A citation-based method for searching scientific literature

Lei Gu, Riki Kawaguchi, Joseph Caprioli, Natik Piri. Sci Rep 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Downregulation of splicing regulator RBFOX1 compromises visual depth perception.
Lei Gu, Dean Bok, Fei Yu, Joseph Caprioli, Natik Piri. PLoS One 2018
8
100

RBFOX3/NeuN is dispensable for visual function.
Yi-Sian Lin, Kuan-Ting Kuo, Shih-Kuo Chen, Hsien-Sung Huang. PLoS One 2018
5
100

A new view of transcriptome complexity and regulation through the lens of local splicing variations.
Jorge Vaquero-Garcia, Alejandro Barrera, Matthew R Gazzara, Juan González-Vallinas, Nicholas F Lahens, John B Hogenesch, Kristen W Lynch, Yoseph Barash. Elife 2016
114
50



The CRB1 Complex: Following the Trail of Crumbs to a Feasible Gene Therapy Strategy.
Peter M Quinn, Lucie P Pellissier, Jan Wijnholds. Front Neurosci 2017
24
50

Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.
G J Farrar, J B Findlay, R Kumar-Singh, P Kenna, M M Humphries, E Sharpe, P Humphries. Hum Mol Genet 1992
17
50

Evolutionary dynamics of gene and isoform regulation in Mammalian tissues.
Jason Merkin, Caitlin Russell, Ping Chen, Christopher B Burge. Science 2012
476
50

Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt Disease.
Silvia Albert, Alejandro Garanto, Riccardo Sangermano, Mubeen Khan, Nathalie M Bax, Carel B Hoyng, Jana Zernant, Winston Lee, Rando Allikmets, Rob W J Collin,[...]. Am J Hum Genet 2018
43
50

Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease.
Riccardo Sangermano, Nathalie M Bax, Miriam Bauwens, L Ingeborgh van den Born, Elfride De Baere, Alejandro Garanto, Rob W J Collin, Angelique S A Goercharn-Ramlal, Anke H A den Engelsman-van Dijk, Klaus Rohrschneider,[...]. Ophthalmology 2016
51
50

Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa.
Adriana Buskin, Lili Zhu, Valeria Chichagova, Basudha Basu, Sina Mozaffari-Jovin, David Dolan, Alastair Droop, Joseph Collin, Revital Bronstein, Sudeep Mehrotra,[...]. Nat Commun 2018
54
50

Targeted knockdown of Cerkl, a retinal dystrophy gene, causes mild affectation of the retinal ganglion cell layer.
Alejandro Garanto, Javier Vicente-Tejedor, Marina Riera, Pedro de la Villa, Roser Gonzàlez-Duarte, Román Blanco, Gemma Marfany. Biochim Biophys Acta 2012
25
50

A general role for splicing enhancers in exon definition.
Bianca J Lam, Klemens J Hertel. RNA 2002
56
50

PRPF31 reduction causes mis-splicing of the phototransduction genes in human organotypic retinal culture.
Leila Azizzadeh Pormehr, Shahin Ahmadian, Narsis Daftarian, Seyed Ahmad Mousavi, Mahshid Shafiezadeh. Eur J Hum Genet 2020
5
50


Dynamic landscape of alternative polyadenylation during retinal development.
Wenyan Hu, Shengguo Li, Ji Yeon Park, Sridhar Boppana, Ting Ni, Miaoxin Li, Jun Zhu, Bin Tian, Zhi Xie, Mengqing Xiang. Cell Mol Life Sci 2017
11
50

The hnRNP family: insights into their role in health and disease.
Thomas Geuens, Delphine Bouhy, Vincent Timmerman. Hum Genet 2016
289
50

Antisense Oligonucleotide-Based Splice Correction of a Deep-Intronic Mutation in CHM Underlying Choroideremia.
Alejandro Garanto, Saskia D van der Velde-Visser, Frans P M Cremers, Rob W J Collin. Adv Exp Med Biol 2018
18
50

The spliceosome: design principles of a dynamic RNP machine.
Markus C Wahl, Cindy L Will, Reinhard Lührmann. Cell 2009
50

