A citation-based method for searching scientific literature

Lin Li, Catherine Cheng, Chun-hong Xia, Thomas W White, Daniel A Fletcher, Xiaohua Gong. PLoS One 2010
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Congenital cataracts and their molecular genetics.
J Fielding Hejtmancik. Semin Cell Dev Biol 2008
257
22

Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice.
X Gong, E Li, G Klier, Q Huang, Y Wu, H Lei, N M Kumar, J Horwitz, N B Gilula. Cell 1997
334
22

Focus on lens connexins.
Viviana M Berthoud, Anaclet Ngezahayo. BMC Cell Biol 2017
44
22

Functions of the intermediate filament cytoskeleton in the eye lens.
Shuhua Song, Andrew Landsbury, Ralf Dahm, Yizhi Liu, Qingjiong Zhang, Roy A Quinlan. J Clin Invest 2009
105
16

Global data on visual impairment in the year 2002.
Serge Resnikoff, Donatella Pascolini, Daniel Etya'ale, Ivo Kocur, Ramachandra Pararajasegaram, Gopal P Pokharel, Silvio P Mariotti. Bull World Health Organ 2004
16


New genetic model rat for congenital cataracts due to a connexin 46 (Gja3 ) mutation.
Manabu Yoshida, Yuji Harada, Sachiko Kaidzu, Akihiro Ohira, Junichi Masuda, Toru Nabika. Pathol Int 2005
16
18

Disruption of Gja8 (alpha8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation.
Pei Rong, Xin Wang, Ingrid Niesman, Ying Wu, Lucio E Benedetti, Irene Dunia, Esther Levy, Xiaohua Gong. Development 2002
139
16

The effects of age on lens transport.
Junyuan Gao, Huan Wang, Xiurong Sun, Kulandaiappan Varadaraj, Leping Li, Thomas W White, Richard T Mathias. Invest Ophthalmol Vis Sci 2013
35
16

Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.
Lin Li, Bo Chang, Catherine Cheng, Da Chang, Norman L Hawes, Chun-hong Xia, Xiaohua Gong. Invest Ophthalmol Vis Sci 2008
16
18

Connexin46fs380 causes progressive cataracts.
Viviana M Berthoud, Peter J Minogue, Helena Yu, Joseph I Snabb, Eric C Beyer. Invest Ophthalmol Vis Sci 2014
15
20

Disruption of the lens circulation causes calcium accumulation and precipitates in connexin mutant mice.
Junyuan Gao, Peter J Minogue, Eric C Beyer, Richard T Mathias, Viviana M Berthoud. Am J Physiol Cell Physiol 2018
16
18

Altered ubiquitin causes perturbed calcium homeostasis, hyperactivation of calpain, dysregulated differentiation, and cataract.
Ke Liu, Lei Lyu, David Chin, Junyuan Gao, Xiurong Sun, Fu Shang, Andrea Caceres, Min-Lee Chang, Sheldon Rowan, Junmin Peng,[...]. Proc Natl Acad Sci U S A 2015
37
16

Connections between connexins, calcium, and cataracts in the lens.
Junyuan Gao, Xiurong Sun, Francisco J Martinez-Wittinghan, Xiaohua Gong, Thomas W White, Richard T Mathias. J Gen Physiol 2004
96
16

Calcium and the physiology of cataract.
G Duncan, T J Jacob. Ciba Found Symp 1984
100
16

Physiological and Optical Alterations Precede the Appearance of Cataracts in Cx46fs380 Mice.
Peter J Minogue, Junyuan Gao, Rebecca K Zoltoski, Layne A Novak, Richard T Mathias, Eric C Beyer, Viviana M Berthoud. Invest Ophthalmol Vis Sci 2017
11
27

The Connexin50D47A Mutant Causes Cataracts by Calcium Precipitation.
Viviana M Berthoud, Junyuan Gao, Peter J Minogue, Oscar Jara, Richard T Mathias, Eric C Beyer. Invest Ophthalmol Vis Sci 2019
11
27

The lens circulation.
Richard T Mathias, Joerg Kistler, Paul Donaldson. J Membr Biol 2007
183
16


Cat-Map: putting cataract on the map.
Alan Shiels, Thomas M Bennett, J Fielding Hejtmancik. Mol Vis 2010
201
11

Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.
S Amer Riazuddin, Afshan Yasmeen, Wenliang Yao, Yuri V Sergeev, Qingjiong Zhang, Fareeha Zulfiqar, Assad Riaz, Sheikh Riazuddin, J Fielding Hejtmancik. Invest Ophthalmol Vis Sci 2005
88
11

Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3).
Zhou Zhou, Shanshan Hu, Binbin Wang, Nan Zhou, Shiyi Zhou, Xu Ma, Yanhua Qi. Mol Vis 2010
16
12

