A citation-based method for searching scientific literature

Riccardo Della Nave, Andrea Ginestroni, Carlo Tessa, Elena Salvatore, Domenico De Grandis, Rosaria Plasmati, Fabrizio Salvi, Giuseppe De Michele, Maria Teresa Dotti, Silvia Piacentini, Mario Mascalchi. Neuroimage 2008
Times Cited: 66







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



Times Cited
  Times     Co-cited
Similarity


Diffusion tensor imaging of spinocerebellar ataxias types 1 and 2.
M L Mandelli, T De Simone, L Minati, M G Bruzzone, C Mariotti, R Fancellu, M Savoiardo, M Grisoli. AJNR Am J Neuroradiol 2007
50
44

Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
T Klockgether, M Skalej, D Wedekind, A R Luft, D Welte, J B Schulz, M Abele, K Bürk, F Laccone, A Brice,[...]. Brain 1998
132
31

Brain structural damage in spinocerebellar ataxia type 2. A voxel-based morphometry study.
Riccardo Della Nave, Andrea Ginestroni, Carlo Tessa, Mirco Cosottini, Marco Giannelli, Elena Salvatore, Ferdinando Sartucci, Giuseppe De Michele, Maria Teresa Dotti, Silvia Piacentini,[...]. Mov Disord 2008
37
56

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
941
31

Atrophy pattern in SCA2 determined by voxel-based morphometry.
Christian Brenneis, Sylvia M Bösch, Michael Schocke, Gregor K Wenning, Werner Poewe. Neuroreport 2003
77
31

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, Tanja Schmitz-Hübsch, Maryla Rakowicz, Caterina Mariotti, Ludger Schöls, Dagmar Timmann, Bart van de Warrenburg, Alexandra Dürr,[...]. Neuroimage 2010
111
30

Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
L Guerrini, F Lolli, A Ginestroni, G Belli, R Della Nave, C Tessa, S Foresti, M Cosottini, S Piacentini, F Salvi,[...]. Brain 2004
78
27

Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data.
Stephen M Smith, Mark Jenkinson, Heidi Johansen-Berg, Daniel Rueckert, Thomas E Nichols, Clare E Mackay, Kate E Watkins, Olga Ciccarelli, M Zaheer Cader, Paul M Matthews,[...]. Neuroimage 2006
27

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
P Trouillas, T Takayanagi, M Hallett, R D Currier, S H Subramony, K Wessel, A Bryer, H C Diener, S Massaquoi, C M Gomez,[...]. J Neurol Sci 1997
890
27

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Kathrin Reetz, Ana S Costa, Shahram Mirzazade, Anna Lehmann, Agnes Juzek, Maria Rakowicz, Romana Boguslawska, Ludger Schöls, Christoph Linnemann, Caterina Mariotti,[...]. Brain 2013
86
25

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
108
24

Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry.
Riccardo Della Nave, Andrea Ginestroni, Carlo Tessa, Elena Salvatore, Ilaria Bartolomei, Fabrizio Salvi, Maria Teresa Dotti, Giuseppe De Michele, Silvia Piacentini, Mario Mascalchi. Neuroimage 2008
81
22

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
657
22

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
161
21

Pontine and cerebellar atrophy correlate with clinical disability in SCA2.
S H Ying, S I Choi, S L Perlman, R W Baloh, D S Zee, A W Toga. Neurology 2006
28
46

Advances in functional and structural MR image analysis and implementation as FSL.
Stephen M Smith, Mark Jenkinson, Mark W Woolrich, Christian F Beckmann, Timothy E J Behrens, Heidi Johansen-Berg, Peter R Bannister, Marilena De Luca, Ivana Drobnjak, David E Flitney,[...]. Neuroimage 2004
19

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
K Bürk, M Abele, M Fetter, J Dichgans, M Skalej, F Laccone, O Didierjean, A Brice, T Klockgether. Brain 1996
177
19

Gray matter volume deficits in spinocerebellar ataxia: an optimized voxel based morphometric study.
Gaurav Goel, Pramod Kumar Pal, Shivashankar Ravishankar, Ganesan Venkatasubramanian, Peruvumba N Jayakumar, Nithin Krishna, Meera Purushottam, Jitender Saini, Mohammed Faruq, Mitali Mukherji,[...]. Parkinsonism Relat Disord 2011
44
29

Brain structural damage in spinocerebellar ataxia type 1 : a VBM study.
Andrea Ginestroni, Riccardo Della Nave, Carlo Tessa, Marco Giannelli, Domenico De Grandis, Rosaria Plasmati, Fabrizio Salvi, Silvia Piacentini, Mario Mascalchi. J Neurol 2008
20
60

Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients.
Federico D'Agata, Paola Caroppo, Andrea Boghi, Mario Coriasco, Marcella Caglio, Bruno Baudino, Katiuscia Sacco, Franco Cauda, Elisabetta Geda, Mauro Bergui,[...]. Brain Struct Funct 2011
32
34

