A citation-based method for searching scientific literature

Emma Perkins, Daumante Suminaite, Mandy Jackson. J Physiol 2016
Times Cited: 18



Yvonne L Clarkson, Emma M Perkins, Callum J Cairncross, Alastair R Lyndon, Paul A Skehel, Mandy Jackson. Hum Mol Genet 2014
Times Cited: 18




List of shared articles



Times cited

Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia.
Francesco Nicita, Marta Nardella, Emanuele Bellacchio, Paolo Alfieri, Gaetano Terrone, Giorgia Piccini, Federica Graziola, Claudio Pignata, Alessandro Capuano, Enrico Bertini,[...]. Clin Genet 2019
14

Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia.
Andrea Accogli, Judith St-Onge, Nassima Addour-Boudrahem, Joël Lafond-Lapalme, Alexandre Dionne Laporte, Guy A Rouleau, Jean-Baptiste Rivière, Myriam Srour. J Child Neurol 2020
5

Critical roles of αII spectrin in brain development and epileptic encephalopathy.
Yu Wang, Tuo Ji, Andrew D Nelson, Katarzyna Glanowska, Geoffrey G Murphy, Paul M Jenkins, Jack M Parent. J Clin Invest 2018
32