A citation-based method for searching scientific literature

Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali, Liana Veneziano, Tiziana Sacco, Enrica Boda, Alessandro Brussino, Florian Bonn, Barbara Castellotti, Silvia Baratta, Caterina Mariotti, Cinzia Gellera, Valentina Fracasso, Stefania Magri, Thomas Langer, Paolo Plevani, Stefano Di Donato, Marco Muzi-Falconi, Franco Taroni. Nat Genet 2010
Times Cited: 208



Claudia Cagnoli, Giovanni Stevanin, Alessandro Brussino, Marco Barberis, Cecilia Mancini, Russell L Margolis, Susan E Holmes, Marcello Nobili, Sylvie Forlani, Sergio Padovan, Patrizia Pappi, Cécile Zaros, Isabelle Leber, Pascale Ribai, Luisa Pugliese, Corrado Assalto, Alexis Brice, Nicola Migone, Alexandra Dürr, Alfredo Brusco. Hum Mutat 2010
Times Cited: 58




List of shared articles



Times cited

Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia.
Han-Lin Chiang, Jong-Ling Fuh, Yu-Shuen Tsai, Bing-Wen Soong, Yi-Chu Liao, Yi-Chung Lee. J Neurol Sci 2021
0


Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy.
Majida Charif, Arnaud Chevrollier, Naïg Gueguen, Céline Bris, David Goudenège, Valérie Desquiret-Dumas, Stéphanie Leruez, Estelle Colin, Audrey Meunier, Catherine Vignal,[...]. Neurol Genet 2020
13

Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias.
Katherine J Robinson, Maxinne Watchon, Angela S Laird. Front Neurosci 2020
2

Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity.
Cecilia Mancini, Eriola Hoxha, Luisa Iommarini, Alessandro Brussino, Uwe Richter, Francesca Montarolo, Claudia Cagnoli, Roberta Parolisi, Diana Iulia Gondor Morosini, Valentina Nicolò,[...]. Neurobiol Dis 2019
12

Mitochondrial stress response triggered by defects in protein synthesis quality control.
Uwe Richter, Kah Ying Ng, Fumi Suomi, Paula Marttinen, Taina Turunen, Christopher Jackson, Anu Suomalainen, Helena Vihinen, Eija Jokitalo, Tuula A Nyman,[...]. Life Sci Alliance 2019
15

Clinical Characteristics and Possible Drug Targets in Autosomal Dominant Spinocerebellar Ataxias.
Laszlo Szpisjak, Denes Zadori, Peter Klivenyi, Laszlo Vecsei. CNS Neurol Disord Drug Targets 2019
3

Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation.
Susanna Tulli, Andrea Del Bondio, Valentina Baderna, Davide Mazza, Franca Codazzi, Tyler Mark Pierson, Alessandro Ambrosi, Dagmar Nolte, Cyril Goizet, Camilo Toro,[...]. J Med Genet 2019
10

Astrocyte-specific deletion of the mitochondrial m-AAA protease reveals glial contribution to neurodegeneration.
Sara Murru, Simon Hess, Esther Barth, Eva R Almajan, Désirée Schatton, Steffen Hermans, Susanne Brodesser, Thomas Langer, Peter Kloppenburg, Elena I Rugarli. Glia 2019
15

Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2.
Sinem Tunc, Marija Dulovic-Mahlow, Hauke Baumann, Magdalena Khira Baaske, Magdalena Jahn, Johanna Junker, Alexander Münchau, Norbert Brüggemann, Katja Lohmann. Cerebellum 2019
6

Upregulation of Peroxiredoxin 3 Protects Afg3l2-KO Cortical Neurons In Vitro from Oxidative Stress: A Paradigm for Neuronal Cell Survival under Neurodegenerative Conditions.
Barbara Bettegazzi, Ilaria Pelizzoni, Floramarida Salerno Scarzella, Lisa Michelle Restelli, Daniele Zacchetti, Francesca Maltecca, Giorgio Casari, Fabio Grohovaz, Franca Codazzi. Oxid Med Cell Longev 2019
1

Spinocerebellar ataxias.
Bing-Wen Soong, Patrick J Morrison. Handb Clin Neurol 2018
29

Dissecting Substrate Specificities of the Mitochondrial AFG3L2 Protease.
Bojian Ding, Dwight W Martin, Anthony J Rampello, Steven E Glynn. Biochemistry 2018
7

Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation.
Stefania Magri, Valentina Fracasso, Massimo Plumari, Enrico Alfei, Daniele Ghezzi, Cinzia Gellera, Paola Rusmini, Angelo Poletti, Daniela Di Bella, Antonio E Elia,[...]. Hum Mutat 2018
17

AAA Proteases: Guardians of Mitochondrial Function and Homeostasis.
Magdalena Opalińska, Hanna Jańska. Cells 2018
14

SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy.
Kirsten Svenstrup, Troels Tolstrup Nielsen, Frederik Aidt, Nina Rostgaard, Morten Duno, Flemming Wibrand, Tua Vinther-Jensen, Ian Law, John Vissing, Peter Roos,[...]. Cerebellum 2017
11

Multifunctional Mitochondrial AAA Proteases.
Steven E Glynn. Front Mol Biosci 2017
30

Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation.
Laszlo Szpisjak, Viola L Nemeth, Noemi Szepfalusi, Denes Zadori, Zoltan Maroti, Tibor Kalmar, Laszlo Vecsei, Peter Klivenyi. Cerebellum 2017
5

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
Esther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, Michiel R Fokkens, Juha M Karjalainen, Cleo J L M Smeets, Jelkje J de Boer-Bergsma, Gerben van der Vries, Dennis Dooijes, Giovana B Bampi,[...]. Brain 2017
55

Non-syndromic isolated dominant optic atrophy caused by the p.R468C mutation in the AFG3 like matrix AAA peptidase subunit 2 gene.
Davide Colavito, Veronica Maritan, Agnese Suppiej, Elda Del Giudice, Monica Mazzarolo, Stefania Miotto, Sofia Farina, Maurizio Dalle Carbonare, Stefano Piermarocchi, Alberta Leon. Biomed Rep 2017
11

Mitochondrial Proteases as Emerging Pharmacological Targets.
Lara Gibellini, Sara De Biasi, Milena Nasi, Anna Iannone, Andrea Cossarizza, Marcello Pinti. Curr Pharm Des 2016
11

Mitochondrial Quality Control Proteases in Neuronal Welfare.
Roman M Levytskyy, Edward M Germany, Oleh Khalimonchuk. J Neuroimmune Pharmacol 2016
20

MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 Diseases.
Letterio Salvatore Politi, Stefania Bianchi Marzoli, Claudia Godi, Marta Panzeri, Paola Ciasca, Gianluca Brugnara, Anna Castaldo, Daniela Di Bella, Franco Taroni, Lorenzo Nanetti,[...]. Invest Ophthalmol Vis Sci 2016
4