Claudio Graziano

2.6k total citations
77 papers, 1.2k citations indexed

About

Claudio Graziano is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Claudio Graziano has authored 77 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 32 papers in Genetics and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Claudio Graziano's work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (9 papers) and Hearing, Cochlea, Tinnitus, Genetics (7 papers). Claudio Graziano is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (9 papers) and Hearing, Cochlea, Tinnitus, Genetics (7 papers). Claudio Graziano collaborates with scholars based in Italy, United States and United Kingdom. Claudio Graziano's co-authors include Marco Seri, Kristen L. Nowak, Nigel G. Laing, Pamela Magini, Suzanne Lillis, Alan H. Beggs, Stella Mitrani‐Rosenbaum, Danielle E. Dye, Nicole Monnier and Thomas Winder and has published in prestigious journals such as Journal of Clinical Oncology, Blood and International Journal of Molecular Sciences.

In The Last Decade

Claudio Graziano

73 papers receiving 1.2k citations

Peers

Countries citing papers authored by Claudio Graziano

Since Specialization

Citations

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

Fields of papers citing papers by Claudio Graziano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudio Graziano

This figure shows the co-authorship network connecting the top 25 collaborators of Claudio Graziano. A scholar is included among the top collaborators of Claudio Graziano 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 Claudio Graziano. Claudio Graziano 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	Low WT1 Expression Identifies a Subset of Acute Myeloid Leukemia with a Distinct Genotype 2025 ·Cancers ·Michela Rondoni, Giovanni Marconi, Annalisa Nicoletti, Barbara Giannini, Elisa Zuffa, (unknown), (unknown), (unknown), Federica Monaco, (unknown), Serena Rocchi, Beatrice Anna Zannetti, (unknown), Claudio Graziano, Monica Bocchia, Francesco Lanza	0
2	Molecular and Clinical Features of Adrenocortical Tumors in Beckwith–Wiedemann Spectrum 2024 ·Cancers ·Diana Carli, (unknown), (unknown), (unknown), Stefano Vallero, Elisa Tirtei, (unknown), Simona Cardaropoli, Francesca Montanari, Claudio Graziano, Paola Quarello, (unknown), Angela Sparago, Giovanni Battista Ferrero, Franca Fagioli, Alessandro Mussa	0
3	Landscape of Constitutional SOX4 Variation in Human Disorders 2024 ·Genes ·(unknown), Claudio Graziano	4
4	Modifiers of Autosomal Dominant Polycystic Kidney Disease Severity: The Role of PKD1 Hypomorphic Alleles 2023 ·Genes ·(unknown), Francesca Montanari, (unknown), Irene Capelli, Claudio La Scola, Andrea Pasini, Claudio Graziano	3
5	The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 2023 ·Biomedicines ·Beatrice Spedicati, (unknown), (unknown), (unknown), Stefania Lenarduzzi, Claudio Graziano, Livia Garavelli, Sara Miccoli, Stefania Bigoni, Anna Morgan, Giorgia Girotto	5
6	A Male Child with Infantile Epilepsy due to a Mosaic Missense Variant of PCDH19 2023 ·Molecular Syndromology ·(unknown), Raffaella Minardi, Antonella Boni, Jacopo Pruccoli, Antonella Pini, Laura Licchetta, Francesca Bisulli, Claudio Graziano, Marco Seri	1
7	HDAC9structural variants disruptingTWIST1transcriptional regulation lead to craniofacial and limb malformations 2022 ·Genome Research ·(unknown), Idit Dahan, (unknown), (unknown), Sarah Vergult, Marta Vidal‐García, Pamela Magini, Claudio Graziano, (unknown), (unknown), Anna Maria Nardone, Francesco Brancati, Alberto Fernández‐Jaén, (unknown), Benedikt Hallgrímsson, Ramon Y. Birnbaum	11
8	There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss 2021 ·Biomedicines ·Anna Morgan, Flavio Faletra, (unknown), Martina La Bianca, Laura Licchetta, Paolo Gasparini, Claudio Graziano, Giorgia Girotto	2
9	A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops 2021 ·Genes ·Daniele Castiglia, Paola Fortugno, Angelo Giuseppe Condorelli, Sabina Barresi, Naomi De Luca, Simone Pizzi, Iria Neri, Claudio Graziano, Diletta Trojan, Diego Ponzin, Sabrina Rossi, Giovanna Zambruno, Marco Tartaglia	7
10	Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study 2019 ·Sleep Medicine ·(unknown), (unknown), (unknown), Silvia Bonetti, (unknown), Ivan Ivanovski, Stefano Giuseppe Caraffi, Lucio Giordano, Patrizia Accorsi, Salvatore Savasta, Federico Raviglione, Antonella Boni, Daniele Grioni, Claudio Graziano, Livia Garavelli, Duccio Maria Cordelli	5
11	De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism 2019 ·The American Journal of Human Genetics ·(unknown), Baojin Yao, (unknown), Tommaso Pippucci, (unknown), Joshua D. Smith, (unknown), Susanne J. Kühl, John Dean, Daniela T. Pilz, Susan Holder, Alisdair McNeill, Claudio Graziano, Véronique Lefèbvre	6
12	<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
13	Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants 2018 ·Journal of Clinical Immunology ·Elisa Adele Colombo, Nursel Elçioğlu, Claudio Graziano, (unknown), (unknown), Iria Neri, Elena Facchini, Mariangela Greco, Cristina Gervasini, Lidia Larizza	6
14	Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 2015 ·Molecular Cytogenetics ·Pamela Magini, Monica Poscente, Simona Ferrari, Manuela Vargiolu, Elena Bacchelli, Claudio Graziano, Anita Wischmeijer, Daniela Turchetti, Elisabetta Malaspina, Valentina Marchiani, Duccio Maria Cordelli, Emilio Franzonı, G. Cara Romeo, Marco Seri	15
15	Genetics of human enteric neuropathies 2012 ·Progress in Neurobiology ·Emanuele Panza, Charles H. Knowles, Claudio Graziano, Nikhil Thapar, Alan J. Burns, Marco Seri, Vincenzo Stanghellini, Roberto De Giorgio	30
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	Mutations and polymorphisms of the skeletal muscle Î±-actin gene (ACTA1) 2009 ·Human Mutation ·Nigel G. Laing, Danielle E. Dye, Carina Wallgren‐Pettersson, Gabriele Richard, Nicole Monnier, Suzanne Lillis, Thomas Winder, (unknown), Claudio Graziano, Stella Mitrani‐Rosenbaum, (unknown), John C. Sparrow, Alan H. Beggs, Kristen L. Nowak	173
18	Functional polymorphisms of the microsomal epoxide hydrolase gene: A reappraisal on a early-onset lung cancer patients series 2008 ·Lung Cancer ·Claudio Graziano, Camilla Comin, (unknown), Luca Novelli, Letterio S. Politi, Luca Messerini, (unknown), Berardino Porfirio	22
19	A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation 2007 ·American Journal of Medical Genetics Part A ·Claudio Graziano, Angela D’Elia, Laura Mazzanti, (unknown), (unknown), Emanuela Scarano, Daniela Turchetti, Emilio Franzonı, G. Cara Romeo, Giuseppe Damante, Marco Seri	25
20	Study of endocrinological functions and sexual behaviour in carbon disulphide workers. 1978 ·PubMed ·(unknown), Pier Alberto Bertazzi, M Tomasini, (unknown), Claudio Graziano, Rosangela Invernizzi, Rovílson Gilioli	23

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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