Antonio Novelli

15.4k total citations
305 papers, 3.4k citations indexed

About

Antonio Novelli is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Antonio Novelli has authored 305 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 173 papers in Genetics, 155 papers in Molecular Biology and 33 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Antonio Novelli's work include Genomic variations and chromosomal abnormalities (90 papers), Genetics and Neurodevelopmental Disorders (58 papers) and Congenital heart defects research (52 papers). Antonio Novelli is often cited by papers focused on Genomic variations and chromosomal abnormalities (90 papers), Genetics and Neurodevelopmental Disorders (58 papers) and Congenital heart defects research (52 papers). Antonio Novelli collaborates with scholars based in Italy, United States and France. Antonio Novelli's co-authors include Bruno Dallapiccola, Laura Bernardini, M. Cristina Digilio, Anna Capalbo, Sara Loddo, Agatino Battaglia, Viola Alesi, Emanuele Agolini, Giuseppe Novelli and Anwar Baban and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Antonio Novelli

280 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antonio Novelli Italy 27 1.7k 1.5k 423 276 258 305 3.4k
Erik A. Sistermans Netherlands 37 2.7k 1.6× 2.9k 1.8× 1.0k 2.4× 199 0.7× 395 1.5× 123 5.6k
Swaroop Aradhya United States 26 1.9k 1.1× 1.2k 0.7× 590 1.4× 70 0.3× 219 0.8× 85 2.8k
Marwan Shinawi United States 32 1.5k 0.9× 2.4k 1.5× 375 0.9× 50 0.2× 415 1.6× 137 4.3k
Bruce Bennetts Australia 31 1.4k 0.8× 1.3k 0.8× 246 0.6× 67 0.2× 471 1.8× 101 3.2k
Kenjiro Kosaki Japan 35 1.8k 1.1× 2.7k 1.8× 591 1.4× 85 0.3× 335 1.3× 363 5.2k
Tibor A. Rauch United States 28 887 0.5× 2.7k 1.8× 182 0.4× 87 0.3× 311 1.2× 50 3.6k
Giuseppe Zampino Italy 30 1.1k 0.6× 3.1k 2.0× 377 0.9× 153 0.6× 1.4k 5.5× 184 4.7k
Maja Di Rocco Italy 34 860 0.5× 1.5k 1.0× 350 0.8× 55 0.2× 205 0.8× 147 3.6k
Dorit Lev Israel 39 1.0k 0.6× 2.0k 1.3× 1.6k 3.8× 358 1.3× 120 0.5× 188 4.9k
Paul J. Benke United States 24 828 0.5× 2.0k 1.3× 348 0.8× 113 0.4× 174 0.7× 54 3.0k

Countries citing papers authored by Antonio Novelli

Since Specialization
Citations

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

Fields of papers citing papers by Antonio Novelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Novelli

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Novelli. A scholar is included among the top collaborators of Antonio Novelli 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 Antonio Novelli. Antonio Novelli 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.
Grati, Francesca Romana, Antonio Capalbo, Maria Carla Pittalis, et al.. (2025). Prenatal diagnosis following preimplantation genetic testing (PGT): recommendations of the Italian Society of Human Genetics (SIGU). Journal of Assisted Reproduction and Genetics. 42(3). 1015–1024. 1 indexed citations
2.
Baldo, Giada Del, Andrea Carai, Antonella Cacchione, et al.. (2024). A second case report of medulloblastoma in a patient carrying biallelic pathogenic MUTYH germline variants. Neuropathology and Applied Neurobiology. 50(2). e12968–e12968.
3.
Stregapede, Fabrizia, Vito Luigi Colona, Francesco Nicita, et al.. (2024). POLR3B de novo variants are a rare cause of infantile myoclonic epilepsy. Seizure. 121. 141–146.
4.
Gnazzo, Maria, et al.. (2024). Usmani‐Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant. Clinical Genetics. 106(1). 109–113.
5.
Micale, Lucia, Carmela Fusco, Maria Lisa Dentici, et al.. (2024). Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomalies. European Journal of Human Genetics. 33(6). 718–726. 1 indexed citations
6.
Travaglini, Lorena, Marina Macchiaiolo, Giacomo Garone, et al.. (2024). Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes. 15(4). 508–508.
7.
Cocciadiferro, Dario, Tommaso Mazza, Nicola Ullmann, et al.. (2024). Two Novel Biallelic Variants in the FARSA Gene: The First Italian Case and a Literature Review. Genes. 15(12). 1573–1573.
8.
Calcagni, Giulio, Federica Ferrigno, Maria Lisa Dentici, et al.. (2024). Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome. Diagnostics. 14(6). 594–594. 1 indexed citations
9.
Bernardini, Laura, Marzia Pollazzon, Maria Grazia Giuffrida, et al.. (2023). Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes. Genes. 14(8). 1526–1526. 2 indexed citations
10.
Rapini, Novella, Patrizia Ippolita Patera, Riccardo Schiaffini, et al.. (2022). Monogenic diabetes clinic (MDC): 3-year experience. Acta Diabetologica. 60(1). 61–70. 6 indexed citations
11.
Siano, Maria, Ilaria Maggio, Roberta Petillo, et al.. (2022). De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome 2: Case Report and Literature Review. Pediatric Reports. 14(1). 131–139. 16 indexed citations
12.
Baban, Anwar, Viola Alesi, Silvia Genovese, et al.. (2022). Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients. Journal of Cardiovascular Development and Disease. 9(10). 332–332. 4 indexed citations
13.
Silvetti, Massimo Stefano, Rachele Adorisio, May El Hachem, et al.. (2022). Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?. Journal of Cardiovascular Development and Disease. 9(2). 47–47. 14 indexed citations
14.
Agolini, Emanuele, Elena Botta, M. Cristina Digilio, et al.. (2021). Expansion of the clinical and molecular spectrum of an XPD ‐related disorder linked to biallelic mutations in ERCC2 gene. Clinical Genetics. 99(6). 842–848. 5 indexed citations
15.
Alesi, Viola, et al.. (2021). A New Intronic Variant in ECEL1 in Two Patients with Distal Arthrogryposis Type 5D. International Journal of Molecular Sciences. 22(4). 2106–2106. 4 indexed citations
16.
Alfieri, Paolo, Maria Lisa Dentici, M. Cristina Digilio, et al.. (2021). Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study. Journal of Clinical Medicine. 10(7). 1523–1523. 2 indexed citations
17.
Pascolini, Giulia, Emanuele Agolini, Antonio Novelli, Silvia Majore, & Paola Grammatico. (2020). The p.Arg377Trp variant in ACTL6A underlines a recognizable BAF‐opathy phenotype. Clinical Genetics. 97(4). 672–674. 3 indexed citations
18.
Brasch‐Andersen, Charlotte, Helen Cox, Michael Parker, et al.. (2020). A new 1p36.13‐1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis. Clinical Genetics. 97(6). 927–932. 2 indexed citations
19.
Alfieri, Paolo, Lorenzo Sinibaldi, Giovanni Valeri, et al.. (2020). Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases. Genes Brain & Behavior. 19(7). e12687–e12687. 5 indexed citations
20.
Agolini, Emanuele, Claudio Cherchi, Emanuele Bellacchio, et al.. (2019). Expanding the clinical and molecular spectrum of lethal congenital contracture syndrome 8 associated with biallelic variants of ADCY6. Clinical Genetics. 97(4). 649–654. 4 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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