A citation-based method for searching scientific literature

Nagini Sarvananthan, Mylvaganam Surendran, Eryl O Roberts, Sunila Jain, Shery Thomas, Nitant Shah, Frank A Proudlock, John R Thompson, Rebecca J McLean, Christopher Degg, Geoffrey Woodruff, Irene Gottlob. Invest Ophthalmol Vis Sci 2009
Times Cited: 94







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



Times Cited
  Times     Co-cited
Similarity


Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, Uma Mallya, Steven Lisgo, Chris J Talbot, Eryl O Roberts, Musarat Awan, Mylvaganam Surendran, Rebecca J McLean,[...]. Nat Genet 2006
121
39

Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
Shery Thomas, Frank A Proudlock, Nagini Sarvananthan, Eryl O Roberts, Musarat Awan, Rebecca McLean, Mylvaganam Surendran, A S Anil Kumar, Shegufta J Farooq, Chris Degg,[...]. Brain 2008
58
46

Motor and sensory characteristics of infantile nystagmus.
R V Abadi, A Bjerre. Br J Ophthalmol 2002
126
23

Congenital nystagmus waveforms and foveation strategy.
L F Dell'Osso, R B Daroff. Doc Ophthalmol 1975
262
21

Social and visual function in nystagmus.
R F Pilling, J R Thompson, I Gottlob. Br J Ophthalmol 2005
46
41

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development.
Joanne Betts-Henderson, Stefano Bartesaghi, Moira Crosier, Susan Lindsay, Hai-Lan Chen, Paolo Salomoni, Irene Gottlob, Pierluigi Nicotera. Hum Mol Genet 2010
51
37

Living with nystagmus: a qualitative study.
Rebecca Jane McLean, Kate C Windridge, Irene Gottlob. Br J Ophthalmol 2012
32
59

Congenital nystagmus: randomized, controlled, double-masked trial of memantine/gabapentin.
Rebecca McLean, Frank Proudlock, Shery Thomas, Chris Degg, Irene Gottlob. Ann Neurol 2007
77
22

Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus.
James E Self, Fatima Shawkat, Crispin T Malpas, N Simon Thomas, Christopher M Harris, Peter R Hodgkins, Xiaoli Chen, Dorothy Trump, Andrew J Lotery. Arch Ophthalmol 2007
31
48


Waveform characteristics in congenital nystagmus.
R V Abadi, C M Dickinson. Doc Ophthalmol 1986
119
13

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3.
A Cabot, J M Rozet, S Gerber, I Perrault, D Ducroq, A Smahi, E Souied, A Munnich, J Kaplan. Am J Hum Genet 1999
64
20

Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus.
Baorong Zhang, Zhirong Liu, Guohua Zhao, Xin Xie, Xinzhen Yin, Zhengmao Hu, Shanhu Xu, Qian Li, Fei Song, Jun Tian,[...]. Mol Vis 2007
36
33

Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online.
Daniel F Schorderet, Leila Tiab, Marie-Claire Gaillard, Birgit Lorenz, Georges Klainguti, John B Kerrison, Elias I Traboulsi, Francis L Munier. Hum Mutat 2007
34
35


Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
Mervyn G Thomas, Anil Kumar, Sarim Mohammad, Frank A Proudlock, Elizabeth C Engle, Caroline Andrews, Wai-Man Chan, Shery Thomas, Irene Gottlob. Ophthalmology 2011
207
12

Abnormal retinal development associated with FRMD7 mutations.
Mervyn G Thomas, Moira Crosier, Susan Lindsay, Anil Kumar, Masasuke Araki, Bart P Leroy, Rebecca J McLean, Viral Sheth, Gail Maconachie, Shery Thomas,[...]. Hum Mol Genet 2014
33
36

Nystagmus in childhood.
Eleni Papageorgiou, Rebecca J McLean, Irene Gottlob. Pediatr Neonatol 2014
42
28

A developmental model of infantile nystagmus.
Chris Harris, David Berry. Semin Ophthalmol 2006
24
45

FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.
Qingjiong Zhang, Xueshan Xiao, Shiqiang Li, Xiangming Guo. Mol Vis 2007
27
40

Clinical and oculomotor characteristics of albinism compared to FRMD7 associated infantile nystagmus.
Anil Kumar, Irene Gottlob, Rebecca J McLean, Shery Thomas, Mervyn G Thomas, Frank A Proudlock. Invest Ophthalmol Vis Sci 2011
36
30

Congenital motor nystagmus linked to Xq26-q27.
J B Kerrison, M R Vagefi, M M Barmada, I H Maumenee. Am J Hum Genet 1999
60
16

