Lucia Perone

525 total citations
21 papers, 361 citations indexed

About

Lucia Perone is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lucia Perone has authored 21 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lucia Perone's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (5 papers). Lucia Perone is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (5 papers). Lucia Perone collaborates with scholars based in Italy, Denmark and United Kingdom. Lucia Perone's co-authors include Andrea Riccio, Maria Vittoria Cubellis, Flavia Cerrato, Fortunato Lonardo, Generoso Andria, Orazio Palumbo, Massimo Carella, Angela Sparago, Silvia Russo and Margherita Silengo and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Lucia Perone

21 papers receiving 333 citations

Peers

Lucia Perone

GENET

PPCH

A. Kuechler Germany

N. A. Skryabin Russia

Mônica M. França Brazil

Nicholas M. Robert Canada

Ying Peng China

Yanan Hai China

Jonathan J. Wilde United States

Hazel L. Kinnell United Kingdom

Xiangfan Zhang Canada

Dale McAninch Australia

A. Kuechler Germany

Lucia Perone

290 ×1.3

GENET

273 ×1.4

91 ×1.1

PPCH

50 ×1.1

133 ×3.8

Citations per year, relative to Lucia Perone Lucia Perone (= 1×) peers A. Kuechler

Countries citing papers authored by Lucia Perone

Since Specialization

Citations

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

Fields of papers citing papers by Lucia Perone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Perone

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Perone. A scholar is included among the top collaborators of Lucia Perone 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 Lucia Perone. Lucia Perone 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

Alfieri, Mariaevelina, Daniela Iaconis, Roberta Tammaro, et al.. (2020). The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progression. Tissue and Cell. 64. 101369–101369. 13 indexed citations

Martone, Julie, Alessandro Rosa, Valerio Di Carlo, et al.. (2020). Trans‐generational epigenetic regulation associated with the amelioration of Duchenne Muscular Dystrophy. EMBO Molecular Medicine. 12(8). e12063–e12063. 10 indexed citations

Parisi, Silvia, Elena V. Polishchuk, Maria Gallo, et al.. (2018). Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells. Scientific Reports. 8(1). 6247–6247. 31 indexed citations

Grandone, Anna, Francesca Del Vecchio Blanco, Annalaura Torella, et al.. (2016). Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature. Hormone Research in Paediatrics. 86(5). 330–336. 1 indexed citations

Boonen, Susanne E., Andrea Freschi, Rikke Christensen, et al.. (2016). Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes. Clinical Epigenetics. 8(1). 69–69. 6 indexed citations

Miceli, Marco, Gianluigi Franci, Carmela Dell’Aversana, et al.. (2013). MePR: A Novel Human Mesenchymal Progenitor Model with Characteristics of Pluripotency. Stem Cells and Development. 22(17). 2368–2383. 17 indexed citations

Savarese, Marco, Anna Grandone, Lucia Perone, et al.. (2013). Familial trisomy 6p in mother and daughter. American Journal of Medical Genetics Part A. 161(7). 1675–1681. 13 indexed citations

Chiesa, Nicoletta, Agostina De Crescenzo, Kankadeb Mishra, et al.. (2011). The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases. Human Molecular Genetics. 21(1). 10–25. 98 indexed citations

Lonardo, Fortunato, Lucia Perone, Roberto Ciccone, et al.. (2011). Clinical, cytogenetic and molecular-cytogenetic characterization of a patient with a de novo tandem proximal-intermediate duplication of 16q and review of the literature. American Journal of Medical Genetics Part A. 155(4). 769–777. 21 indexed citations

10.

Lonardo, Fortunato, Giancarlo Parenti, Daniela V. Luquetti, et al.. (2007). Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD. European Journal of Medical Genetics. 50(4). 301–308. 32 indexed citations

11.

Morleo, Manuela, Tiziano Pramparo, Lucia Perone, et al.. (2005). Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization of 11 cases. American Journal of Medical Genetics Part A. 137A(2). 190–198. 26 indexed citations

12.

Melis, Daniela, Maria Pia Sperandeo, Lucia Perone, et al.. (2005). Mosaic 13q13.2-ter deletion restricted to tissues of ectodermal and mesodermal origins. Clinical Dysmorphology. 15(1). 13–18. 5 indexed citations

13.

Rossi, Massimiliano, et al.. (2002). Unbalanced translocation (3;5)(q26.1;p14): A clinical report. American Journal of Medical Genetics. 110(4). 353–358. 6 indexed citations

14.

Sperandeo, Maria Pia, Paola Ungaro, Maria Vernucci, et al.. (2000). Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes. The American Journal of Human Genetics. 66(3). 841–847. 29 indexed citations

15.

Melis, Daniela, Lucia Perone, Maria Pia Sperandeo, et al.. (1998). Mild phenotype associated with an interstitial deletion of the long arm of chromosome 1.. Journal of Medical Genetics. 35(12). 1047–1049. 10 indexed citations

16.

Sebastio, Gianfranco, Lucia Perone, Vito Guzzetta, et al.. (1996). Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21) (p16.3;q22.1): Relevance to the Wolf-Hirschhorn and Down syndrome critical regions. American Journal of Medical Genetics. 63(2). 366–372. 2 indexed citations

17.

Striano, Salvatore, P. Ruosi, Vito Guzzetta, et al.. (1996). Cutis Verticis Gyrata—Mental Deficiency Syndrome: A Patient with Drug‐Resistant Epilepsy and Polymicrogyria. Epilepsia. 37(3). 284–286. 11 indexed citations

18.

Lonardo, Fortunato, et al.. (1988). A malformed girl with a de novo proximal 6q deletion.. PubMed. 31(1). 57–9. 15 indexed citations

19.

Gentile, Guendalina, et al.. (1987). Cytogenetic study of a cell line of human penile cancer.. PubMed. 30(3). 164–9. 11 indexed citations

20.

Perone, Lucia, et al.. (1986). Double independent balanced translocation in a girl with mild phenotypical stigmata.. PubMed. 29(1). 62–4. 2 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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