A citation-based method for searching scientific literature

J Fielding Hejtmancik. Semin Cell Dev Biol 2008
Times Cited: 260







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



Times Cited
  Times     Co-cited
Similarity


Cat-Map: putting cataract on the map.
Alan Shiels, Thomas M Bennett, J Fielding Hejtmancik. Mol Vis 2010
205
28

Molecular characteristics of inherited congenital cataracts.
Bingyu Huang, Weigong He. Eur J Med Genet 2010
61
37

Personalized diagnosis and management of congenital cataract by next-generation sequencing.
Rachel L Gillespie, James O'Sullivan, Jane Ashworth, Sanjeev Bhaskar, Simon Williams, Susmito Biswas, Elias Kehdi, Simon C Ramsden, Jill Clayton-Smith, Graeme C Black,[...]. Ophthalmology 2014
107
21

Genetics of human cataract.
A Shiels, J F Hejtmancik. Clin Genet 2013
98
20

Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.
Alan S Ma, John R Grigg, Gladys Ho, Ivan Prokudin, Elizabeth Farnsworth, Katherine Holman, Anson Cheng, Frank A Billson, Frank Martin, Clare Fraser,[...]. Hum Mutat 2016
82
23

The genetic and molecular basis of congenital cataract.
Alessandro Santana, Mauro Waiswo. Arq Bras Oftalmol 2011
56
32

Mutations and mechanisms in congenital and age-related cataracts.
Alan Shiels, J Fielding Hejtmancik. Exp Eye Res 2017
109
18

Crystallin gene mutations in Indian families with inherited pediatric cataract.
Ramachandran Ramya Devi, Wenliang Yao, Perumalsamy Vijayalakshmi, Yuri V Sergeev, Periasamy Sundaresan, J Fielding Hejtmancik. Mol Vis 2008
128
17

Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract.
Lars Hansen, Annemette Mikkelsen, Peter Nürnberg, Gudrun Nürnberg, Iram Anjum, Hans Eiberg, Thomas Rosenberg. Invest Ophthalmol Vis Sci 2009
81
19

Global prevalence of childhood cataract: a systematic review.
S Sheeladevi, J G Lawrenson, A R Fielder, C M Suttle. Eye (Lond) 2016
107
16


Childhood blindness in the context of VISION 2020--the right to sight.
C Gilbert, A Foster. Bull World Health Organ 2001
604
15

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
14

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
14

Elimination of cataract blindness: a global perspective entering the new millenium.
D J Apple, J Ram, A Foster, Q Peng. Surv Ophthalmol 2000
91
14

Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS gene.
Wenmin Sun, Xueshan Xiao, Shiqiang Li, Xiangming Guo, Qingjiong Zhang. PLoS One 2014
38
34

Genetic origins of cataract.
Alan Shiels, J Fielding Hejtmancik. Arch Ophthalmol 2007
128
12

Aetiology of congenital and paediatric cataract in an Australian population.
M G Wirth, I M Russell-Eggitt, J E Craig, J E Elder, D A Mackey. Br J Ophthalmol 2002
118
12

Epidemiology and molecular genetics of congenital cataracts.
Jun Yi, Jun Yun, Zhi-Kui Li, Chang-Tai Xu, Bo-Rong Pan. Int J Ophthalmol 2011
42
28

Clinical and experimental advances in congenital and paediatric cataracts.
Amanda Churchill, Jochen Graw. Philos Trans R Soc Lond B Biol Sci 2011
67
17

Lanosterol reverses protein aggregation in cataracts.
Ling Zhao, Xiang-Jun Chen, Jie Zhu, Yi-Bo Xi, Xu Yang, Li-Dan Hu, Hong Ouyang, Sherrina H Patel, Xin Jin, Danni Lin,[...]. Nature 2015
231
12

