A citation-based method for searching scientific literature

Dwan A Gerido, Caterina Sellitto, Leping Li, Thomas W White. Invest Ophthalmol Vis Sci 2003
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity



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
337
52

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
141
41

Genetic factors influence cataract formation in alpha 3 connexin knockout mice.
X Gong, K Agopian, N M Kumar, N B Gilula. Dev Genet 1999
66
38


A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.
Bo Chang, Xin Wang, Norman L Hawes, Ryan Ojakian, Muriel T Davisson, Woo-Kuen Lo, Xiaohua Gong. Hum Mol Genet 2002
63
33

A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract.
E C Steele, M F Lyon, J Favor, P V Guillot, Y Boyd, R L Church. Curr Eye Res 1998
77
30


Connexin46 mutations in autosomal dominant congenital cataract.
D Mackay, A Ionides, Z Kibar, G Rouleau, V Berry, A Moore, A Shiels, S Bhattacharya. Am J Hum Genet 1999
232
27

Physiological properties of the normal lens.
R T Mathias, J L Rae, G J Baldo. Physiol Rev 1997
313
27

Defining a link between gap junction communication, proteolysis, and cataract formation.
A Baruch, D Greenbaum, E T Levy, P A Nielsen, N B Gilula, N M Kumar, M Bogyo. J Biol Chem 2001
93
27

Dominant cataracts result from incongruous mixing of wild-type lens connexins.
Francisco J Martinez-Wittinghan, Caterina Sellitto, Leping Li, Xiaohua Gong, Peter R Brink, Richard T Mathias, Thomas W White. J Cell Biol 2003
48
25

Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.
J Graw, J Löster, D Soewarto, H Fuchs, B Meyer, A Reis, E Wolf, R Balling, M Hrabé de Angelis. Exp Eye Res 2001
44
25



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
22


Gap junctional coupling in lenses from alpha(8) connexin knockout mice.
G J Baldo, X Gong, F J Martinez-Wittinghan, N M Kumar, N B Gilula, R T Mathias. J Gen Physiol 2001
76
22

Loss of function and impaired degradation of a cataract-associated mutant connexin50.
Viviana M Berthoud, Peter J Minogue, Jun Guo, Edward K Williamson, Xiaorong Xu, Lisa Ebihara, Eric C Beyer. Eur J Cell Biol 2003
73
22

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
22

A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract.
A Arora, P J Minogue, X Liu, M A Reddy, J R Ainsworth, S S Bhattacharya, A R Webster, D M Hunt, L Ebihara, A T Moore,[...]. J Med Genet 2006
68
22


Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract.
A V Polyakov, I A Shagina, O V Khlebnikova, O V Evgrafov. Clin Genet 2001
69
19

Molecular solutions to mammalian lens transparency.
P Donaldson, J Kistler, R T Mathias. News Physiol Sci 2001
133
19


Heteromeric connexons in lens gap junction channels.
J X Jiang, D A Goodenough. Proc Natl Acad Sci U S A 1996
216
19

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.
A Arora, P J Minogue, X Liu, P K Addison, I Russel-Eggitt, A R Webster, D M Hunt, L Ebihara, E C Beyer, V M Berthoud,[...]. J Med Genet 2008
61
19

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Oliver Puk, Jana Löster, Claudia Dalke, Dian Soewarto, Helmut Fuchs, Birgit Budde, Peter Nürnberg, Eckhard Wolf, Martin Hrabé de Angelis, Jochen Graw. Invest Ophthalmol Vis Sci 2008
23
30

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
19

Gap junctional coupling in lenses lacking alpha3 connexin.
X Gong, G J Baldo, N M Kumar, N B Gilula, R T Mathias. Proc Natl Acad Sci U S A 1998
92
16

Lens gap junctional coupling is modulated by connexin identity and the locus of gene expression.
Francisco J Martinez-Wittinghan, Caterina Sellitto, Thomas W White, Richard T Mathias, David Paul, Daniel A Goodenough. Invest Ophthalmol Vis Sci 2004
37
16


Lens organelle degradation.
Steven Bassnett. Exp Eye Res 2002
208
16

Plasma membrane channels formed by connexins: their regulation and functions.
Juan C Saez, Viviana M Berthoud, Maria C Branes, Agustin D Martinez, Eric C Beyer. Physiol Rev 2003
892
16

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.
K P Burdon, M G Wirth, D A Mackey, I M Russell-Eggitt, J E Craig, J E Elder, J L Dickinson, M M Sale. J Med Genet 2004
50
16

A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.
Haisong Jiang, Yiping Jin, Lei Bu, Weiying Zhang, Jing Liu, Bin Cui, Xiangyin Kong, Landian Hu. Mol Vis 2003
46
16


A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.
C E Willoughby, Sara Arab, R Gandhi, S Zeinali, Seddigheh Arab, D Luk, G Billingsley, F L Munier, E Héon. J Med Genet 2003
53
16

Molecular mechanism underlying a Cx50-linked congenital cataract.
J D Pal, V M Berthoud, E C Beyer, D Mackay, A Shiels, L Ebihara. Am J Physiol 1999
62
16

Connexin50 is essential for normal postnatal lens cell proliferation.
Caterina Sellitto, Leping Li, Thomas W White. Invest Ophthalmol Vis Sci 2004
59
16


A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.
P K F Addison, V Berry, K R Holden, D Espinal, B Rivera, H Su, A K Srivastava, S S Bhattacharya. Mol Vis 2006
33
18

Cardiac malformation in neonatal mice lacking connexin43.
A G Reaume, P A de Sousa, S Kulkarni, B L Langille, D Zhu, T C Davies, S C Juneja, G M Kidder, J Rossant. Science 1995
16

Knock-in of alpha3 connexin prevents severe cataracts caused by an alpha8 point mutation.
Chun-hong Xia, Debra Cheung, Adam M DeRosa, Bo Chang, Woo-Kuen Lo, Thomas W White, Xiaohua Gong. J Cell Sci 2006
26
23

Connexin channel permeability to cytoplasmic molecules.
Andrew L Harris. Prog Biophys Mol Biol 2007
334
16

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
58
16

Connexins in lens development and cataractogenesis.
Xiaohua Gong, Catherine Cheng, Chun-hong Xia. J Membr Biol 2007
69
16

An aberrant sequence in a connexin46 mutant underlies congenital cataracts.
Peter J Minogue, Xiaoqin Liu, Lisa Ebihara, Eric C Beyer, Viviana M Berthoud. J Biol Chem 2005
50
16

Lens gap junctions in growth, differentiation, and homeostasis.
Richard T Mathias, Thomas W White, Xiaohua Gong. Physiol Rev 2010
159
16



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.