Sergio Cocozza

8.0k citations

101 papers · 3.3k indexed · 1 hit paper · h-index 30

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 2%
- Neurological diseases and metabolism
- Neurological disorders and treatments

Papers in ⓘ

Cellular and Molecular Neuroscience 37
- Genetic Neurodegenerative Diseases 34
- Hereditary Neurological Disorders 12
Molecular Biology 70
- Mitochondrial Function and Pathology 27
- Epigenetics and DNA Methylation 19
- RNA modifications and cancer 8
- DNA Repair Mechanisms 7
- Genomics and Chromatin Dynamics 7

Co-authors: Antonella Monticelli (51 shared papers)Alessandro Filla (22 shared papers)Giuseppe De Michele (20 shared papers)Francesca Cavalcanti (11 shared papers)Luigi Pianese (13 shared papers)G Campanella (6 shared papers)Giorgio Casari (3 shared papers)Maurizio De Fusco (2 shared papers)
Journals: PLoS ONE (7 papers)Scientific Reports (5 papers)Nucleic Acids Research (5 papers)Journal of Neurology (4 papers)Neurology (4 papers)
Partner nations: Italy United States United Kingdom

In The Last Decade

Sergio Cocozza

99 papers receiving 3.2k citations

Hit Papers

align trajectories log scale

Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease 1998 · 586 citations

Peers

Countries citing papers authored by Sergio Cocozza

Since Specialization

Citations

This map shows the geographic impact of Sergio Cocozza'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 Sergio Cocozza with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sergio Cocozza more than expected).

Fields of papers citing papers by Sergio Cocozza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sergio Cocozza. 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 Sergio Cocozza. The network helps show where Sergio Cocozza may publish in the future.