A nationwide Danish study of 1027 cases of congenital/infantile cataracts: etiological and clinical classifications.
Birgitte Haargaard, Jan Wohlfahrt, Hans C Fledelius, Thomas Rosenberg, Mads Melbye. Ophthalmology 2004
97
12

Genetics of Congenital Cataract.
Francesco Pichi, Andrea Lembo, Massimiliano Serafino, Paolo Nucci. Dev Ophthalmol 2016
46
23

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
10

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
19

Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.
Linda M Reis, Rebecca C Tyler, Sanaa Muheisen, Victor Raggio, Leonardo Salviati, Dennis P Han, Deborah Costakos, Hagith Yonath, Sarah Hall, Patricia Power,[...]. Hum Genet 2013
56
17



Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.
Olga Messina-Baas, Sergio A Cuevas-Covarrubias. Mol Syndromol 2017
34
29

Targeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype-Phenotype Correlations in 27 Chinese Han Families.
Yi Zhai, Jinyu Li, Wangshu Yu, Sha Zhu, Yinhui Yu, Menghan Wu, Guizhen Sun, Xiaohua Gong, Ke Yao. Sci Rep 2017
29
34

Ageing and vision: structure, stability and function of lens crystallins.
Hans Bloemendal, Wilfried de Jong, Rainer Jaenicke, Nicolette H Lubsen, Christine Slingsby, Annette Tardieu. Prog Biophys Mol Biol 2004
614
9

Mutation analysis of 12 genes in Chinese families with congenital cataracts.
Wenmin Sun, Xueshan Xiao, Shiqiang Li, Xiangming Guo, Qingjiong Zhang. Mol Vis 2011
43
20

Molecular genetics of congenital nuclear cataract.
Hao Deng, Lamei Yuan. Eur J Med Genet 2014
42
21

Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.
Ramya Devi Ramachandran, Vijayalakshmi Perumalsamy, J Fielding Hejtmancik. Hum Genet 2007
82
10

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
9


Distribution of gene mutations in sporadic congenital cataract in a Han Chinese population.
Dan Li, Siying Wang, Hongfei Ye, Yating Tang, Xiaodi Qiu, Qi Fan, Xianfang Rong, Xin Liu, Yuhong Chen, Jin Yang,[...]. Mol Vis 2016
35
25

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
8

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
8

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
8

Epidemiology of cataract in childhood: a global perspective.
A Foster, C Gilbert, J Rahi. J Cataract Refract Surg 1997
191
8

Infantile cataracts.
S R Lambert, A V Drack. Surv Ophthalmol 1996
247
8

Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family.
Haiba Kaul, S Amer Riazuddin, Mariam Shahid, Samra Kousar, Nadeem H Butt, Ahmad U Zafar, Shaheen N Khan, Tayyab Husnain, Javed Akram, J Fielding Hejtmancik,[...]. Mol Vis 2010
82
9

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
8

Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataract.
Donna S Mackay, Thomas M Bennett, Susan M Culican, Alan Shiels. Hum Genomics 2014
32
25

A novel mutation in major intrinsic protein of the lens gene (MIP) underlies autosomal dominant cataract in a Chinese family.
Feng Gu, Hong Zhai, Dan Li, Luxin Zhao, Chao Li, Shangzhi Huang, Xu Ma. Mol Vis 2007
58
12

Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms.
Sathiyavedu T Santhiya, Ganesan Senthil Kumar, Pridhvi Sudhakar, Navnit Gupta, Norman Klopp, Thomas Illig, Torben Söker, Marco Groth, Matthias Platzer, Puthiya M Gopinath,[...]. Mol Vis 2010
33
21

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
7

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.
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. Br J Ophthalmol 2004
60
11

Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literature.
Yoko Narumi, Sachiko Nishina, Motoharu Tokimitsu, Yoko Aoki, Rika Kosaki, Keiko Wakui, Noriyuki Azuma, Toshinori Murata, Fumio Takada, Yoshimitsu Fukushima,[...]. Am J Med Genet A 2014
25
28


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.