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

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

#	Work	Indexed citations
1	Myoclonic reflex and non‐reflex seizures in a female child with Coffin–Lowry syndrome: Clinical vignette 2025 ·Epileptic Disorders ·(unknown), (unknown), Carlotta Spagnoli, (unknown), A Cavalli, Stefano Giuseppe Caraffi, (unknown), (unknown), Roberta Russo, Iris Scala, Roberta Zuntini, Livia Garavelli, Daniele Frattini, Carlo Fusco	1
2	Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures 2023 ·Frontiers in Neurology ·(unknown), Marzia Pollazzon, Cecilia Mancini, (unknown), (unknown), Simone Pizzi, Daniele Frattini, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Roberta Zuntini, (unknown), Marcello Niceta, Francesca Clementina Radio, Marco Tartaglia, Livia Garavelli, Carlo Fusco	3
3	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 2023 ·Frontiers in Genetics ·Roberta Zuntini, (unknown), Lucia Pedace, Evelina Miele, Stefano Giuseppe Caraffi, (unknown), (unknown), Simone Pizzi, Francesca Clementina Radio, Angelica Barone, Simonetta Piana, Patrizia Bertolini, Domenico Corradi, (unknown), Caterina Longo, Alberico Motolese, Orsetta Zuffardi, Marco Tartaglia, Livia Garavelli	1
4	Characterization of BRCA Deficiency in Ovarian Cancer 2023 ·Cancers ·Giovanna Barbero, Roberta Zuntini, Pamela Magini, (unknown), (unknown), Anna Myriam Perrone, Daniela Rubino, (unknown), Antonio De Leo, Claudio Ceccarelli, Lea Godino, Sara Miccoli, Simona Ferrari, Donatella Santini, Pierandrea De Iaco, Claudio Zamagni, (unknown), Daniela Turchetti	1
5	Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the SOX2 Gene: Ultrasound, Pathological, and Cytogenetic Findings 2023 ·Fetal and Pediatric Pathology ·Maria Paola Bonasoni, Giuseppina Comitini, (unknown), (unknown), (unknown), (unknown), Stefano Giuseppe Caraffi, Roberta Zuntini, Marzia Pollazzon, Andrea Palicelli, Livia Garavelli	1
6	Developmental and epileptic encephalopathy in a young Italian woman with a de novo missense variant in the CLCN4 gene: A case report 2023 ·Brain and Development ·Jessica Rossi, Marco Russo, Giuseppe Gobbi, Antonio Terracciano, Roberta Zuntini, Stefano Giuseppe Caraffi, Antonio Novelli, Livia Garavelli, Franco Valzania, Romana Rizzi	0
7	PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis 2021 ·Frontiers in Medicine ·(unknown), Elena Bonora, Iria Neri, Annalucia Virdi, Alba Guglielmo, (unknown), Claudio Ceccarelli, Laura Benedetta Amato, Anna Lanzoni, Sara Miccoli, Giuseppe Gasparre, Roberta Zuntini, Daniela Turchetti	6
8	Intrahepatic cholangiocarcinoma development in a patient with a novel BAP1 germline mutation and low exposure to asbestos 2020 ·Cancer Genetics ·Giovanni Brandi, (unknown), Andrea Palloni, Daniela Turchetti, Roberta Zuntini, Federica Pedica, Giorgio Frega, Stefania De Lorenzo, Francesca Abbati, Alessandro Rizzo, Mariacristina Di Marco, Francesco Massari, Simona Tavolari	13
9	<b><i>HDAC8</i></b> Loss of Function and <b><i>SHOX</i></b> Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype 2018 ·Cytogenetic and Genome Research ·(unknown), Elena Bonora, Annamaria Perri, Emanuela Scarano, Laura Mazzanti, (unknown), Roberta Zuntini, Soara Menabò, Claudio Graziano	3
10	Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients 2018 ·European Journal of Human Genetics ·(unknown), Sara Miccoli, Anna Prossomariti, Tommaso Pippucci, Elena Bonora, (unknown), Flavia Palombo, Roberta Zuntini, Tiziana Balbi, Claudio Ceccarelli, Franco Bazzoli, Luigi Ricciardiello, Daniela Turchetti, Giulia Piazzi	25
11	Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help? 2018 ·Frontiers in Genetics ·Roberta Zuntini, Simona Ferrari, Elena Bonora, (unknown), (unknown), (unknown), Lea Godino, Sara Miccoli, Daniela Turchetti	10
12	A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy 2017 ·Journal of the Neurological Sciences ·(unknown), Claudio Graziano, Giovanna Cenacchi, Duccio Maria Cordelli, Roberta Zuntini, Valentina Papa, Anna Maria Magistà, Monica Gagliardi, (unknown), Aldo Quattrone, Grazia Annesi	8
13	A unique combination of rare mitochondrial ribosomal RNA variants affects the kinetics of complex I assembly 2016 ·The International Journal of Biochemistry & Cell Biology ·Anna Maria Porcelli, Maria Antonietta Calvaruso, Luisa Iommarini, Ivana Kurelac, Roberta Zuntini, Simona Ferrari, Giuseppe Gasparre	2
14	Consanguinity and Polygenic Diseases: A Model for Antibody Deficiencies 2014 ·Human Heredity ·(unknown), Roberta Zuntini, Caterina Cancrini, Andrea Finocchi, Giulia Angelino, Paolo Rossi, Simona Ferrari	3
15	Where Birt–Hogg–Dubé meets Cowden Syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours 2013 ·European Journal of Human Genetics ·(unknown), Martin Lang, Ivana Kurelac, Elisa Mariani, Flora Guerra, Roberta Zuntini, Giovanni Tallini, Alan Mackay, Jorge S. Reis‐Filho, Marco Seri, Daniela Turchetti, Giuseppe Gasparre	19
16	Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion 2011 ·Journal of Medical Genetics ·(unknown), Roberta Zuntini, Pamela Magini, Claudio Ceccarelli, Iria Neri, Serenella Cerasoli, Claudio Graziano, Giuseppe Gasparre, Daniela Turchetti	13
17	An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene 2009 ·Genes and Immunity ·Marco Sazzini, Roberta Zuntini, Shirin Farjadian, Isabella Quinti, Giampaolo Ricci, (unknown), Sérgio Ferrari, Francesc Calafell, Donata Luiselli	10
18	Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity 2008 ·European Journal of Neurology ·Tommaso Pippucci, Emanuele Panza, Eva Pompilii, Vincenzo Donadio, Antonella Borreca, Carla Babalini, Carlo Patrono, Roberta Zuntini, Toshitaka Kawarai, Giorgio Bernardi, Rocco Liguori, G. Cara Romeo, P. Montagna, Antonio Orlacchio, Marco Seri	12
19	An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells 2008 ·Human Mutation ·Giuseppe Gasparre, Luisa Iommarini, Anna Maria Porcelli, Martin Lang, Gian Gaetano Ferri, Ivana Kurelac, Roberta Zuntini, Elisa Mariani, (unknown), Ernesto Pasquini, Gianandrea Pasquinelli, Anna Ghelli, Elena Bonora, Claudio Ceccarelli, Michela Rugolo, Nunzio Salfi, Giovanni Romeo, Valério Carelli	44
20	Mutations of the Igβ gene cause agammaglobulinemia in man 2007 ·The Journal of Experimental Medicine ·Simona Ferrari, Vassilios Lougaris, Stefano Giuseppe Caraffi, Roberta Zuntini, Jianying Yang, Annarosa Soresina, Jordi Antón, (unknown), Cesare Rossi, Michael Reth, Alessandro Plebani	54

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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