Reduction of choroidal neovascularization in mice by adeno-associated virus-delivered anti-vascular endothelial growth factor short hairpin RNA.
Anne Louise Askou, Jean-Antoine C Pournaras, Maria Pihlmann, Jesper D Svalgaard, Yvan Arsenijevic, Corinne Kostic, Toke Bek, Frederik Dagnaes-Hansen, Jacob Giehm Mikkelsen, Thomas Gryesten Jensen,[...]. J Gene Med 2012
36
50

Alternative splicing of the LIM-homeodomain transcription factor Isl1 in the mouse retina.
Irene E Whitney, Amanda G Kautzman, Benjamin E Reese. Mol Cell Neurosci 2015
6
50

Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure.
Serge A van de Pavert, Albena Kantardzhieva, Anna Malysheva, Jan Meuleman, Inge Versteeg, Christiaan Levelt, Jan Klooster, Sylvia Geiger, Mathias W Seeliger, Penny Rashbass,[...]. J Cell Sci 2004
178
50

Microexons: at the nexus of nervous system development, behaviour and autism spectrum disorder.
Thomas Gonatopoulos-Pournatzis, Benjamin J Blencowe. Curr Opin Genet Dev 2020
4
50

Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies.
Xavier Gerard, Alejandro Garanto, Jean-Michel Rozet, Rob W J Collin. Adv Exp Med Biol 2016
15
50

Intergenic mRNA molecules resulting from trans-splicing.
Csaba Finta, Peter G Zaphiropoulos. J Biol Chem 2002
105
50

Complex inheritance of ABCA4 disease: four mutations in a family with multiple macular phenotypes.
Winston Lee, Yajing Xie, Jana Zernant, Bo Yuan, Srilaxmi Bearelly, Stephen H Tsang, James R Lupski, Rando Allikmets. Hum Genet 2016
26
50

The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.
Dimitra Athanasiou, Monica Aguila, James Bellingham, Wenwen Li, Caroline McCulley, Philip J Reeves, Michael E Cheetham. Prog Retin Eye Res 2018
101
50

ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease.
Riccardo Sangermano, Mubeen Khan, Stéphanie S Cornelis, Valerie Richelle, Silvia Albert, Alejandro Garanto, Duaa Elmelik, Raheel Qamar, Dorien Lugtenberg, L Ingeborgh van den Born,[...]. Genome Res 2018
52
50

The role of alternative splicing coupled to nonsense-mediated mRNA decay in human disease.
Paulo J da Costa, Juliane Menezes, Luísa Romão. Int J Biochem Cell Biol 2017
27
50

RNA therapeutics for retinal diseases.
Michael C Gemayel, Ashay D Bhatwadekar, Thomas Ciulla. Expert Opin Biol Ther 2021
1
100

Neuronal-specific microexon splicing of TAF1 mRNA is directly regulated by SRRM4/nSR100.
Simona Capponi, Nadja Stöffler, Manuel Irimia, Frederik M A Van Schaik, Mercedes M Ondik, Martin L Biniossek, Lisa Lehmann, Julia Mitschke, Marit W Vermunt, Menno P Creyghton,[...]. RNA Biol 2020
2
50

Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
P McWilliam, G J Farrar, P Kenna, D G Bradley, M M Humphries, E M Sharp, D J McConnell, M Lawler, D Sheils, C Ryan. Genomics 1989
175
50

Nr2e3 functional domain ablation by CRISPR-Cas9D10A identifies a new isoform and generates retinitis pigmentosa and enhanced S-cone syndrome models.
Izarbe Aísa-Marín, M José López-Iniesta, Santiago Milla, Jaume Lillo, Gemma Navarro, Pedro de la Villa, Gemma Marfany. Neurobiol Dis 2020
3
50

ASCOT identifies key regulators of neuronal subtype-specific splicing.
Jonathan P Ling, Christopher Wilks, Rone Charles, Patrick J Leavey, Devlina Ghosh, Lizhi Jiang, Clayton P Santiago, Bo Pang, Anand Venkataraman, Brian S Clark,[...]. Nat Commun 2020
7
50

Splicing in the pathogenesis, diagnosis and treatment of ciliopathies.
Gabrielle Wheway, Jenny Lord, Diana Baralle. Biochim Biophys Acta Gene Regul Mech 2019
7
50

AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring the Common Leber Congenital Amaurosis CEP290 Mutation.
Xavier Gerard, Isabelle Perrault, Sylvain Hanein, Eduardo Silva, Karine Bigot, Sabine Defoort-Delhemmes, Marlèene Rio, Arnold Munnich, Daniel Scherman, Josseline Kaplan,[...]. Mol Ther Nucleic Acids 2012
70
50

Short-interfering RNAs induce retinal degeneration via TLR3 and IRF3.
Mark E Kleinman, Hiroki Kaneko, Won Gil Cho, Sami Dridi, Benjamin J Fowler, Alexander D Blandford, Romulo J C Albuquerque, Yoshio Hirano, Hiroko Terasaki, Mineo Kondo,[...]. Mol Ther 2012
67
50

Identification of splice defects due to noncanonical splice site or deep-intronic variants in ABCA4.
Zeinab Fadaie, Mubeen Khan, Marta Del Pozo-Valero, Stéphanie S Cornelis, Carmen Ayuso, Frans P M Cremers, Susanne Roosing, The Abca Study Group. Hum Mutat 2019
16
50

Exon-skipping variant of RGR opsin in human retina and pigment epithelium.
Henry K W Fong, Meng-Yin Lin, Sujay Pandey. Exp Eye Res 2006
8
50

Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA.
Gaby Tanner, Esther Glaus, Daniel Barthelmes, Marius Ader, Johannes Fleischhauer, Franco Pagani, Wolfgang Berger, John Neidhardt. Hum Mutat 2009
41
50

A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs.
Martina Huranová, Jarmila Hnilicová, Branislav Fleischer, Zuzana Cvacková, David Stanek. Hum Mol Genet 2009
23
50

Usher syndrome type 2 caused by activation of an USH2A pseudoexon: implications for diagnosis and therapy.
Christel Vaché, Thomas Besnard, Pauline le Berre, Gema García-García, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Hanno Jörn Bolz, Jose Millan,[...]. Hum Mutat 2012
68
50

Integrative transcriptome sequencing identifies trans-splicing events with important roles in human embryonic stem cell pluripotency.
Chan-Shuo Wu, Chun-Ying Yu, Ching-Yu Chuang, Michael Hsiao, Cheng-Fu Kao, Hung-Chih Kuo, Trees-Juen Chuang. Genome Res 2014
63
50

Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation.
Radulfus Wn Slijkerman, Christel Vaché, Margo Dona, Gema García-García, Mireille Claustres, Lisette Hetterschijt, Theo A Peters, Bas P Hartel, Ronald Je Pennings, José M Millan,[...]. Mol Ther Nucleic Acids 2016
58
50

Avoiding the Pitfalls of siRNA Delivery to the Retinal Pigment Epithelium with Physiologically Relevant Cell Models.
Eva Ramsay, Manuela Raviña, Sanjay Sarkhel, Sarah Hehir, Neil R Cameron, Tanja Ilmarinen, Heli Skottman, Jørgen Kjems, Arto Urtti, Marika Ruponen,[...]. Pharmaceutics 2020
2
50

Targeted deletion of an NRL- and CRX-regulated alternative promoter specifically silences FERM and PDZ domain containing 1 (Frmpd1) in rod photoreceptors.
Christie K Campla, Hannah Mast, Lijin Dong, Jingqi Lei, Stephanie Halford, Sumathi Sekaran, Anand Swaroop. Hum Mol Genet 2019
4
50

Expression of Kir7.1 and a novel Kir7.1 splice variant in native human retinal pigment epithelium.
Dongli Yang, Anuradha Swaminathan, Xiaoming Zhang, Bret A Hughes. Exp Eye Res 2008
20
50

RBFOX and PTBP1 proteins regulate the alternative splicing of micro-exons in human brain transcripts.
Yang I Li, Luis Sanchez-Pulido, Wilfried Haerty, Chris P Ponting. Genome Res 2015
79
50

Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?
Eranga N Vithana, Leen Abu-Safieh, Lucia Pelosini, Elizabeth Winchester, Dan Hornan, Alan C Bird, David M Hunt, Stephen A Bustin, Shomi S Bhattacharya. Invest Ophthalmol Vis Sci 2003
92
50

Regulation of Neuronal Differentiation, Function, and Plasticity by Alternative Splicing.
Elisabetta Furlanis, Peter Scheiffele. Annu Rev Cell Dev Biol 2018
37
50


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.