Roberta Pietrobono

889 total citations
20 papers, 641 citations indexed

About

Roberta Pietrobono is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Roberta Pietrobono has authored 20 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Cognitive Neuroscience. Recurrent topics in Roberta Pietrobono's work include Genetics and Neurodevelopmental Disorders (10 papers), Epigenetics and DNA Methylation (7 papers) and Autism Spectrum Disorder Research (7 papers). Roberta Pietrobono is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Epigenetics and DNA Methylation (7 papers) and Autism Spectrum Disorder Research (7 papers). Roberta Pietrobono collaborates with scholars based in Italy, United States and Netherlands. Roberta Pietrobono's co-authors include Giovanni Neri, Pietro Chiurazzi, Maria Grazia Pomponi, Ben A. Oostra, Elisabetta Tabolacci, C.E. Bakker, Umberto Moscato, Antonio Terracciano, Francesca Zalfa and Claudia Bagni and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and Journal of Neurology.

In The Last Decade

Roberta Pietrobono

20 papers receiving 635 citations

Peers

Countries citing papers authored by Roberta Pietrobono

Since Specialization

Citations

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

Fields of papers citing papers by Roberta Pietrobono

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Pietrobono

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Pietrobono. A scholar is included among the top collaborators of Roberta Pietrobono 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 Roberta Pietrobono. Roberta Pietrobono 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	Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype 2022 ·Genes ·(unknown), Elisabetta Tabolacci, (unknown), Maria Grazia Pomponi, Roberta Pietrobono, Giovanni Neri, (unknown), (unknown), Cristina Grippaudo, (unknown), Alessia De Vita, (unknown), Alessandro Arcovito, Wanda Lattanzi, Maurizio Genuardi, Pietro Chiurazzi	1
2	Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis 2021 ·Genes ·Elisabetta Tabolacci, Maria Grazia Pomponi, (unknown), Roberta Pietrobono, Daniela Orteschi, (unknown), (unknown), (unknown), Marika Pane, Eugenio Mercuri, Giovanni Neri, Maurizio Genuardi, Pietro Chiurazzi, Marcella Zollino	3
3	Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families 2020 ·Genes ·Elisabetta Tabolacci, Roberta Pietrobono, (unknown), (unknown), (unknown), Matteo Della Monica, Maria Grazia Pomponi, Maurizio Genuardi, Giovanni Neri, Pietro Chiurazzi	10
4	Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation 2019 ·European Journal of Human Genetics ·Elisabetta Tabolacci, Maria Grazia Pomponi, (unknown), Roberta Pietrobono, (unknown), (unknown), Fiorella Gurrieri, Giovanni Neri, Maurizio Genuardi, Pietro Chiurazzi	5
5	Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome 2019 ·European Journal of Human Genetics ·Eugenio Sangiorgi, Alessia Azzarà, (unknown), Roberta Pietrobono, Donato Rigante, Elena Verrecchia, Ludovico Luca Sicignano, Maurizio Genuardi, Fiorella Gurrieri, Raffaele Manna	23
6	Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue 2016 ·American Journal of Medical Genetics Part A ·(unknown), Maria Grazia Pomponi, Roberta Pietrobono, Elisabetta Tabolacci, Giovanni Neri	12
7	A Novel Intragenic Deletion in Ophn1 in A Boy with Developmental Delay, Strabismus and Cerebellar Hypoplasia 2015 ·Luisa Ronzoni, Lidia Pezzani, Donatella Milani, Pietro Chiurazzi, Maria Grazia Pomponi, Roberta Pietrobono, Maurizio Viri, Susanna Esposito	2
