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



Joyce van de Leemput, Jayanth Chandran, Melanie A Knight, Lynne A Holtzclaw, Sonja Scholz, Mark R Cookson, Henry Houlden, Katrina Gwinn-Hardy, Hon-Chung Fung, Xian Lin, Dena Hernandez, Javier Simon-Sanchez, Nick W Wood, Paola Giunti, Ian Rafferty, John Hardy, Elsdon Storey, R J McKinlay Gardner, Susan M Forrest, Elizabeth M C Fisher, James T Russell, Huaibin Cai, Andrew B Singleton. PLoS Genet 2007
Times Cited: 180




List of shared articles



Times cited

Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.
Giacomo Garone, Alessandro Capuano, Lorena Travaglini, Federica Graziola, Fabrizia Stregapede, Ginevra Zanni, Federico Vigevano, Enrico Bertini, Francesco Nicita. Int J Mol Sci 2020
8

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

Ion channel dysfunction in cerebellar ataxia.
David D Bushart, Vikram G Shakkottai. Neurosci Lett 2019
16

Spinocerebellar ataxia: an update.
Roisin Sullivan, Wai Yan Yau, Emer O'Connor, Henry Houlden. J Neurol 2019
33

Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA).
Francesca Prestori, Francesco Moccia, Egidio D'Angelo. Int J Mol Sci 2019
4





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

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
19

Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias.
Renu Kumari, Deepak Kumar, Samir K Brahmachari, Achal K Srivastava, Mohammed Faruq, Mitali Mukerji. J Genet 2018
0

Keeping Our Calcium in Balance to Maintain Our Balance.
Melanie D Mark, Jan Claudius Schwitalla, Michelle Groemmke, Stefan Herlitze. Biochem Biophys Res Commun 2017
17

Cellular defects by deletion of ANO10 are due to deregulated local calcium signaling.
Podchanart Wanitchakool, Jiraporn Ousingsawat, Lalida Sirianant, Inês Cabrita, Diana Faria, Rainer Schreiber, Karl Kunzelmann. Cell Signal 2017
24

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