Maria Iascone

4.0k total citations
115 papers, 1.5k citations indexed

About

Maria Iascone is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Maria Iascone has authored 115 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 39 papers in Genetics and 30 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Maria Iascone's work include Cardiomyopathy and Myosin Studies (18 papers), Genomics and Rare Diseases (15 papers) and Genomic variations and chromosomal abnormalities (13 papers). Maria Iascone is often cited by papers focused on Cardiomyopathy and Myosin Studies (18 papers), Genomics and Rare Diseases (15 papers) and Genomic variations and chromosomal abnormalities (13 papers). Maria Iascone collaborates with scholars based in Italy, United States and United Kingdom. Maria Iascone's co-authors include Laura Pezzoli, Daniela Marchetti, Paolo Ferrazzi, Michele Senni, Attilio Iacovoni, Paolo Spirito, Samuele Pentiricci, Maria Elena Sana, Simona Vittorini and Anna Cereda and has published in prestigious journals such as Circulation, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Maria Iascone

104 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Iascone Italy 20 608 472 320 268 265 115 1.5k
Chengqi Xu China 21 639 1.1× 280 0.6× 120 0.4× 140 0.5× 164 0.6× 78 1.2k
Aileen M. Healy United States 13 567 0.9× 262 0.6× 223 0.7× 135 0.5× 156 0.6× 18 1.4k
Salma M. Wakil Saudi Arabia 19 517 0.9× 135 0.3× 268 0.8× 293 1.1× 115 0.4× 67 1.2k
Jared M. Evans United States 25 1.2k 1.9× 446 0.9× 189 0.6× 145 0.5× 136 0.5× 43 1.7k
Lora Jh Bean United States 24 862 1.4× 176 0.4× 606 1.9× 210 0.8× 139 0.5× 58 1.6k
Mitsuhiro Kamisago Japan 16 1.4k 2.3× 1.1k 2.3× 240 0.8× 335 1.3× 349 1.3× 36 2.2k
Urban Hellman Sweden 17 908 1.5× 183 0.4× 108 0.3× 178 0.7× 107 0.4× 47 1.3k
Marleen Renard Belgium 21 347 0.6× 263 0.6× 104 0.3× 138 0.5× 138 0.5× 50 1.5k
Melissa Swinnen Belgium 16 600 1.0× 561 1.2× 80 0.3× 61 0.2× 217 0.8× 24 1.2k
Koshiro Monzen Japan 16 1.2k 1.9× 351 0.7× 183 0.6× 202 0.8× 300 1.1× 25 1.4k

Countries citing papers authored by Maria Iascone

Since Specialization
Citations

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

Fields of papers citing papers by Maria Iascone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Iascone

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Iascone. A scholar is included among the top collaborators of Maria Iascone 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 Maria Iascone. Maria Iascone 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.
Pezzani, Lidia, Angelo Selicorni, Maria Francesca Bedeschi, et al.. (2025). Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies—30 Years' Experience From a Third Level Center. Clinical Genetics. 109(4). 707–716.
2.
Teutonico, Federica, Ugo Cavallari, Paola Doneda, et al.. (2024). Early onset epileptic and developmental encephalopathy and MOGS variants: a new diagnosis in the whole exome sequencing (WES) ERA. Neurogenetics. 25(3). 281–286.
3.
Pezzoli, Laura, Lidia Pezzani, Antonella Lettieri, et al.. (2024). Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter. Orphanet Journal of Rare Diseases. 19(1). 481–481. 1 indexed citations
4.
5.
Spaccini, Luigina, et al.. (2023). Case report: Early-onset parkinsonism among the neurological features in children with PHACTR1 variants. Frontiers in Neurology. 14. 1181015–1181015.
6.
Masnada, Silvia, Paola Anna Erba, Anna Camporesi, et al.. (2023). FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy. Neurological Sciences. 44(9). 3037–3043. 4 indexed citations
7.
Jokela, Manu, Meriel McEntagart, Tessa Homfray, et al.. (2023). The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum. Journal of Medical Genetics. 60(9). 866–873. 8 indexed citations
8.
Rinaldi, Berardo, M. Rimoldi, Roberta Villa, et al.. (2023). Chung–Jansen syndrome can mimic Cornelia de Lange syndrome: Another player among chromatinopathies?. American Journal of Medical Genetics Part A. 191(6). 1586–1592. 4 indexed citations
9.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2023). Comparison of first‐tier whole‐exome sequencing with a multi‐step traditional approach for diagnosing paediatric outpatients: An Italian prospective study. Molecular Genetics & Genomic Medicine. 12(1). e2316–e2316. 4 indexed citations
10.
Girolami, Francesca, Maria Iascone, Laura Pezzoli, et al.. (2022). Indicazioni all’esecuzione del test genetico nella diagnosi delle cardiomiopatie ad esordio pediatrico: percorso clinico della Società Italiana di Cardiologia Pediatrica. Giornale italiano di cardiologia. 23(7). 505–515. 2 indexed citations
11.
Consales, Alessandra, Roberta Villa, Nicoletta Resta, et al.. (2022). Prenatal overgrowth and polydramnios: Would you think about Noonan syndrome?. SHILAP Revista de lepidopterología. 10(8). e6256–e6256. 2 indexed citations
12.
Iascone, Maria, Luigina Spaccini, Davide Tonduti, et al.. (2022). Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child. Genes. 13(3). 442–442. 14 indexed citations
13.
Geroldi, Alessandro, Paola Origone, Anna Pichiecchio, et al.. (2021). A novel mutation in COL3A1 associates to vascular Ehlers–Danlos syndrome with predominant musculoskeletal involvement. Molecular Genetics & Genomic Medicine. 9(9). e1753–e1753. 7 indexed citations
14.
Li, Rachel, Scott A. Turner, Richard H. van Jaarsveld, et al.. (2020). HNRNPH1 ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome. Clinical Genetics. 98(1). 91–98. 18 indexed citations
15.
Peron, Angela, et al.. (2020). PIGW‐related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literature. American Journal of Medical Genetics Part A. 182(6). 1477–1482. 8 indexed citations
16.
Dordoni, Chiara, Federico Prefumo, Maria Iascone, et al.. (2019). Prenatal findings in oral‐facial‐digital syndrome type VI: Report of three cases and literature review. Prenatal Diagnosis. 39(8). 652–655. 2 indexed citations
17.
Pezzani, Lidia, Daniela Marchetti, Anna Cereda, et al.. (2018). Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy. American Journal of Medical Genetics Part A. 176(12). 2867–2871. 24 indexed citations
18.
Sana, Maria Elena, Andrea Spitaleri, Dimitrios Spiliotopoulos, et al.. (2014). Identification of a novel de novo deletion in RAF1 associated with biventricular hypertrophy in Noonan syndrome. American Journal of Medical Genetics Part A. 164(8). 2069–2073. 5 indexed citations
19.
Iascone, Maria, et al.. (2009). Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.. PubMed. 126(2). 351–351. 3 indexed citations
20.
Chessa, Massimo, et al.. (2000). Familial occurrence of isolated right ventricular hypoplasia. American Journal of Medical Genetics. 90(5). 356–357. 11 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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