8	Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p 2013 ·European Journal of Human Genetics ·Fiorella Gurrieri, Marcella Zollino, Antonio Oliva, Vincenzo L. Pascali, Daniela Orteschi, Roberta Pietrobono, Antonia Camporeale, (unknown), Sara Partemi, Ramón Brugada, Fulvio Bellocci, Giovanni Neri	32
9	Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 2012 ·Journal of Neurology ·Massimo Santoro, Marcella Masciullo, Roberta Pietrobono, Giulia Conte, Anna Modoni, Maria Laura Ester Bianchi, Valentina Rizzo, Maria Grazia Pomponi, Giorgio Tasca, Giovanni Neri, Gabriella Silvestri	31
10	Simpson–Golabi–Behmel syndrome type 1 in a 27‐week macrosomic preterm newborn: The diagnostic value of rib malformations and index nail and finger hypoplasia 2012 ·American Journal of Medical Genetics Part A ·Livia Garavelli, (unknown), (unknown), Simonetta Rosato, Anita Wischmeijer, (unknown), (unknown), (unknown), Francesca Forzano, Roberta Pietrobono, Maria Grazia Pomponi, Elena Andreucci, Annick Toutain, Andrea Superti‐Furga, Giovanni Neri	13
11	The Simpson–Golabi–Behmel syndrome: A clinical case and a detective story 2010 ·American Journal of Medical Genetics Part A ·Fiorella Gurrieri, Maria Grazia Pomponi, Roberta Pietrobono, Emanuela Lucci‐Cordisco, Evelina Silvestri, (unknown), Giovanni Neri	9
12	A premature infant with Costello syndrome due to a rare G13C HRAS mutation 2009 ·American Journal of Medical Genetics Part A ·Maria Piccione, Ettore Piro, Maria Grazia Pomponi, (unknown), Roberta Pietrobono, (unknown), (unknown), Giovanni Neri, Giovanni Corsello	9
13	Correlation between GJB2 mutations and audiological deficits: personal experience 2008 ·European Archives of Oto-Rhino-Laryngology ·Pasqualina Maria Picciotti, Roberta Pietrobono, Giovanni Neri, Gaetano Paludetti, Anna Rita Fetoni, Francesca Cianfrone, Maria Grazia Pomponi	9
14	A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy 2007 ·European Journal of Human Genetics ·Elisabetta Tabolacci, Maria Grazia Pomponi, Roberta Pietrobono, Pietro Chiurazzi, Giovanni Neri	22
15	A truncating mutation in the IL1RAPL1 gene is responsible for X‐linked mental retardation in the MRX21 family 2006 ·American Journal of Medical Genetics Part A ·Elisabetta Tabolacci, Maria Grazia Pomponi, Roberta Pietrobono, Antonio Terracciano, Pietro Chiurazzi, Giovanni Neri	41
16	Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments 2005 ·European Journal of Human Genetics ·Elisabetta Tabolacci, Roberta Pietrobono, Umberto Moscato, Ben A. Oostra, Pietro Chiurazzi, Giovanni Neri	67
17	Molecular dissection of the events leading to inactivation of the FMR1 gene 2004 ·Human Molecular Genetics ·Roberta Pietrobono, Elisabetta Tabolacci, Francesca Zalfa, Ilaria Zito, Antonio Terracciano, Umberto Moscato, Claudia Bagni, Ben A. Oostra, Pietro Chiurazzi, Giovanni Neri	94
18	Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine 2002 ·Nucleic Acids Research ·Roberta Pietrobono	85
19	Recombinant GroES in combination with CpG oligodeoxynucleotides protects mice against Mycobacterium avium infection 2002 ·Journal of Medical Microbiology ·Lanfranco Fattorini, Roberta Creti, Roberto Nisini, Roberta Pietrobono, (unknown), Annarita Stringaro, Giuseppe Arancia, Ottaviano Serlupi‐Crescenzi, Elisabetta Iona, Graziella Orefici	6
20	Synergistic Effect of Histone Hyperacetylation and DNA Demethylation in the Reactivation of the FMR1 Gene 1999 ·Human Molecular Genetics ·Pietro Chiurazzi, Maria Grazia Pomponi, Roberta Pietrobono, C.E. Bakker, Giovanni Neri, Ben A. Oostra	167

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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