A citation-based method for searching scientific literature

Sara Salinas, Christos Proukakis, Andrew Crosby, Thomas T Warner. Lancet Neurol 2008
Times Cited: 357







List of co-cited articles
538 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
301
24

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
207
21

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
186
21

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
133
17

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
113
17

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.
Samuel Shribman, Evan Reid, Andrew H Crosby, Henry Houlden, Thomas T Warner. Lancet Neurol 2019
80
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
345
15

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

Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.
Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, Gabriel Novaes de Rezende Batistella, Thiago Bortholin, Acary Souza Bulle Oliveira. Cerebellum 2017
114
13

Clinical and genetic study of hereditary spastic paraplegia in Canada.
Nicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, Anna Szuto, Shiyi Chen, Anil Venkitachalam, Jean-Denis Brisson, Jodi Warman-Chardon, Sohnee Ahmed, Setareh Ashtiani,[...]. Neurol Genet 2016
55
23


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
160
11


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
227
10

Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin.
Genny Orso, Diana Pendin, Song Liu, Jessica Tosetto, Tyler J Moss, Joseph E Faust, Massimo Micaroni, Anastasia Egorova, Andrea Martinuzzi, James A McNew,[...]. Nature 2009
322
10

Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China.
En-Lin Dong, Chong Wang, Shuang Wu, Ying-Qian Lu, Xiao-Hong Lin, Hui-Zhen Su, Miao Zhao, Jin He, Li-Xiang Ma, Ning Wang,[...]. Mol Neurodegener 2018
48
20

Hereditary spastic paraplegia.
Craig Blackstone. Handb Clin Neurol 2018
70
14



Hereditary spastic paraparesis: a review of new developments.
C McDermott, K White, K Bushby, P Shaw. J Neurol Neurosurg Psychiatry 2000
183
9

The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
G C Deluca, G C Ebers, M M Esiri. Neuropathol Appl Neurobiol 2004
131
8

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
J Hazan, N Fonknechten, D Mavel, C Paternotte, D Samson, F Artiguenave, C S Davoine, C Cruaud, A Dürr, P Wincker,[...]. Nat Genet 1999
466
8

Cellular pathways of hereditary spastic paraplegia.
Craig Blackstone. Annu Rev Neurosci 2012
197
8

Hereditary spastic paraplegias: membrane traffic and the motor pathway.
Craig Blackstone, Cahir J O'Kane, Evan Reid. Nat Rev Neurosci 2011
208
8

Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons.
Steven Havlicek, Zacharias Kohl, Himanshu K Mishra, Iryna Prots, Esther Eberhardt, Naime Denguir, Holger Wend, Sonja Plötz, Leah Boyer, Maria C N Marchetto,[...]. Hum Mol Genet 2014
78
10

Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia.
Marie Coutelier, Cyril Goizet, Alexandra Durr, Florence Habarou, Sara Morais, Alexandre Dionne-Laporte, Feifei Tao, Juliette Konop, Marion Stoll, Perrine Charles,[...]. Brain 2015
55
12


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
99
7

Functional effects of botulinum toxin type-A treatment and subsequent stretching of spastic calf muscles: a study in patients with hereditary spastic paraplegia.
Mark de Niet, Susanne T de Bot, Bart P C van de Warrenburg, Vivian Weerdesteyn, Alexander C Geurts. J Rehabil Med 2015
14
50

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
7

Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegia.
Kyle R Denton, Ling Lei, Jeremy Grenier, Vladimir Rodionov, Craig Blackstone, Xue-Jun Li. Stem Cells 2014
87
8

Hereditary spastic paraplegia: More than an upper motor neuron disease.
L Parodi, S Fenu, G Stevanin, A Durr. Rev Neurol (Paris) 2017
43
16

A class of dynamin-like GTPases involved in the generation of the tubular ER network.
Junjie Hu, Yoko Shibata, Peng-Peng Zhu, Christiane Voss, Neggy Rismanchi, William A Prinz, Tom A Rapoport, Craig Blackstone. Cell 2009
380
7

The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genes.
Lorena Travaglini, Chiara Aiello, Fabrizia Stregapede, Adele D'Amico, Viola Alesi, Andrea Ciolfi, Alessandro Bruselles, Michela Catteruccia, Simone Pizzi, Ginevra Zanni,[...]. Neurogenetics 2018
26
26

Quantitative and functional analyses of spastin in the nervous system: implications for hereditary spastic paraplegia.
Joanna M Solowska, Gerardo Morfini, Aditi Falnikar, B Timothy Himes, Scott T Brady, Dongyang Huang, Peter W Baas. J Neurosci 2008
85
7

Hereditary spastic paraplegia.
John K Fink. Curr Neurol Neurosci Rep 2006
193
6

Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A.
Peng-Peng Zhu, Kyle R Denton, Tyler Mark Pierson, Xue-Jun Li, Craig Blackstone. Hum Mol Genet 2014
42
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
6

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
G Casari, M De Fusco, S Ciarmatori, M Zeviani, M Mora, P Fernandez, G De Michele, A Filla, S Cocozza, R Marconi,[...]. Cell 1998
608
6

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
41
14

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
6


A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.
Anne Tarrade, Coralie Fassier, Sabrina Courageot, Delphine Charvin, Jérémie Vitte, Leticia Peris, Alain Thorel, Etienne Mouisel, Nuria Fonknechten, Natacha Roblot,[...]. Hum Mol Genet 2006
134
6

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.
Paul R Kasher, Kurt J De Vos, Stephen B Wharton, Catherine Manser, Ellen J Bennett, Megan Bingley, Jonathan D Wood, Roy Milner, Christopher J McDermott, Christopher C J Miller,[...]. J Neurochem 2009
103
6

Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial.
Ludger Schöls, Tim W Rattay, Peter Martus, Christoph Meisner, Jonathan Baets, Imma Fischer, Christine Jägle, Matthew J Fraidakis, Andrea Martinuzzi, Jonas Alex Saute,[...]. Brain 2017
54
11

Atlastin GTPases are required for Golgi apparatus and ER morphogenesis.
Neggy Rismanchi, Cynthia Soderblom, Julia Stadler, Peng-Peng Zhu, Craig Blackstone. Hum Mol Genet 2008
143
6


Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.
Felipe Franco da Graça, Thiago Junqueira Ribeiro de Rezende, Luiz Felipe Rocha Vasconcellos, José Luiz Pedroso, Orlando Graziani P Barsottini, Marcondes C França. Front Neurol 2019
34
17


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.