A citation-based method for searching scientific literature

Letterio Salvatore Politi, Stefania Bianchi Marzoli, Claudia Godi, Marta Panzeri, Paola Ciasca, Gianluca Brugnara, Anna Castaldo, Daniela Di Bella, Franco Taroni, Lorenzo Nanetti, Caterina Mariotti. Invest Ophthalmol Vis Sci 2016
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials.
Roberto Rodríguez-Labrada, Luis Velázquez-Pérez, Georg Auburger, Ulf Ziemann, Nalia Canales-Ochoa, Jacqueline Medrano-Montero, Yaimeé Vázquez-Mojena, Yanetza González-Zaldivar. Mov Disord 2016
25
50

Vestibulo-ocular arreflexia in families with spinocerebellar ataxia type 3 (Machado-Joseph disease).
C R Gordon, V Joffe, G Vainstein, N Gadoth. J Neurol Neurosurg Psychiatry 2003
34
50

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.
S Rivaud-Pechoux, A Dürr, B Gaymard, G Cancel, C J Ploner, Y Agid, A Brice, C Pierrot-Deseilligny. Ann Neurol 1998
61
50

Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias.
Pamela Federighi, Gabriele Cevenini, Maria T Dotti, Francesca Rosini, Elena Pretegiani, Antonio Federico, Alessandra Rufa. Brain 2011
40
50

Fast versus slow: different saccadic behavior in cerebellar ataxias.
Alessandra Rufa, Pamela Federighi. Ann N Y Acad Sci 2011
9
50

Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.
K Bürk, M Fetter, M Abele, F Laccone, A Brice, J Dichgans, T Klockgether. J Neurol 1999
106
50


Oculomotor phenotypes in autosomal dominant ataxias.
N Buttner, D Geschwind, J C Jen, S Perlman, S M Pulst, R W Baloh. Arch Neurol 1998
97
50

Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2.
Luis Velázquez-Pérez, Carola Seifried, Nieves Santos-Falcón, Michael Abele, Ulf Ziemann, Luis Enrique Almaguer, Edilberto Martínez-Góngora, Gilberto Sánchez-Cruz, Nalia Canales, Ruth Pérez-González,[...]. Ann Neurol 2004
65
50

The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease).
U Rüb, E R Brunt, K Gierga, C Schultz, H Paulson, R A I de Vos, H Braak. J Chem Neuroanat 2003
25
50

Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1.
W Klostermann, C Zühlke, W Heide, D Kömpf, K Wessel. J Neurol 1997
25
50

Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
Caterina Mariotti, Alfredo Brusco, Daniela Di Bella, Claudia Cagnoli, Marco Seri, Cinzia Gellera, Stefano Di Donato, Franco Taroni. Cerebellum 2008
37
50

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
T Matsuura, T Yamagata, D L Burgess, A Rasmussen, R P Grewal, K Watase, M Khajavi, A E McCall, C F Davis, L Zu,[...]. Nat Genet 2000
347
50

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.
A Rasmussen, T Matsuura, L Ruano, P Yescas, A Ochoa, T Ashizawa, E Alonso. Ann Neurol 2001
87
50

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.
Michael F Waters, Natali A Minassian, Giovanni Stevanin, Karla P Figueroa, John P A Bannister, Dagmar Nolte, Allan F Mock, Virgilio Gerald H Evidente, Dominic B Fee, Ulrich Müller,[...]. Nat Genet 2006
203
50

Spinocerebellar ataxia type 15.
R J McKinlay Gardner, Melanie A Knight, Kenju Hara, Shoji Tsuji, Susan M Forrest, Elsdon Storey. Cerebellum 2005
23
50

Spinocerebellar ataxia type 15.
Elsdon Storey, R J McKinlay Gardner. Handb Clin Neurol 2012
15
50

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, M Yamada, H Takahashi, S Tsuji. Hum Mol Genet 1999
278
50

Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
Keiko Hiramoto, Hideshi Kawakami, Kimiko Inoue, Takahiro Seki, Hirofumi Maruyama, Hiroyuki Morino, Masayasu Matsumoto, Kaoru Kurisu, Norio Sakai. Mov Disord 2006
27
50

