Cinzia Galasso

1.0k total citations
37 papers, 651 citations indexed

About

Cinzia Galasso is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Cinzia Galasso has authored 37 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 17 papers in Molecular Biology and 6 papers in Psychiatry and Mental health. Recurrent topics in Cinzia Galasso's work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (13 papers) and Congenital heart defects research (7 papers). Cinzia Galasso is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (13 papers) and Congenital heart defects research (7 papers). Cinzia Galasso collaborates with scholars based in Italy, Denmark and United States. Cinzia Galasso's co-authors include Paolo Curatolo, Marta Elena Santarone, Romina Moavero, Adriana Lo‐Castro, Arthur R. Brothman, Agatino Battaglia, John C. Carey, David Viskochil, Giuseppe Marangi and Marina Murdolo and has published in prestigious journals such as PEDIATRICS, Scientific Reports and Journal of Biomechanics.

In The Last Decade

Cinzia Galasso

34 papers receiving 627 citations

Peers

Cinzia Galasso

GENET

PPCH

PMH

Milen Velinov United States

A. C. Warren United States

Amy Yang United States

Melissa T. Carter Canada

Deborah Barbouth United States

Angela Peron Italy

Elisabeth Gabau Spain

Maria Teresa Bonati Italy

Carlos Eduardo Steiner Brazil

Milen Velinov United States

Cinzia Galasso

476 ×1.3

GENET

413 ×1.7

103 ×0.6

PPCH

68 ×0.6

PMH

51 ×0.6

Citations per year, relative to Cinzia Galasso Cinzia Galasso (= 1×) peers Milen Velinov

Countries citing papers authored by Cinzia Galasso

Since Specialization

Citations

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

Fields of papers citing papers by Cinzia Galasso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cinzia Galasso

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

Siracusano, Martina, Assia Riccioni, Romina Moavero, et al.. (2025). Autism spectrum disorder and 3p24.3p23 triplication: a case report. Journal of Medical Case Reports. 19(1). 106–106.

Frattale, Ilaria, Martina Siracusano, Assia Riccioni, et al.. (2024). Sleep disturbances and behavioral symptoms in pediatric Sotos syndrome. Frontiers in Neurology. 15. 1360055–1360055. 1 indexed citations

Riccioni, Assia, Martina Siracusano, Ilaria Frattale, et al.. (2023). Short report: Autistic symptoms in Sotos syndrome, preliminary results from a case-control study. Research in Developmental Disabilities. 145. 104655–104655.

Vacca, Mariacarolina, Mariana Fernandes, Andrea Ballesio, et al.. (2023). Clinical, Sociodemographic, and Psychological Factors Associated with Transition Readiness in Patients with Epilepsy. Brain Sciences. 14(1). 21–21. 2 indexed citations

Lintas, Carla, Angelo Facchiano, Alessia Azzarà, et al.. (2023). Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability. Genes. 14(7). 1353–1353. 3 indexed citations

Galasso, Cinzia, et al.. (2023). Presence of neurologic signs in children with neurofibromatosis type 1. Minerva Pediatrics. 75(1). 1–7. 1 indexed citations

Pierro, Donato Di, Chiara Ciaccio, Diego Sbardella, et al.. (2019). Effects of oral administration of common antioxidant supplements on the energy metabolism of red blood cells. Attenuation of oxidative stress-induced changes in Rett syndrome erythrocytes by CoQ10. Molecular and Cellular Biochemistry. 463(1-2). 101–113. 18 indexed citations

Ricci, Mariachiara, et al.. (2018). Wearable-based electronics to objectively support diagnosis of motor impairments in school-aged children. Journal of Biomechanics. 83. 243–252. 31 indexed citations

Ciaccio, Chiara, Donato Di Pierro, Diego Sbardella, et al.. (2017). Oxygen exchange and energy metabolism in erythrocytes of Rett syndrome and their relationships with respiratory alterations. Molecular and Cellular Biochemistry. 426(1-2). 205–213. 5 indexed citations

10.

Moavero, Romina, Marta Elena Santarone, Cinzia Galasso, & Paolo Curatolo. (2017). Cognitive and behavioral effects of new antiepileptic drugs in pediatric epilepsy. Brain and Development. 39(6). 464–469. 103 indexed citations

11.

Sbardella, Diego, Grazia Raffaella Tundo, Luisa Campagnolo, et al.. (2017). Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome. Scientific Reports. 7(1). 12297–12297. 37 indexed citations

12.

Porfirio, Maria Cristina, et al.. (2012). Attention-deficit hyperactivity disorder and binge eating disorder in a patient with 2q21.1–q22.2 deletion. Psychiatric Genetics. 22(4). 202–205. 7 indexed citations

13.

Pasini, Augusto, et al.. (2012). Detecting anxiety symptoms in children and youths with neurofibromatosis type I. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(7). 869–873. 22 indexed citations

14.

Lo‐Castro, Adriana, Cinzia Galasso, Alberto Verrotti, et al.. (2011). De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems. European Journal of Medical Genetics. 54(3). 329–332. 13 indexed citations

15.

Zollino, Marcella, Marina Murdolo, Giuseppe Marangi, et al.. (2008). On the nosology and pathogenesis of Wolf–Hirschhorn syndrome: Genotype–phenotype correlation analysis of 80 patients and literature review. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 148C(4). 257–269. 112 indexed citations

16.

Galasso, Cinzia, et al.. (2007). Anophthalmia-Waardenburg Syndrome With Expanding Phenotype: Does Neural Crest Play a Role?. Journal of Child Neurology. 22(11). 1252–1255. 4 indexed citations

17.

Galasso, Cinzia, et al.. (2006). Interstitial deletion of a proximal 3p: A clinically recognisable syndrome. Brain and Development. 29(5). 312–316. 10 indexed citations

18.

Arpino, Carla, et al.. (2005). Lack of association between IDE genetic variability and Down's syndrome. Neuroscience Letters. 382(1-2). 93–95. 2 indexed citations

19.

Galasso, Cinzia, et al.. (1995). Growth Hormone and Dysmorphic Syndromes. Hormone Research. 44(3). 42–48. 7 indexed citations

20.

Scirè, Giuseppe, Bruno Dallapiccola, Paola Iannetti, et al.. (1994). Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions. American Journal of Medical Genetics. 52(4). 478–482. 41 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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