Co-authors

The 25 scholars most cited alongside Sergio Cocozza, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sergio Cocozza Line = papers co-authored together Sergio Cocozza links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 101 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease Cell ·Giorgio Casari, Maurizio De Fusco, Sonia Ciarmatori, Massimo Zeviani, Marina Mora, Patricio Fernández‐Silva, Giuseppe De Michele, Alessandro Filla, Sergio Cocozza, R. Marconi, A. Dürr, Bertrand Fontaine, Andrea Ballabio Hit paper breakdown →	1998	586
2	The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia. PubMed ·Alessandro Filla, Giuseppe De Michele, Francesca Cavalcanti, Luigi Pianese, Antonella Monticelli, G Campanella, Sergio Cocozza	1996	389
3	Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder Scientific Reports ·Lorena Coretti, Claudia Cristiano, Ermanno Florio, Giovanni Scala, Adriano Lama, Simona Keller, Mariella Cuomo, Roberto Russo, Raffaela Pero, Orlando Paciello, Giuseppina Mattace Raso, Rosaria Meli, Sergio Cocozza, Antonio Calignano, Lorenzo Chiariotti, Francesca Lembo	2017	140
4	Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARγ pathway as a therapeutic target in Friedreich’s ataxia Human Molecular Genetics ·Giovanni Coppola, Daniele Marmolino, Daning Lu, Qing Wang, Miriam Cnop, Myriam Rai, Fabio Acquaviva, Sergio Cocozza, Massimo Pandolfo, Daniel H. Geschwind	2009	100
5	A New Locus for Autosomal Recessive Hereditary Spastic Paraplegia Maps to Chromosome 16q24.3 The American Journal of Human Genetics ·Giuseppe De Michele, Maurizio De Fusco, Francesca Cavalcanti, Alessandro Filla, R. Marconi, Giampiero Volpe, Antonella Monticelli, Andrea Ballabio, Giorgio Casari, Sergio Cocozza	1998	93
6	Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients Annals of Neurology ·Irene De Biase, Astrid Rasmussen, Dan Endres, Sahar Al‐Mahdawi, Antonella Monticelli, Sergio Cocozza, Mark A. Pook, Sanjay I. Bidichandani	2007	92
7	Genome-wide mapping of 8-oxo-7,8-dihydro-2′-deoxyguanosine reveals accumulation of oxidatively-generated damage at DNA replication origins within transcribed long genes of mammalian cells Nucleic Acids Research ·Stefano Amente, Giacomo Di Palo, Giovanni Scala, Tiziana Castrignanò, Francesca Gorini, Sergio Cocozza, Angela Moresano, Piero Pucci, Bin Ma, Irina Stepanov, Luigi Lania, Pier Giuseppe Pelicci, Gaetano Ivan Dellino, Barbara Majello	2018	92
8	Early‐onset ataxia with cardiomyopathy and retained tendon reflexes maps to the friedreich's ataxia locus on chromosome 9q Annals of Neurology ·Francesc Palau, Giuseppe De Michele, Juan J. Vílchez, Massimo Pandolfo, Eugègnia Monrós, Sergio Cocozza, Patricia Smeyers, José Lopez‐Arlandis, G Campanella, Stefano Di Donato, Alessandro Filla	1995	68
9	Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life Genomics ·Irene De Biase, Astrid Rasmussen, Antonella Monticelli, Sahar Al‐Mahdawi, Mark A. Pook, Sergio Cocozza, Sanjay I. Bidichandani	2007	66
10	Nucleotide distance influences co-methylation between nearby CpG sites Genomics ·Ornella Affinito, Domenico Palumbo, Annalisa Fierro, Mariella Cuomo, Giulia De Riso, Antonella Monticelli, Gennaro Miele, Lorenzo Chiariotti, Sergio Cocozza	2019	56
11	Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2 Journal of Cell Science ·Fabio Acquaviva, Irene De Biase, Luigi Nezi, Giuseppina Ruggiero, Fabiana Tatangelo, Carmela Pisano, Antonella Monticelli, Corrado Garbi, Angela M. Acquaviva, Sergio Cocozza	2005	56
12	The complete structure of the rat thyroglobulin gene. Proceedings of the National Academy of Sciences ·Anna Maria Musti, E V Avvedimento, Claudio Polistina, Valeria M. Ursini, Silvana Obici, Lucio Nitsch, Sergio Cocozza, Roberto Di Lauro	1986	56
13	DiGeorge anomaly associated with 10p deletion American Journal of Medical Genetics ·Giuseppe Monaco, Claudio Pignata, Elena Rossi, Ornella Mascellaro, Sergio Cocozza, F Ciccimarra	1991	51
14	The genomic landscape of 8-oxodG reveals enrichment at specific inherently fragile promoters Nucleic Acids Research ·Francesca Gorini, Giovanni Scala, Giacomo Di Palo, Gaetano Ivan Dellino, Sergio Cocozza, Pier Giuseppe Pelicci, Luigi Lania, Barbara Majello, Stefano Amente	2020	51
15	Recombinant Human Erythropoietin Increases Frataxin Protein Expression Without Increasing mRNA Expression The Cerebellum ·Fabio Acquaviva, Imma Castaldo, Alessandro Filla, Manuela Giacchetti, Daniele Marmolino, Antonella Monticelli, Michele Pinelli, Francesco Saccà, Sergio Cocozza	2008	50
16	Relative Frequencies of CAG Expansions in Spinocerebellar Ataxia and Dentatorubropallidoluysian Atrophy in 116 Italian Families European Neurology ·Alessandro Filla, Caterina Mariotti, Giuseppe Caruso, Giovanni Coppola, Sergio Cocozza, Imma Castaldo, Olga Calabrese, Elena Salvatore, Giuseppe De Michele, M. C. Riggio, Davide Pareyson, Cinzia Gellera, Stefano Di Donato	2000	49
17	Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families Journal of Neurology ·Alessandro Filla, Giuseppe De Michele, Lucio Santoro, Olga Calabrese, Imma Castaldo, Salvatore Giuffrida, Domenico A. Restivo, Luigi Serlenga, D. F. Condorelli, Ubaldo Bonuccelli, Raffaele Scala, Giovanni Coppola, Giuseppe Caruso, Sergio Cocozza	1999	48
18	A Combined Nucleic Acid and Protein Analysis in Friedreich Ataxia: Implications for Diagnosis, Pathogenesis and Clinical Trial Design PLoS ONE ·Francesco Saccà, Giorgia Puorro, Antonella Antenora, Angela Marsili, Alessandra Denaro, Raffaele Piro, Pierpaolo Sorrentino, Chiara Pane, Alessandra Tessa, Vincenzo Brescia Morra, Sergio Cocozza, Giuseppe De Michele, Filippo M. Santorelli, Alessandro Filla	2011	47
19	NIDDM Associated With Mutation in Tyrosine Kinase Domain of Insulin Receptor Gene Diabetes ·Sergio Cocozza, Antonio Porcellini, Gabriele Riccardi, Antonella Monticelli, Gianluigi Condorelli, Assiamira Ferrara, Luigi Pianese, Claudia Miele, Brunella Capaldo, Francesco Bèguinot, S Varrone	1992	46
20	Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients Journal of the Neurological Sciences ·A. Perretti, Lucio Santoro, Bernardo Lanzillo, Alessandro Filla, Giovanna De Michele, F Barbieri, Gianvito Martino, M. Ragno, Sergio Cocozza, Giuseppe Caruso	1996	44

About Sergio Cocozza

Sergio Cocozza is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Biochemistry and Neurology, having authored 101 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (34 papers), Mitochondrial Function and Pathology (27 papers), Epigenetics and DNA Methylation (19 papers), Hereditary Neurological Disorders (12 papers), Endoplasmic Reticulum Stress and Disease (11 papers), RNA modifications and cancer (8 papers), DNA Repair Mechanisms (7 papers) and Genomics and Chromatin Dynamics (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.7k citations), Neurology (351 citations), Molecular Biology (2.4k citations), Neurology (526 citations) and Clinical Biochemistry (209 citations). Sergio Cocozza has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Antonella Monticelli, Alessandro Filla, Giuseppe De Michele, Francesca Cavalcanti, Luigi Pianese, G Campanella, Giorgio Casari, Maurizio De Fusco, R. Marconi and Andrea Ballabio. Their work appears in journals such as PLoS ONE, Scientific Reports, Nucleic Acids Research, Journal of Neurology and Neurology.

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