Quantitative measurement of saccade amplitude, duration, and velocity.
R W Baloh, A W Sills, W E Kumley, V Honrubia. Neurology 1975
283
25

Dynamic properties of horizontal and vertical eye movements in parkinsonian syndromes.
K G Rottach, D E Riley, A O DiScenna, A Z Zivotofsky, R J Leigh. Ann Neurol 1996
127
25

Brainstem serotonergic neurons in chronic alcoholics with and without the memory impairment of Korsakoff's psychosis.
G Halliday, J Ellis, R Heard, D Caine, C Harper. J Neuropathol Exp Neurol 1993
61
25


The disturbance of gaze in progressive supranuclear palsy: implications for pathogenesis.
Athena L Chen, David E Riley, Susan A King, Anand C Joshi, Alessandro Serra, Ke Liao, Mark L Cohen, Jorge Otero-Millan, Susana Martinez-Conde, Michael Strupp,[...]. Front Neurol 2010
74
25


Eye movement abnormalities in stiff person syndrome.
John R Economides, Jonathan C Horton. Neurology 2005
28
25

The neuroanatomical basis of slow saccades in spinocerebellar ataxia type 2 (Wadia-subtype).
S Geiner, A K E Horn, N H Wadia, H Sakai, J A Büttner-Ennever. Prog Brain Res 2008
26
25

Mapping the oculomotor system.
Jean A Büttner-Ennever. Prog Brain Res 2008
22
25

Opsoclonus-myoclonus-ataxia syndrome with autoantibodies to glutamic acid decarboxylase.
Ioannis Markakis, Eleni Alexiou, Michael Xifaras, Georgios Gekas, Antonios Rombos. Clin Neurol Neurosurg 2008
41
25



Connections of cat omnipause neurons.
C R Kaneko, A F Fuchs. Brain Res 1982
34
25


Spread deficits in initiation, speed and accuracy of horizontal and vertical automatic saccades in dementia with lewy bodies.
Zoi Kapoula, Qing Yang, Marine Vernet, Benedicte Dieudonné, Sandrine Greffard, Marc Verny. Front Neurol 2010
12
25

Atypical Wernicke's encephalopathy showing involvement of substantia nigra.
Bhagheerathi Kalidass, Rajani Sunnathkal, Dr Vital Rangashamanna, Rajesh Paraswani. J Neuroimaging 2012
9
25

Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2.
L Velázquez-Pérez, C Seifried, M Abele, F Wirjatijasa, R Rodríguez-Labrada, N Santos-Falcón, G Sánchez-Cruz, L Almaguer-Mederos, R Tejeda, N Canales-Ochoa,[...]. Clin Neurophysiol 2009
54
25

Present concepts of oculomotor organization.
U Büttner, J A Büttner-Ennever. Prog Brain Res 2006
77
25



A rare saccade velocity profile in Stiff-Person Syndrome with cerebellar degeneration.
Ari Z Zivotofsky, Tali Siman-Tov, Natan Gadoth, Carlos R Gordon. Brain Res 2006
25
25



Multiple step pattern as a biomarker in Parkinson disease.
Tanya Blekher, Marjorie Weaver, Jason Rupp, William C Nichols, Siu L Hui, Jacqueline Gray, Robert D Yee, Joanne Wojcieszek, Tatiana Foroud. Parkinsonism Relat Disord 2009
37
25

Evolution of abnormal eye movements in Wernicke's encephalopathy: correlation with serial MRI findings.
Kitae Kim, Dong Hoon Shin, Yeong-Bae Lee, Kee-Hyung Park, Hyeon-Mi Park, Dong-Jin Shin, Ji-Soo Kim. J Neurol Sci 2012
15
25



Neuro-otological and neuropathological findings in two cases with Machado-Joseph disease.
T Murofushi, M Mizuno, T Hayashida, M Yamane, R Osanai, K Ito, K Kaga. Acta Otolaryngol Suppl 1995
10
25



Corticobasal degeneration.
Robert K Mahapatra, Mark J Edwards, Jonathan M Schott, Kailash P Bhatia. Lancet Neurol 2004
103
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.