Simonetta Rosato

713 total citations
27 papers, 269 citations indexed

About

Simonetta Rosato is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Simonetta Rosato has authored 27 papers receiving a total of 269 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Simonetta Rosato's work include Genomic variations and chromosomal abnormalities (7 papers), Hedgehog Signaling Pathway Studies (4 papers) and Connective tissue disorders research (4 papers). Simonetta Rosato is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Hedgehog Signaling Pathway Studies (4 papers) and Connective tissue disorders research (4 papers). Simonetta Rosato collaborates with scholars based in Italy, Switzerland and United States. Simonetta Rosato's co-authors include Livia Garavelli, Anita Wischmeijer, Andrea Superti‐Furga, Marzia Pollazzon, Caterina Longo, Simonetta Piana, Ivan Ivanovski, Giuseppe Argenziano, Iris Zalaudek and Gerardo Ferrara and has published in prestigious journals such as Cancer Research, Breast Cancer Research and Treatment and Cytogenetic and Genome Research.

In The Last Decade

Simonetta Rosato

25 papers receiving 267 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Simonetta Rosato Italy 11 144 121 44 41 38 27 269
Ching‐In Lau United Kingdom 14 251 1.7× 48 0.4× 45 1.0× 24 0.6× 15 0.4× 22 401
Anisha Solanki United Kingdom 13 239 1.7× 39 0.3× 70 1.6× 18 0.4× 13 0.3× 16 369
Yao‐Shan Fan United States 9 94 0.7× 48 0.4× 34 0.8× 9 0.2× 28 0.7× 19 275
Colin Kwok United Kingdom 11 273 1.9× 68 0.6× 33 0.8× 136 3.3× 34 0.9× 19 480
Paul Oei New Zealand 11 73 0.5× 96 0.8× 50 1.1× 9 0.2× 18 0.5× 19 256
Valérie Raclin France 8 196 1.4× 110 0.9× 46 1.0× 27 0.7× 8 0.2× 9 276
S. Larkins United Kingdom 8 121 0.8× 112 0.9× 20 0.5× 24 0.6× 8 0.2× 12 258
José Ignacio Saldaña United Kingdom 11 232 1.6× 51 0.4× 34 0.8× 13 0.3× 8 0.2× 12 329
Jadwiga Żebracka‐Gala Poland 8 164 1.1× 113 0.9× 25 0.6× 24 0.6× 10 0.3× 12 302
Maria Aggelakopoulou Greece 9 109 0.8× 45 0.4× 62 1.4× 16 0.4× 24 0.6× 12 345

Countries citing papers authored by Simonetta Rosato

Since Specialization
Citations

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

Fields of papers citing papers by Simonetta Rosato

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simonetta Rosato

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

All Works

20 of 20 papers shown
1.
Caraffi, Stefano Giuseppe, Simonetta Rosato, Carlotta Spagnoli, et al.. (2025). Axonal motor polyneuropathy in a 13 years old Girl with a de Novo variant in ADNP. Neurogenetics. 26(1). 32–32.
2.
Melli, Beatrice, Fabiana Castiglione, Andrea Palicelli, et al.. (2024). Clinical exome next‑generation sequencing panel for hereditary pheochromocytoma and paraganglioma diagnosis. Experimental and Therapeutic Medicine. 29(2). 34–34. 2 indexed citations
3.
Bernardini, Laura, Marzia Pollazzon, Maria Grazia Giuffrida, et al.. (2023). Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes. Genes. 14(8). 1526–1526. 2 indexed citations
4.
Rosato, Simonetta, Sheila Unger, Belinda Campos‐Xavier, et al.. (2022). Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features. Genes. 13(2). 261–261. 9 indexed citations
5.
Pollazzon, Marzia, Stefano Giuseppe Caraffi, Silvia Faccioli, et al.. (2021). Clinical and Genetic Findings in a Series of Eight Families with Arthrogryposis. Genes. 13(1). 29–29. 10 indexed citations
6.
Errichiello, Edoardo, Stefano Giuseppe Caraffi, Simonetta Rosato, et al.. (2020). Improving the phenotype description of Basel-Vanagaite-Smirin-Yosef syndrome, MED25-related: polymicrogyria as a distinctive neuroradiological finding. Neurogenetics. 22(1). 19–25. 1 indexed citations
7.
Ivanovski, Ivan, Stefano Giuseppe Caraffi, Elisa Magnani, et al.. (2019). Alazami syndrome: the first case of papillary thyroid carcinoma. Journal of Human Genetics. 65(2). 133–141. 15 indexed citations
8.
Ivanovski, Ivan, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.. (2018). Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes. American Journal of Medical Genetics Part A. 176(5). 1166–1174. 13 indexed citations
9.
Ivanovski, Ivan, Olivera Djurić, Stefano Giuseppe Caraffi, et al.. (2018). Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 34–34. 4 indexed citations
10.
Pollazzon, Marzia, Simonetta Rosato, Ivan Ivanovski, et al.. (2018). Complex cranio-vertebral malformation: disruption sequence or iniencephaly?. Clinical Dysmorphology. 27(3). 105–108.
11.
Garavelli, Livia, Ivan Ivanovski, Marzia Pollazzon, et al.. (2016). Natural history and life-threatening complications in Myhre syndrome and review of the literature. European Journal of Pediatrics. 175(10). 1307–1315. 18 indexed citations
12.
Ivanovski, Ivan, Alessandro Iodice, Simonetta Rosato, et al.. (2016). Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review. Molecular Syndromology. 7(6). 337–343. 3 indexed citations
13.
Riccardi, Federica, Gianna Franca Rivolta, Vera Uliana, et al.. (2015). Cryptic 13q34 and 4q35.2 Deletions in an Italian Family. Cytogenetic and Genome Research. 147(1). 24–30. 6 indexed citations
14.
Lallas, Aimilios, Elvira Moscarella, Giuseppe Argenziano, et al.. (2013). Dermoscopy of uncommon skin tumours. Australasian Journal of Dermatology. 55(1). 53–62. 45 indexed citations
15.
Garavelli, Livia, Simonetta Rosato, Anita Wischmeijer, et al.. (2012). 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. American Journal of Medical Genetics Part A. 158A(9). 2245–2249. 13 indexed citations
16.
Garavelli, Livia, Simonetta Rosato, Anita Wischmeijer, et al.. (2011). 22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review. Molecular Syndromology. 2(1). 35–44. 18 indexed citations
17.
Garavelli, Livia, Anita Wischmeijer, Simonetta Rosato, et al.. (2010). Al‐Awadi–Raas‐Rothschild (limb/pelvis/uterus–hypoplasia/aplasia) syndrome and WNT7A mutations: Genetic homogeneity and nosological delineation. American Journal of Medical Genetics Part A. 155(2). 332–336. 15 indexed citations
18.
Garavelli, Livia, Maria Rosaria D’Apice, Francesca Rivieri, et al.. (2009). Mandibuloacral dysplasia type A in childhood. American Journal of Medical Genetics Part A. 149A(10). 2258–2264. 30 indexed citations
19.
Seymour, Ian, Silvia Casadei, Valentina Zampiga, et al.. (2007). Results of a population-based screening for hereditary breast cancer in a region of North-Central Italy: contribution of BRCA1/2 germ-line mutations. Breast Cancer Research and Treatment. 112(2). 343–349. 5 indexed citations
20.
Casadei, Silvia, Ian Seymour, Simonetta Rosato, et al.. (2004). Analysis of single nucleotide polymorphisms in coding and non-coding regions of human BRCA1 and BRCA2 genes. Cancer Research. 64. 301–301. 1 indexed citations

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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