Berardo Rinaldi

506 total citations
26 papers, 170 citations indexed

About

Berardo Rinaldi is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Berardo Rinaldi has authored 26 papers receiving a total of 170 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Berardo Rinaldi's work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Berardo Rinaldi is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Berardo Rinaldi collaborates with scholars based in Italy, France and Denmark. Berardo Rinaldi's co-authors include Maria Francesca Bedeschi, Orsetta Zuffardi, Livia Garavelli, Palma Finelli, Roberta Villa, Sabrina Giglio, Annalisa Vetro, Edoardo Errichiello, Hugo de Jonge and Patrizia Morbini and has published in prestigious journals such as PLoS Genetics, The Journal of Pathology and Human Genetics.

In The Last Decade

Berardo Rinaldi

21 papers receiving 167 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Berardo Rinaldi Italy 7 99 90 32 15 12 26 170
Milena Mariani Italy 9 165 1.7× 90 1.0× 19 0.6× 15 1.0× 9 0.8× 26 236
Jillene Kogan United States 9 105 1.1× 94 1.0× 29 0.9× 34 2.3× 10 0.8× 13 217
Jennifer Glass United States 4 66 0.7× 61 0.7× 24 0.8× 18 1.2× 5 0.4× 6 237
Eda Ütine Türkiye 9 96 1.0× 99 1.1× 10 0.3× 20 1.3× 12 1.0× 24 218
Katharina M. Roetzer Austria 8 96 1.0× 112 1.2× 19 0.6× 13 0.9× 9 0.8× 15 220
Tomi L. Toler United States 7 105 1.1× 139 1.5× 23 0.7× 50 3.3× 13 1.1× 10 275
Érika L. Freitas Brazil 10 112 1.1× 122 1.4× 18 0.6× 32 2.1× 5 0.4× 16 260
Ikumi Hori Japan 11 157 1.6× 158 1.8× 9 0.3× 28 1.9× 10 0.8× 25 258
Dhanya Lakshmi Narayanan India 10 135 1.4× 88 1.0× 13 0.4× 22 1.5× 27 2.3× 42 261
Bianca Russell United States 7 77 0.8× 71 0.8× 8 0.3× 20 1.3× 11 0.9× 18 142

Countries citing papers authored by Berardo Rinaldi

Since Specialization
Citations

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

Fields of papers citing papers by Berardo Rinaldi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Berardo Rinaldi

This figure shows the co-authorship network connecting the top 25 collaborators of Berardo Rinaldi. A scholar is included among the top collaborators of Berardo Rinaldi 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 Berardo Rinaldi. Berardo Rinaldi 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.
Allegri, Anna Elsa Maria, Maria Francesca Bedeschi, Michaela Veronika Gonfiantini, et al.. (2025). Integrating vosoritide therapy with limb surgery in paediatric patients with achondroplasia: real-life experiences. Orphanet Journal of Rare Diseases. 20(1). 369–369.
2.
Picciolli, Irene, Berardo Rinaldi, Anwar Baban, et al.. (2024). Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 156–156. 1 indexed citations
3.
Cogliati, Francesca, Letizia Straniero, Valeria Rimoldi, et al.. (2024). Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(6). e32976–e32976. 2 indexed citations
4.
Rinaldi, Berardo, M. Rimoldi, Roberta Villa, et al.. (2023). Chung–Jansen syndrome can mimic Cornelia de Lange syndrome: Another player among chromatinopathies?. American Journal of Medical Genetics Part A. 191(6). 1586–1592. 4 indexed citations
5.
Bedeschi, Maria Francesca, Claudia Izzi, Chiara Dordoni, et al.. (2023). Identification of bi‐allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3. Clinical Genetics. 104(2). 230–237. 1 indexed citations
6.
Giunti, Laura, Chiara Caporalini, Anna Maria Buccoliero, et al.. (2023). SMARCE1-related meningiomas: A clear example of cancer predisposing syndrome. European Journal of Medical Genetics. 66(7). 104784–104784. 1 indexed citations
7.
Rimoldi, M., Berardo Rinaldi, Roberta Villa, et al.. (2022). Congenital diaphragmatic hernia in Coffin Siris syndrome: Further evidence from two cases. American Journal of Medical Genetics Part A. 191(2). 605–611.
8.
Costanza, Jole, Patrizia Colapietro, Emanuele Micaglio, et al.. (2022). Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology. Genes & Genomics. 45(5). 637–655. 2 indexed citations
9.
Hamanaka, Kohei, Keita Miyoshi, Jiahui Sun, et al.. (2022). Amelioration of a neurodevelopmental disorder by carbamazepine in a case having a gain-of-function GRIA3 variant. Human Genetics. 141(2). 283–293. 2 indexed citations
10.
Rinaldi, Berardo, Elena Freri, Arianna Tucci, et al.. (2021). Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene. Neurogenetics. 23(1). 27–35. 2 indexed citations
11.
Rinaldi, Berardo, Rosamaria Silipigni, Luca Bergamaschi, et al.. (2021). Incidental finding of APC deletion in a child: double trouble or double chance? – a case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 31–31. 5 indexed citations
12.
Sun, Jiahui, Jiang Chen, Carolyn M. Brown, et al.. (2021). X-linked neonatal-onset epileptic encephalopathy associated with a gain-of-function variant p.R660T in GRIA3. PLoS Genetics. 17(6). e1009608–e1009608. 12 indexed citations
13.
Rinaldi, Berardo, Rosamaria Silipigni, Luca Bergamaschi, et al.. (2021). Correction to: Incidental finding of APC deletion in a child: double trouble or double chance? – a case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 185–185.
14.
Lisi, Cláudio Sérgio, et al.. (2020). Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study. PubMed. 72(2). 73–78.
15.
Rinaldi, Berardo, et al.. (2019). BCAP31-related syndrome: The first de novo report. European Journal of Medical Genetics. 63(2). 103732–103732. 8 indexed citations
16.
Zampini, Laura, et al.. (2017). Developmental trends of communicative skills in children with chromosome 14 aberrations. European Journal of Pediatrics. 176(4). 455–464. 3 indexed citations
17.
Vetro, Annalisa, Didier Goidin, Ivan Limongelli, et al.. (2017). Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH. Clinical Genetics. 93(3). 545–556. 10 indexed citations
18.
Rinaldi, Berardo, Sergio Amarri, Chiara Baldo, et al.. (2017). Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force. Orphanet Journal of Rare Diseases. 12(1). 69–69. 14 indexed citations
19.
Foiadelli, Thomas, et al.. (2015). Paediatric clinically isolated syndromes: report of seven cases, differential diagnosis and literature review. Child s Nervous System. 32(1). 69–77. 4 indexed citations
20.
Calabrese, G, Marco Cavallini, Vincenzo Montano, et al.. (2014). Relationship between primary headache and nutrition: a questionnaire about dietary habits of patients with headache. Neurological Sciences. 35(S1). 159–161. 4 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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