A citation-based method for searching scientific literature

O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
Times Cited: 978



K Nakamura, S Y Jeong, T Uchihara, M Anno, K Nagashima, T Nagashima, S Ikeda, S Tsuji, I Kanazawa. Hum Mol Genet 2001
Times Cited: 382




List of shared articles



Times cited

Targeting Expanded Repeats by Small Molecules in Repeat Expansion Disorders.
Masayuki Nakamori, Hideki Mochizuki. Mov Disord 2021
0

Zebrafish Models of Autosomal Dominant Ataxias.
Ana Quelle-Regaldie, Daniel Sobrido-Cameán, Antón Barreiro-Iglesias, María Jesús Sobrido, Laura Sánchez. Cells 2021
1

Conventional MRI findings in hereditary degenerative ataxias: a pictorial review.
Sirio Cocozza, Giuseppe Pontillo, Giovanna De Michele, Martina Di Stasi, Elvira Guerriero, Teresa Perillo, Chiara Pane, Anna De Rosa, Lorenzo Ugga, Arturo Brunetti. Neuroradiology 2021
0

An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics.
Sanjog R Chintalaphani, Sandy S Pineda, Ira W Deveson, Kishore R Kumar. Acta Neuropathol Commun 2021
0

Receptor protein tyrosine phosphatases control Purkinje neuron firing.
Alexander S Brown, Pratap Meera, Gabe Quinones, Jessica Magri, Thomas S Otis, Stefan M Pulst, Anthony E Oro. Cell Cycle 2020
0

Pathogenic mechanisms underlying spinocerebellar ataxia type 1.
Leon Tejwani, Janghoo Lim. Cell Mol Life Sci 2020
0

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
31

Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias.
Katherine J Robinson, Maxinne Watchon, Angela S Laird. Front Neurosci 2020
1

Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias.
Ronald A M Buijsen, Lodewijk J A Toonen, Sarah L Gardiner, Willeke M C van Roon-Mom. Neurotherapeutics 2019
32

Repeat variations in polyglutamine disease-associated genes and cognitive function in old age.
Sarah L Gardiner, Stella Trompet, Behnam Sabayan, Merel W Boogaard, J Wouter Jukema, P Eline Slagboom, Raymund A C Roos, Jeroen van der Grond, N Ahmad Aziz. Neurobiol Aging 2019
1


Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease.
Sarah L Gardiner, Aster V E Harder, Yvonne J M Campman, Stella Trompet, Jacobijn Gussekloo, Martine J van Belzen, Merel W Boogaard, Raymund A C Roos, Iris E Jansen, Yolande A L Pijnenburg,[...]. Neurobiol Aging 2019
5


From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
Maria Pennuto, Carlo Rinaldi. Mol Cell Endocrinol 2018
8

Polyglutamine expansion diseases: More than simple repeats.
Alexandra Silva, Ana Viana de Almeida, Sandra Macedo-Ribeiro. J Struct Biol 2018
12


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

Discovery of Therapeutic Approaches for Polyglutamine Diseases: A Summary of Recent Efforts.
Sofia Esteves, Sara Duarte-Silva, Patrícia Maciel. Med Res Rev 2017
11


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
24