A citation-based method for searching scientific literature

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, Richard P Gale, Robert D Reinecke, Geoffrey Woodruff, Andrea Langmann, Susanne Lindner, Sunila Jain, Patrick Tarpey, F Lucy Raymond, Irene Gottlob. Brain 2008
Times Cited: 58







List of co-cited articles
467 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
72

The prevalence of nystagmus: the Leicestershire nystagmus survey.
Nagini Sarvananthan, Mylvaganam Surendran, Eryl O Roberts, Sunila Jain, Shery Thomas, Nitant Shah, Frank A Proudlock, John R Thompson, Rebecca J McLean, Christopher Degg,[...]. Invest Ophthalmol Vis Sci 2009
95
46

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
43

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
50

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
51

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
45


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
45

Congenital nystagmus waveforms and foveation strategy.
L F Dell'Osso, R B Daroff. Doc Ophthalmol 1975
262
24

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
24

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
43

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
36

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
208
20

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
18

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
32

Congenital nystagmus: randomized, controlled, double-masked trial of memantine/gabapentin.
Rebecca McLean, Frank Proudlock, Shery Thomas, Chris Degg, Irene Gottlob. Ann Neurol 2007
77
18

Congenital Nystagmus Gene FRMD7 Is Necessary for Establishing a Neuronal Circuit Asymmetry for Direction Selectivity.
Keisuke Yonehara, Michele Fiscella, Antonia Drinnenberg, Federico Esposti, Stuart Trenholm, Jacek Krol, Felix Franke, Brigitte Gross Scherf, Akos Kusnyerik, Jan Müller,[...]. Neuron 2016
64
18

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
27

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
38

A developmental model of infantile nystagmus.
Chris Harris, David Berry. Semin Ophthalmol 2006
24
37

Motor and sensory characteristics of infantile nystagmus.
R V Abadi, A Bjerre. Br J Ophthalmol 2002
126
15


A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmus.
Xiang He, Feng Gu, Ze Wang, Chong Wang, Yi Tong, Yujing Wang, Juhua Yang, Wei Liu, Meng Zhang, Xu Ma. Genet Test 2008
19
47


Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus.
Basamat AlMoallem, Miriam Bauwens, Sophie Walraedt, Patricia Delbeke, Julie De Zaeytijd, Philippe Kestelyn, Françoise Meire, Sandra Janssens, Caroline van Cauwenbergh, Hannah Verdin,[...]. Invest Ophthalmol Vis Sci 2015
14
64


Social and visual function in nystagmus.
R F Pilling, J R Thompson, I Gottlob. Br J Ophthalmol 2005
46
17

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
19

FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.
Qingjiong Zhang, Xueshan Xiao, Shiqiang Li, Xiangming Guo. Mol Vis 2007
27
29

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
20

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
13

Aetiology of infantile nystagmus.
Irene Gottlob, Frank A Proudlock. Curr Opin Neurol 2014
26
30

Development and clinical utility of a novel diagnostic nystagmus gene panel using targeted next-generation sequencing.
Mervyn G Thomas, Gail DE Maconachie, Viral Sheth, Rebecca J McLean, Irene Gottlob. Eur J Hum Genet 2017
27
29

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

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
20


A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family.
Wei Du, Juan Bu, Jiamei Dong, Yanlei Jia, Jing Li, Chen Liang, Shancheng Si, Lejin Wang. Mol Vis 2011
9
77

Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmus.
Uppala Radhakrishna, Uppala Ratnamala, Samuel Deutsch, Lucia Bartoloni, Murali R Kuracha, Raminder Singh, Jasjit Banwait, Dhundy K Bastola, Kaid Johar, Swapan K Nath,[...]. Eur J Hum Genet 2012
11
63

FERM domain containing protein 7 interacts with the Rho GDP dissociation inhibitor and specifically activates Rac1 signaling.
Jiali Pu, Yanfang Mao, Xiaoguang Lei, Yaping Yan, Xiaoxiong Lu, Jun Tian, Xinzhen Yin, Guohua Zhao, Baorong Zhang. PLoS One 2013
14
50

Potential of handheld optical coherence tomography to determine cause of infantile nystagmus in children by using foveal morphology.
Helena Lee, Viral Sheth, Mashal Bibi, Gail Maconachie, Aarti Patel, Rebecca J McLean, Michel Michaelides, Mervyn G Thomas, Frank A Proudlock, Irene Gottlob. Ophthalmology 2013
40
17

A unifying neurologic mechanism for infantile nystagmus.
Michael C Brodsky, Louis F Dell'Osso. JAMA Ophthalmol 2014
23
30



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
10


The effects of gabapentin and memantine in acquired and congenital nystagmus: a retrospective study.
T Shery, F A Proudlock, N Sarvananthan, R J McLean, I Gottlob. Br J Ophthalmol 2006
40
15

Latent, manifest latent, and congenital nystagmus.
L F Dell'Osso, D Schmidt, R B Daroff. Arch Ophthalmol 1979
95
10

Waveform characteristics in congenital nystagmus.
R V Abadi, C M Dickinson. Doc Ophthalmol 1986
119
10

Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.
N K Ragge, C Hartley, A M Dearlove, J Walker, I Russell-Eggitt, C M Harris. J Med Genet 2003
24
25


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.