A citation-based method for searching scientific literature

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



Francois-Dominique Jacob, Eugenia S Ho, Mayra Martinez-Ojeda, Basil T Darras, Omar S Khwaja. J Child Neurol 2013
Times Cited: 27




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

Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report.
Tomoko Mizuno, Ayako Kashimada, Toshihiro Nomura, Kengo Moriyama, Haruna Yokoyama, Setsuko Hasegawa, Masatoshi Takagi, Shuki Mizutani. Brain Dev 2019
8

Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral Neuropathy.
Carlotta Spagnoli, Daniele Frattini, Fabrizio Gozzi, Susanna Rizzi, Grazia Gabriella Salerno, Luca Cimino, Carlo Fusco. Cerebellum 2021
0

A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.
Mohammad A Al-Muhaizea, Faten AlMutairi, Rawan Almass, Safinaz AlHarthi, Mazhor S Aldosary, Maysoon Alsagob, Ali AlOdaib, Dilek Colak, Namik Kaya. Cerebellum 2018
11