A citation-based method for searching scientific literature

Eric D Wieben, Ross A Aleff, Nirubol Tosakulwong, Malinda L Butz, W Edward Highsmith, Albert O Edwards, Keith H Baratz. PLoS One 2012
Times Cited: 145







List of co-cited articles
1293 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


E2-2 protein and Fuchs's corneal dystrophy.
Keith H Baratz, Nirubol Tosakulwong, Euijung Ryu, William L Brown, Kari Branham, Wei Chen, Khoa D Tran, Katharina E Schmid-Kubista, John R Heckenlively, Anand Swaroop,[...]. N Engl J Med 2010
181
46

RNA toxicity and missplicing in the common eye disease fuchs endothelial corneal dystrophy.
Jintang Du, Ross A Aleff, Elisabetta Soragni, Krishna Kalari, Jinfu Nie, Xiaojia Tang, Jaime Davila, Jean-Pierre Kocher, Sanjay V Patel, Joel M Gottesfeld,[...]. J Biol Chem 2015
83
46


TCF4 Triplet Repeat Expansion and Nuclear RNA Foci in Fuchs' Endothelial Corneal Dystrophy.
V Vinod Mootha, Imran Hussain, Khrishen Cunnusamy, Eric Graham, Xin Gong, Sudha Neelam, Chao Xing, Ralf Kittler, W Matthew Petroll. Invest Ophthalmol Vis Sci 2015
55
58

Corneal endothelial dystrophy. A study of 64 families.
J H Krachmer, J J Purcell, C W Young, K D Bucher. Arch Ophthalmol 1978
236
31

Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant.
Chao Xing, Xin Gong, Imran Hussain, Chiea-Chuen Khor, Donald T H Tan, Tin Aung, Jodhbir S Mehta, Eranga N Vithana, V Vinod Mootha. Invest Ophthalmol Vis Sci 2014
45
66

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.
Natalie A Afshari, Robert P Igo, Nathan J Morris, Dwight Stambolian, Shiwani Sharma, V Lakshmi Pulagam, Steven Dunn, John F Stamler, Barbara J Truitt, Jacqueline Rimmler,[...]. Nat Commun 2017
66
43

Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.
S Amer Riazuddin, David S Parker, Elyse J McGlumphy, Edwin C Oh, Benjamin W Iliff, Thore Schmedt, Ula Jurkunas, Robert Schleif, Nicholas Katsanis, John D Gottsch. Am J Hum Genet 2012
112
28

Correlation of Severity of Fuchs Endothelial Corneal Dystrophy With Triplet Repeat Expansion in TCF4.
Ahmed Z Soliman, Chao Xing, Salma H Radwan, Xin Gong, V Vinod Mootha. JAMA Ophthalmol 2015
41
68

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
S Biswas, F L Munier, J Yardley, N Hart-Holden, R Perveen, P Cousin, J E Sutphin, B Noble, M Batterbury, C Kielty,[...]. Hum Mol Genet 2001
274
27

Trinucleotide Repeat Expansion in the Transcription Factor 4 (TCF4) Gene Leads to Widespread mRNA Splicing Changes in Fuchs' Endothelial Corneal Dystrophy.
Eric D Wieben, Ross A Aleff, Xiaojia Tang, Malinda L Butz, Krishna R Kalari, Edward W Highsmith, Jin Jen, George Vasmatzis, Sanjay V Patel, Leo J Maguire,[...]. Invest Ophthalmol Vis Sci 2017
41
65

Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
S Amer Riazuddin, Norann A Zaghloul, Amr Al-Saif, Lisa Davey, Bill H Diplas, Danielle N Meadows, Allen O Eghrari, Mollie A Minear, Yi-Ju Li, Gordon K Klintworth,[...]. Am J Hum Genet 2010
137
26

Evidence of oxidative stress in the pathogenesis of fuchs endothelial corneal dystrophy.
Ula V Jurkunas, Maya S Bitar, Toshinari Funaki, Behrooz Azizi. Am J Pathol 2010
189
26

Mutations in AGBL1 cause dominant late-onset Fuchs corneal dystrophy and alter protein-protein interaction with TCF4.
S Amer Riazuddin, Shivakumar Vasanth, Nicholas Katsanis, John D Gottsch. Am J Hum Genet 2013
63
36

