A citation-based method for searching scientific literature

Shea Ping Yip, Choi Chu Li, Wai Chi Yiu, Wing Hong Hung, Wai Wa Lam, Man Chi Lai, Po Wah Ng, Wai Yan Fung, Patrick H W Chu, Bo Jiang, Henry H L Chan, Maurice K H Yap. Ophthalmic Physiol Opt 2013
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Mutations in NYX of individuals with high myopia, but without night blindness.
Qingjiong Zhang, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Zhikuan Yang, Shizhou Huang, Rafael C Caruso, Tianqin Guan, Yuri Sergeev, Xiangming Guo,[...]. Mol Vis 2007
32
61

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
239
44

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013
89
44

CSNB1 in Chinese families associated with novel mutations in NYX.
Xueshan Xiao, Xiaoyun Jia, Xiangming Guo, Shiqiang Li, Zhikuan Yang, Qingjiong Zhang. J Hum Genet 2006
13
53

A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites.
Jillian N Pearring, Pasano Bojang, Yin Shen, Chieko Koike, Takahisa Furukawa, Scott Nawy, Ronald G Gregg. J Neurosci 2011
64
38


Mutations in LRPAP1 are associated with severe myopia in humans.
Mohammed A Aldahmesh, Arif O Khan, Hisham Alkuraya, Nouran Adly, Shamsa Anazi, Ahmed A Al-Saleh, Jawahir Y Mohamed, Hadia Hijazi, Sarita Prabakaran, Marlene Tacke,[...]. Am J Hum Genet 2013
65
33

Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.
Dan Jiang, Jiali Li, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Xiangming Guo, Qingjiong Zhang. Invest Ophthalmol Vis Sci 2014
67
33

A common NYX mutation in Flemish patients with X linked CSNB.
B P Leroy, B S Budde, M Wittmer, E De Baere, W Berger, C Zeitz. Br J Ophthalmol 2009
13
38

Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.
Ronald G Gregg, Maarten Kamermans, Jan Klooster, Peter D Lukasiewicz, Neal S Peachey, Kirstan A Vessey, Maureen A McCall. J Neurophysiol 2007
72
27

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
186
27

Sequence variations of GRM6 in patients with high myopia.
Xiaoyu Xu, Shiqiang Li, Xueshan Xiao, Panfeng Wang, Xiangming Guo, Qingjiong Zhang. Mol Vis 2009
19
27

Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.
Jiali Li, Bei Gao, Liping Guan, Xueshan Xiao, Jianguo Zhang, Shiqiang Li, Hui Jiang, Xiaoyun Jia, Jianhua Yang, Xiangming Guo,[...]. Invest Ophthalmol Vis Sci 2015
26
27

NYX mutations in four families with high myopia with or without CSNB1.
Lin Zhou, Tuo Li, Xiusheng Song, Yin Li, Hongyan Li, Handong Dan. Mol Vis 2015
10
50

Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1.
Q Zhang, X Guo, X Xiao, X Jia, S Li, J F Hejtmancik. J Med Genet 2006
84
22

SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia.
Hui Guo, Xuemin Jin, Tengfei Zhu, Tianyun Wang, Ping Tong, Lei Tian, Yu Peng, Liangdan Sun, Anran Wan, Jingjing Chen,[...]. J Med Genet 2014
55
22

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.
S Annunen, J Körkkö, M Czarny, M L Warman, H G Brunner, H Kääriäinen, J B Mulliken, L Tranebjaerg, D G Brooks, G F Cox,[...]. Am J Hum Genet 1999
162
22

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Virginie J M Verhoeven, Pirro G Hysi, Robert Wojciechowski, Qiao Fan, Jeremy A Guggenheim, René Höhn, Stuart MacGregor, Alex W Hewitt, Abhishek Nag, Ching-Yu Cheng,[...]. Nat Genet 2013
299
22

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.
Khanh-Nhat Tran-Viet, Caldwell Powell, Veluchamy A Barathi, Thomas Klemm, Sebastian Maurer-Stroh, Vachiranee Limviphuvadh, Vincent Soler, Candice Ho, Tammy Yanovitch, Georg Schneider,[...]. Am J Hum Genet 2013
70
22

RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.
Thiran Jayasundera, Kari E H Branham, Mohammad Othman, William R Rhoades, Athanasios J Karoukis, Hemant Khanna, Anand Swaroop, John R Heckenlively. Arch Ophthalmol 2010
44
22

Multiple molecular mechanisms underlying subdiagnostic variants of Marfan syndrome.
R A Montgomery, M T Geraghty, E Bull, B D Gelb, M Johnson, I McIntosh, C A Francomano, H C Dietz. Am J Hum Genet 1998
60
22

Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.
Amy K Kiefer, Joyce Y Tung, Chuong B Do, David A Hinds, Joanna L Mountain, Uta Francke, Nicholas Eriksson. PLoS Genet 2013
193
22

Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome.
H C Dietz, I McIntosh, L Y Sakai, G M Corson, S C Chalberg, R E Pyeritz, C A Francomano. Genomics 1993
250
22

Exome sequencing identifies ZNF644 mutations in high myopia.
Yi Shi, Yingrui Li, Dingding Zhang, Hao Zhang, Yuanfeng Li, Fang Lu, Xiaoqi Liu, Fei He, Bo Gong, Li Cai,[...]. PLoS Genet 2011
138
22