Progression of brain atrophy in spinocerebellar ataxia type 2: a longitudinal tensor-based morphometry study.
Mario Mascalchi, Stefano Diciotti, Marco Giannelli, Andrea Ginestroni, Andrea Soricelli, Emanuele Nicolai, Marco Aiello, Carlo Tessa, Lucia Galli, Maria Teresa Dotti,[...]. PLoS One 2014
31
35

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
878
15

Gray and white matter alterations in spinocerebellar ataxia type 7: an in vivo DTI and VBM study.
Sarael Alcauter, Fernando A Barrios, Rosalinda Díaz, Juan Fernández-Ruiz. Neuroimage 2011
50
20

Longitudinal study of cognitive and psychiatric functions in spinocerebellar ataxia types 1 and 2.
Roberto Fancellu, Dominga Paridi, Chiara Tomasello, Marta Panzeri, Anna Castaldo, Silvia Genitrini, Paola Soliveri, Floriano Girotti. J Neurol 2013
52
19


Voxel-based morphometry--the methods.
J Ashburner, K J Friston. Neuroimage 2000
13

Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.
Ina Klinke, Martina Minnerop, Tanja Schmitz-Hübsch, Marc Hendriks, Thomas Klockgether, Ullrich Wüllner, Christoph Helmstaedter. Cerebellum 2010
80
13

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.
A Dürr, D Smadja, G Cancel, A Lezin, G Stevanin, J Mikol, R Bellance, G G Buisson, H Chneiweiss, J Dellanave. Brain 1995
166
13

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.
Kathrin Reetz, Rebekka Lencer, Johannes M Hagenah, Christian Gaser, Vera Tadic, Uwe Walter, Alexander Wolters, Susanne Steinlechner, Christine Zühlke, Katja Brockmann,[...]. Cerebellum 2010
25
36

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
214
13

Progression of microstructural damage in spinocerebellar ataxia type 2: a longitudinal DTI study.
M Mascalchi, N Toschi, M Giannelli, A Ginestroni, R Della Nave, E Nicolai, A Bianchi, C Tessa, E Salvatore, M Aiello,[...]. AJNR Am J Neuroradiol 2015
21
42

The cerebellar cognitive affective syndrome.
J D Schmahmann, J C Sherman. Brain 1998
12

ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias.
Riccardo Della Nave, Silvia Foresti, Carlo Tessa, Marco Moretti, Andrea Ginestroni, Cinzia Gavazzi, Laura Guerrini, Fabrizio Salvi, Silvia Piacentini, Mario Mascalchi. Neuroimage 2004
38
21

Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: a voxel-based morphometry study.
Carsten Lukas, Ludger Schöls, Barbara Bellenberg, Udo Rüb, Horst Przuntek, Gebhard Schmid, Odo Köster, Boris Suchan. Neurosci Lett 2006
55
14


Acquisition and voxelwise analysis of multi-subject diffusion data with tract-based spatial statistics.
Stephen M Smith, Heidi Johansen-Berg, Mark Jenkinson, Daniel Rueckert, Thomas E Nichols, Karla L Miller, Matthew D Robson, Derek K Jones, Johannes C Klein, Andreas J Bartsch,[...]. Nat Protoc 2007
443
12

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.
K Bürk, C Globas, S Bösch, T Klockgether, C Zühlke, I Daum, J Dichgans. J Neurol 2003
131
12

Magnetic resonance and nuclear medicine imaging in ataxias.
Mario Mascalchi, Alessandra Vella. Handb Clin Neurol 2012
24
33

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
10

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
168
10


A voxel-based morphometric study of ageing in 465 normal adult human brains.
C D Good, I S Johnsrude, J Ashburner, R N Henson, K J Friston, R S Frackowiak. Neuroimage 2001
10

Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.
K Iwabuchi, K Tsuchiya, T Uchihara, S Yagishita. Rev Neurol (Paris) 1999
75
10


Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.
S Gilman, A A Sima, L Junck, K J Kluin, R A Koeppe, M E Lohman, R Little. Ann Neurol 1996
112
10


Supratentorial atrophy in spinocerebellar ataxia type 2: MRI study of 20 patients.
S Giuffrida, R Saponara, D A Restivo, A Trovato Salinaro, L Tomarchio, P Pugliares, G Fabbri, C Maccagnano. J Neurol 1999
45
15

Improved optimization for the robust and accurate linear registration and motion correction of brain images.
Mark Jenkinson, Peter Bannister, Michael Brady, Stephen Smith. Neuroimage 2002
10

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, H Przuntek, J T Epplen, O Riess. Ann Neurol 1997
243
10

A multimodal evaluation of microstructural white matter damage in spinocerebellar ataxia type 3.
Rachel P Guimarães, Anelyssa D'Abreu, Clarissa L Yasuda, Marcondes C França, Beatriz H B Silva, Fabio A M Cappabianco, Felipe P G Bergo, Iscia T Lopes-Cendes, Fernando Cendes. Mov Disord 2013
51
13


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.