A citation-based method for searching scientific literature

Joanne Betts-Henderson, Stefano Bartesaghi, Moira Crosier, Susan Lindsay, Hai-Lan Chen, Paolo Salomoni, Irene Gottlob, Pierluigi Nicotera. Hum Mol Genet 2010
Times Cited: 51







List of co-cited articles
241 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
82

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
43

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
94
37

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
50

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

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
47

FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.
Qingjiong Zhang, Xueshan Xiao, Shiqiang Li, Xiangming Guo. Mol Vis 2007
27
55

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
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
53

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
48

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
61

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
23


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
37

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
92

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
35


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
19

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
52

The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane.
A H Chishti, A C Kim, S M Marfatia, M Lutchman, M Hanspal, H Jindal, S C Liu, P S Low, G A Rouleau, N Mohandas,[...]. Trends Biochem Sci 1998
421
17

A novel FERM domain including guanine nucleotide exchange factor is involved in Rac signaling and regulates neurite remodeling.
Tateki Kubo, Toshihide Yamashita, Atsushi Yamaguchi, Hideki Sumimoto, Ko Hosokawa, Masaya Tohyama. J Neurosci 2002
57
17

Frmd7 expression in developing mouse brain.
J Self, H M Haitchi, H Griffiths, S T Holgate, D E Davies, A Lotery. Eye (Lond) 2010
11
81

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
22

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

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
23

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

X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7.
Alan Shiels, Thomas M Bennett, Jessica B Prince, Lawrence Tychsen. Mol Vis 2007
13
61

Congenital nystagmus waveforms and foveation strategy.
L F Dell'Osso, R B Daroff. Doc Ophthalmol 1975
262
15


Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmus.
John H Fingert, Ben Roos, Mari E Eyestone, Joshua D Pham, Mei L Mellot, Edwin Stone. Ophthalmic Genet 2010
15
46

Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutation in the FRMD7 gene.
Y Kaplan, I Vargel, T Kansu, B Akin, E Rohmann, S Kamaci, E Uz, T Ozcelik, B Wollnik, N A Akarsu. Br J Ophthalmol 2008
16
43

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
13

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
22

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
14



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
11

A developmental model of infantile nystagmus.
Chris Harris, David Berry. Semin Ophthalmol 2006
24
25

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
54

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
16

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
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
63
11

A hypothetical explanation of congenital nystagmus.
L M Optican, D S Zee. Biol Cybern 1984
73
9

Nystagmus in infancy.
I Casteels, C M Harris, F Shawkat, D Taylor. Br J Ophthalmol 1992
55
9


Albino mice as an animal model for infantile nystagmus syndrome.
Ghislaine L Traber, Chien-Cheng Chen, Ying-Yu Huang, Marcella Spoor, Jeanine Roos, Maarten A Frens, Dominik Straumann, Christian Grimm. Invest Ophthalmol Vis Sci 2012
12
41

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
35


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
16

Localizing forms of nystagmus: symptoms, diagnosis, and treatment.
Andrew G Lee, Paul W Brazis. Curr Neurol Neurosci Rep 2006
18
22


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.