High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2.
Shikma Mordechai, Libe Gradstein, Annika Pasanen, Rivka Ofir, Khalil El Amour, Jaime Levy, Nadav Belfair, Tova Lifshitz, Sara Joshua, Ginat Narkis,[...]. Am J Hum Genet 2011
73
22

Evaluation of 12 myopia-associated genes in Chinese patients with high myopia.
Jiali Li, Dan Jiang, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Xiangming Guo, Qingjiong Zhang. Invest Ophthalmol Vis Sci 2015
39
22

Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations.
Zi-Bing Jin, Xiao-Qiang Liu, Mutsuko Hayakawa, Akira Murakami, Nobuhisa Nao-i. Mol Vis 2006
34
22

Myopia.
Ian G Morgan, Kyoko Ohno-Matsui, Seang-Mei Saw. Lancet 2012
915
22

Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes.
Wenmin Sun, Li Huang, Yan Xu, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Bei Gao, Panfeng Wang, Xiangming Guo, Qingjiong Zhang. Invest Ophthalmol Vis Sci 2015
48
22

Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness.
Shuzhen Dai, Ming Ying, Kai Wang, Liming Wang, Ruifang Han, Peng Hao, Ningdong Li. Sci Rep 2015
5
80

Localization of nyctalopin in the mammalian retina.
Catherine W Morgans, Gaoying Ren, Lakshmi Akileswaran. Eur J Neurosci 2006
56
16

Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1.
Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, Xiaoyun Jia, Xiangming Guo. J Hum Genet 2007
24
16

A genome-wide scan maps a novel high myopia locus to 5p15.
Ching Yan Lam, Pancy O S Tam, Dorothy S P Fan, Bao Jian Fan, Dan Yi Wang, Coral W S Lee, Chi Pui Pang, Dennis S C Lam. Invest Ophthalmol Vis Sci 2008
64
16


A second locus for familial high myopia maps to chromosome 12q.
T L Young, S M Ronan, A B Alvear, S C Wildenberg, W S Oetting, L D Atwood, D J Wilkin, R A King. Am J Hum Genet 1998
204
16

New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.
Prasuna Paluru, Shawn M Ronan, Elise Heon, Marcella Devoto, Scott C Wildenberg, Genaro Scavello, Ann Holleschau, Outi Mäkitie, William G Cole, Richard A King,[...]. Invest Ophthalmol Vis Sci 2003
145
16

Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.
Sudha Nallasamy, Prasuna C Paluru, Marcella Devoto, Nora F Wasserman, Jie Zhou, Terri L Young. Mol Vis 2007
71
16

Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
Prasuna C Paluru, Sudha Nallasamy, Marcella Devoto, Eric F Rappaport, Terri L Young. Invest Ophthalmol Vis Sci 2005
98
16

A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.
Qingjiong Zhang, Xiangming Guo, Xueshan Xiao, Xiaoyun Jia, Shiqiang Li, J Fielding Hejtmancik. Mol Vis 2005
94
16

Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Mieke M C Bijveld, Ralph J Florijn, Arthur A B Bergen, L Ingeborgh van den Born, Maarten Kamermans, Liesbeth Prick, Frans C C Riemslag, Mary J van Schooneveld, Astrid M L Kappers, Maria M van Genderen. Ophthalmology 2013
57
16

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.
Christina Zeitz, Roberta Minotti, Silke Feil, Gábor Mátyás, Frans P M Cremers, Carel B Hoyng, Wolfgang Berger. Mol Vis 2005
30
16

The leucine-rich repeat: a versatile binding motif.
B Kobe, J Deisenhofer. Trends Biochem Sci 1994
941
16

Clinical and genetic characterization of a Chinese family with CSNB1.
Ruifang Sui, Fengrong Li, Jialiang Zhao, Ruxin Jiang. Adv Exp Med Biol 2008
4
75

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, Ralph J Florijn, Jillian N Pearring, Francoise M Meire, Maureen A McCall, Frans C C Riemslag, Ronald G Gregg, Arthur A B Bergen,[...]. Am J Hum Genet 2009
148
16

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
Ariana Hemara-Wahanui, Stanislav Berjukow, Carolyn I Hope, Peter K Dearden, Shu-Biao Wu, Jane Wilson-Wheeler, Dianne M Sharp, Patricia Lundon-Treweek, Gillian M Clover, Jean-Charles Hoda,[...]. Proc Natl Acad Sci U S A 2005
99
16

Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract.
H Guo, P Tong, Y Peng, T Wang, Y Liu, J Chen, Y Li, Q Tian, Y Hu, Y Zheng,[...]. Clin Genet 2014
39
16

The Stickler syndrome: genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1.
Ruth M Liberfarb, Howard P Levy, Peter S Rose, Douglas J Wilkin, Joie Davis, Joan Z Balog, Andrew J Griffith, Yvonne M Szymko-Bennett, Jennifer J Johnston, Clair A Francomano,[...]. Genet Med 2003
52
16

Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa.
A Yokoyama, F Maruiwa, M Hayakawa, A Kanai, R Vervoort, A F Wright, K Yamada, N Niikawa, N Naōi. Am J Med Genet 2001
30
16

Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.
Zhikuan Yang, Xueshan Xiao, Shiqiang Li, Qingjiong Zhang. Mol Vis 2009
45
16

A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon.
N N Ahmad, D M McDonald-McGinn, E H Zackai, R G Knowlton, D LaRossa, J DiMascio, D J Prockop. Am J Hum Genet 1993
107
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.