A citation-based method for searching scientific literature

I K Svenson, A E Ashley-Koch, P C Gaskell, T J Riney, W J Cumming, H M Kingston, E L Hogan, R M Boustany, J M Vance, M A Nance, M A Pericak-Vance, D A Marchuk. Am J Hum Genet 2001
Times Cited: 104







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



Times Cited
  Times     Co-cited
Similarity


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
460
62

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
N Fonknechten, D Mavel, P Byrne, C S Davoine, C Cruaud, D Bönsch, D Samson, P Coutinho, M Hutchinson, P McMonagle,[...]. Hum Mol Genet 2000
217
53


Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis.
J C Lindsey, M E Lusher, C J McDermott, K D White, E Reid, D C Rubinsztein, R Bashir, J Hazan, P J Shaw, K M Bushby. J Med Genet 2000
103
37

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
S Sauter, B Miterski, S Klimpe, D Bönsch, L Schöls, A Visbeck, T Papke, H C Hopf, W Engel, T Deufel,[...]. Hum Mutat 2002
81
37

Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.
Inge A Meijer, Collette K Hand, P Cossette, Denise A Figlewicz, Guy A Rouleau. Arch Neurol 2002
61
40

Hereditary spastic paraplegia caused by mutations in the SPG4 gene.
J Bürger, N Fonknechten, M Hoeltzenbein, L Neumann, E Bratanoff, J Hazan, A Reis. Eur J Hum Genet 2000
61
39

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.
X Zhao, D Alvarado, S Rainier, R Lemons, P Hedera, C H Weber, T Tukel, M Apak, T Heiman-Patterson, L Ming,[...]. Nat Genet 2001
248
24

Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing.
Katia J Evans, Edgar R Gomes, Steven M Reisenweber, Gregg G Gundersen, Brett P Lauring. J Cell Biol 2005
153
24


Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus.
Pamela Claudiani, Elena Riano, Alessia Errico, Gennaro Andolfi, Elena I Rugarli. Exp Cell Res 2005
78
26

Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.
A Hentati, H X Deng, H Zhai, W Chen, Y Yang, W Y Hung, A C Azim, S Bohlega, R Tandan, C Warner,[...]. Neurology 2000
50
40

Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus.
Delphine Charvin, Carmen Cifuentes-Diaz, Nuria Fonknechten, Vandana Joshi, Jamilé Hazan, Judith Melki, Sandrine Betuing. Hum Mol Genet 2003
63
30

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
Evan Reid, Mark Kloos, Allison Ashley-Koch, Lori Hughes, Simon Bevan, Ingrid K Svenson, Felicia Lennon Graham, Perry C Gaskell, Andrew Dearlove, Margaret A Pericak-Vance,[...]. Am J Hum Genet 2002
356
18

Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon.
Alessia Errico, Pamela Claudiani, Marilena D'Addio, Elena I Rugarli. Hum Mol Genet 2004
96
18

Hereditary spastic paraparesis: a review of new developments.
C McDermott, K White, K Bushby, P Shaw. J Neurol Neurosurg Psychiatry 2000
180
17

A second leaky splice-site mutation in the spastin gene.
I K Svenson, A E Ashley-Koch, M A Pericak-Vance, D A Marchuk. Am J Hum Genet 2001
27
62

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.
Christopher J McDermott, Andrew J Grierson, Jonathan D Wood, Megan Bingley, Stephen B Wharton, Katharine M D Bushby, Pamela J Shaw. Ann Neurol 2003
83
20

The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.
Nick Trotta, Genny Orso, Maria Giovanna Rossetto, Andrea Daga, Kendal Broadie. Curr Biol 2004
182
17

The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.
Evan Reid, James Connell, Thomas L Edwards, Simon Duley, Stephanie E Brown, Christopher M Sanderson. Hum Mol Genet 2005
142
17

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia.
C Beetz, A O H Nygren, J Schickel, M Auer-Grumbach, K Bürk, G Heide, J Kassubek, S Klimpe, T Klopstock, F Kreuz,[...]. Neurology 2006
106
16

Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing.
Susan Roehl White, Katia J Evans, Jeffrey Lary, James L Cole, Brett Lauring. J Cell Biol 2007
110
15

Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia.
Moneef Shoukier, Juergen Neesen, Simone M Sauter, Loukas Argyriou, Nadine Doerwald, D V Krishna Pantakani, Ashraf U Mannan. Eur J Hum Genet 2009
58
25

