A citation-based method for searching scientific literature

Anne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray-Pedersen, Michael Abdelnoor, Chantal M E Tallaksen. Brain 2009
Times Cited: 127







List of co-cited articles
867 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
291
25


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
71
29

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
Giovanni Stevanin, Hamid Azzedine, Paola Denora, Amir Boukhris, Meriem Tazir, Alexander Lossos, Alberto Luis Rosa, Israela Lerer, Abdelmadjid Hamri, Paulo Alegria,[...]. Brain 2008
151
18

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
Giovanni Stevanin, Filippo M Santorelli, Hamid Azzedine, Paula Coutinho, Jacques Chomilier, Paola S Denora, Elodie Martin, Anne-Marie Ouvrard-Hernandez, Alessandra Tessa, Naïma Bouslam,[...]. Nat Genet 2007
225
17


Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
Josef Finsterer, Wolfgang Löscher, Stefan Quasthoff, Julia Wanschitz, Michaela Auer-Grumbach, Giovanni Stevanin. J Neurol Sci 2012
183
15

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity.
A Boukhris, G Stevanin, I Feki, P Denora, N Elleuch, M I Miladi, C Goizet, J Truchetto, S Belal, A Brice,[...]. Clin Genet 2009
39
35

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms.
Sara Salinas, Christos Proukakis, Andrew Crosby, Thomas T Warner. Lancet Neurol 2008
352
14

Hereditary ataxias and spastic paraplegias: methodological aspects of a prevalence study in Portugal.
M C Silva, P Coutinho, C D Pinheiro, J M Neves, P Serrano. J Clin Epidemiol 1997
62
20

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Gaia Novarino, Ali G Fenstermaker, Maha S Zaki, Matan Hofree, Jennifer L Silhavy, Andrew D Heiberg, Mostafa Abdellateef, Basak Rosti, Eric Scott, Lobna Mansour,[...]. Science 2014
340
13

Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.
Viviana Pensato, Barbara Castellotti, Cinzia Gellera, Davide Pareyson, Claudia Ciano, Lorenzo Nanetti, Ettore Salsano, Giuseppe Piscosquito, Elisa Sarto, Marica Eoli,[...]. Brain 2014
97
13

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
671
12

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
B P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, H Scheffer, E R Brunt, P F Ippel, J A Maat-Kievit, D Dooijes, N C Notermans, D Lindhout,[...]. Neurology 2002
161
12


The prevalence of hereditary spastic paraplegia and the occurrence of SPG4 mutations in Estonia.
Mark Braschinsky, Siiri-Merike Luus, Katrin Gross-Paju, Sulev Haldre. Neuroepidemiology 2009
23
52

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, Martha A Nance, Perry C Gaskell, Jeffery M Vance, Allison E Ashley-Koch, Margaret A Pericak-Vance. Am J Hum Genet 2006
163
12


The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland.
P McMonagle, S Webb, M Hutchinson. J Neurol Neurosurg Psychiatry 2002
48
25

CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
Cyril Goizet, Amir Boukhris, Alexandra Durr, Christian Beetz, Jeremy Truchetto, Christelle Tesson, Maria Tsaousidou, Sylvie Forlani, Lucie Guyant-Maréchal, Bertrand Fontaine,[...]. Brain 2009
78
14

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.
Christian Beetz, Rebecca Schüle, Tine Deconinck, Khanh-Nhat Tran-Viet, Hui Zhu, Berry P H Kremer, Suzanna G M Frints, Wendy A G van Zelst-Stams, Paula Byrne, Susanne Otto,[...]. Brain 2008
129
11

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.
C Goizet, A Boukhris, D Maltete, L Guyant-Maréchal, J Truchetto, E Mundwiller, S Hanein, P Jonveaux, F Roelens, J Loureiro,[...]. Neurology 2009
58
18

Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.
Sylvain Hanein, Elodie Martin, Amir Boukhris, Paula Byrne, Cyril Goizet, Abdelmadjid Hamri, Ali Benomar, Alexander Lossos, Paola Denora, José Fernandez,[...]. Am J Hum Genet 2008
139
11

The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity.
R Schüle, T Holland-Letz, S Klimpe, J Kassubek, T Klopstock, V Mall, S Otto, B Winner, L Schöls. Neurology 2006
154
11

Autosomal dominant spastic paraplegias: a review of 89 families resulting from a portuguese survey.
José Leal Loureiro, Eva Brandão, Luis Ruano, Ana F Brandão, Ana M Lopes, Carolina Thieleke-Matos, Leonor Miller-Fleming, Vitor T Cruz, Mafalda Barbosa, Isabel Silveira,[...]. JAMA Neurol 2013
40
27

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy.
A Filla, G De Michele, R Marconi, L Bucci, C Carillo, A E Castellano, L Iorio, C Kniahynicki, F Rossi, G Campanella. J Neurol 1992
79
12

