A citation-based method for searching scientific literature

Bing-Wen Soong, Patrick J Morrison. Handb Clin Neurol 2018
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinho. Neuroepidemiology 2014
243
35

Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
907
21

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
14

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
14



Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
207
14

Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.
Tetsuo Ashizawa, Karla P Figueroa, Susan L Perlman, Christopher M Gomez, George R Wilmot, Jeremy D Schmahmann, Sarah H Ying, Theresa A Zesiewicz, Henry L Paulson, Vikram G Shakkottai,[...]. Orphanet J Rare Dis 2013
71
10

The spinocerebellar ataxias.
Henry L Paulson. J Neuroophthalmol 2009
107
10

Spinocerebellar ataxia.
Thomas Klockgether, Caterina Mariotti, Henry L Paulson. Nat Rev Dis Primers 2019
112
10

Spinocerebellar ataxias: prospects and challenges for therapy development.
Tetsuo Ashizawa, Gülin Öz, Henry L Paulson. Nat Rev Neurol 2018
70
10


Recessive ataxias.
Matthis Synofzik, Andrea H Németh. Handb Clin Neurol 2018
34
10

Polyglutamine spinocerebellar ataxias - from genes to potential treatments.
Henry L Paulson, Vikram G Shakkottai, H Brent Clark, Harry T Orr. Nat Rev Neurosci 2017
128
10

The cerebellar cognitive affective syndrome.
J D Schmahmann, J C Sherman. Brain 1998
10

Hereditary ataxias: overview.
Suman Jayadev, Thomas D Bird. Genet Med 2013
119
10

Neuroradiological Findings in the Spinocerebellar Ataxias.
Alex Tiburtino Meira, Walter Oleschko Arruda, Sergio Eiji Ono, Arnolfo de Carvalho Neto, Salmo Raskin, Carlos Henrique F Camargo, Hélio Afonso G Teive. Tremor Other Hyperkinet Mov (N Y) 2019
11
27

Spinocerebellar ataxias: an update.
Bing-wen Soong, Henry L Paulson. Curr Opin Neurol 2007
91
7

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles,[...]. Neurology 2008
167
7

The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family.
Chin-Song Lu, Hsiu-Chen Chang, Pei-Chi Kuo, Yu-Lun Liu, Wen-Shiang Wu, Yi-Hsin Weng, Tzu-Chen Yen, Yah-Huei Wu Chou. Parkinsonism Relat Disord 2004
36
7

Comparison of cerebellar ataxias: A three-year prospective longitudinal assessment.
Yi-chung Lee, Yi-chu Liao, Po-shan Wang, I-Hui Lee, Kon-ping Lin, Bing-wen Soong. Mov Disord 2011
41
7

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Anna Sulek, Alexandra Durr, Perrine Charles,[...]. Lancet Neurol 2013
105
7

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
Hirofumi Maruyama, Yuishin Izumi, Hiroyuki Morino, Masaya Oda, Hiromasa Toji, Shigenobu Nakamura, Hideshi Kawakami. Am J Med Genet 2002
70
7


The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.
H Jacobi, P Bauer, P Giunti, R Labrum, M G Sweeney, P Charles, A Dürr, C Marelli, C Globas, C Linnemann,[...]. Neurology 2011
120
7

A longitudinal investigation into cognition and disease progression in spinocerebellar ataxia types 1, 2, 3, 6, and 7.
Amy Moriarty, Arron Cook, Helen Hunt, Matthew E Adams, Lisa Cipolotti, Paola Giunti. Orphanet J Rare Dis 2016
33
7

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
Arndt Rolfs, Arnulf H Koeppen, Ingrid Bauer, Peter Bauer, Sven Buhlmann, Helge Topka, Ludger Schöls, Olaf Riess. Ann Neurol 2003
151
7

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael H Parkinson, Alexandra Durr, Alexis Brice, Perrine Charles,[...]. Lancet Neurol 2015
108
7

Mini-review: spinocerebellar ataxias: an update of SCA genes.
Alexis Trott, Lucien J Houenou. Recent Pat DNA Gene Seq 2012
13
15