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.
Surya Prakash G Ponnam, Kekunnaya Ramesha, Sushma Tejwani, Balasubramanya Ramamurthy, Chitra Kannabiran. J Med Genet 2007
56
11

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.
V Berry, D Mackay, S Khaliq, P J Francis, A Hameed, K Anwar, S Q Mehdi, R J Newbold, A Ionides, A Shiels,[...]. Hum Genet 1999
118
11

Epidemiology of cataract in childhood: a global perspective.
A Foster, C Gilbert, J Rahi. J Cataract Refract Surg 1997
186
11

Mutation analysis of CRYAA, CRYGC, and CRYGD associated with autosomal dominant congenital cataract in Brazilian families.
Alessandro Santana, Mauro Waiswol, Enyr Saran Arcieri, José Paulo Cabral de Vasconcellos, Mônica Barbosa de Melo. Mol Vis 2009
52
11


Removal of Hsf4 leads to cataract development in mice through down-regulation of gamma S-crystallin and Bfsp expression.
Xiaohe Shi, Bin Cui, Zhugang Wang, Lin Weng, Zhongping Xu, Jinjin Ma, Guotong Xu, Xiangyin Kong, Landian Hu. BMC Mol Biol 2009
57
11

Two affected siblings with nuclear cataract associated with a novel missense mutation in the CRYGD gene.
Olga Maud Messina-Baas, Luz Maria Gonzalez-Huerta, Sergio Alberto Cuevas-Covarrubias. Mol Vis 2006
35
11

Molecular basis of a progressive juvenile-onset hereditary cataract.
A Pande, J Pande, N Asherie, A Lomakin, O Ogun, J A King, N H Lubsen, D Walton, G B Benedek. Proc Natl Acad Sci U S A 2000
125
11

SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
11

Posttranslational modifications in lens fiber connexins identified by off-line-HPLC MALDI-quadrupole time-of-flight mass spectrometry.
David Shearer, Werner Ens, Ken Standing, Gunnar Valdimarsson. Invest Ophthalmol Vis Sci 2008
38
11

Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family.
Xiaohui Zhang, Lina Wang, Jun Wang, Bing Dong, Yang Li. Mol Vis 2012
11
18

A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract.
Jun Wang, Xu Ma, Feng Gu, Ning-pu Liu, Xiao-lin Hao, Kai-jie Wang, Ning-li Wang, Si-quan Zhu. Chin Med J (Engl) 2007
26
11

Clinical and experimental advances in congenital and paediatric cataracts.
Amanda Churchill, Jochen Graw. Philos Trans R Soc Lond B Biol Sci 2011
67
11

Absence of alpha3 (Cx46) and alpha8 (Cx50) connexins leads to cataracts by affecting lens inner fiber cells.
Chun-hong Xia, Catherine Cheng, Qingling Huang, Debra Cheung, Lin Li, Irene Dunia, Lucio E Benedetti, Joseph Horwitz, Xiaohua Gong. Exp Eye Res 2006
46
11


Inbred FVB/N mice are mutant at the cp49/Bfsp2 locus and lack beaded filament proteins in the lens.
Vladimir N Simirskii, Robert S Lee, Eric F Wawrousek, Melinda K Duncan. Invest Ophthalmol Vis Sci 2006
46
11

Lens intermediate filaments.
Paul G FitzGerald. Exp Eye Res 2009
31
11

An essential role for FGF receptor signaling in lens development.
Michael L Robinson. Semin Cell Dev Biol 2006
102
11

Tmod1 and CP49 synergize to control the fiber cell geometry, transparency, and mechanical stiffness of the mouse lens.
David S Gokhin, Roberta B Nowak, Nancy E Kim, Ernest E Arnett, Albert C Chen, Robert L Sah, John I Clark, Velia M Fowler. PLoS One 2012
39
11

Connexins in lens development and cataractogenesis.
Xiaohua Gong, Catherine Cheng, Chun-hong Xia. J Membr Biol 2007
66
11

Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study.
Zhou Zhou, Binbin Wang, Shanshan Hu, Chunmei Zhang, Xu Ma, Yanhua Qi. Mol Vis 2011
24
11


Physiological properties of the normal lens.
R T Mathias, J L Rae, G J Baldo. Physiol Rev 1997
312
11


Loss of cytoskeletal proteins and lens cell opacification in the selenite cataract model.
H Matsushima, L L David, T Hiraoka, J I Clark. Exp Eye Res 1997
55
11

Calcium content and distribution in human cataract.
K R Hightower, V N Reddy. Exp Eye Res 1982
66
11


Connexin50D47A decreases levels of fiber cell connexins and impairs lens fiber cell differentiation.
Viviana M Berthoud, Peter J Minogue, Helena Yu, Richard Schroeder, Joseph I Snabb, Eric C Beyer. Invest Ophthalmol Vis Sci 2013
28
11


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.