Roberta Zuntini

1.0k total citations
39 papers, 669 citations indexed

About

Roberta Zuntini is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Roberta Zuntini has authored 39 papers receiving a total of 669 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 8 papers in Immunology. Recurrent topics in Roberta Zuntini's work include Immunodeficiency and Autoimmune Disorders (6 papers), BRCA gene mutations in cancer (5 papers) and PI3K/AKT/mTOR signaling in cancer (5 papers). Roberta Zuntini is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (6 papers), BRCA gene mutations in cancer (5 papers) and PI3K/AKT/mTOR signaling in cancer (5 papers). Roberta Zuntini collaborates with scholars based in Italy, United States and Germany. Roberta Zuntini's co-authors include Simona Ferrari, Isabella Quinti, Alessandro Plebani, Simona Cascioli, Rita Carsetti, Maria Cagliuso, Ezio Giorda, G Seganti, Cinzia Auriti and Federica Capolunghi and has published in prestigious journals such as The Journal of Experimental Medicine, Journal of Clinical Oncology and The Journal of Immunology.

In The Last Decade

Roberta Zuntini

37 papers receiving 659 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roberta Zuntini Italy	14	278	235	145	107	81	39	669
Vishal Sindhava United States	16	499 1.8×	182 0.8×	109 0.8×	88 0.8×	47 0.6×	25	730
Wolfgang Schuh Germany	20	677 2.4×	423 1.8×	107 0.7×	99 0.9×	91 1.1×	45	1.2k
Emma Ivansson Sweden	16	178 0.6×	196 0.8×	117 0.8×	205 1.9×	47 0.6×	30	712
Florence Bardin France	17	275 1.0×	404 1.7×	94 0.6×	42 0.4×	161 2.0×	30	1.0k
Mario Pujato United States	11	157 0.6×	250 1.1×	86 0.6×	55 0.5×	21 0.3×	20	594
Long Vien United States	9	330 1.2×	374 1.6×	139 1.0×	29 0.3×	34 0.4×	11	778
Hongshan Zhao China	18	120 0.4×	544 2.3×	113 0.8×	111 1.0×	35 0.4×	42	843
Daniel Rodríguez‐Pinto United States	11	519 1.9×	208 0.9×	279 1.9×	82 0.8×	28 0.3×	12	988
Ana Berta Sousa Portugal	16	278 1.0×	591 2.5×	253 1.7×	28 0.3×	92 1.1×	46	1000
Ariel Madrigal United States	9	626 2.3×	430 1.8×	161 1.1×	82 0.8×	20 0.2×	17	1.1k

Countries citing papers authored by Roberta Zuntini

Since Specialization

Citations

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

Fields of papers citing papers by Roberta Zuntini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Zuntini

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

Spagnoli, Carlotta, A Cavalli, Stefano Giuseppe Caraffi, et al.. (2025). Myoclonic reflex and non‐reflex seizures in a female child with Coffin–Lowry syndrome: Clinical vignette. Epileptic Disorders. 27(2). 299–303. 1 indexed citations

Pollazzon, Marzia, Cecilia Mancini, Simone Pizzi, et al.. (2023). Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures. Frontiers in Neurology. 14. 1207176–1207176. 3 indexed citations

Zuntini, Roberta, Lucia Pedace, Evelina Miele, et al.. (2023). Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation. Frontiers in Genetics. 14. 1231434–1231434. 1 indexed citations

Barbero, Giovanna, Roberta Zuntini, Pamela Magini, et al.. (2023). Characterization of BRCA Deficiency in Ovarian Cancer. Cancers. 15(5). 1530–1530. 1 indexed citations

Bonasoni, Maria Paola, Giuseppina Comitini, Stefano Giuseppe Caraffi, et al.. (2023). Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the SOX2 Gene: Ultrasound, Pathological, and Cytogenetic Findings. Fetal and Pediatric Pathology. 42(6). 979–989. 1 indexed citations

Rossi, Jessica, Marco Russo, Giuseppe Gobbi, et al.. (2023). Developmental and epileptic encephalopathy in a young Italian woman with a de novo missense variant in the CLCN4 gene: A case report. Brain and Development. 45(8). 445–450.

Bonora, Elena, Iria Neri, Annalucia Virdi, et al.. (2021). PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis. Frontiers in Medicine. 8. 688105–688105. 6 indexed citations

Brandi, Giovanni, Andrea Palloni, Daniela Turchetti, et al.. (2020). Intrahepatic cholangiocarcinoma development in a patient with a novel BAP1 germline mutation and low exposure to asbestos. Cancer Genetics. 248-249. 57–62. 13 indexed citations

Bonora, Elena, Annamaria Perri, Emanuela Scarano, et al.. (2018). HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype. Cytogenetic and Genome Research. 157(3). 135–140. 3 indexed citations

10.

Miccoli, Sara, Anna Prossomariti, Tommaso Pippucci, et al.. (2018). Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients. European Journal of Human Genetics. 26(3). 387–395. 25 indexed citations

11.

Zuntini, Roberta, Simona Ferrari, Elena Bonora, et al.. (2018). Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?. Frontiers in Genetics. 9. 378–378. 10 indexed citations

12.

Graziano, Claudio, Giovanna Cenacchi, Duccio Maria Cordelli, et al.. (2017). A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy. Journal of the Neurological Sciences. 381. 209–212. 8 indexed citations

13.

Porcelli, Anna Maria, Maria Antonietta Calvaruso, Luisa Iommarini, et al.. (2016). A unique combination of rare mitochondrial ribosomal RNA variants affects the kinetics of complex I assembly. The International Journal of Biochemistry & Cell Biology. 75. 117–122. 2 indexed citations

14.

Zuntini, Roberta, Caterina Cancrini, Andrea Finocchi, et al.. (2014). Consanguinity and Polygenic Diseases: A Model for Antibody Deficiencies. Human Heredity. 77(1-4). 144–149. 3 indexed citations

15.

Lang, Martin, Ivana Kurelac, Elisa Mariani, et al.. (2013). Where Birt–Hogg–Dubé meets Cowden Syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours. European Journal of Human Genetics. 21(10). 1169–1172. 19 indexed citations

16.

Zuntini, Roberta, Pamela Magini, Claudio Ceccarelli, et al.. (2011). Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion. Journal of Medical Genetics. 48(11). 779–782. 13 indexed citations

17.

Sazzini, Marco, Roberta Zuntini, Shirin Farjadian, et al.. (2009). An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. Genes and Immunity. 10(6). 566–578. 10 indexed citations

18.

Pippucci, Tommaso, Emanuele Panza, Eva Pompilii, et al.. (2008). Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. European Journal of Neurology. 16(1). 121–126. 12 indexed citations

19.

Gasparre, Giuseppe, Luisa Iommarini, Anna Maria Porcelli, et al.. (2008). An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. Human Mutation. 30(3). 391–396. 44 indexed citations

20.

Ferrari, Simona, Vassilios Lougaris, Stefano Giuseppe Caraffi, et al.. (2007). Mutations of the Igβ gene cause agammaglobulinemia in man. The Journal of Experimental Medicine. 204(9). 2047–2051. 54 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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