A citation-based method for searching scientific literature

A Shiels, D Mackay, A Ionides, V Berry, A Moore, S Bhattacharya. Am J Hum Genet 1998
Times Cited: 292







List of co-cited articles
1307 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
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
29

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
Ramachandran Ramya Devi, Perumalsamy Vijayalakshmi. Mol Vis 2006
67
43

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
42

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
26

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
47

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
27

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
34

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


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
23

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
23

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
23

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
37

CRYBA4, a novel human cataract gene, is also involved in microphthalmia.
Gail Billingsley, Sathiyavedu T Santhiya, Andrew D Paterson, Koji Ogata, Shoshana Wodak, S Mohsen Hosseini, Shyam Manohar Manisastry, Perumalsamy Vijayalakshmi, Pudhiya Mundyat Gopinath, Jochen Graw,[...]. Am J Hum Genet 2006
74
29

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
36


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
20

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD.
E V Semina, R E Ferrell, H A Mintz-Hittner, P Bitoun, W L Alward, R S Reiter, C Funkhauser, S Daack-Hirsch, J C Murray. Nat Genet 1998
295
20

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
55

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

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
19

Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.
Robyn V Jamieson, Rahat Perveen, Bronwyn Kerr, Martin Carette, Jill Yardley, Elise Heon, M Gabriela Wirth, Veronica van Heyningen, Di Donnai, Francis Munier,[...]. Hum Mol Genet 2002
201
19

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
21

Congenital cataracts and their molecular genetics.
J Fielding Hejtmancik. Semin Cell Dev Biol 2008
260
19

The EPHA2 gene is associated with cataracts linked to chromosome 1p.
Alan Shiels, Thomas M Bennett, Harry L S Knopf, Giovanni Maraini, Anren Li, Xiaodong Jiao, J Fielding Hejtmancik. Mol Vis 2008
119
19


CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q.
Alan Shiels, Thomas M Bennett, Harry L S Knopf, Koki Yamada, Koh-ichiro Yoshiura, Norio Niikawa, Soomin Shim, Phyllis I Hanson. Am J Hum Genet 2007
84
21

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
17

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
36

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
34

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
51

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
17

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
40

Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.
Ramya Devi Ramachandran, Vijayalakshmi Perumalsamy, J Fielding Hejtmancik. Hum Genet 2007
82
20

Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2.
P M Jakobs, J F Hess, P G FitzGerald, P Kramer, R G Weleber, M Litt. Am J Hum Genet 2000
137
17

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
William A Paznekas, Simeon A Boyadjiev, Robert E Shapiro, Otto Daniels, Bernd Wollnik, Catherine E Keegan, Jeffrey W Innis, Mary Beth Dinulos, Cathy Christian, Mark C Hannibal,[...]. Am J Hum Genet 2003
464
17

A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
Vanita Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, Karl Sperling. Mol Vis 2008
36
47

A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract.
Ming Yan, Chenling Xiong, Shui Qing Ye, Yongmei Chen, Min Ke, Fang Zheng, Xin Zhou. Mol Vis 2008
32
53

Cat-Map: putting cataract on the map.
Alan Shiels, Thomas M Bennett, J Fielding Hejtmancik. Mol Vis 2010
205
17

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
25



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
15

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
53



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.