Ugo Cavallari

1.6k total citations
30 papers, 967 citations indexed

About

Ugo Cavallari is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Ugo Cavallari has authored 30 papers receiving a total of 967 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Ugo Cavallari's work include Antiplatelet Therapy and Cardiovascular Diseases (6 papers), Atherosclerosis and Cardiovascular Diseases (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Ugo Cavallari is often cited by papers focused on Antiplatelet Therapy and Cardiovascular Diseases (6 papers), Atherosclerosis and Cardiovascular Diseases (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Ugo Cavallari collaborates with scholars based in Italy, United States and Spain. Ugo Cavallari's co-authors include Pier Franco Pignatti, Elisabetta Trabetti, Roberto Corrocher, Domenico Girelli, Nicola Martinelli, Oliviero Olivieri, Dominick J. Angiolillo, Giovanni Malerba, Michele Biscuola and Camino Bañuelos and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Ugo Cavallari

26 papers receiving 933 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ugo Cavallari Italy	16	428	219	191	189	154	30	967
Concetta Di Febbo Italy	18	255 0.6×	184 0.8×	215 1.1×	82 0.4×	65 0.4×	31	1.0k
Michele Nutini Italy	8	218 0.5×	152 0.7×	226 1.2×	99 0.5×	83 0.5×	9	1.0k
P.D. Winocour Canada	20	493 1.2×	238 1.1×	268 1.4×	384 2.0×	74 0.5×	57	1.4k
Sandra Austin United States	12	431 1.0×	134 0.6×	365 1.9×	74 0.4×	63 0.4×	15	1.4k
Shahida Shafi United Kingdom	14	198 0.5×	193 0.9×	325 1.7×	139 0.7×	60 0.4×	29	808
A J Marcus United States	7	296 0.7×	137 0.6×	206 1.1×	88 0.5×	85 0.6×	10	1.0k
Scott Gleim United States	18	172 0.4×	137 0.6×	357 1.9×	89 0.5×	41 0.3×	29	873
Cornelius F.H. Mueller Germany	15	229 0.5×	124 0.6×	344 1.8×	67 0.4×	84 0.5×	19	892
K Tack-Goldman United States	10	463 1.1×	222 1.0×	214 1.1×	64 0.3×	63 0.4×	13	1.0k

Countries citing papers authored by Ugo Cavallari

Since Specialization

Citations

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

Fields of papers citing papers by Ugo Cavallari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ugo Cavallari

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

Teutonico, Federica, Ugo Cavallari, Paola Doneda, et al.. (2024). Early onset epileptic and developmental encephalopathy and MOGS variants: a new diagnosis in the whole exome sequencing (WES) ERA. Neurogenetics. 25(3). 281–286.

Mauri, Lucia, Simone Gana, Alessandra Longo, et al.. (2024). Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract. Clinical Genetics. 106(4). 403–412. 2 indexed citations

Mauri, Gianluca, Giorgio Patelli, Francesco Rizzetto, et al.. (2023). Multimodal treatment with curative intent in a germline BRCA2 mutant metastatic ampullary adenocarcinoma: a case report. World Journal of Surgical Oncology. 21(1). 118–118.

Ćorić, Marijana, Laura Calabresi, Chiara Pavanello, et al.. (2022). Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency. SHILAP Revista de lepidopterología. 49. 28–31. 1 indexed citations

Ciaccio, Claudia, Serena Redaelli, Angela Bentivegna, et al.. (2020). Unbalanced X;Autosome Translocations May Lead to Mild Phenotypes and Are Associated with Autoimmune Diseases. Cytogenetic and Genome Research. 160(2). 80–84. 3 indexed citations

Marini, Valéria, Carmen Fucile, Francesca Mattioli, et al.. (2019). Combined evaluation of genotype and phenotype of thiopurine S-methyltransferase (TPMT) in the clinical management of patients in chronic therapy with azathioprine. Drug Metabolism and Personalized Therapy. 34(1). 2 indexed citations

Zuradelli, Monica, Bernard Peissel, Siranoush Manoukian, et al.. (2010). Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristics. Breast Cancer Research and Treatment. 124(1). 251–258. 27 indexed citations

Lalatta, Faustina, Ugo Cavallari, Barbara Gentilin, et al.. (2010). Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis. European Journal of Pediatrics. 169(10). 1255–1261. 19 indexed citations

Martinelli, Nicola, Elisabetta Trabetti, Mirko Pinotti, et al.. (2008). Combined Effect of Hemostatic Gene Polymorphisms and the Risk of Myocardial Infarction in Patients with Advanced Coronary Atherosclerosis. PLoS ONE. 3(2). e1523–e1523. 33 indexed citations

10.

Natacci, Federica, Ugo Cavallari, Maria Francesca Bedeschi, et al.. (2008). Germline mosaicism in achondroplasia detected in sperm DNA of the father of three affected sibs. American Journal of Medical Genetics Part A. 146A(6). 784–786. 14 indexed citations

11.

Malerba, Giovanni, Luciano Xumerle, Norman Klopp, et al.. (2008). SNPs of the FADS Gene Cluster are Associated with Polyunsaturated Fatty Acids in a Cohort of Patients with Cardiovascular Disease. Lipids. 43(4). 289–299. 191 indexed citations

12.

Girelli, Domenico, Nicola Martinelli, Elisabetta Trabetti, et al.. (2007). ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study. European Journal of Human Genetics. 15(9). 959–966. 36 indexed citations

13.

Bernardo, Esther, Dominick J. Angiolillo, Celia Ramírez, et al.. (2006). Influence of the CD14 C260T Promoter Polymorphism on C-Reactive Protein Levels in Patients With Coronary Artery Disease. The American Journal of Cardiology. 98(9). 1182–1184. 9 indexed citations

14.

Bernardo, Esther, Dominick J. Angiolillo, Celia Ramírez, et al.. (2006). Lack of association between gene sequence variations of platelet membrane receptors and aspirin responsiveness detected by the PFA-100 system in patients with coronary artery disease. Platelets. 17(8). 586–590. 19 indexed citations

15.

Bedeschi, Maria Francesca, Fabienne Escande, Melissa Bellini, et al.. (2006). Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expression. Clinical Dysmorphology. 15(4). 239–241.

16.

Grati, Francesca Romana, Faustina Lalatta, Licia Turolla, et al.. (2005). Three cases with de novo 6q imbalance and variable prenatal phenotype. American Journal of Medical Genetics Part A. 136A(3). 254–258. 18 indexed citations

17.

Trabetti, Elisabetta, Michele Biscuola, Ugo Cavallari, et al.. (2005). On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease. European Journal of Human Genetics. 14(1). 127–130. 46 indexed citations

18.

Angiolillo, Dominick J., Antonio Fernández‐Ortíz, Esther Bernardo, et al.. (2005). Lack of association between the P2Y12 receptor gene polymorphism and platelet response to clopidogrel in patients with coronary artery disease. Thrombosis Research. 116(6). 491–497. 116 indexed citations

19.

Martinelli, Nicola, Domenico Girelli, Oliviero Olivieri, et al.. (2005). Interaction between metabolic syndrome and PON1 polymorphisms as a determinant of the risk of coronary artery disease. Clinical and Experimental Medicine. 5(1). 20–30. 20 indexed citations

20.

Grati, Francesca Romana, Silvia Maria Sirchia, Barbara Gentilin, et al.. (2003). Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies. European Journal of Human Genetics. 12(4). 272–278. 15 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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