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: 1248







List of shared articles



Times cited

Rare CACNA1A mutations leading to congenital ataxia.
Mercè Izquierdo-Serra, José M Fernández-Fernández, Mercedes Serrano. Pflugers Arch 2020
3

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

Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA).
Francesca Prestori, Francesco Moccia, Egidio D'Angelo. Int J Mol Sci 2019
5

m-AAA proteases, mitochondrial calcium homeostasis and neurodegeneration.
Maria Patron, Hans-Georg Sprenger, Thomas Langer. Cell Res 2018
41

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