A citation-based method for searching scientific literature

Stephen T Hansen, Pratap Meera, Thomas S Otis, Stefan M Pulst. Hum Mol Genet 2013
Times Cited: 104



Yi-Chung Lee, Alexandra Durr, Karen Majczenko, Yen-Hua Huang, Yu-Chao Liu, Cheng-Chang Lien, Pei-Chien Tsai, Yaeko Ichikawa, Jun Goto, Marie-Lorraine Monin, Jun Z Li, Ming-Yi Chung, Emeline Mundwiller, Vikram Shakkottai, Tze-Tze Liu, Christelle Tesson, Yi-Chun Lu, Alexis Brice, Shoji Tsuji, Margit Burmeister, Giovanni Stevanin, Bing-Wen Soong. Ann Neurol 2012
Times Cited: 98




List of shared articles



Times cited

Antisense Oligonucleotide Therapy Targeted Against ATXN3 Improves Potassium Channel-Mediated Purkinje Neuron Dysfunction in Spinocerebellar Ataxia Type 3.
David D Bushart, Annie J Zalon, Hongjiu Zhang, Logan M Morrison, Yuanfang Guan, Henry L Paulson, Vikram G Shakkottai, Hayley S McLoughlin. Cerebellum 2021
1

Consensus Paper: Strengths and Weaknesses of Animal Models of Spinocerebellar Ataxias and Their Clinical Implications.
Jan Cendelin, Marija Cvetanovic, Mandi Gandelman, Hirokazu Hirai, Harry T Orr, Stefan M Pulst, Michael Strupp, Filip Tichanek, Jan Tuma, Mario Manto. Cerebellum 2021
0

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

Ion channel dysfunction in cerebellar ataxia.
David D Bushart, Vikram G Shakkottai. Neurosci Lett 2019
19

Autosomal-dominant cerebellar ataxias.
Andrew Mundwiler, Vikram G Shakkottai. Handb Clin Neurol 2018
13

Targeting potassium channels to treat cerebellar ataxia.
David D Bushart, Ravi Chopra, Vikrant Singh, Geoffrey G Murphy, Heike Wulff, Vikram G Shakkottai. Ann Clin Transl Neurol 2018
28

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

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


Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner.
Anna Duarri, Meng-Chin A Lin, Michiel R Fokkens, Michel Meijer, Cleo J L M Smeets, Esther A R Nibbeling, Erik Boddeke, Richard J Sinke, Harm H Kampinga, Diane M Papazian,[...]. Cell Mol Life Sci 2015
19

Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.
A Matilla-Dueñas, T Ashizawa, A Brice, S Magri, K N McFarland, M Pandolfo, S M Pulst, O Riess, D C Rubinsztein, J Schmidt,[...]. Cerebellum 2014
75

Coexpression networks predict ataxia genes.
Stefan M Pulst, Lance T Pflieger. JAMA Neurol 2014
0