Rosanna Bagnulo

998 total citations
36 papers, 515 citations indexed

About

Rosanna Bagnulo is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Rosanna Bagnulo has authored 36 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Genetics and 9 papers in Pathology and Forensic Medicine. Recurrent topics in Rosanna Bagnulo's work include Genetic factors in colorectal cancer (9 papers), Cancer Genomics and Diagnostics (7 papers) and Cancer-related Molecular Pathways (4 papers). Rosanna Bagnulo is often cited by papers focused on Genetic factors in colorectal cancer (9 papers), Cancer Genomics and Diagnostics (7 papers) and Cancer-related Molecular Pathways (4 papers). Rosanna Bagnulo collaborates with scholars based in Italy, United States and Russia. Rosanna Bagnulo's co-authors include Cristiano Simone, Nicoletta Resta, Alessandro Stella, Francesco Susca, Ginevra Guanti, Giovanna Forte, Daria Carmela Loconte, Patrizia Lastella, Antonio Matrone and Valentina Grossi and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Rosanna Bagnulo

35 papers receiving 510 citations

Peers

Rosanna Bagnulo

ONCOL

PFM

EPIDE

GENET

Laurence Lasorsa France

Céline J. Rocca United States

Concetta Cuozzo Italy

Sharon Amir Israel

Gülden Dınız Türkiye

Taiji Hamada Japan

Alun R. Wang United States

Chiara Verdelli Italy

Chun Cao Switzerland

Xueyan Guo China

Laurence Lasorsa France

Rosanna Bagnulo

369 ×1.3

136 ×1.3

ONCOL

62 ×0.7

PFM

51 ×0.5

EPIDE

69 ×0.9

GENET

Citations per year, relative to Rosanna Bagnulo Rosanna Bagnulo (= 1×) peers Laurence Lasorsa

Countries citing papers authored by Rosanna Bagnulo

Since Specialization

Citations

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

Fields of papers citing papers by Rosanna Bagnulo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rosanna Bagnulo

This figure shows the co-authorship network connecting the top 25 collaborators of Rosanna Bagnulo. A scholar is included among the top collaborators of Rosanna Bagnulo 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 Rosanna Bagnulo. Rosanna Bagnulo 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

Carli, Diana, Marilidia Piglionica, Stefania Martino, et al.. (2025). Expanding the phenotypic spectrum of PROS: reclassifying isolated lateralised overgrowth. Journal of Medical Genetics. 62(4). 276–280.

Piglionica, Marilidia, et al.. (2024). Molecular Basis and Diagnostic Approach to Isolated and Syndromic Lateralized Overgrowth in Childhood. The Journal of Pediatrics. 274. 114177–114177. 1 indexed citations

Forleo, Cinzia, Sandro Sorrentino, Ilaria Dentamaro, et al.. (2024). Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience. Biomedicines. 12(6). 1293–1293. 5 indexed citations

Martino, Stefania, Pietro D’Addabbo, Francesca Clementina Radio, et al.. (2024). Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency. International Journal of Molecular Sciences. 25(17). 9637–9637. 3 indexed citations

Bukvić, Nenad, Massimiliano Chetta, Rosanna Bagnulo, et al.. (2023). What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis. Genes. 14(1). 165–165. 3 indexed citations

Infantino, Vittoria, Anna Santarsiero, Robert H. Mach, et al.. (2023). Sigma-2 Receptor Ligand Binding Modulates Association between TSPO and TMEM97. International Journal of Molecular Sciences. 24(7). 6381–6381. 8 indexed citations

Piglionica, Marilidia, Rosanna Bagnulo, Simona Cardaropoli, et al.. (2023). The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowth. Genes Chromosomes and Cancer. 62(12). 703–709. 5 indexed citations

Forte, Giovanna, Valentina Grossi, Candida Fasano, et al.. (2022). Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes. Genes & Diseases. 10(4). 1187–1189. 1 indexed citations

Loconte, Daria Carmela, Rosalba De Nola, Francesca Arezzo, et al.. (2022). Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers. Cancers. 14(2). 365–365. 6 indexed citations

10.

Summa, Simona De, Nicoletta Resta, Maria Digennaro, et al.. (2021). Spectrum of Germline Pathogenic Variants in BRCA1/2 Genes in the Apulian Southern Italy Population: Geographic Distribution and Evidence for Targeted Genetic Testing. Cancers. 13(18). 4714–4714. 5 indexed citations

11.

Guaraldi, Federica, Giovanni Di Nardo, Luigi Tarani, et al.. (2017). Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation. European Journal of Medical Genetics. 60(7). 380–384. 6 indexed citations

12.

Loconte, Daria Carmela, Valentina Grossi, Cristina Bozzao, et al.. (2015). Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors. PLoS ONE. 10(4). e0123092–e0123092. 52 indexed citations

13.

Loconte, Daria Carmela, Patrizia Lastella, Carmela Di Gregorio, et al.. (2014). A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage. Human Pathology. 45(10). 2162–2167. 6 indexed citations

14.

Forte, Giovanna, Valentina Grossi, Giuseppe Lucisano, et al.. (2014). Characterization of the rs2802292 SNP identifies FOXO3Aas a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes. BMC Cancer. 14(1). 661–661. 11 indexed citations

15.

Yalçın, Şule, Arbay Ö. Çiftçi, İbrahim Karnak, et al.. (2011). The association of adrenocortical carcinoma and thyroid cancer in a child with Peutz-Jeghers syndrome. Journal of Pediatric Surgery. 46(3). 570–573. 6 indexed citations

16.

Resta, Nicoletta, Roberto Giorda, Rosanna Bagnulo, et al.. (2010). Breakpoint determination of 15 large deletions in Peutz–Jeghers subjects. Human Genetics. 128(4). 373–382. 21 indexed citations

17.

Marignani, Paola A., Rosanna Bagnulo, Eleonora Ferrari, et al.. (2007). Novel splice isoforms of STRADα differentially affect LKB1 activity, complex assembly and subcellular localization.. Cancer Biology & Therapy. 6(10). 1627–1631. 16 indexed citations

18.

Resta, Nicoletta, Francesco Susca, Marilena Carmela Di Giacomo, et al.. (2006). A homozygous frameshift mutation in the ESCO2 gene: Evidence of intertissue and interindividual variation in Nmd efficiency. Journal of Cellular Physiology. 209(1). 67–73. 45 indexed citations

19.

Matrone, Antonio, Alessandro Stella, Beatrice Nico, et al.. (2006). A novel cell type-specific role of p38α in the control of autophagy and cell death in colorectal cancer cells. Cell Death and Differentiation. 14(4). 693–702. 112 indexed citations

20.

Giacomo, Marilena Carmela Di, et al.. (2006). Tumor-specific hyperactive low-molecular-weight cyclin E isoform detection and characterization in non-metastatic colorectal tumors. Cancer Biology & Therapy. 5(2). 198–203. 23 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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