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
84
16

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
J K Fink, T Heiman-Patterson, T Bird, F Cambi, M P Dubé, D A Figlewicz, J K Fink, J L Haines, T Heiman-Patterson, A Hentati,[...]. Neurology 1996
167
13


The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.
Stephen B Wharton, Christopher J McDermott, Andrew J Grierson, Jonathan D Wood, Catherine Gelsthorpe, Paul G Ince, Pamela J Shaw. J Neuropathol Exp Neurol 2003
69
18

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
Ingrid K Svenson, Mark T Kloos, P Craig Gaskell, Martha A Nance, James Y Garbern, Shin-ichi Hisanaga, Margaret A Pericak-Vance, Allison E Ashley-Koch, Douglas A Marchuk. Neurogenetics 2004
61
21

Clinical features of hereditary spastic paraplegia due to spastin mutation.
C J McDermott, C E Burness, J Kirby, L E Cox, D G Rao, C Hewamadduma, B Sharrack, M Hadjivassiliou, P F Chinnery, A Dalton,[...]. Neurology 2006
84
15



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
79
15

Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation.
F M Santorelli, C Patrono, D Fortini, A Tessa, G Comanducci, E Bertini, A Pierallini, G A Amabile, C Casali. Neurology 2000
36
30

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia.
Francesca D Ciccarelli, Christos Proukakis, Heema Patel, Harold Cross, Shakil Azam, Michael A Patton, Peer Bork, Andrew H Crosby. Genomics 2003
110
11

The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo.
Jonathan D Wood, Jennifer A Landers, Megan Bingley, Christopher J McDermott, Vickie Thomas-McArthur, Lisa J Gleadall, Pamela J Shaw, Vincent T Cunliffe. Hum Mol Genet 2006
103
11


Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegia.
Joanna M Solowska, James Y Garbern, Peter W Baas. Hum Mol Genet 2010
38
28

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
599
10

Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations.
P McMonagle, P C Byrne, B Fitzgerald, S Webb, N A Parfrey, M Hutchinson. Neurology 2000
33
30

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.
Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, Costa Georgopoulos, Debbie Ang, Marit Nyholm Nielsen, Claire-Sophie Davoine, Alexis Brice, Bertrand Fontaine, Niels Gregersen,[...]. Am J Hum Genet 2002
242
10

The AAA team: related ATPases with diverse functions.
S Patel, M Latterich. Trends Cell Biol 1998
419
10

Identification of nuclear localisation sequences in spastin (SPG4) using a novel Tetra-GFP reporter system.
Christian Beetz, Michael Brodhun, Konstantin Moutzouris, Michael Kiehntopf, Alexander Berndt, Dirk Lehnert, Thomas Deufel, Martin Bastmeyer, Jörg Schickel. Biochem Biophys Res Commun 2004
39
25

Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function.
Nina Tang Sherwood, Qi Sun, Mingshan Xue, Bing Zhang, Kai Zinn. PLoS Biol 2004
186
10

Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases.
C Depienne, C Tallaksen, J Y Lephay, B Bricka, S Poea-Guyon, B Fontaine, P Labauge, A Brice, A Durr. J Med Genet 2006
68
14

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners.
Christopher M Sanderson, James W Connell, Thomas L Edwards, Nicholas A Bright, Simon Duley, Amanda Thompson, J Paul Luzio, Evan Reid. Hum Mol Genet 2006
115
10

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
123
10

X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.
M Jouet, A Rosenthal, G Armstrong, J MacFarlane, R Stevenson, J Paterson, A Metzenberg, V Ionasescu, K Temple, S Kenwrick. Nat Genet 1994
332
9

Recent advances in hereditary spastic paraplegia.
C M Tallaksen, A Dürr, A Brice. Curr Opin Neurol 2001
63
14

Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegia.
Clarice Patrono, Carlo Casali, Alessandra Tessa, Federica Cricchi, Daniela Fortini, Rosalba Carrozzo, Gabriele Siciliano, Enrico Bertini, Filippo M Santorelli. J Neurol 2002
18
50

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.
Heema Patel, Harold Cross, Christos Proukakis, Ruth Hershberger, Peer Bork, Francesca D Ciccarelli, Michael A Patton, Victor A McKusick, Andrew H Crosby. Nat Genet 2002
174
9


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.