Daniela Leone

1.0k total citations
18 papers, 273 citations indexed

About

Daniela Leone is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Daniela Leone has authored 18 papers receiving a total of 273 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Daniela Leone's work include Neurogenetic and Muscular Disorders Research (5 papers), Neonatal and fetal brain pathology (4 papers) and Infant Development and Preterm Care (4 papers). Daniela Leone is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Neonatal and fetal brain pathology (4 papers) and Infant Development and Preterm Care (4 papers). Daniela Leone collaborates with scholars based in Italy, United States and United Kingdom. Daniela Leone's co-authors include Eugenio Mercuri, Marika Pane, Francesca Gallini, Laura Cesarini, Daniela Ricci, Costantino Romagnoli, Roberto De Sanctis, Lavinia Fanelli, Concetta Palermo and Simona Lucibello and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Archives of Disease in Childhood.

In The Last Decade

Daniela Leone

18 papers receiving 270 citations

Peers

Daniela Leone

PPCH

GENET

SURGE

PRM

Giacomo Talenti Italy

Cesar Alves United States

R. Lévy France

Rosa Morabito Italy

A Arivazhagan India

Charles‐Joris Roux France

Handan Güleryüz Türkiye

Özdem Ertürk Çetin Türkiye

Gholamreza Zamani Iran

Sasha Burn United Kingdom

Giacomo Talenti Italy

Daniela Leone

81 ×0.9

125 ×1.5

PPCH

69 ×0.9

GENET

57 ×0.9

SURGE

37 ×0.8

PRM

Citations per year, relative to Daniela Leone Daniela Leone (= 1×) peers Giacomo Talenti

Countries citing papers authored by Daniela Leone

Since Specialization

Citations

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

Fields of papers citing papers by Daniela Leone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Leone

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Leone. A scholar is included among the top collaborators of Daniela Leone 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 Daniela Leone. Daniela Leone is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Coratti, Giorgia, María Luisa Scattoni, Marika Pane, et al.. (2025). Neurodevelopmental and mental disorders in children with type I and presymptomatic spinal muscular atrophy. Scientific Reports. 15(1). 26984–26984. 3 indexed citations

Berti, Beatrice, Daniela Verrigni, Alessia Nasca, et al.. (2024). De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting. International Journal of Molecular Sciences. 25(14). 7782–7782. 2 indexed citations

Berti, Beatrice, Lavinia Fanelli, Roberta Onesimo, et al.. (2022). Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patients. Archives of Disease in Childhood. 107(10). 912–916. 9 indexed citations

Berti, Beatrice, Lavinia Fanelli, Roberto De Sanctis, et al.. (2021). Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New Module. Journal of Neuromuscular Diseases. 8(4). 589–601. 22 indexed citations

Ricci, Daniela, Simona Lucibello, Lorenzo Orazi, et al.. (2020). Early visual and neuro-development in preterm infants with and without retinopathy. Early Human Development. 148. 105134–105134. 9 indexed citations

Buonsenso, Danilo, Beatrice Berti, Concetta Palermo, et al.. (2020). Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophy. Pediatric Pulmonology. 55(7). 1781–1788. 19 indexed citations

Lamendola, Priscilla, G. A. Lanza, Angelo Villano, et al.. (2020). Duchenne muscular dystrophy: preliminary experience with sacubitril-valsartan in patients with asymptomatic left ventricular dysfunction.. PubMed. 24(17). 9112–9115. 2 indexed citations

Romeo, Domenico M., Giuseppina Leo, Leonardo Lapenta, et al.. (2019). Sleep disorders in low-risk preschool very preterm children. Sleep Medicine. 63. 137–141. 7 indexed citations

Sanctis, Roberto De, Marika Pane, Giorgia Coratti, et al.. (2017). Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy. Neuromuscular Disorders. 28(1). 24–28. 38 indexed citations

10.

Seferian, A., C. Lilien, Thomas Voït, et al.. (2016). Longitudinal results of magneto-inertial motion analysis in Duchenne muscular dystrophy ambulant patients. Neuromuscular Disorders. 26. S184–S185. 1 indexed citations

11.

Alfieri, Paolo, Giorgia Piccini, Maria Luigia Gambardella, et al.. (2014). Behavioral Profile in RASopathies. American Journal of Medical Genetics Part A. 164(4). 934–942. 64 indexed citations

12.

Trani, Michela Di, et al.. (2014). Comorbid Depressive Disorders in ADHD: The Role of ADHD Severity, Subtypes and Familial Psychiatric Disorders. Psychiatry Investigation. 11(2). 137–137. 9 indexed citations

13.

Donfrancesco, Renato, et al.. (2014). Bipolar Disorder in Children With ADHD: A Clinical Sample Study. Journal of Attention Disorders. 21(9). 715–720. 7 indexed citations

14.

Leone, Daniela, Claudia Brogna, Daniela Ricci, et al.. (2012). Development of clinical signs in low risk term born infants with neonatal hyperexcitability. Early Human Development. 89(2). 65–68. 5 indexed citations

15.

Ricci, Daniela, Domenico M. Romeo, Francesca Serrao, et al.. (2010). Early assessment of visual function in preterm infants: How early is early?. Early Human Development. 86(1). 29–33. 23 indexed citations

16.

Luciano, Rita, Giovanni Baranello, L. Masini, et al.. (2007). Antenatal Post-hemorrhagic Ventriculomegaly: A Prospective Follow-up Study. Neuropediatrics. 38(3). 137–142. 10 indexed citations

17.

Ricci, Daniela, Domenico M. Romeo, Francesca Serrao, et al.. (2007). Application of a neonatal assessment of visual function in a population of low risk full-term newborn. Early Human Development. 84(4). 277–280. 20 indexed citations

18.

Ricci, Daniela, Frances M. Cowan, Marika Pane, et al.. (2006). Neurological Examination at 6 to 9 Months in Infants with Cystic Periventricular Leukomalacia. Neuropediatrics. 37(4). 247–252. 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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