Cinzia Gellera

16.8k total citations · 1 hit paper
155 papers, 5.5k citations indexed

About

Cinzia Gellera is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Cinzia Gellera has authored 155 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Molecular Biology, 73 papers in Cellular and Molecular Neuroscience and 57 papers in Neurology. Recurrent topics in Cinzia Gellera's work include Genetic Neurodegenerative Diseases (64 papers), Mitochondrial Function and Pathology (52 papers) and Amyotrophic Lateral Sclerosis Research (29 papers). Cinzia Gellera is often cited by papers focused on Genetic Neurodegenerative Diseases (64 papers), Mitochondrial Function and Pathology (52 papers) and Amyotrophic Lateral Sclerosis Research (29 papers). Cinzia Gellera collaborates with scholars based in Italy, United States and United Kingdom. Cinzia Gellera's co-authors include Stefano DiDonato, Franco Taroni, Caterina Mariotti, Massimo Zeviani, Barbara Castellotti, Serenella Servidei, Enrico Bertini, Stefano Di Donato, Salvatore DiMauro and Vincenzo Silani and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Cinzia Gellera

155 papers receiving 5.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1989 483 citations Cinzia Gellera, Stefano DiDonato et al. profile →

Peers

Countries citing papers authored by Cinzia Gellera

Since Specialization

Citations

This map shows the geographic impact of Cinzia Gellera's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Cinzia Gellera with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cinzia Gellera more than expected).

Fields of papers citing papers by Cinzia Gellera

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cinzia Gellera. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Cinzia Gellera. The network helps show where Cinzia Gellera may publish in the future.

