A citation-based method for searching scientific literature

Raphael Hourez, Laurent Servais, David Orduz, David Gall, Isabelle Millard, Alban de Kerchove d'Exaerde, Guy Cheron, Harry T Orr, Massimo Pandolfo, Serge N Schiffmann. J Neurosci 2011
Times Cited: 86



Emma M Perkins, Yvonne L Clarkson, Nancy Sabatier, David M Longhurst, Christopher P Millward, Jennifer Jack, Junko Toraiwa, Mitsunori Watanabe, Jeffrey D Rothstein, Alastair R Lyndon, David J A Wyllie, Mayank B Dutia, Mandy Jackson. J Neurosci 2010
Times Cited: 83




List of shared articles



Times cited


MTSS1/Src family kinase dysregulation underlies multiple inherited ataxias.
Alexander S Brown, Pratap Meera, Banu Altindag, Ravi Chopra, Emma M Perkins, Sharan Paul, Daniel R Scoles, Eric Tarapore, Jessica Magri, Haoran Huang,[...]. Proc Natl Acad Sci U S A 2018
8


Mechanisms underlying synaptic vulnerability and degeneration in neurodegenerative disease.
T H Gillingwater, T M Wishart. Neuropathol Appl Neurobiol 2013
47

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

Precision medicine in spinocerebellar ataxias: treatment based on common mechanisms of disease.
David D Bushart, Geoffrey G Murphy, Vikram G Shakkottai. Ann Transl Med 2016
15

IP3 receptor mutations and brain diseases in human and rodents.
Chihiro Hisatsune, Katsuhiko Mikoshiba. J Neurochem 2017
28

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

Cellular and circuit mechanisms underlying spinocerebellar ataxias.
Pratap Meera, Stefan M Pulst, Thomas S Otis. J Physiol 2016
33


Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2.
James M Dell'Orco, Stefan M Pulst, Vikram G Shakkottai. Hum Mol Genet 2017
27