Expansion of CTG18.1 Trinucleotide Repeat in TCF4 Is a Potent Driver of Fuchs' Corneal Dystrophy.
Shivakumar Vasanth, Allen O Eghrari, Briana C Gapsis, Jiangxia Wang, Nicolas F Haller, Walter J Stark, Nicholas Katsanis, S Amer Riazuddin, John D Gottsch. Invest Ophthalmol Vis Sci 2015
33
69

SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Eranga N Vithana, Patricio E Morgan, Vedam Ramprasad, Donald T H Tan, Victor H K Yong, Divya Venkataraman, Anandalakshmi Venkatraman, Gary H F Yam, Soumittra Nagasamy, Ricky W K Law,[...]. Hum Mol Genet 2008
179
23

Oligonucleotides targeting TCF4 triplet repeat expansion inhibit RNA foci and mis-splicing in Fuchs' dystrophy.
Jiaxin Hu, Ziye Rong, Xin Gong, Zhengyang Zhou, Vivek K Sharma, Chao Xing, Jonathan K Watts, David R Corey, V Vinod Mootha. Hum Mol Genet 2018
31
74

Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity.
Christina Zarouchlioti, Beatriz Sanchez-Pintado, Nathaniel J Hafford Tear, Pontus Klein, Petra Liskova, Kalyan Dulla, Ma'ayan Semo, Anthony A Vugler, Kirithika Muthusamy, Lubica Dudakova,[...]. Am J Hum Genet 2018
36
63

Genetic association of TCF4 intronic polymorphisms, CTG18.1 and rs17089887, with Fuchs' endothelial corneal dystrophy in an Indian population.
Gargi Gouranga Nanda, Biswajit Padhy, Sujata Samal, Sujata Das, Debasmita Pankaj Alone. Invest Ophthalmol Vis Sci 2014
39
56

Global Survey of Corneal Transplantation and Eye Banking.
Philippe Gain, Rémy Jullienne, Zhiguo He, Mansour Aldossary, Sophie Acquart, Fabrice Cognasse, Gilles Thuret. JAMA Ophthalmol 2016
625
21

Trinucleotide Repeat Expansion in the TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy in Japanese.
Masakazu Nakano, Naoki Okumura, Hiroko Nakagawa, Noriko Koizumi, Yoko Ikeda, Morio Ueno, Kengo Yoshii, Hiroko Adachi, Ross A Aleff, Malinda L Butz,[...]. Invest Ophthalmol Vis Sci 2015
35
57

Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy.
John D Gottsch, Olof H Sundin, Sammy H Liu, Albert S Jun, Karl W Broman, Walter J Stark, Elizabeth C L Vito, Amol K Narang, John M Thompson, Malcolm Magovern. Invest Ophthalmol Vis Sci 2005
148
20

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
20

Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy.
S Amer Riazuddin, Eranga N Vithana, Li-Fong Seet, Yangjian Liu, Amr Al-Saif, Li Wei Koh, Yee Meng Heng, Tin Aung, Danielle N Meadows, Allen O Eghrari,[...]. Hum Mutat 2010
93
20

Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy.
V Vinod Mootha, Brock Hansen, Ziye Rong, Pradeep P Mammen, Zhengyang Zhou, Chao Xing, Xin Gong. Invest Ophthalmol Vis Sci 2017
26
69

Prevalence and risk factors for cornea guttata in the Reykjavik Eye Study.
Gunnar M Zoega, Aya Fujisawa, Hiroshi Sasaki, Akiko Kubota, Kazuyuki Sasaki, Kazuko Kitagawa, Fridbert Jonasson. Ophthalmology 2006
91
19

Central cornea guttata. Incidence in the general population.
D W Lorenzetti, M H Uotila, N Parikh, H E Kaufman. Am J Ophthalmol 1967
112
17

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
585
17

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
843
17

Unfolded protein response in fuchs endothelial corneal dystrophy: a unifying pathogenic pathway?
Christoph Engler, Clare Kelliher, Arielle R Spitze, Caroline L Speck, Charles G Eberhart, Albert S Jun. Am J Ophthalmol 2010
76
22

CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs' dystrophy.
Sabine Foja, Mirjam Luther, Katrin Hoffmann, Andreas Rupprecht, Claudia Gruenauer-Kloevekorn. Graefes Arch Clin Exp Ophthalmol 2017
19
89

