Ornella Galesi

1.3k total citations
17 papers, 198 citations indexed

About

Ornella Galesi is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Ornella Galesi has authored 17 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Ornella Galesi's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genomics and Rare Diseases (4 papers). Ornella Galesi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genomics and Rare Diseases (4 papers). Ornella Galesi collaborates with scholars based in Italy, United States and United Kingdom. Ornella Galesi's co-authors include Marco Fichera, Corrado Romano, Francesco Calı̀, Lucia Castiglia, A Alberti, Daniela Benedetto, Maurizio Elia, Pasquale Striano, Michela Malacarne and S Musumeci and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Autism and Developmental Disorders and Epilepsia.

In The Last Decade

Ornella Galesi

16 papers receiving 198 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ornella Galesi Italy 9 155 107 42 22 14 17 198
Magdalena Bartnik Poland 10 168 1.1× 140 1.3× 56 1.3× 37 1.7× 8 0.6× 23 266
Yoko Hiraki Japan 10 131 0.8× 97 0.9× 22 0.5× 18 0.8× 21 1.5× 17 219
Michèle Mathieu‐Dramard France 9 170 1.1× 200 1.9× 44 1.0× 22 1.0× 25 1.8× 15 363
Diane Hu‐Lince United States 7 144 0.9× 143 1.3× 22 0.5× 13 0.6× 9 0.6× 7 253
Eve Õiglane‐Shlik Estonia 10 185 1.2× 177 1.7× 76 1.8× 16 0.7× 10 0.7× 17 320
Fernanda T. Bellucco Brazil 9 140 0.9× 107 1.0× 43 1.0× 56 2.5× 12 0.9× 24 233
Mariana Moysés‐Oliveira Brazil 11 206 1.3× 130 1.2× 53 1.3× 35 1.6× 16 1.1× 45 300
Patricia A. Eng United States 5 243 1.6× 134 1.3× 104 2.5× 49 2.2× 16 1.1× 5 298
Noriko Sangu Japan 9 115 0.7× 101 0.9× 23 0.5× 17 0.8× 17 1.2× 17 191
Mylène Béri France 7 150 1.0× 79 0.7× 65 1.5× 11 0.5× 8 0.6× 8 175

Countries citing papers authored by Ornella Galesi

Since Specialization
Citations

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

Fields of papers citing papers by Ornella Galesi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ornella Galesi

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

All Works

17 of 17 papers shown
1.
Failla, Pinella, Ornella Galesi, Donatella Greco, et al.. (2024). Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis. International Journal of Molecular Sciences. 25(24). 13471–13471.
2.
Failla, Pinella, et al.. (2023). Trait − driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & Genomics. 45(4). 491–505. 4 indexed citations
3.
Bertini, Veronica, Alessandro Orsini, Alice Bonuccelli, et al.. (2022). Phenotypic Spectrum of NFIA Haploinsufficiency: Two Additional Cases and Review of the Literature. Genes. 13(12). 2249–2249. 4 indexed citations
4.
Galesi, Ornella, et al.. (2022). Dyslexia and Attention Deficit Hyperactivity Disorder Associated to a De Novo 1p34.3 Microdeletion. Genes. 13(11). 1926–1926. 1 indexed citations
5.
Capra, Anna Paola, Silvana Briuglia, Chiara Baldo, et al.. (2021). 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes. 12(5). 652–652. 12 indexed citations
6.
Scuderi, Carmela, Mirella Vinci, Lucia Castiglia, et al.. (2019). Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorder. European Journal of Human Genetics. 27(4). 594–602. 19 indexed citations
7.
8.
Vinci, Mirella, Lucia Castiglia, Lucia Grillo, et al.. (2016). Identification of novel mutations in L1CAM gene by a DHPLC-based assay. Genes & Genomics. 38(12). 1159–1164. 1 indexed citations
9.
Benedetto, Daniela, S Musumeci, Emanuela Avola, et al.. (2014). Definition of minimal duplicated region encompassing the XIAP and STAG2 genes in the Xq25 microduplication syndrome. American Journal of Medical Genetics Part A. 164(8). 1923–1930. 9 indexed citations
10.
Mazzone, Luigi, et al.. (2012). Brief Report: Peculiar Evolution of Autistic Behaviors in Two Unrelated Children with Brachidactyly-Mental Retardation Syndrome. Journal of Autism and Developmental Disorders. 42(10). 2202–2207. 4 indexed citations
11.
Concolino, Daniela, Maria Anna Rapsomaniki, Rosa Marotta, et al.. (2011). A de novo 8q22.2-24.3 duplication in a patient with mild phenotype. European Journal of Medical Genetics. 55(1). 67–70. 17 indexed citations
12.
Striano, Pasquale, Maria Margherita Mancardi, Marco Fichera, et al.. (2008). Partial monosomy Xq(Xq23→qter) and trisomy 4p(4p15.33→pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features. Brain and Development. 30(6). 425–429. 9 indexed citations
13.
Grosso, Salvatore, Marco Fichera, Ornella Galesi, et al.. (2008). Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation. Developmental Medicine & Child Neurology. 50(6). 473–476. 6 indexed citations
14.
Alberti, A, Corrado Romano, Francesco Calı̀, et al.. (2007). 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features. Clinical Genetics. 71(2). 177–182. 45 indexed citations
15.
Bella, Maria Antonietta Di, Francesco Calı̀, Gregorio Seidita, et al.. (2006). Screening of subtelomeric rearrangements in autistic disorder: Identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(6). 584–590. 11 indexed citations
16.
Elia, Maurizio, Pasquale Striano, Marco Fichera, et al.. (2006). 6q Terminal Deletion Syndrome Associated with a Distinctive EEG and Clinical Pattern: A Report of Five Cases. Epilepsia. 47(5). 830–838. 38 indexed citations
17.
Borgione, Eugenia, Mariangela Lo Giudice, Lucia Castiglia, et al.. (2003). Mutational analysis of the ATRX gene by DGGE: A powerful diagnostic approach for the ATRX syndrome. Human Mutation. 21(5). 529–534. 7 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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