A citation-based method for searching scientific literature

Dong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, Xiao-Jian Tan, Laura Bylenok, David Nochlin, Mark Matsushita, Hillary Lipe, John Wolff, Magali Fernandez, P J Cimino, Thomas D Bird, Wendy H Raskind. Am J Hum Genet 2003
Times Cited: 175



S E Holmes, E E O'Hearn, M G McInnis, D A Gorelick-Feldman, J J Kleiderlein, C Callahan, N G Kwak, R G Ingersoll-Ashworth, M Sherr, A J Sumner, A H Sharp, U Ananth, W K Seltzer, M A Boss, A M Vieria-Saecker, J T Epplen, O Riess, C A Ross, R L Margolis. Nat Genet 1999
Times Cited: 318




List of shared articles



Times cited

Cerebellar Development and Circuit Maturation: A Common Framework for Spinocerebellar Ataxias.
Francesca Binda, Carla Pernaci, Smita Saxena. Front Neurosci 2020
2

Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias.
Katherine J Robinson, Maxinne Watchon, Angela S Laird. Front Neurosci 2020
2


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

Spinocerebellar ataxias.
Bing-Wen Soong, Patrick J Morrison. Handb Clin Neurol 2018
28

Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
Esther A R Nibbeling, Cathérine C S Delnooz, Tom J de Koning, Richard J Sinke, Hyder A Jinnah, Marina A J Tijssen, Dineke S Verbeek. Neurosci Biobehav Rev 2017
26

A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
Marie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, Juliette Konop, Claire-Sophie Davoine, Christelle Tesson, Rémi Valter, Mathieu Anheim, Anthony Behin, Giovanni Castelnovo,[...]. Brain 2017
56


Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.
Emma Perkins, Daumante Suminaite, Mandy Jackson. J Physiol 2016
18

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.
Connie Marras, Anthony Lang, Bart P van de Warrenburg, Carolyn M Sue, Sarah J Tabrizi, Lars Bertram, Saadet Mercimek-Mahmutoglu, Darius Ebrahimi-Fakhari, Thomas T Warner, Alexandra Durr,[...]. Mov Disord 2016
123

Genetic cerebellar ataxias.
Elsdon Storey. Semin Neurol 2014
28

Epidemiology and population genetics of degenerative ataxias.
Jorge Sequeiros, Sandra Martins, Isabel Silveira. Handb Clin Neurol 2012
36

Spinocerebellar ataxia type 5.
Katherine A Dick, Yoshio Ikeda, John W Day, Laura P W Ranum. Handb Clin Neurol 2012
20

Spinocerebellar ataxia 13 and 25.
Giovanni Stevanin, Alexandra Dürr. Handb Clin Neurol 2012
8

Spinocerebellar degenerations.
Susan L Perlman. Handb Clin Neurol 2011
10

Autosomal dominant cerebellar ataxias.
C Marelli, C Cazeneuve, A Brice, G Stevanin, A Dürr. Rev Neurol (Paris) 2011
7

Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
Nathaniel Robb Whaley, Shinsuke Fujioka, Zbigniew K Wszolek. Orphanet J Rare Dis 2011
33

Genetics of the dominant ataxias.
Dineke S Verbeek, Bart P C van de Warrenburg. Semin Neurol 2011
21

Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias.
Antoni Matilla-Dueñas, Ivelisse Sánchez, Marc Corral-Juan, Antoni Dávalos, Ramiro Alvarez, Pilar Latorre. Cerebellum 2010
62

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling.
Stephanie Schorge, Joyce van de Leemput, Andrew Singleton, Henry Houlden, John Hardy. Trends Neurosci 2010
61


SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
Mohammed Faruq, Vinod Scaria, Inder Singh, Shivani Tyagi, Achal K Srivastava, Mitali Mukerji. Hum Mutat 2009
20

Genetics and pathogenesis of inherited ataxias and spastic paraplegias.
Carmen Espinós, Francesc Palau. Adv Exp Med Biol 2009
6

Therapeutic prospects for spinocerebellar ataxia type 2 and 3.
Ilya Bezprozvanny, Thomas Klockgether. Drugs Future 2009
13