Roberta Gioia

1.3k citations

28 papers · 825 indexed · h-index 16

Impact in

Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms
Genetics top 10%
- Connective tissue disorders research
- Neurogenetic and Muscular Disorders Research
- Mesenchymal stem cell research

Papers in ⓘ

Developmental Neuroscience 6
- Neurogenesis and neuroplasticity mechanisms 6
Genetics 6
- Connective tissue disorders research 10
- Neurogenetic and Muscular Disorders Research 6

Co-authors: Antonella Forlino (16 shared papers)Antonio Rossi (12 shared papers)Roberta Besio (11 shared papers)Stefania Corti (3 shared papers)Monica Nizzardo (3 shared papers)Giacomo P. Comi (3 shared papers)Federica Rizzo (2 shared papers)Elena Abati (2 shared papers)
Journals: Human Molecular Genetics (2 papers)International Journal of Molecular Sciences (2 papers)Frontiers in Endocrinology (2 papers)PLoS ONE (2 papers)Stem Cells (1 paper)
Partner nations: Italy United States Germany

In The Last Decade

Roberta Gioia

28 papers receiving 817 citations

Peers

Countries citing papers authored by Roberta Gioia

Since Specialization

Citations

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

Fields of papers citing papers by Roberta Gioia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Roberta Gioia, 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 Roberta Gioia Line = papers co-authored together Roberta Gioia 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 28 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Neural Stem Cell Transplantation for Neurodegenerative Diseases International Journal of Molecular Sciences ·Roberta Gioia, Fabio Biella, Gaia Citterio, Federica Rizzo, Elena Abati, Monica Nizzardo, Nereo Bresolin, Giacomo P. Comi, Stefania Corti	2020	177
2	In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfecta Blood ·Cristina Panaroni, Roberta Gioia, Anna Lupi, Roberta Besio, Steven A. Goldstein, Jaclynn M. Kreider, Sergey Leikin, Juan Carlos Vera, Edward L. Mertz, Egon Perilli, Fabio Baruffaldi, Isabella Villa, Aurora Farina, Marco Casasco, Giuseppe Cetta, Antonio Rossi, Annalisa Frattini, Joan C. Marini, Paolo Vezzoni, Antonella Forlino	2009	70
3	The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta Human Molecular Genetics ·Roberta Gioia, Francesca Tonelli, Ilaria Ceppi, Marco Biggiogera, Sergey Leikin, Shannon Fisher, Elena Tenedini, Timur Yorgan, Thorsten Schinke, Kun Tian, Jean‐Marc Schwartz, Fabiana Forte, Raimund Wagener, Simona Villani, Antonio Rossi, Antonella Forlino	2017	66
4	Severely Impaired Bone Material Quality in Chihuahua Zebrafish Resembles Classical Dominant Human Osteogenesis Imperfecta Journal of Bone and Mineral Research ·Imke A.K. Fiedler, Felix N. Schmidt, Eva Maria Wölfel, Christine Plumeyer, Petar Milovanović, Roberta Gioia, Francesca Tonelli, Hrishikesh Bale, Katharina Jähn, Roberta Besio, Antonella Forlino, Björn Busse	2018	58
5	Impaired Osteoblastogenesis in a Murine Model of Dominant Osteogenesis Imperfecta: A New Target for Osteogenesis Imperfecta Pharmacological Therapy Stem Cells ·Roberta Gioia, Cristina Panaroni, Roberta Besio, Giovanni Palladini, Giampaolo Merlini, Vincenzo Giansanti, A. Ivana Scovassi, Simona Villani, Isabella Villa, Anna Villa, Paolo Vezzoni, Ruggero Tenni, Antonio Rossi, Joan C. Marini, Antonella Forlino	2012	54
6	TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy Neurological Sciences ·Jacopo C. DiFrancesco, Francesca Novara, Orsetta Zuffardi, Antonella Forlino, Roberta Gioia, Federica Cossu, Martino Bolognesi, Simona Andreoni, Enrico Saracchi, Barbara Frigeni, T. Stellato, Markus Tolnay, David T. Winkler, Paolo Remida, Giuseppe Isimbaldi, Carlo Ferrarese	2014	40
7	RNS60 exerts therapeutic effects in the SOD1 ALS mouse model through protective glia and peripheral nerve rescue Journal of Neuroinflammation ·Antonio Vallarola, Francesca Sironi, Massimo Tortarolo, Noemi Gatto, Roberta Gioia, Laura Pasetto, Massimiliano De Paola, Alessandro Mariani, Supurna Ghosh, Richard L. Watson, Andreas Kalmes, Valentina Bonetto, Caterina Bendotti	2018	36
8	Multiple intracerebroventricular injections of human umbilical cord mesenchymal stem cells delay motor neurons loss but not disease progression of SOD1G93A mice Stem Cell Research ·Francesca Sironi, Antonio Vallarola, Martina Bruna Violatto, Laura Talamini, Mattia Freschi, Roberta Gioia, Chiara Capelli, Azzurra Agostini, Davide Moscatelli, Massimo Tortarolo, Paolo Bigini, Martino Introna, Caterina Bendotti	2017	33
9	Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype Matrix Biology ·Francesca Tonelli, Silvia Cotti, Laura Leoni, Roberta Besio, Roberta Gioia, Loredana Marchese, Sofia Giorgetti, Simona Villani, Charlotte Gistelinck, Raimund Wagener, Birgit Kobbe, Imke A.K. Fiedler, Daria Larionova, Björn Busse, David R. Eyre, Antonio Rossi, P. Eckhard Witten, Antonella Forlino	2020	30
