Andrea Bartuli

3.5k total citations
78 papers, 1.6k citations indexed

About

Andrea Bartuli is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Andrea Bartuli has authored 78 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 20 papers in Surgery and 20 papers in Genetics. Recurrent topics in Andrea Bartuli's work include Metabolism and Genetic Disorders (12 papers), Lipoproteins and Cardiovascular Health (8 papers) and Vascular Malformations and Hemangiomas (7 papers). Andrea Bartuli is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Lipoproteins and Cardiovascular Health (8 papers) and Vascular Malformations and Hemangiomas (7 papers). Andrea Bartuli collaborates with scholars based in Italy, United States and Netherlands. Andrea Bartuli's co-authors include Carlo Dionisi‐Vici, Valério Nobili, Anna Alisi, Stefano Picca, Alberto Villani, Paola Sabrina Buonuomo, Paola Dongiovanni, Silvia Fargion, Luca Valenti and E. Galmozzi and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Hepatology.

In The Last Decade

Andrea Bartuli

73 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrea Bartuli Italy 24 453 415 391 346 343 78 1.6k
Norbert Vaessen Netherlands 19 410 0.9× 137 0.3× 330 0.8× 366 1.1× 66 0.2× 30 1.7k
Joachim Misselwitz Germany 27 529 1.2× 253 0.6× 159 0.4× 168 0.5× 64 0.2× 51 2.4k
Erfan Nur Netherlands 20 310 0.7× 147 0.4× 94 0.2× 161 0.5× 92 0.3× 103 1.6k
Michael Haidinger Austria 20 319 0.7× 595 1.4× 250 0.6× 558 1.6× 93 0.3× 49 1.9k
P. Pola Italy 23 366 0.8× 833 2.0× 253 0.6× 97 0.3× 101 0.3× 71 1.8k
Susanne Rasoul‐Rockenschaub Austria 26 370 0.8× 683 1.6× 488 1.2× 120 0.3× 34 0.1× 56 1.9k
Kari Otterdal Norway 27 553 1.2× 273 0.7× 296 0.8× 123 0.4× 41 0.1× 63 2.2k
Adam M. Zawada Germany 23 558 1.2× 347 0.8× 463 1.2× 97 0.3× 37 0.1× 52 2.3k
Paola Barsotti Italy 20 293 0.6× 149 0.4× 172 0.4× 99 0.3× 194 0.6× 48 1.3k
Francesco L. Ierino Australia 24 383 0.8× 1.0k 2.5× 141 0.4× 85 0.2× 43 0.1× 82 2.1k

Countries citing papers authored by Andrea Bartuli

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Bartuli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Bartuli

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Bartuli. A scholar is included among the top collaborators of Andrea Bartuli 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 Andrea Bartuli. Andrea Bartuli 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.
Ruzzini, Laura, et al.. (2025). Management of a case of melorheostosis deformity and pain with intramedullary nailing. European Journal of Medical Genetics. 75. 105018–105018.
2.
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.
3.
Calcagni, Giulio, Federica Ferrigno, Maria Lisa Dentici, et al.. (2024). Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome. Diagnostics. 14(6). 594–594. 1 indexed citations
4.
Galeotti, Angela, Giovanni Carlo De Vincentiis, Giuseppe Marzo, et al.. (2024). Use of an Orthodontic and Otolaryngological Approach in an Infant with Holoprosencephaly. Children. 11(5). 554–554.
5.
Baban, Anwar, Marianna Cicenia, Antonino Romanzo, et al.. (2024). Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care. Journal of Cardiovascular Development and Disease. 11(4). 114–114. 1 indexed citations
6.
Leoni, Chiara, Marilidia Piglionica, Maurizio De Pellegrin, et al.. (2023). Work-Up and Treatment Strategies for Individuals with PIK3CA-Related Disorders: A Consensus of Experts from the Scientific Committee of the Italian Macrodactyly and PROS Association. Genes. 14(12). 2134–2134. 6 indexed citations
7.
Onesimo, Roberta, Valentina Trevisan, Chiara Leoni, et al.. (2023). From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome. Genes. 14(10). 1843–1843. 6 indexed citations
8.
Iarossi, Giancarlo, Lorenzo Sinibaldi, Chiara Passarelli, et al.. (2022). A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients. Diagnostics. 12(9). 2183–2183. 2 indexed citations
9.
Buonuomo, Paola Sabrina, Giovanna Leone, Michaela Veronika Gonfiantini, et al.. (2021). Evolocumab in the management of children <10 years of age affected by homozygous familial hypercholesterolemia. Atherosclerosis. 324. 148–150. 2 indexed citations
10.
Rossi, Michela, Paola Sabrina Buonuomo, Giulia Battafarano, et al.. (2021). Dysregulated miRNAs in bone cells of patients with Gorham‐Stout disease. The FASEB Journal. 35(3). e21424–e21424. 12 indexed citations
11.
Vecchio, Davide, et al.. (2020). Deciphering the Invdupdel(8p) Genotype–Phenotype Correlation: Our Opinion. Brain Sciences. 10(7). 451–451. 5 indexed citations
12.
Santos, Raúl D., Andrea Ruzza, G. Kees Hovingh, et al.. (2020). Evolocumab in Pediatric Heterozygous Familial Hypercholesterolemia. New England Journal of Medicine. 383(14). 1317–1327. 115 indexed citations
13.
Pepe, Jessica, Michela Rossi, Giulia Battafarano, et al.. (2020). Characterization of Extracellular Vesicles in Osteoporotic Patients Compared to Osteopenic and Healthy Controls. Journal of Bone and Mineral Research. 37(11). 2186–2200. 23 indexed citations
14.
Macchiaiolo, Marina, Michaela Veronika Gonfiantini, Paola Sabrina Buonuomo, et al.. (2020). Langerhans cell histiocytosis in a young patient with Pitt–Hopkins syndrome. American Journal of Medical Genetics Part A. 182(11). 2746–2750.
15.
Dentici, Maria Lisa, Sabina Barresi, Marcello Niceta, et al.. (2019). Expanding the clinical spectrum associated with PACS2 mutations. Clinical Genetics. 95(4). 525–531. 17 indexed citations
16.
Rossi, Michela, Paola Sabrina Buonuomo, Giulia Battafarano, et al.. (2019). Dissecting the mechanisms of bone loss in Gorham-Stout disease. Bone. 130. 115068–115068. 29 indexed citations
17.
Callea, Francesco, Isabella Giovannoni, Sinan Sarı, et al.. (2017). Fibrinogen Gamma Chain Mutations Provoke Fibrinogen and Apolipoprotein B Plasma Deficiency and Liver Storage. International Journal of Molecular Sciences. 18(12). 2717–2717. 18 indexed citations
18.
Gonfiantini, Michaela Veronika, Marco Armando, Marina Macchiaiolo, et al.. (2015). Borderline cognitive level in a family with Bazex‐Dupré‐Christol syndrome. American Journal of Medical Genetics Part A. 167(7). 1637–1643. 2 indexed citations
19.
Macchiaiolo, Marina, Maurizio Mennini, M. Cristina Digilio, et al.. (2013). Thricho‐rhino‐phalangeal syndrome and severe osteoporosis: A rare association or a feature? An effective therapeutic approach with biphosphonates. American Journal of Medical Genetics Part A. 164(3). 760–763. 7 indexed citations
20.
Saudubray, Jean‐Marie, Delphine Martin, F Poggi-Travert, et al.. (1997). Clinical presentations of inherited mitochondrial fatty acid oxidation disorders: An update. 12(1). 34–40. 5 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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