Cellular pathways of hereditary spastic paraplegia.
Craig Blackstone. Annu Rev Neurosci 2012
193
10

Hereditary spastic paraplegias: membrane traffic and the motor pathway.
Craig Blackstone, Cahir J O'Kane, Evan Reid. Nat Rev Neurosci 2011
207
10

Hereditary spastic paraplegias.
A E Harding. Semin Neurol 1993
125
10

Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
Maria K Tsaousidou, Karim Ouahchi, Tom T Warner, Yi Yang, Michael A Simpson, Nigel G Laing, Philip A Wilkinson, Ricardo E Madrid, Heema Patel, Faycal Hentati,[...]. Am J Hum Genet 2008
120
9



Sporadic ataxias in Japan--a population-based epidemiological study.
Shoji Tsuji, Osamu Onodera, Jun Goto, Masatoyo Nishizawa. Cerebellum 2008
91
9

A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia.
Alessia Arnoldi, Alessandra Tonelli, Francesca Crippa, Gaetano Villani, Consiglia Pacelli, Manuela Sironi, Uberto Pozzoli, Maria Grazia D'Angelo, Giovanni Meola, Andrea Martinuzzi,[...]. Hum Mutat 2008
69
13

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).
Katherine J Dick, Matthias Eckhardt, Coro Paisán-Ruiz, Aisha Alkhayat Alshehhi, Christos Proukakis, Naomi A Sibtain, Helena Maier, Reza Sharifi, Michael A Patton, Wafa Bashir,[...]. Hum Mutat 2010
134
9

Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature.
Rami Abou Jamra, Orianne Philippe, Annick Raas-Rothschild, Sebastian H Eck, Elisabeth Graf, Rebecca Buchert, Guntram Borck, Arif Ekici, Felix F Brockschmidt, Markus M Nöthen,[...]. Am J Hum Genet 2011
142
9

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy.
Stephan Klebe, Christel Depienne, Sylvie Gerber, Georges Challe, Mathieu Anheim, Perrine Charles, Estelle Fedirko, Elodie Lejeune, Julien Cottineau, Alfredo Brusco,[...]. Brain 2012
112
9

Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms.
Temistocle Lo Giudice, Federica Lombardi, Filippo Maria Santorelli, Toshitaka Kawarai, Antonio Orlacchio. Exp Neurol 2014
202
9

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
999
8

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
126
8

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia.
Christel Depienne, Estelle Fedirko, Sylvie Forlani, Cécile Cazeneuve, Pascale Ribaï, Imed Feki, Chantal Tallaksen, Karine Nguyen, Bruno Stankoff, Merle Ruberg,[...]. J Med Genet 2007
87
9

Prevalence of hereditary ataxias and paraplegias in the province of Torino, Italy.
F Brignolio, M Leone, A Tribolo, M G Rosso, P Meineri, D Schiffer. Ital J Neurol Sci 1986
29
27

Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
R Sridharan, K Radhakrishnan, P P Ashok, M E Mousa. Brain 1985
37
21

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years.
M Namekawa, P Ribai, I Nelson, S Forlani, F Fellmann, C Goizet, C Depienne, G Stevanin, M Ruberg, A Dürr,[...]. Neurology 2006
82
9

Neuropathy target esterase gene mutations cause motor neuron disease.
Shirley Rainier, Melanie Bui, Erin Mark, Donald Thomas, Debra Tokarz, Lei Ming, Colin Delaney, Rudy J Richardson, James W Albers, Nori Matsunami,[...]. Am J Hum Genet 2008
158
8

Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy.
Annemieke J M H Verkerk, Rachel Schot, Belinda Dumee, Karlijn Schellekens, Sigrid Swagemakers, Aida M Bertoli-Avella, Maarten H Lequin, Jeroen Dudink, Paul Govaert, A L van Zwol,[...]. Am J Hum Genet 2009
106
8

Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.
Cyril Goizet, Amir Boukhris, Emeline Mundwiller, Chantal Tallaksen, Sylvie Forlani, Annick Toutain, Nathalie Carriere, Véronique Paquis, Christel Depienne, Alexandra Durr,[...]. Hum Mutat 2009
91
8

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.
Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, Janel O Johnson, Camilo Toro, Katherine V Bricceno, Carlo Rinaldi, Katherine G Meilleur, Modibo Sangaré, Oumarou Diallo,[...]. Hum Mutat 2013
58
13


Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
Eleanna Kara, Arianna Tucci, Claudia Manzoni, David S Lynch, Marilena Elpidorou, Conceicao Bettencourt, Viorica Chelban, Andreea Manole, Sherifa A Hamed, Nourelhoda A Haridy,[...]. Brain 2016
108
8


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.