dudinsky, Joseph Fogerty, Robert Gaivin, Brian D Perkins. Invest Ophthalmol Vis Sci 2016
19
33

POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
M Mancuso, M Filosto, M Bellan, R Liguori, P Montagna, A Baruzzi, S DiMauro, V Carelli. Neurology 2004
61
33

Wwox-Brca1 interaction: role in DNA repair pathway choice.
M S Schrock, B Batar, J Lee, T Druck, B Ferguson, J H Cho, K Akakpo, H Hagrass, N A Heerema, F Xia,[...]. Oncogene 2017
30
33

Niemann-Pick disease type C.
Marie T Vanier. Orphanet J Rare Dis 2010
656
33

Zebrafish models for personalized psychiatry: Insights from individual, strain and sex differences, and modeling gene x environment interactions.
Andrey D Volgin, Oleg A Yakovlev, Konstantin A Demin, Murilo S de Abreu, Polina A Alekseeva, Ashton J Friend, Anton M Lakstygal, Tamara G Amstislavskaya, Wandong Bao, Cai Song,[...]. J Neurosci Res 2019
28
33

Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency.
Ming-Yang Chang, Tsu-Lin Ma, Cheng-Chieh Hung, Ya-Chung Tian, Yung-Chang Chen, Chih-Wei Yang, Yi-Chuan Cheng. Sci Rep 2017
40
33

A familial late‑onset hereditary ataxia mimicking pontocerebellar hypoplasia caused by a novel TSEN54 mutation.
Yi Qian, Haiyong Wang, Tao Jin, Yiqing Wang, Lizheng Fang, Yuhao Chen, Liying Chen. Mol Med Rep 2014
4
33

Serotonin Promotes Development and Regeneration of Spinal Motor Neurons in Zebrafish.
Antón Barreiro-Iglesias, Karolina S Mysiak, Angela L Scott, Michell M Reimer, Yujie Yang, Catherina G Becker, Thomas Becker. Cell Rep 2015
35
33

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4.
John A Sayer, Edgar A Otto, John F O'Toole, Gudrun Nurnberg, Michael A Kennedy, Christian Becker, Hans Christian Hennies, Juliana Helou, Massimo Attanasio, Blake V Fausett,[...]. Nat Genet 2006
402
33

Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia.
Jijun Wan, Janos Steffen, Michael Yourshaw, Hafsa Mamsa, Erik Andersen, Sabine Rudnik-Schöneborn, Kate Pope, Katherine B Howell, Catriona A McLean, Andrew J Kornberg,[...]. Brain 2016
46
33

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.
Federico Sicca, Elena Ambrosini, Maria Marchese, Luigi Sforna, Ilenio Servettini, Giulia Valvo, Maria Stefania Brignone, Angela Lanciotti, Francesca Moro, Alessandro Grottesi,[...]. Sci Rep 2016
42
33

Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration.
Alfonso Saera-Vila, Phillip E Kish, Ke'ale W Louie, Steven J Grzegorski, Daniel J Klionsky, Alon Kahana. Autophagy 2016
37
33


SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy.
Gavin Charlesworth, Bettina Balint, Niccolò E Mencacci, Lucinda Carr, Nicholas W Wood, Kailash P Bhatia. Mov Disord 2016
33
33

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
Rita Horvath, Gavin Hudson, Gianfrancesco Ferrari, Nancy Fütterer, Sofia Ahola, Eleonora Lamantea, Holger Prokisch, Hanns Lochmüller, Robert McFarland, V Ramesh,[...]. Brain 2006
290
33


Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.
Claudia Gonzaga-Jauregui, Tamar Harel, Tomasz Gambin, Maria Kousi, Laurie B Griffin, Ludmila Francescatto, Burcak Ozes, Ender Karaca, Shalini N Jhangiani, Matthew N Bainbridge,[...]. Cell Rep 2015
157
33

Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes.
Robert B Hufnagel, Gavin Arno, Nichole D Hein, Joshua Hersheson, Megana Prasad, Yvonne Anderson, Laura A Krueger, Louise C Gregory, Corinne Stoetzel, Thomas J Jaworek,[...]. J Med Genet 2015
56
33

Basal body stability and ciliogenesis requires the conserved component Poc1.
Chad G Pearson, Daniel P S Osborn, Thomas H Giddings, Philip L Beales, Mark Winey. J Cell Biol 2009
93
33

Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for in vivo screening of candidate therapeutic compounds.
Wei-Chia Tseng, Hannah E Loeb, Wuhong Pei, Chon-Hwa Tsai-Morris, Lisha Xu, Celine V Cluzeau, Christopher A Wassif, Benjamin Feldman, Shawn M Burgess, William J Pavan,[...]. Dis Model Mech 2018
27
33

Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish.
Elena V Semina, Dmitry V Bosenko, Natalya C Zinkevich, Kelly A Soules, David R Hyde, Thomas S Vihtelic, Gregory B Willer, Ronald G Gregg, Brian A Link. Dev Biol 2006
55
33

Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).
Yu Sun, Rowida Almomani, Guido J Breedveld, Gijs W E Santen, Emmelien Aten, Dirk J Lefeber, Jorrit I Hoff, Esther Brusse, Frans W Verheijen, Rob M Verdijk,[...]. Hum Mutat 2013
53
33

Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration.
Valentina Muto, Elisabetta Flex, Zachary Kupchinsky, Guido Primiano, Hamid Galehdari, Mohammadreza Dehghani, Serena Cecchetti, Giovanna Carpentieri, Teresa Rizza, Neda Mazaheri,[...]. Neurology 2018
23
33

Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease.
Elena Buglo, Evan Sarmiento, Nicole Belliard Martuscelli, David W Sant, Matt C Danzi, Alexander J Abrams, Julia E Dallman, Stephan Züchner. PLoS One 2020
16
33

CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.
Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N Robinson. PLoS Genet 2009
93
33

Evolutionary conserved role of ptf1a in the specification of exocrine pancreatic fates.
Elisabetta Zecchin, Anastasia Mavropoulos, Nathalie Devos, Alida Filippi, Natascia Tiso, Dirk Meyer, Bernard Peers, Marino Bortolussi, Francesco Argenton. Dev Biol 2004
85
33


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.