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
7

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner.
Anna Duarri, Meng-Chin A Lin, Michiel R Fokkens, Michel Meijer, Cleo J L M Smeets, Esther A R Nibbeling, Erik Boddeke, Richard J Sinke, Harm H Kampinga, Diane M Papazian,[...]. Cell Mol Life Sci 2015
19
10


Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxia.
Conceição Bettencourt, Mina Ryten, Paola Forabosco, Stephanie Schorge, Joshua Hersheson, John Hardy, Henry Houlden. JAMA Neurol 2014
39
7

Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features.
Matthis Synofzik, Christian Beetz, Claudia Bauer, Michael Bonin, Elena Sanchez-Ferrero, Tanja Schmitz-Hübsch, Ullrich Wüllner, Thomas Nägele, Olaf Riess, Ludger Schöls,[...]. J Med Genet 2011
36
7

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients.
Rebecca Schüle, Sarah Wiethoff, Peter Martus, Kathrin N Karle, Susanne Otto, Stephan Klebe, Sven Klimpe, Constanze Gallenmüller, Delia Kurzwelly, Dorothea Henkel,[...]. Ann Neurol 2016
100
7

Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study.
Paula Coutinho, Luis Ruano, José L Loureiro, Vitor T Cruz, José Barros, Assunção Tuna, Clara Barbot, João Guimarães, Isabel Alonso, Isabel Silveira,[...]. JAMA Neurol 2013
66
7

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.
E Sánchez-Ferrero, E Coto, C Beetz, J Gámez, A I Corao, M Díaz, J Esteban, E del Castillo, G Moris, J Infante,[...]. Clin Genet 2013
63
7

Spinocerebellar ataxia: an update.
Roisin Sullivan, Wai Yan Yau, Emer O'Connor, Henry Houlden. J Neurol 2019
48
7


Cerebellar ataxia: abnormal control of interaction torques across multiple joints.
A J Bastian, T A Martin, J G Keating, W T Thach. J Neurophysiol 1996
345
7

Cerebellar control of balance and locomotion.
Susanne M Morton, Amy J Bastian. Neuroscientist 2004
237
7

Cerebellum and procedural learning: evidence from focal cerebellar lesions.
M Molinari, M G Leggio, A Solida, R Ciorra, S Misciagna, M C Silveri, L Petrosini. Brain 1997
228
7


Scales for the clinical evaluation of cerebellar disorders.
Katrin Bürk, Deborah A Sival. Handb Clin Neurol 2018
10
20

Non-invasive cerebellar stimulation--a consensus paper.
G Grimaldi, G P Argyropoulos, A Boehringer, P Celnik, M J Edwards, R Ferrucci, J M Galea, S J Groiss, K Hiraoka, P Kassavetis,[...]. Cerebellum 2014
144
7

The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin.
M C Moreira, C Barbot, N Tachi, N Kozuka, E Uchida, T Gibson, P Mendonça, M Costa, J Barros, T Yanagisawa,[...]. Nat Genet 2001
313
7

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.
Maria-Céu Moreira, Sandra Klur, Mitsunori Watanabe, Andrea H Németh, Isabelle Le Ber, José-Carlos Moniz, Christine Tranchant, Patrick Aubourg, Meriem Tazir, Lüdger Schöls,[...]. Nat Genet 2004
326
7

Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: a genotype-phenotype study.
Mijke M M Verhagen, James I Last, Frans B L Hogervorst, Dominique F C M Smeets, Nel Roeleveld, Frans Verheijen, Coriene E Catsman-Berrevoets, Nico M Wulffraat, Jan M Cobben, Johan Hiel,[...]. Hum Mutat 2012
88
7

Autosomal dominant cerebellar ataxias: Imaging biomarkers with high effect sizes.
Isaac M Adanyeguh, Vincent Perlbarg, Pierre-Gilles Henry, Daisy Rinaldi, Elodie Petit, Romain Valabregue, Alexis Brice, Alexandra Durr, Fanny Mochel. Neuroimage Clin 2018
37
7

Diffusion tensor imaging of spinocerebellar ataxia type 12.
Haitao Li, Jingjing Ma, Xiaoning Zhang. Med Sci Monit 2014
9
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.