Co-authorship network of co-authors of Cinzia Gellera

This figure shows the co-authorship network connecting the top 25 collaborators of Cinzia Gellera. A scholar is included among the top collaborators of Cinzia Gellera based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Cinzia Gellera. Cinzia Gellera is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Severe epilepsy phenotypes in adults with succinic semialdehyde dehydrogenase deficiency: Novel clinical and therapeutic insights from an Italian multicenter retrospective cohort study 2025 ·Seizure ·Laura Canafoglia, Mario Mastrangelo, Marco Russo, Jacopo C. DiFrancesco, Andrea Stabile, Fabio Martino Doniselli, Roberta Di Giacomo, Giuseppe Didato, Silvia Esposito, Claudio Caccia, Francesco Pisani, Emilio Russo, Romana Rizzi, Cinzia Gellera, Barbara Castellotti	2
2	Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach 2024 ·Epilepsia Open ·Barbara Castellotti, Francesca Ragona, Elena Freri, (unknown), (unknown), (unknown), Roberta Solazzi, Silvana Franceschetti, Franco Taroni, Laura Canafoglia, Cinzia Gellera, Tiziana Granata, Jacopo C. DiFrancesco	2
3	A novel KCNC1 gain‐of‐function variant causing developmental and epileptic encephalopathy: “Precision medicine” approach with fluoxetine 2023 ·Epilepsia ·Paolo Ambrosino, Francesca Ragona, Ilaria Mosca, (unknown), Laura Canafoglia, Roberta Solazzi, Ilaria Rivolta, Elena Freri, Tiziana Granata, (unknown), Barbara Castellotti, Cinzia Gellera, Maria Virginia Soldovieri, Jacopo C. DiFrancesco, Maurizio Taglialatela	10
4	Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes 2023 ·Epilepsia Open ·Barbara Castellotti, Laura Canafoglia, Elena Freri, (unknown), (unknown), Stefania Magri, Jacopo C. DiFrancesco, Martina Fanella, Carlo Di Bonaventura, Alessandra Morano, Tiziana Granata, Cinzia Gellera, Silvana Franceschetti, Roberto Michelucci	6
5	MiR-146a in ALS: Contribution to Early Peripheral Nerve Degeneration and Relevance as Disease Biomarker 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Paola Cavalcante, Letizia Scandiffio, (unknown), Viviana Pensato, Cinzia Gellera, Nilo Riva, Angelo Quattrini, Eleonora Dalla Bella, Giuseppe Lauria, Renato Mantegazza, Silvia Bonanno, Stefania Marcuzzo	3
6	Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 Variants 2022 ·Neurology ·Eleonora Dalla Bella, Enrica Bersano, Maria Grazia Bruzzone, Cinzia Gellera, Viviana Pensato, Giuseppe Lauria, Monica Consonni	11
7	Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms 2020 ·Journal of Clinical Medicine ·Viviana Pensato, Stefania Magri, Eleonora Dalla Bella, Pierpaola Tannorella, Enrica Bersano, Gianni Sorarú, Marta Gatti, Nicola Ticozzi, Franco Taroni, Giuseppe Lauria, Caterina Mariotti, Cinzia Gellera	23
8	Teaching NeuroImages: Symmetrical abnormalities of the globi pallidi in succinic semialdehyde dehydrogenase deficiency 2020 ·Neurology ·Silvia Esposito, Marco Moscatelli, Claudio Caccia, (unknown), Chiara Pantaleoni, Anna Ardissone, Cinzia Gellera, Laura Farina	2
9	Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I 2020 ·Journal of Clinical Medicine ·Rosario Mosca, Diantha van de Vlekkert, Yvan Campos, (unknown), (unknown), (unknown), Emil Kakkis, Cynthia J. Tifft, Camilo Toro, (unknown), Cinzia Gellera, Laura Canafoglia, Gepke Visser, Ida Annunziata, Alessandra d’Azzo	15
10	Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 2020 ·Pharmacological Research ·Maria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, Ilaria Rivolta, Ilaria Mosca, Anna Binda, (unknown), Francesca Ragona, Laura Canafoglia, (unknown), Roberta Solazzi, Tiziana Granata, Barbara Castellotti, (unknown), Cinzia Gellera, Audrey Labalme, Gaëtan Lesca, Jacopo C. DiFrancesco, Maurizio Taglialatela	13
11	Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients 2020 ·Biomedicines ·Silvia Bonanno, Stefania Marcuzzo, (unknown), (unknown), Riccardo Masson, Riccardo Zanin, Maria Teresa Arnoldi, Francesca Andreetta, Ornella Simoncini, Anna Venerando, Cinzia Gellera, Chiara Pantaleoni, Renato Mantegazza, Pia Bernasconi, Giovanni Baranello, Lorenzo Maggi	38
12	Glutamine Synthetase 1 Increases Autophagy Lysosomal Degradation of Mutant Huntingtin Aggregates in Neurons, Ameliorating Motility in a Drosophila Model for Huntington’s Disease 2020 ·Cells ·(unknown), Chiara Paiardi, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), M. Gioria, Maria Enrica Pasini, Daniela Grifoni, Maria A. Vanoni, Cinzia Gellera, Franco Taroni, Paola Bellosta	20
13	Stance instability in preclinical SCA1 mutation carriers: A 4-year prospective posturography study 2017 ·Gait & Posture ·Lorenzo Nanetti, D. Alpini, Valentina Elisabetta Di Mattei, Anna Castaldo, (unknown), Greta Brenna, Cinzia Gellera, Caterina Mariotti	11
14	Granny trips down: is she carrying the big bad wolf? 2012 ·Neurological Sciences ·Lucio Tremolizzo, (unknown), Graziella Uziel, Barbara Castellotti, Cinzia Gellera, Carlo Ferrarese, Ildebrando Appollonio	2
15	Novel and recurrent spastin mutations in a large series of SPG4 Italian families 2012 ·Neuroscience Letters ·Lorenzo Nanetti, Silvia Baratta, Marta Panzeri, Chiara Tomasello, Carlo Lovati, Jacopo Azzollini, Cinzia Gellera, Daniela Di Bella, Franco Taroni, Caterina Mariotti	5
16	Paroxysmal exercise-induced dyskinesia with self-limiting partial epilepsy: A novel GLUT-1 mutation with benign phenotype 2011 ·Parkinsonism & Related Disorders ·Tommaso Bovi, Alfonso Fasano, (unknown), Cinzia Gellera, Barbara Castellotti, Elena Fontana, Michèle Tinazzi	12
17	A Simple Multiplex Real-Time PCR Methodology for the SMN1 Gene Copy Number Quantification 2009 ·Genetic Testing and Molecular Biomarkers ·(unknown), Federico Pozzo, (unknown), (unknown), Cinzia Gellera, Giuseppe Damante, Renata Lonigro	15
18	The gender effect in juvenile Huntington disease patients of Italian origin 2003 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Milena Cannella, Cinzia Gellera, Vittorio Maglione, Patrizia Giallonardo, Giuliana Cislaghi, M. Muglia, Aldo Quattrone, Francesco Pierelli, Stefano Di Donato, Ferdinando Squitieri	42
19	Autosomal dominant cerebellar ataxias: Genotype frequency and clinical/molecular correlations 1997 ·The Italian Journal of Neurological Sciences ·Davide Pareyson, Cinzia Gellera, Barbara Castellotti, (unknown), (unknown), (unknown), F. Girotti, Caterina Mariotti, Stefano DiDonato	1
20	Lethal carnitine palmitoyltransferase (CPT) II deficiency in newborns: A molecular-genetic study 1994 ·The American Journal of Human Genetics ·Franco Taroni, Cinzia Gellera, Patrizia Cavadini	19

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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