Giulia Pascolini

459 total citations
27 papers, 176 citations indexed

About

Giulia Pascolini is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Giulia Pascolini has authored 27 papers receiving a total of 176 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 3 papers in Genetics. Recurrent topics in Giulia Pascolini's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Giulia Pascolini is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Giulia Pascolini collaborates with scholars based in Italy, Lebanon and United States. Giulia Pascolini's co-authors include Paola Grammatico, Marco Castori, Silvia Morlino, Carlo Blundo, Silvia Majore, Antonio Novelli, Vincenzo Leuzzi, Antonio Pizzuti, Emanuele Agolini and Nicole Fleischer and has published in prestigious journals such as Archives of Oral Biology, Clinical Genetics and Acta Dermato Venereologica.

In The Last Decade

Giulia Pascolini

22 papers receiving 172 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giulia Pascolini Italy 7 89 69 33 21 20 27 176
George Karamanolis Greece 8 22 0.2× 43 0.6× 70 2.1× 59 2.8× 15 0.8× 20 247
Alice S. Brooks Netherlands 10 116 1.3× 112 1.6× 297 9.0× 37 1.8× 4 0.2× 15 447
Stefano Petrocchi Italy 8 129 1.4× 84 1.2× 31 0.9× 7 0.3× 15 236
Jamal Ghoumid France 11 160 1.8× 209 3.0× 62 1.9× 6 0.3× 2 0.1× 34 352
Monica J. Basehore United States 7 61 0.7× 84 1.2× 18 0.5× 2 0.1× 2 0.1× 15 264
Jennifer Keller‐Ramey United States 8 62 0.7× 71 1.0× 21 0.6× 7 0.3× 8 162
Lavinia Caba Romania 11 119 1.3× 140 2.0× 40 1.2× 2 0.1× 2 0.1× 37 283
Maria Pina Simula Italy 6 15 0.2× 19 0.3× 28 0.8× 64 3.0× 12 0.6× 14 194
Ana Vieira Portugal 4 9 0.1× 63 0.9× 47 1.4× 13 0.6× 4 0.2× 5 246
Ingrid Scurr United Kingdom 8 52 0.6× 111 1.6× 23 0.7× 11 0.6× 16 191

Countries citing papers authored by Giulia Pascolini

Since Specialization
Citations

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

Fields of papers citing papers by Giulia Pascolini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulia Pascolini

This figure shows the co-authorship network connecting the top 25 collaborators of Giulia Pascolini. A scholar is included among the top collaborators of Giulia Pascolini 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 Giulia Pascolini. Giulia Pascolini 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.
Abdul‐Rahman, Omar, Giulia Pascolini, Giovanni Di Zenzo, et al.. (2025). Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene. American Journal of Medical Genetics Part A. 197(11). e64171–e64171.
2.
Gizzi, G., et al.. (2025). Keratitis, Ichthyosis, and Deafness Syndrome with Endocarditis and Myelitis: A Rare Case Report. Case Reports in Dermatology. 17(1). 291–298.
3.
Gnazzo, Maria, et al.. (2024). Usmani‐Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant. Clinical Genetics. 106(1). 109–113.
4.
Pascolini, Giulia, Giovanni Luca Scaglione, Balasubramanian Chandramouli, et al.. (2024). Broadening the PHIP-Associated Neurodevelopmental Phenotype. Children. 11(11). 1395–1395. 1 indexed citations
5.
Pascolini, Giulia, et al.. (2024). Clinical Improvement of Bullous Pemphigoid with Hyperkeratosis and Palmoplantar Keratoderma in Two Patients Treated with Dupilumab. Acta Dermato Venereologica. 104. adv40984–adv40984.
6.
Pascolini, Giulia, et al.. (2024). The face of Non‐photosensitive trichothiodystrophy phenotypic spectrum: A subsequent study on paediatric population. Molecular Genetics & Genomic Medicine. 12(8). e2501–e2501. 2 indexed citations
7.
Pascolini, Giulia, et al.. (2024). Extended phenotypic characterization of a novel Helsmoortel‐van der Aa syndrome case series. American Journal of Medical Genetics Part A. 194(5). e63539–e63539. 2 indexed citations
8.
Pascolini, Giulia, et al.. (2023). Facial clues to the photosensitive trichothiodystrophy phenotype in childhood. Journal of Human Genetics. 68(6). 437–443. 2 indexed citations
9.
Pascolini, Giulia, Mauro Calvani, & Paola Grammatico. (2022). First Italian experience using the automated craniofacial gestalt analysis on a cohort of pediatric patients with multiple anomaly syndromes. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 91–91. 2 indexed citations
10.
Pascolini, Giulia, et al.. (2021). Clinical and Molecular Aspects of the Neurodevelopmental Disorder Associated with PAK3 Perturbation. Journal of Molecular Neuroscience. 71(12). 2474–2481. 5 indexed citations
11.
Pascolini, Giulia, Emanuele Agolini, Antonio Novelli, Silvia Majore, & Paola Grammatico. (2020). The p.Arg377Trp variant in ACTL6A underlines a recognizable BAF‐opathy phenotype. Clinical Genetics. 97(4). 672–674. 3 indexed citations
12.
Majore, Silvia, Emanuele Agolini, Lucia Micale, et al.. (2020). Clinical presentation and molecular characterization of a novel patient with variant POC1A ‐ related syndrome. Clinical Genetics. 99(4). 540–546. 9 indexed citations
13.
Pascolini, Giulia, Emanuele Agolini, Nicole Fleischer, et al.. (2020). Further delineation of the neurodevelopmental phenotypic spectrum associated to 14q11.2 microduplication. Neurological Sciences. 41(12). 3751–3753. 2 indexed citations
14.
Pascolini, Giulia, Nicole Fleischer, Alessandro Ferraris, Silvia Majore, & Paola Grammatico. (2019). The facial dysmorphology analysis technology in intellectual disability syndromes related to defects in the histones modifiers. Journal of Human Genetics. 64(8). 721–728. 8 indexed citations
15.
Pascolini, Giulia, Irene Bottillo, Luigi Laino, et al.. (2019). Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion. European Journal of Medical Genetics. 63(3). 103739–103739. 5 indexed citations
16.
Pascolini, Giulia, Silvia Majore, Irene Bottillo, et al.. (2019). Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene. Psychiatric Genetics. 29(3). 86–90. 1 indexed citations
17.
Pascolini, Giulia, Emanuele Agolini, Silvia Majore, et al.. (2018). Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement. European Journal of Paediatric Neurology. 22(3). 552–557. 15 indexed citations
18.
Margiotti, Katia, Giulia Pascolini, Federica Consoli, et al.. (2017). Lack of pathogenic mutations in SOS1 gene in phenytoin-induced gingival overgrowth patients. Archives of Oral Biology. 80. 160–163. 2 indexed citations
19.
Castori, Marco, Silvia Morlino, Giulia Pascolini, Carlo Blundo, & Paola Grammatico. (2015). Gastrointestinal and nutritional issues in joint hypermobility syndrome/ehlers–danlos syndrome, hypermobility type. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 54–75. 64 indexed citations
20.
Castori, Marco, Francesca Servadei, Luigi Laino, et al.. (2015). Axial skeletogenesis in human autosomal aneuploidies: A radiographic study of 145 second trimester fetuses. American Journal of Medical Genetics Part A. 170(3). 676–687. 11 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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