A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus.
Rachel J Watkins, Rajashree Patil, Benjamin T Goult, Mervyn G Thomas, Irene Gottlob, Sue Shackleton. Hum Mol Genet 2013
36
27

A hypothetical explanation of congenital nystagmus.
L M Optican, D S Zee. Biol Cybern 1984
73
12

Oculomotor instabilities in zebrafish mutant belladonna: a behavioral model for congenital nystagmus caused by axonal misrouting.
Ying-Yu Huang, Oliver Rinner, Patrik Hedinger, Shih-Chii Liu, Stephan C F Neuhauss. J Neurosci 2006
34
26

Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus.
Ningdong Li, Liming Wang, Lihong Cui, Li Zhang, Suzhen Dai, Hongyan Li, Xia Chen, Lina Zhu, James F Hejtmancik, Kanxing Zhao. Mol Vis 2008
26
34



The Role of FRMD7 in Idiopathic Infantile Nystagmus.
Rachel J Watkins, Mervyn G Thomas, Chris J Talbot, Irene Gottlob, Sue Shackleton. J Ophthalmol 2012
29
31


Aetiology of infantile nystagmus.
Irene Gottlob, Frank A Proudlock. Curr Opin Neurol 2014
26
34

Ocular and vision defects in preschool children.
M Stayte, B Reeves, C Wortham. Br J Ophthalmol 1993
66
12

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.
Mervyn G Thomas, Moira Crosier, Susan Lindsay, Anil Kumar, Shery Thomas, Masasuke Araki, Chris J Talbot, Rebecca J McLean, Mylvaganam Surendran, Katie Taylor,[...]. Brain 2011
32
25

Nystagmus in infancy.
I Casteels, C M Harris, F Shawkat, D Taylor. Br J Ophthalmol 1992
55
14


Infantile and acquired nystagmus in childhood.
Oliver Ehrt. Eur J Paediatr Neurol 2012
24
33

FARP2 triggers signals for Sema3A-mediated axonal repulsion.
Toshihiko Toyofuku, Junko Yoshida, Tamiko Sugimoto, Hong Zhang, Atsushi Kumanogoh, Masatsugu Hori, Hitoshi Kikutani. Nat Neurosci 2005
170
7

Horizontal rectus tenotomy in patients with congenital nystagmus: results in 10 adults.
Richard W Hertle, Louis F Dell'Osso, Edmond J FitzGibbon, Darby Thompson, Dongsheng Yang, Susan D Mellow. Ophthalmology 2003
74
9

The nature of head postures in congenital nystagmus.
R V Abadi, J Whittle. Arch Ophthalmol 1991
32
21

Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus.
C Klein, P Vieregge, W Heide, B Kemper, M Hagedorn-Greiwe, J Hagenah, C Vollmer, X O Breakefield, D Kömpf, L Ozelius. Genomics 1998
27
25

A gene for autosomal dominant congenital nystagmus localizes to 6p12.
J B Kerrison, V J Arnould, M M Barmada, R K Koenekoop, B J Schmeckpeper, I H Maumenee. Genomics 1996
41
17

A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.
Xiang He, Feng Gu, Yujing Wang, Jinting Yan, Meng Zhang, Shangzhi Huang, Xu Ma. Mol Vis 2008
21
33

Therapy for nystagmus.
Matthew J Thurtell, R John Leigh. J Neuroophthalmol 2010
16
43

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.
Jing Yu Liu, Xiang Ren, Xiufeng Yang, Tangying Guo, Qi Yao, Lin Li, Xiaohua Dai, Mingchang Zhang, Lejin Wang, Mugen Liu,[...]. J Hum Genet 2007
40
17

Expression and localization of FRMD7 in human fetal brain, and a role for F-actin.
Jiali Pu, Yingzhi Li, Zhirong Liu, Yaping Yan, Jun Tian, Sheng Chen, Baorong Zhang. Mol Vis 2011
13
53

Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome.
M T Bassi, M V Schiaffino, A Renieri, F De Nigris, L Galli, M Bruttini, M Gebbia, A A Bergen, R A Lewis, A Ballabio. Nat Genet 1995
166
7


Combined gaze-angle and vergence variation in infantile nystagmus: two therapies that improve the high-visual-acuity field and methods to measure it.
Alessandro Serra, Louis F Dell'Osso, Jonathan B Jacobs, Robert A Burnstine. Invest Ophthalmol Vis Sci 2006
26
26

The diagnosis and treatment of infantile nystagmus syndrome (INS).
Sangeeta Khanna, Louis F Dell'Osso. ScientificWorldJournal 2006
13
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.