A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
76

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
73




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
59

Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population.
Ramachandran Ramya Devi, Chandrashekar Reena, Perumalsamy Vijayalakshmi. Mol Vis 2005
42
59

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
44

Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract.
Z W Ma, J Q Zheng, J Li, X R Li, X Tang, X Y Yuan, X M Zhang, H M Sun. Br J Ophthalmol 2005
28
71

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
60

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
40

The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46.
Lars Hansen, Wenliang Yao, Hans Eiberg, Mikkel Funding, Ruth Riise, Klaus Wilbrandt Kjaer, James Fielding Hejtmancik, Thomas Rosenberg. Mol Vis 2006
36
52

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
38

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
38

Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.
M Litt, R Carrero-Valenzuela, D M LaMorticella, D W Schultz, T N Mitchell, P Kramer, I H Maumenee. Hum Mol Genet 1997
218
34

A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
Kamlesh Guleria, Karl Sperling, Daljit Singh, Raymonda Varon, Jai Rup Singh, Vanita Vanita. Mol Vis 2007
31
48

Molecular genetic basis of inherited cataract and associated phenotypes.
M Ashwin Reddy, Peter J Francis, Vanita Berry, Shomi S Bhattacharya, Anthony T Moore. Surv Ophthalmol 2004
178
29


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
29

A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.
Kamlesh Guleria, Vanita Vanita, Daljit Singh, Jai Rup Singh. Mol Vis 2007
16
87

Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.
Lei Bu, Yiping Jin, Yuefeng Shi, Renyuan Chu, Airong Ban, Hans Eiberg, Lisa Andres, Haisong Jiang, Guangyong Zheng, Meiqian Qian,[...]. Nat Genet 2002
208
27

The gamma-crystallins and human cataracts: a puzzle made clearer.
E Héon, M Priston, D F Schorderet, G D Billingsley, P O Girard, N Lubsen, F L Munier. Am J Hum Genet 1999
228
27


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
27


Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
Ramachandran Ramya Devi, Perumalsamy Vijayalakshmi. Mol Vis 2006
67
27

Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.
V Berry, P Francis, M A Reddy, D Collyer, E Vithana, I MacKay, G Dawson, A H Carey, A Moore, S S Bhattacharya,[...]. Am J Hum Genet 2001
192
25

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
M Litt, P Kramer, D M LaMorticella, W Murphey, E W Lovrien, R G Weleber. Hum Mol Genet 1998
376
25

Connexin46 mutations linked to congenital cataract show loss of gap junction channel function.
J D Pal, X Liu, D Mackay, A Shiels, V M Berthoud, E C Beyer, L Ebihara. Am J Physiol Cell Physiol 2000
72
25


A nonsense mutation in CRYBB1 associated with autosomal dominant cataract linked to human chromosome 22q.
Donna S Mackay, Olivera B Boskovska, Harry L S Knopf, Kirsten J Lampi, Alan Shiels. Am J Hum Genet 2002
107
23

Connexin disorders of the ear, skin, and lens.
Dwan A Gerido, Thomas W White. Biochim Biophys Acta 2004
124
23

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
23

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
23

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
89
23

A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
Vanita Vanita, Hans Christian Hennies, Daljit Singh, Peter Nürnberg, Karl Sperling, Jai Rup Singh. Mol Vis 2006
34
32

Heteromeric connexons in lens gap junction channels.
J X Jiang, D A Goodenough. Proc Natl Acad Sci U S A 1996
216
21

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
21


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
21

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
21

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
22

Physiological properties of the normal lens.
R T Mathias, J L Rae, G J Baldo. Physiol Rev 1997
313
21

Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.
D Gill, R Klose, F L Munier, M McFadden, M Priston, G Billingsley, N Ducrey, D F Schorderet, E Héon. Invest Ophthalmol Vis Sci 2000
124
21

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
21

Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.
Lars Hansen, Wenliang Yao, Hans Eiberg, Klaus Wilbrandt Kjaer, Kirsten Baggesen, J Fielding Hejtmancik, Thomas Rosenberg. Invest Ophthalmol Vis Sci 2007
113
21

A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2.
Y P Conley, D Erturk, A Keverline, T S Mah, A Keravala, L R Barnes, A Bruchis, J F Hess, P G FitzGerald, D E Weeks,[...]. Am J Hum Genet 2000
126
19

A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.
Vanita Vanita, Daljit Singh, Peter N Robinson, Karl Sperling, Jai Rup Singh. Am J Med Genet A 2006
70
19


Gamma-S crystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans.
H Sun, Z Ma, Y Li, B Liu, Z Li, X Ding, Y Gao, W Ma, X Tang, X Li,[...]. J Med Genet 2005
90
19


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.