Fabio Acquaviva

1.1k total citations
25 papers, 842 citations indexed

About

Fabio Acquaviva is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Fabio Acquaviva has authored 25 papers receiving a total of 842 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 7 papers in Genetics. Recurrent topics in Fabio Acquaviva's work include Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Fabio Acquaviva is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Fabio Acquaviva collaborates with scholars based in Italy, Belgium and United States. Fabio Acquaviva's co-authors include Daniele Marmolino, Antonella Monticelli, Sergio Cocozza, Massimo Pandolfo, Michele Pinelli, Imma Castaldo, Alessandro Filla, Paola Vergara, Mariateresa Falco and Mario Manto and has published in prestigious journals such as PLoS ONE, Journal of Cell Science and Human Molecular Genetics.

In The Last Decade

Fabio Acquaviva

24 papers receiving 801 citations

Peers

Countries citing papers authored by Fabio Acquaviva

Since Specialization

Citations

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

Fields of papers citing papers by Fabio Acquaviva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabio Acquaviva

This figure shows the co-authorship network connecting the top 25 collaborators of Fabio Acquaviva. A scholar is included among the top collaborators of Fabio Acquaviva 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 Fabio Acquaviva. Fabio Acquaviva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 2023 ·Frontiers in Cell and Developmental Biology ·Laura Pignata, (unknown), Fabio Acquaviva, (unknown), (unknown), (unknown), Orazio Palumbo, Pietro Palumbo, Massimo Carella, Angela Sparago, Daniele De Brasi, Flavia Cerrato, Andrea Riccio	2
2	Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum 2022 ·Genes ·(unknown), Laura Pignata, Giuseppina Vitiello, Viola Alesi, Gemma D’Elia, (unknown), Fabio Acquaviva, Daniele De Brasi, Antonio Novelli, Andrea Riccio, Achille Iolascon, Flavia Cerrato	2
3	SNORD116 deletions cause Prader‐Willi syndrome with a mild phenotype and macrocephaly 2017 ·Clinical Genetics ·Paolo Fontana, Marina Grasso, Fabio Acquaviva, Elena Di Gennaro, (unknown), Mariateresa Falco, (unknown), Gioacchino Scarano, Fortunato Lonardo	34
4	<em>RAI1</em> gene mutations: mechanisms of Smith–Magenis Syndrome 2017 ·The Application of Clinical Genetics ·Mariateresa Falco, Sonia Amabile, Fabio Acquaviva	36
5	First evidence of Smith–Magenis syndrome in mother and daughter due to a novel RAI mutation 2016 ·American Journal of Medical Genetics Part A ·Fabio Acquaviva, Maria Elena Sana, Matteo Della Monica, Michele Pinelli, Diana Postorivo, Paolo Fontana, Mariateresa Falco, Anna Maria Nardone, Fortunato Lonardo, Maria Iascone, Gioacchino Scarano	26
6	Phenotypic Screening for Friedreich Ataxia Using Random shRNA Selection 2015 ·SLAS DISCOVERY ·M. Grazia Cotticelli, Fabio Acquaviva, Shujuan J. Xia, (unknown), Yongping Wang, Robert B. Wilson	2
7	Mucopolysaccharidosis type II in a female patient with a reciprocal X;9 translocation and skewed X chromosome inactivation 2014 ·American Journal of Medical Genetics Part A ·Fortunato Lonardo, Paola Di Natale, Susanna Lualdi, Fabio Acquaviva, Cristina Cuoco, (unknown), (unknown), Luigi Michele Pavone, (unknown), Mirella Filocamo, Gioacchino Scarano	27
8	Identification of Candidate Children for Maturity-Onset Diabetes of the Young Type 2 (MODY2) Gene Testing: A Seven-Item Clinical Flowchart (7-iF) 2013 ·PLoS ONE ·Michele Pinelli, Fabio Acquaviva, Fabrizio Barbetti, (unknown), Sergio Cocozza, Maurizio Delvecchio, Enza Mozzillo, (unknown), Francesco Prisco, Ivana Rabbone, Lucia Sacchetti, Nadia Tinto, Sonia Toni, Stefano Zucchini, Dario Iafusco, (unknown)	32
