Flavia Cerrato

2.4k total citations
44 papers, 1.6k citations indexed

About

Flavia Cerrato is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Flavia Cerrato has authored 44 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 39 papers in Molecular Biology and 29 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Flavia Cerrato's work include Genetic Syndromes and Imprinting (41 papers), Epigenetics and DNA Methylation (37 papers) and Prenatal Screening and Diagnostics (28 papers). Flavia Cerrato is often cited by papers focused on Genetic Syndromes and Imprinting (41 papers), Epigenetics and DNA Methylation (37 papers) and Prenatal Screening and Diagnostics (28 papers). Flavia Cerrato collaborates with scholars based in Italy, United States and United Kingdom. Flavia Cerrato's co-authors include Andrea Riccio, Angela Sparago, Margherita Silengo, Giovanni Battista Ferrero, Maria Vernucci, Agostina De Crescenzo, Maria Vittoria Cubellis, Gaetano Verde, Silvia Russo and Orazio Palumbo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Flavia Cerrato

41 papers receiving 1.5k citations

Peers

Countries citing papers authored by Flavia Cerrato

Since Specialization

Citations

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

Fields of papers citing papers by Flavia Cerrato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Flavia Cerrato

This figure shows the co-authorship network connecting the top 25 collaborators of Flavia Cerrato. A scholar is included among the top collaborators of Flavia Cerrato 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 Flavia Cerrato. Flavia Cerrato 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	Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans 2025 ·Epigenetics & Chromatin ·(unknown), Raissa Relator, Michael A. Levy, Ankit Verma, Haley McConkey, Bruno Hay Mele, Laura Pignata, (unknown), (unknown), (unknown), (unknown), Angela Sparago, Claudia Angelini, Flavia Cerrato, Bekim Sadiković, Andrea Riccio	0
2	A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 2024 ·Genes & Development ·(unknown), (unknown), (unknown), (unknown), António Galvão, Dario Acampora, Gianna Rossi, Bruno Hay Mele, (unknown), Scott A. Coonrod, Maria Vittoria Cubellis, Flavia Cerrato, Simon Andrews, Sandra Cecconi, Gavin Kelsey, Andrea Riccio	12
3	Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 2023 ·Cancers ·(unknown), Laura Pignata, Bruno Hay Mele, (unknown), (unknown), Orazio Palumbo, Pietro Palumbo, Massimo Carella, Gioacchino Scarano, Giovanni Battista Rossi, Claudia Angelini, Angela Sparago, Flavia Cerrato, Andrea Riccio	3
4	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
5	Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 2023 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·(unknown), Beatrice Spedicati, Flavio Faletra, Laura Pignata, Flavia Cerrato, Andrea Riccio, Egidio Barbi, Luigi Memo, Laura Travan	0
6	Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome 2021 ·Genes ·Laura Pignata, Angela Sparago, Orazio Palumbo, Elena Andreucci, Elisabetta Lapi, Romano Tenconi, Massimo Carella, Andrea Riccio, Flavia Cerrato	5
7	Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of CDKN1C 2021 ·Genes ·Angela Sparago, Flavia Cerrato, Laura Pignata, Francisco Cammarata‐Scalisi, Livia Garavelli, Carmelo Piscopo, (unknown), Andrea Riccio	3
8	Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 2020 ·Cancers ·Laura Pignata, Orazio Palumbo, Flavia Cerrato, (unknown), Enrique de Álava, Josep Roma, Soledad Gallego, Jaume Mora, Massimo Carella, Andrea Riccio, Gaetano Verde	7
9	Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus 2019 ·Genetics in Medicine ·(unknown), Angela Sparago, Andrea Freschi, (unknown), Saskia M. Maas, Suzanna G.M. Frints, Mariëlle Alders, Laura Pignata, Monica Franzese, Claudia Angelini, Diana Carli, Alessandro Mussa, (unknown), Fulvio Gabbarini, (unknown), Giovanni Battista Ferrero, Jet Bliek, Charles A. Williams, Andrea Riccio, Flavia Cerrato	32
10	The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 2019 ·Clinical Epigenetics ·Angela Sparago, Ankit Verma, Maria Grazia Patricelli, Laura Pignata, Silvia Russo, Luciano Calzari, (unknown), (unknown), Orazio Palumbo, Massimo Carella, Deborah Mackay, Faisal I. Rezwan, Claudia Angelini, Flavia Cerrato, Maria Vittoria Cubellis, Andrea Riccio	24
11	Origins of DNA methylation defects in Wilms tumors 2019 ·Cancer Letters ·Zahra Anvar, (unknown), Josep Roma, Flavia Cerrato, Gaetano Verde	25
12	Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome? 2018 ·Clinical Epigenetics ·Angela Sparago, Flavia Cerrato, Andrea Riccio	24
13	Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 2018 ·PLoS Genetics ·Andrea Freschi, (unknown), (unknown), Folami Ideraabdullah, Angela Sparago, Maria Teresa Gentile, (unknown), (unknown), Luca Colucci-D’Amato, Joanne L. Thorvaldsen, Marisa S. Bartolomei, Andrea Riccio, Flavia Cerrato	12
14	A novel large deletion of the ICR1 region including H19 and putative enhancer elements 2015 ·BMC Medical Genetics ·Helen Fryssira, (unknown), Deniz Kanber, Christalena Sofocleous, (unknown), Christina Kanaka‐Gantenbein, Flavia Cerrato, Hermann‐Josef Lüdecke, Susanne Bens, Andrea Riccio, Karin Buiting	6
15	Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 2012 ·Journal of Medical Genetics ·Agostina De Crescenzo, Angela Sparago, Flavia Cerrato, Orazio Palumbo, Massimo Carella, Marco Miceli, Moshe Bronshtein, Andrea Riccio, Yuval Yaron	33
16	The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases 2011 ·Human Molecular Genetics ·Nicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, Lucia Perone, Massimo Carella, Orazio Palumbo, Alessandro Mussa, Angela Sparago, Flavia Cerrato, Silvia Russo, Elisabetta Lapi, Maria Vittoria Cubellis, Chandrasekhar Kanduri, Margherita Silengo, Andrea Riccio, Giovanni Battista Ferrero	98
17	Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour 2008 ·Human Molecular Genetics ·Flavia Cerrato, Angela Sparago, Gaetano Verde, Agostina De Crescenzo, Valentina Citro, Maria Vittoria Cubellis, (unknown), Luigi Boccuto, Giampiero Neri, Corrado Magnani, Paolo D’Angelo, Paola Collini, Daniela Perotti, Gianfranco Sebastio, Eamonn R. Maher, Andrea Riccio	66
18	MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment 2008 ·European Journal of Human Genetics ·Manuela Priolo, Angela Sparago, Corrado Mammì, Flavia Cerrato, Carmelo Laganà, Andrea Riccio	57
19	The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster 2005 ·Human Molecular Genetics ·Flavia Cerrato, Angela Sparago, (unknown), Xiangang Zou, Wendy Dean, Hiroyuki Sasaki, Paul D. Smith, Rita Genesio, Marianne Brüggemann, Wolf Reik, Andrea Riccio	38
20	Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 2003 ·Human Molecular Genetics ·Flavia Cerrato, Wendy Dean, (unknown), Kazuhiro Kagotani, Kohzoh Mitsuya, Katsuzumi Okumura, Andrea Riccio, Wolf Reik	15

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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