Marta Cerutti

400 total citations
19 papers, 270 citations indexed

About

Marta Cerutti is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Marta Cerutti has authored 19 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Marta Cerutti's work include Protein Tyrosine Phosphatases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Marta Cerutti is often cited by papers focused on Protein Tyrosine Phosphatases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Marta Cerutti collaborates with scholars based in Italy, United States and Canada. Marta Cerutti's co-authors include Angelo Selicorni, Susanna Esposito, Donatella Milani, Francesca Pantaleoni, Laura Cesarini, Daniela Ricci, Paolo Alfieri, Marco Tartaglia, Chiara Leoni and Francesca Menni and has published in prestigious journals such as PEDIATRICS, Journal of Thoracic and Cardiovascular Surgery and Vaccine.

In The Last Decade

Marta Cerutti

18 papers receiving 258 citations

Peers

Countries citing papers authored by Marta Cerutti

Since Specialization

Citations

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

Fields of papers citing papers by Marta Cerutti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Cerutti

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Eosinophilic esophagitis improved by the discontinuation of sublingual immunotherapy for aeroallergens: a case report 2024 ·Frontiers in Pediatrics ·Alice Monzani, Marta Cerutti, (unknown), (unknown), (unknown), (unknown), (unknown), Ivana Rabbone	2
2	Rhinomyiasis: clinical and surgical management 2020 ·BMJ Case Reports ·(unknown), Marta Cerutti, (unknown), Carmine F. Gervasio	1
3	Urotensin II, urotensin-related peptide, and their receptor in aortic valve stenosis 2019 ·Journal of Thoracic and Cardiovascular Surgery ·(unknown), (unknown), Bin Yu, (unknown), (unknown), (unknown), Jean‐Claude Tardif, (unknown), Marta Cerutti, Adel Schwertani	6
4	A rare case of solitary fibrous tumor of parotid gland: diagnostic work-up and treatment 2017 ·Carmine F. Gervasio, Marta Cerutti, (unknown), (unknown), Roberto Albera	6
5	Vaccination coverage of children with rare genetic diseases and attitudes of their parents toward vaccines 2015 ·Human Vaccines & Immunotherapeutics ·Susanna Esposito, Marta Cerutti, Donatella Milani, Francesca Menni, Nicola Principi	11
6	Vaccination coverage of patients with inborn errors of metabolism and the attitudes of their parents towards vaccines 2015 ·Vaccine ·Marta Cerutti, Pascale de Lonlay, Francesca Menni, Rossella Parini, Nicola Principi, Susanna Esposito	12
7	Syndromic obesity: clinical implications of a correct diagnosis 2014 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·Donatella Milani, Marta Cerutti, Lidia Pezzani, Pietro Maffei, Gabriella Milan, Susanna Esposito	16
8	Audiological findings, genotype and clinical severity score in Cornelia de Lange syndrome 2014 ·International Journal of Pediatric Otorhinolaryngology ·Paola Marchisio, Angelo Selicorni, Sonia Bianchini, Donatella Milani, Elena Baggi, Marta Cerutti, Lidia Larizza, Nicola Principi, Susanna Esposito	8
9	Hemostatic Abnormalities in Noonan Syndrome 2014 ·PEDIATRICS ·Andrea Artoni, Angelo Selicorni, Serena M. Passamonti, Anna Lecchi, Paolo Bucciarelli, Marta Cerutti, Paola Cianci, Francesca Gianniello, Ida Martinelli	38
10	Eosinophilic Inflammation of Chronic Rhinosinusitis with Nasal Polyps Is Related to OX40 Ligand Expression 2013 ·Otolaryngology ·Massimiliano Garzaro, Monica Boita, Luca Raimondo, Giuseppe Riva, Marta Cerutti, Giovanni Rolla, Giancarlo Pecorari	1
11	A particular phenotype in a case of Down-Turner syndrome 2012 ·15th International & 14th European Congress of Endocrinology ·S. Bergamaschi, Claudia Giavoli, Eriselda Profka, Emanuele Ferrante, (unknown), Silvana Guerneri, Diogo Milani, Francesca Menni, Marta Cerutti, (unknown), (unknown), Santiago Vallasciani, Alberto Spada, P. Beck‐Peccoz	2
12	De novo Deletion of 1q31.1–q32.1 in a Patient with Developmental Delay and Behavioral Disorders 2012 ·Cytogenetic and Genome Research ·Donatella Milani, Maria Francesca Bedeschi, Maria Iascone, (unknown), Marta Cerutti, Francesca Menni	4
13	Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndrome 2011 ·Human Vaccines ·Susanna Esposito, Angelo Selicorni, Cristina Daleno, (unknown), Marta Cerutti, Carlotta Galeone, Silvia Consolo, Francesca Menni, Nicola Principi	8
14	Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndrome 2009 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Donatella Milani, Anna Cereda, Marta Cerutti, Silvia Maitz, Francesca Menni, Angelo Selicorni	6
15	Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascade 2009 ·American Journal of Medical Genetics Part A ·Laura Cesarini, Paolo Alfieri, Francesca Pantaleoni, Isabella Vasta, Marta Cerutti, Valentina Petrangeli, Paolo Mariotti, Chiara Leoni, Daniela Ricci, Stefano Vicari, Angelo Selicorni, Marco Tartaglia, Eugenio Mercuri, Giuseppe Zampino	73
16	Audiological and vestibular findings in the Kabuki syndrome 2009 ·American Journal of Medical Genetics Part A ·Stefania Barozzi, Federica Di Berardino, (unknown), (unknown), Marta Cerutti, Angelo Selicorni, Antonio Cesarani	13
17	Analysis of congenital heart defects in 87 consecutive patients with Brachmann‐de Lange syndrome 2009 ·American Journal of Medical Genetics Part A ·Angelo Selicorni, (unknown), (unknown), Donatella Milani, Anna Cereda, Marta Cerutti, Silvia Maitz, (unknown), Laura Salvini, (unknown), (unknown), Patrizia Salice, Gian Battista Danzi	30
18	Otitis media with effusion and hearing loss in children with Cornelia de Lange syndrome 2008 ·American Journal of Medical Genetics Part A ·Paola Marchisio, Angelo Selicorni, Lorenzo Pignataro, Donatella Milani, Elena Baggi, (unknown), (unknown), Laura Villa, Pasquale Capaccio, Marta Cerutti, Susanna Esposito, Nicola Principi	12
19	Visual Function in Noonan and LEOPARD Syndrome 2008 ·Neuropediatrics ·Paolo Alfieri, Laura Cesarini, Giuseppe Zampino, Francesca Pantaleoni, Angelo Selicorni, Annabella Salerni, (unknown), Marta Cerutti, Anna Dickmann, F. Colitto, Susanna Staccioli, Chiara Leoni, Daniela Ricci, Claudia Brogna, Marco Tartaglia, Eugenio Mercuri	21

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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