Pio D’Adamo

12.2k total citations
84 papers, 2.8k citations indexed

About

Pio D’Adamo is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Pio D’Adamo has authored 84 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 19 papers in Genetics and 13 papers in Sensory Systems. Recurrent topics in Pio D’Adamo's work include Genetics and Neurodevelopmental Disorders (12 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). Pio D’Adamo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Hearing, Cochlea, Tinnitus, Genetics (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). Pio D’Adamo collaborates with scholars based in Italy, United States and Qatar. Pio D’Adamo's co-authors include Paolo Gasparini, Massimo Zeviani, Daniele Ghezzi, Erika Fernández‐Vizarra, Graziella Uziel, Carmela Lanzara, Valeria Tiranti, Federica Invernizzi, Yvonne Koelliker and Beverly J. Tepper and has published in prestigious journals such as Nature Genetics, The Journal of Immunology and PLoS ONE.

In The Last Decade

Pio D’Adamo

81 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pio D’Adamo Italy 24 1.6k 597 376 351 349 84 2.8k
Isabel Varela‐Nieto Spain 39 2.5k 1.6× 115 0.2× 1.5k 3.9× 202 0.6× 235 0.7× 146 5.2k
Robin R. Hodges United States 32 777 0.5× 180 0.3× 176 0.5× 239 0.7× 74 0.2× 98 2.9k
Nathan Fischel‐Ghodsian United States 47 4.8k 3.0× 877 1.5× 2.1k 5.5× 133 0.4× 884 2.5× 106 6.8k
Sandra T. Cooper Australia 38 2.7k 1.7× 139 0.2× 45 0.1× 77 0.2× 319 0.9× 95 3.6k
Shahid Mahmood Baig Pakistan 26 1.3k 0.8× 47 0.1× 137 0.4× 94 0.3× 536 1.5× 102 2.4k
Atsushi Watanabe Japan 29 1.1k 0.7× 29 0.0× 243 0.6× 195 0.6× 438 1.3× 137 3.0k
Cas Simons Australia 25 2.0k 1.3× 79 0.1× 69 0.2× 70 0.2× 368 1.1× 73 2.8k
Kazumasa Morita Japan 24 2.4k 1.5× 62 0.1× 107 0.3× 126 0.4× 157 0.4× 44 4.6k
Toni R. Prezant United States 20 1.9k 1.2× 372 0.6× 660 1.8× 24 0.1× 232 0.7× 28 2.9k
Jason Perret Belgium 30 1.6k 1.0× 26 0.0× 296 0.8× 381 1.1× 373 1.1× 86 3.3k

Countries citing papers authored by Pio D’Adamo

Since Specialization
Citations

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

Fields of papers citing papers by Pio D’Adamo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pio D’Adamo. 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 Pio D’Adamo. The network helps show where Pio D’Adamo may publish in the future.

Co-authorship network of co-authors of Pio D’Adamo

This figure shows the co-authorship network connecting the top 25 collaborators of Pio D’Adamo. A scholar is included among the top collaborators of Pio D’Adamo 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 Pio D’Adamo. Pio D’Adamo 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.
Ura, Blendi, Pietro Campiglia, Giovanni Peri, et al.. (2025). Deep Proteomics Analysis Unravels the Molecular Signatures of Tonsillar B Cells in PFAPA and OSAS in the Pediatric Population. International Journal of Molecular Sciences. 26(14). 6621–6621.
2.
Lucafò, Marianna, Alessandro Amaddeo, Pio D’Adamo, et al.. (2024). Neuron‐Derived Extracellular Vesicles miRNA Profiles Identify Children Who Experience Adverse Events after Ketamine Administration for Procedural Sedation. Clinical Pharmacology & Therapeutics. 117(1). 174–183. 5 indexed citations
3.
Moura, Ronald, et al.. (2024). Genomic instability in congenital lung malformations in children. Pediatric Surgery International. 40(1). 248–248. 2 indexed citations
4.
Tricarico, Paola Maura, Ronald Moura, Pio D’Adamo, et al.. (2023). Unraveling the Epigenetic Tapestry: Decoding the Impact of Epigenetic Modifications in Hidradenitis Suppurativa Pathogenesis. Genes. 15(1). 38–38. 9 indexed citations
5.
Stazio, Mariateresa Di, Caterina Zanus, Flavio Faletra, et al.. (2023). Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders. Genes. 14(2). 250–250. 3 indexed citations
6.
Pederiva, Federica, Steven S. Rothenberg, Nigel Hall, et al.. (2023). Congenital lung malformations. Nature Reviews Disease Primers. 9(1). 60–60. 33 indexed citations
7.
8.
Brumatti, Liza Vecchi, Valentina Rosolen, Marika Mariuz, et al.. (2020). Impact of Methylmercury and Other Heavy Metals Exposure on Neurocognitive Function in Children Aged 7 Years: Study Protocol of the Follow-up. Journal of Epidemiology. 31(2). 157–163. 10 indexed citations
9.
Navarra, Chiara Ottavia, Marco Bobbo, Pio D’Adamo, et al.. (2020). Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report. BMC Pediatrics. 20(1). 201–201. 5 indexed citations
10.
Stazio, Mariateresa Di, Chiara Collesi, Diego Vozzi, et al.. (2018). TBL1Y: a new gene involved in syndromic hearing loss. European Journal of Human Genetics. 27(3). 466–474. 15 indexed citations
11.
Morgan, Anna, Ilaria Gandin, Pietro Palumbo, et al.. (2015). Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 781. 32–36. 9 indexed citations
12.
Athanasakis, Emmanouil, Danilo Licastro, Flavio Faletra, et al.. (2013). Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection. American Journal of Medical Genetics Part A. 164(1). 170–176. 31 indexed citations
13.
Faletra, Flavio, Giorgia Girotto, Pio D’Adamo, et al.. (2013). A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss. Gene. 534(2). 236–239. 31 indexed citations
14.
Perotti, Daniela, Filippo Spreafico, Federica Torri, et al.. (2012). Genomic profiling by whole‐genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse. Genes Chromosomes and Cancer. 51(7). 644–653. 20 indexed citations
15.
Girotto, Giorgia, Nicola Pirastu, Rossella Sorice, et al.. (2011). Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways: Figure 1. Journal of Medical Genetics. 48(6). 369–374. 59 indexed citations
16.
Ghezzi, Daniele, Irina F. Sevrioukova, Federica Invernizzi, et al.. (2010). Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor. The American Journal of Human Genetics. 86(4). 639–649. 171 indexed citations
17.
Ghezzi, Daniele, Ann Saada, Pio D’Adamo, et al.. (2008). FASTKD2 Nonsense Mutation in an Infantile Mitochondrial Encephalomyopathy Associated with Cytochrome C Oxidase Deficiency. The American Journal of Human Genetics. 83(3). 415–423. 86 indexed citations
18.
Leva, Francesca Di, Pio D’Adamo, Maria Vittoria Cubellis, et al.. (2006). Identification of a Novel Mutation in the Myosin VIIA Motor Domain in a Family with Autosomal Dominant Hearing Loss (DFNA11). Audiology and Neurotology. 11(3). 157–164. 24 indexed citations
19.
Coppola, Giovanni, Chiara Criscuolo, Salvatore Striano, et al.. (2005). Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. Journal of Neurology. 252(8). 897–900. 5 indexed citations
20.
Santoro, Lucio, Fiore Manganelli, Luigi Di Maio, et al.. (2002). Charcot–Marie–Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. Neuromuscular Disorders. 12(4). 399–404. 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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