Rosamaria Silipigni

511 total citations
35 papers, 264 citations indexed

About

Rosamaria Silipigni is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Rosamaria Silipigni has authored 35 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Genetics and 6 papers in Genetics. Recurrent topics in Rosamaria Silipigni's work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (5 papers). Rosamaria Silipigni is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (5 papers). Rosamaria Silipigni collaborates with scholars based in Italy, Germany and United States. Rosamaria Silipigni's co-authors include Silvana Guerneri, Laura Fontana, Silvia Tabano, Monica Miozzo, Chiara Pesenti, Giovanni Marfia, Leda Paganini, Silvano Bòsari, Andrea Terrasi and Peter P. Pramstaller and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Bone and Mineral Research and Cellular and Molecular Life Sciences.

In The Last Decade

Rosamaria Silipigni

32 papers receiving 262 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rosamaria Silipigni Italy 10 144 79 54 50 34 35 264
Ruolan Guo China 11 158 1.1× 120 1.5× 48 0.9× 28 0.6× 62 1.8× 41 332
Bin Mao China 12 143 1.0× 55 0.7× 28 0.5× 32 0.6× 29 0.9× 24 262
Emine İkbal Atlı Türkiye 8 119 0.8× 46 0.6× 33 0.6× 51 1.0× 20 0.6× 48 212
Jocelyne Attia‐Sobol France 8 99 0.7× 64 0.8× 35 0.6× 42 0.8× 40 1.2× 10 240
Caterina Barbieri Italy 9 228 1.6× 79 1.0× 37 0.7× 48 1.0× 24 0.7× 18 392
Angeline Lai Singapore 10 152 1.1× 133 1.7× 28 0.5× 40 0.8× 23 0.7× 31 349
Eyby Leon United States 9 263 1.8× 104 1.3× 18 0.3× 24 0.5× 32 0.9× 29 379
Xike Zhu China 11 170 1.2× 67 0.8× 63 1.2× 27 0.5× 44 1.3× 21 344
Irén Haltrich Hungary 9 103 0.7× 93 1.2× 25 0.5× 16 0.3× 22 0.6× 33 239
Kristbjorn O. Gudmundsson United States 13 195 1.4× 69 0.9× 42 0.8× 66 1.3× 18 0.5× 23 400

Countries citing papers authored by Rosamaria Silipigni

Since Specialization
Citations

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

Fields of papers citing papers by Rosamaria Silipigni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rosamaria Silipigni

This figure shows the co-authorship network connecting the top 25 collaborators of Rosamaria Silipigni. A scholar is included among the top collaborators of Rosamaria Silipigni 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 Rosamaria Silipigni. Rosamaria Silipigni 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.
Pezzani, Lidia, Rosamaria Silipigni, Silvia Russo, et al.. (2024). A long way to syndromic short stature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 192–192.
2.
Cavallieri, Francesco, Edoardo Monfrini, Alessandro Fraternali, et al.. (2024). A Case of 18p Chromosomal Deletion Encompassing GNAL in a Patient With Dystonia-Parkinsonism. Journal of Movement Disorders. 17(2). 236–238. 2 indexed citations
3.
Ciaccio, Claudia, Margherita Estienne, Rosamaria Silipigni, et al.. (2023). Clinical features and magnesium levels: Novel insights in 15q11.2 BP1–BP2 copy number variants. Journal of Intellectual Disability Research. 67(7). 679–689. 1 indexed citations
4.
Volani, Chiara, Andrea Colliva, Alessia Paldino, et al.. (2023). Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation. Stem Cell Research. 71. 103172–103172. 1 indexed citations
5.
Rimoldi, M., Berardo Rinaldi, Roberta Villa, et al.. (2022). Congenital diaphragmatic hernia in Coffin Siris syndrome: Further evidence from two cases. American Journal of Medical Genetics Part A. 191(2). 605–611.
6.
Rizzuti, Mafalda, Valentina Melzi, Delia Gagliardi, et al.. (2022). Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes. Cellular and Molecular Life Sciences. 79(3). 189–189. 27 indexed citations
7.
8.
Rinaldi, Berardo, Rosamaria Silipigni, Luca Bergamaschi, et al.. (2021). Incidental finding of APC deletion in a child: double trouble or double chance? – a case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 31–31. 5 indexed citations
9.
Monfrini, Edoardo, Letizia Straniero, Sara Bonato, et al.. (2019). Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy. Parkinsonism & Related Disorders. 63. 66–72. 18 indexed citations
10.
Zanon, Alessandra, Cláudia B. Volpato, Anne Picard, et al.. (2019). Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene. Stem Cell Research. 41. 101624–101624. 4 indexed citations
11.
Pesenti, Chiara, Stefania Elena Navone, Laura Guarnaccia, et al.. (2019). The Genetic Landscape of Human Glioblastoma and Matched Primary Cancer Stem Cells Reveals Intratumour Similarity and Intertumour Heterogeneity. Stem Cells International. 2019. 1–12. 36 indexed citations
12.
Silipigni, Rosamaria, et al.. (2018). Tetrasomy 18p: The challenges of noninvasive prenatal testing and combined test. Journal of obstetrics and gynaecology research. 45(3). 705–708. 2 indexed citations
13.
Augello, Claudia, Federico Colombo, Andrea Terrasi, et al.. (2018). Expression of C19MC miRNAs in HCC associates with stem-cell features and the cancer-testis genes signature. Digestive and Liver Disease. 50(6). 583–593. 13 indexed citations
14.
Meraviglia, Viviana, Patrizia Benzoni, Benedetta Maria Motta, et al.. (2017). Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene. Stem Cell Research. 27. 25–29. 3 indexed citations
15.
Silipigni, Rosamaria, Edoardo Monfrini, Marco Baccarin, et al.. (2017). Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1. Cytogenetic and Genome Research. 153(2). 73–80. 2 indexed citations
16.
Pezzani, Lidia, Donatella Milani, Francesca Manzoni, et al.. (2015). HOXA genes cluster: clinical implications of the smallest deletion. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 31–31. 8 indexed citations
17.
Silipigni, Rosamaria, Elisa Cattaneo, Marco Baccarin, Monica Fumagalli, & Maria Francesca Bedeschi. (2015). Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features. European Journal of Medical Genetics. 59(1). 39–42. 2 indexed citations
18.
Meraviglia, Viviana, Alessandra Zanon, Alexandros Α. Lavdas, et al.. (2015). Generation of Induced Pluripotent Stem Cells from Frozen Buffy Coats using Non-integrating Episomal Plasmids. Journal of Visualized Experiments. 3 indexed citations
19.
Ronzoni, Luisa, Angela Peron, Vera Bianchi, et al.. (2015). Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis. American Journal of Medical Genetics Part A. 167(7). 1551–1559. 4 indexed citations
20.
Natacci, Federica, Giulia Melloni, Francesca Motta, et al.. (2015). Delineating the Mosaic Trisomy 15 Phenotype Using a Serendipitous Mechanism as a Clue. Cytogenetic and Genome Research. 146(1). 44–50. 2 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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