10	Altered cytoskeletal organization characterized lethal but not surviving Brtl^+/−mice: insight on phenotypic variability in osteogenesis imperfecta Human Molecular Genetics ·Laura Bianchi, Assunta Gagliardi, Silvia Maruelli, Roberta Besio, Claudia Landi, Roberta Gioia, Kenneth M. Kozloff, Basma Khoury, Paul Coucke, Sofie Symoens, Joan C. Marini, Antonio Rossi, Luca Bini, Antonella Forlino	2015	30
11	Characterization of stress response in human retinal epithelial cells Journal of Cellular and Molecular Medicine ·Vincenzo Giansanti, Gloria Elisa Villalpando Rodriguez, M. Savoldelli, Roberta Gioia, Antonella Forlino, Giuliano Mazzini, Marzia Pennati, Nadia Zaffaroni, A. Ivana Scovassi, Alicia Torriglia	2012	29
12	Molecular Mechanisms of Neurogenic Aging in the Adult Mouse Subventricular Zone SHILAP Revista de lepidopterología ·Giuseppe Lupo, Roberta Gioia, Paola S. Nisi, Stefano Biagioni, Emanuele Cacci	2019	27
13	Allele-specific Col1a1 silencing reduces mutant collagen in fibroblasts from Brtl mouse, a model for classical osteogenesis imperfecta European Journal of Human Genetics ·Julie Rousseau, Roberta Gioia, Pierre Layrolle, Blandine Lieubeau, Dominique Heymann, Antonio Rossi, Joan C. Marini, Valérie Trichet, Antonella Forlino	2013	24
14	Kinetic and Structural Evidences on Human Prolidase Pathological Mutants Suggest Strategies for Enzyme Functional Rescue PLoS ONE ·Roberta Besio, Roberta Gioia, Federica Cossu, Enrico Monzani, Stefania Nicolis, Lucia Cucca, Antonella Profumo, Luigi Casella, Ruggero Tenni, Martino Bolognesi, Antonio Rossi, Antonella Forlino	2013	20
15	Differential response to intracellular stress in the skin from osteogenesis imperfecta Brtl mice with lethal and non lethal phenotype: A proteomic approach Journal of Proteomics ·Laura Bianchi, Assunta Gagliardi, Roberta Gioia, Roberta Besio, Chiara Tani, Claudia Landi, Maria Augusta Cipriano, Anna Gimigliano, Antonio Rossi, Joan C. Marini, Antonella Forlino, Luca Bini	2012	19
16	A Mn(II)–Mn(II) center in human prolidase Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ·Roberta Besio, Maria Camilla Baratto, Roberta Gioia, Enrico Monzani, Stefania Nicolis, Lucia Cucca, Antonella Profumo, Luigi Casella, Riccardo Basosi, Ruggero Tenni, Antonio Rossi, Antonella Forlino	2012	17
17	Adult hippocampal neurogenesis and social behavioural deficits in the R451C Neuroligin3 mouse model of autism are reverted by the antidepressant fluoxetine Journal of Neurochemistry ·Roberta Gioia, Tommaso Seri, Tamara Diamanti, Stefania Fimmanò, Marina Vitale, Henrik Ahlenius, Zaal Kokaia, Felice Tirone, Laura Micheli, Stefano Biagioni, Giuseppe Lupo, Arianna Rinaldi, Antonella De Jaco, Emanuele Cacci	2022	14
18	Terminal Differentiation of Adult Hippocampal Progenitor Cells Is a Step Functionally Dissociable from Proliferation and Is Controlled by Tis21, Id3 and NeuroD2 Frontiers in Cellular Neuroscience ·Laura Micheli, Manuela Ceccarelli, Roberta Gioia, Giorgio D’Andrea, Stefano Farioli‐Vecchioli, Marco Costanzi, Daniele Saraulli, Vincenzo Cestari, Felice Tirone	2017	13
19	Improved prolidase activity assay allowed enzyme kinetic characterization and faster prolidase deficiency diagnosis Clinica Chimica Acta ·Roberta Besio, Enrico Monzani, Roberta Gioia, Stefania Nicolis, Antonio Rossi, Luigi Casella, Antonella Forlino	2011	10
20	Egr-1 Maintains NSC Proliferation and Its Overexpression Counteracts Cell Cycle Exit Triggered by the Withdrawal of Epidermal Growth Factor Developmental Neuroscience ·(unknown), Emanuele Cacci, Camilla Toselli, Silvia Cardarelli, A. Bernardi, Roberta Gioia, Mauro Giorgi, Giancarlo Poiana, Stefano Biagioni	2018	10

About Roberta Gioia

Roberta Gioia is a scholar working on Developmental Neuroscience, Genetics, Genetics, Cellular and Molecular Neuroscience and Rheumatology, having authored 28 papers that have together received 825 indexed citations. Recurring topics across this work include Connective tissue disorders research (10 papers), Neurogenesis and neuroplasticity mechanisms (6 papers), Neurogenetic and Muscular Disorders Research (6 papers), Bone and Dental Protein Studies (4 papers), Protease and Inhibitor Mechanisms (4 papers), Pluripotent Stem Cells Research (4 papers), Amyotrophic Lateral Sclerosis Research (3 papers) and Neuropeptides and Animal Physiology (3 papers). The work is most often cited by research in Developmental Neuroscience (123 citations), Genetics (136 citations), Genetics (269 citations), Rheumatology (144 citations) and Neurology (65 citations). Roberta Gioia has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Antonella Forlino, Antonio Rossi, Roberta Besio, Stefania Corti, Monica Nizzardo, Giacomo P. Comi, Federica Rizzo, Elena Abati, Nereo Bresolin and Joan C. Marini. Their work appears in journals such as Human Molecular Genetics, International Journal of Molecular Sciences, Frontiers in Endocrinology, PLoS ONE and Stem Cells.

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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