Maria Piccione

2.2k total citations
78 papers, 1.0k citations indexed

About

Maria Piccione is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maria Piccione has authored 78 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 31 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maria Piccione's work include Genomic variations and chromosomal abnormalities (19 papers), Congenital heart defects research (11 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Maria Piccione is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Congenital heart defects research (11 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Maria Piccione collaborates with scholars based in Italy, United States and Argentina. Maria Piccione's co-authors include Giovanni Corsello, Ettore Piro, Mario Giuffrè, Vincenzo Antona, Michela Malacarne, Mauro Pierluigi, Simona Cavani, L Giuffrè, Cristina Gervasini and Gregorio Serra and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and International Journal of Molecular Sciences.

In The Last Decade

Maria Piccione

70 papers receiving 942 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 Piccione Italy 21 408 384 192 141 103 78 1.0k
Assunta Albanese United Kingdom 20 446 1.1× 338 0.9× 279 1.5× 106 0.8× 137 1.3× 46 1.2k
Charu Deshpande United Kingdom 13 436 1.1× 344 0.9× 122 0.6× 61 0.4× 90 0.9× 24 1.1k
Salvatore Savasta Italy 23 542 1.3× 366 1.0× 182 0.9× 130 0.9× 94 0.9× 120 1.6k
Kathy Hodgkinson Canada 17 469 1.1× 421 1.1× 130 0.7× 99 0.7× 104 1.0× 38 1.4k
Neil Stoodley United Kingdom 17 328 0.8× 185 0.5× 451 2.3× 169 1.2× 54 0.5× 39 1.2k
Stephen R. Braddock United States 25 525 1.3× 538 1.4× 296 1.5× 240 1.7× 112 1.1× 71 1.7k
Géraldine Viot France 21 674 1.7× 647 1.7× 280 1.5× 144 1.0× 109 1.1× 56 1.4k
Patrick Rump Netherlands 21 547 1.3× 487 1.3× 314 1.6× 69 0.5× 77 0.7× 39 1.2k
George McGillivray Australia 22 471 1.2× 641 1.7× 498 2.6× 133 0.9× 58 0.6× 54 1.3k
Andrea D. Praticò Italy 23 396 1.0× 427 1.1× 254 1.3× 208 1.5× 57 0.6× 116 1.3k

Countries citing papers authored by Maria Piccione

Since Specialization
Citations

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

Fields of papers citing papers by Maria Piccione

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Piccione

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Piccione. A scholar is included among the top collaborators of Maria Piccione 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 Piccione. Maria Piccione 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.
Amodio, Emanuele, Claudio Costantino, Mario Giuffrè, et al.. (2026). INVASIVE PNEUMOCOCCAL DISEASES IN CHILDREN AGED 1-59 MONTHS IN SICILY, ITALY: IMPORTANCE OF ACTIVE FAMILY PAEDIATRICIAN SURVEILLANCE AND VACCINATION COVERAGE.. Nova Science Publishers (Nova Science Publishers, Inc.). 9.
2.
Niceta, Marcello, Simone Pizzi, Francesca Clementina Radio, et al.. (2023). Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly. Frontiers in Neurology. 14. 1090082–1090082. 1 indexed citations
3.
Malacarne, Michela, Maria Brigida Lioi, Andrea M. Chiariello, et al.. (2022). Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability. International Journal of Molecular Sciences. 23(6). 3084–3084. 3 indexed citations
4.
Cassarà, Filippo, Michela Malacarne, Domenico Coviello, et al.. (2022). Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid. Life. 13(1). 20–20. 1 indexed citations
5.
Piro, Ettore, et al.. (2022). Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 152–152. 3 indexed citations
6.
Dong, Xiaomin, Natalie B. Tan, Katherine B. Howell, et al.. (2020). Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neurodegenerative Condition with Intracranial Calcification. The American Journal of Human Genetics. 106(4). 559–569. 18 indexed citations
7.
Piccione, Maria, et al.. (2015). 4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization. European Journal of Paediatric Neurology. 19(4). 477–483. 6 indexed citations
8.
Puccio, Giuseppe, et al.. (2013). Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 39(1). 23–23. 16 indexed citations
9.
Corsello, Giovanni, Ettore Piro, Mario Giuffrè, & Maria Piccione. (2013). 16P11.2 MICRODELETION/MICRODUPLICATION SYNDROME: FURTHER CHARACTERIZATIONOF A CRITICAL REGION FOR NEUROPSYCHIATRIC DEVELOPMENT. 29. 1 indexed citations
10.
Piro, Ettore, et al.. (2013). COPY NUMBER VARIATIONS IN THE ETIOLOGY OF AUTISM SPECTRUM DISORDERS. Nova Science Publishers (Nova Science Publishers, Inc.). 29(2). 337–342.
11.
Piro, Ettore, Maria Piccione, Gianluca Marrone, Mario Giuffrè, & Giovanni Corsello. (2013). Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 39(1). 32–32. 18 indexed citations
12.
Piccione, Maria, et al.. (2013). PTEN hamartoma tumor syndromes in childhood: Description of two cases and a proposal for follow‐up protocol. American Journal of Medical Genetics Part A. 161(11). 2902–2908. 27 indexed citations
13.
Piccione, Maria, et al.. (2013). Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future. SHILAP Revista de lepidopterología. 35(3). 105–9. 8 indexed citations
14.
Cavani, Simona, Mauro Pierluigi, Vincenzo Antona, et al.. (2012). Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by fish and array-CGH. Journal of Applied Genetics. 53(3). 285–288. 4 indexed citations
15.
Piccione, Maria, Simona Cavani, Michela Malacarne, et al.. (2011). Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders. Journal of Genetics. 90(3). 473–477. 4 indexed citations
16.
Piccione, Maria, et al.. (2011). Silver Russell syndrome. Atlas of Genetics and Cytogenetics in Oncology and Haematology. 2 indexed citations
17.
Piccione, Maria, Vincenzo Antona, Marcello Niceta, et al.. (2008). Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome. European Journal of Pediatrics. 168(9). 1135–1139. 11 indexed citations
18.
Andria, Generoso, Daniela Concolino, Maria Piccione, et al.. (2003). Down syndrome and breastfeeding. Acta Paediatrica. 92(12). 1479–1481. 31 indexed citations
19.
Piro, Ettore, et al.. (1991). Kabuki make-up (Niikawa-Kuroki) syndrome: Clinical and radiological observations in two sicilian children. Pediatric Radiology. 21(6). 428–431. 25 indexed citations
20.
Piccione, Maria, et al.. (1975). [Fast-acting antidepressive agents: comparison of trazodone and desipramine in a controlled double-blind trial].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 72(1). 43–53. 1 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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