Repeat-Associated Non-ATG (RAN) Translation in Fuchs' Endothelial Corneal Dystrophy.
Elisabetta Soragni, Lina Petrosyan, Tommy A Rinkoski, Eric D Wieben, Keith H Baratz, Michael P Fautsch, Joel M Gottesfeld. Invest Ophthalmol Vis Sci 2018
30
56

Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.
Yi-Ju Li, Mollie A Minear, Jacqueline Rimmler, Bei Zhao, Elmer Balajonda, Michael A Hauser, R Rand Allingham, Allen O Eghrari, S Amer Riazuddin, Nicholas Katsanis,[...]. PLoS One 2011
61
24


A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
15

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.
Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, Shuichi Asakawa, Taro Ishiguro, Taiji Tsunemi, Makoto Takahashi, Tohru Matsuura, Kevin M Flanigan, Sawa Iwasaki,[...]. Am J Hum Genet 2009
181
15

Fuchs' endothelial dystrophy of the cornea.
A P Adamis, V Filatov, B J Tripathi, R C Tripathi. Surv Ophthalmol 1993
199
15

Repeat expansion diseases.
Henry Paulson. Handb Clin Neurol 2018
146
15

Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13.
Olof H Sundin, Albert S Jun, Karl W Broman, Sammy H Liu, Siobhan E Sheehan, Elizabeth C L Vito, Walter J Stark, John D Gottsch. Invest Ophthalmol Vis Sci 2006
92
15

Corneal endothelial cell apoptosis in patients with Fuchs' dystrophy.
V M Borderie, M Baudrimont, A Vallée, T L Ereau, F Gray, L Laroche. Invest Ophthalmol Vis Sci 2000
93
15

Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese.
Anbupalam Thalamuthu, Chiea Chuen Khor, Divya Venkataraman, Li Wei Koh, Donald T H Tan, Tin Aung, Jodhbir S Mehta, Eranga N Vithana. Invest Ophthalmol Vis Sci 2011
42
33

An alpha 2 collagen VIII transgenic knock-in mouse model of Fuchs endothelial corneal dystrophy shows early endothelial cell unfolded protein response and apoptosis.
Albert S Jun, Huan Meng, Naren Ramanan, Mario Matthaei, Shukti Chakravarti, Richard Bonshek, Graeme C M Black, Rhonda Grebe, Martha Kimos. Hum Mol Genet 2012
74
18

Involvement of ZEB1 and Snail1 in excessive production of extracellular matrix in Fuchs endothelial corneal dystrophy.
Naoki Okumura, Ryuki Minamiyama, Leona Ty Ho, EunDuck P Kay, Satoshi Kawasaki, Theofilos Tourtas, Ursula Schlötzer-Schrehardt, Friedrich E Kruse, Robert D Young, Andrew J Quantock,[...]. Lab Invest 2015
57
24

A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.
Olof H Sundin, Karl W Broman, Howard H Chang, Elizabeth C L Vito, Walter J Stark, John D Gottsch. Invest Ophthalmol Vis Sci 2006
85
15

Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus.
S Amer Riazuddin, Elyse J McGlumphy, William S Yeo, Jiangxia Wang, Nicholas Katsanis, John D Gottsch. Invest Ophthalmol Vis Sci 2011
53
24

Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy.
Jodhbir S Mehta, Eranga N Vithana, Donald T H Tan, Victor H K Yong, Gary H F Yam, Ricky W K Law, Wesley G W Chong, Calvin P Pang, Tin Aung. Invest Ophthalmol Vis Sci 2008
62
20

Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process.
Abraham Kuot, Alex W Hewitt, Kim Griggs, Sonja Klebe, Richard Mills, Vishal Jhanji, Jamie E Craig, Shiwani Sharma, Kathryn P Burdon. Eur J Hum Genet 2012
50
26

Fuchs endothelial corneal dystrophy.
Hussain Elhalis, Behrooz Azizi, Ula V Jurkunas. Ocul Surf 2010
116
13

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
J D Brook, M E McCurrach, H G Harley, A J Buckler, D Church, H Aburatani, K Hunter, V P Stanton, J P Thirion, T Hudson. Cell 1992
13

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
M D Koob, M L Moseley, L J Schut, K A Benzow, T D Bird, J W Day, L P Ranum. Nat Genet 1999
455
13


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.