9	Science, art, and mistery in the statues and in the anatomical machines of the prince of sansevero: The masterpieces of the “Sansevero Chapel” 2013 ·American Journal of Medical Genetics Part A ·Matteo Della Monica, Domenico Galzerano, (unknown), Fabio Acquaviva, Giovanni De Gregorio, Fortunato Lonardo, (unknown), (unknown), (unknown), Gioacchino Scarano	3
10	Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit 2010 ·Movement Disorders ·Francesco Saccà, (unknown), Giuseppe De Michele, Fabio Acquaviva, Antonella Antenora, Guido Carlomagno, Sergio Cocozza, Alessandra Denaro, (unknown), Angela Marsili, Gaetano Perrotta, Giorgia Puorro, Antonio Cittadini, Alessandro Filla	38
11	PGC-1alpha Down-Regulation Affects the Antioxidant Response in Friedreich's Ataxia 2010 ·PLoS ONE ·Daniele Marmolino, Mario Manto, Fabio Acquaviva, Paola Vergara, (unknown), Antonella Monticelli, Massimo Pandolfo	124
12	Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARγ pathway as a therapeutic target in Friedreich’s ataxia 2009 ·Human Molecular Genetics ·Giovanni Coppola, Daniele Marmolino, Daning Lu, Qing Wang, Miriam Cnop, Myriam Rai, Fabio Acquaviva, Sergio Cocozza, Massimo Pandolfo, Daniel H. Geschwind	100
13	Friedreich’s Ataxia: From the (GAA) n Repeat Mediated Silencing to New Promising Molecules for Therapy 2009 ·The Cerebellum ·Daniele Marmolino, Fabio Acquaviva	25
14	DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients 2008 ·Journal of Medical Genetics ·Imma Castaldo, Michele Pinelli, Antonella Monticelli, Fabio Acquaviva, (unknown), Alessandro Filla, Silvana Sacchetti, (unknown), Vittorio Enrico Avvedimento, Lorenzo Chiariotti, Sirio Cocozza	82
15	Recombinant Human Erythropoietin Increases Frataxin Protein Expression Without Increasing mRNA Expression 2008 ·The Cerebellum ·Fabio Acquaviva, Imma Castaldo, Alessandro Filla, (unknown), Daniele Marmolino, Antonella Monticelli, Michele Pinelli, Francesco Saccà, Sergio Cocozza	50
16	PPAR-γ Agonist Azelaoyl PAF Increases Frataxin Protein and mRNA Expression. New Implications for the Friedreich’s Ataxia Therapy 2008 ·The Cerebellum ·Daniele Marmolino, Fabio Acquaviva, Michele Pinelli, Antonella Monticelli, Imma Castaldo, Alessandro Filla, Sergio Cocozza	43
17	PGE₂inhibits apoptosis in human adenocarcinoma Caco-2 cell line through Ras-PI3K association and cAMP-dependent kinase A activation 2007 ·American Journal of Physiology-Gastrointestinal and Liver Physiology ·Vincenza Leone, (unknown), Paolo Ricchi, Fabio Acquaviva, Maria Giannouli, (unknown), (unknown), Angela M. Acquaviva	73
18	β2-adrenergic receptor and UCP3 variants modulate the relationship between age and type 2 diabetes mellitus 2006 ·BMC Medical Genetics ·Michele Pinelli, (unknown), Fabio Acquaviva, Sergio Cocozza, Giovanna Donnarumma, Emanuela Lapice, Gabriele Riccardi, Geremia Romano, Olga Vaccaro, Antonella Monticelli	25
19	Aspirin reduces the outcome of anticancer therapy in Meth A–bearing mice through activation of AKT-glycogen synthase kinase signaling 2006 ·Molecular Cancer Therapeutics ·(unknown), Giuseppe Matarese, Vincenza Leone, Tiziana Di Matola, Fabio Acquaviva, Angela M. Acquaviva, Paolo Ricchi	7
20	Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2 2005 ·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	56

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.

Explore authors with similar magnitude of impact