Lucia Mauri

1.0k total citations
33 papers, 461 citations indexed

About

Lucia Mauri is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Epidemiology. According to data from OpenAlex, Lucia Mauri has authored 33 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Cardiology and Cardiovascular Medicine and 9 papers in Epidemiology. Recurrent topics in Lucia Mauri's work include Congenital Heart Disease Studies (7 papers), melanin and skin pigmentation (5 papers) and Connexins and lens biology (4 papers). Lucia Mauri is often cited by papers focused on Congenital Heart Disease Studies (7 papers), melanin and skin pigmentation (5 papers) and Connexins and lens biology (4 papers). Lucia Mauri collaborates with scholars based in Italy, France and Germany. Lucia Mauri's co-authors include Alain Fraisse, Sébastien Hascoët, Younès Boudjemline, Jean‐Benoît Thambo, Gabriele Vignati, Jérôme Petit, Julien Mancini, Jean‐Yves Riou, Emmanuelle Fournier and Philippe Brenot and has published in prestigious journals such as European Heart Journal, Gene and The Annals of Thoracic Surgery.

In The Last Decade

Lucia Mauri

33 papers receiving 455 citations

Peers

Lucia Mauri
R Florio United Kingdom
Kim Km South Korea
Eckart Thein Germany
V Rychterová Czechia
Deepak Srivastava United States
Toru Iwasa Japan
K. S. Iyer India
Anette Richter Germany
Sneha Raju Canada
Pietro Bajona United States
R Florio United Kingdom
Lucia Mauri
Citations per year, relative to Lucia Mauri Lucia Mauri (= 1×) peers R Florio

Countries citing papers authored by Lucia Mauri

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Mauri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Mauri

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Mauri. A scholar is included among the top collaborators of Lucia Mauri 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 Lucia Mauri. Lucia Mauri 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.
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
2.
Galli, Jessica, et al.. (2023). Oculocutaneous albinism: the neurological, behavioral, and neuro-ophthalmological perspective. European Journal of Pediatrics. 182(6). 2723–2733. 1 indexed citations
3.
Ouldali, Naïm, Rosa Maria Dellepiane, Sofia Torreggiani, et al.. (2022). Development of a score for early identification of children with Kawasaki disease requiring second-line treatment in multi-ethnic populations in Europe: A multicentre retrospective cohort study. The Lancet Regional Health - Europe. 22. 100481–100481. 6 indexed citations
4.
Annoni, G, Francesca De Rienzo, Lorenza Pugni, et al.. (2022). Enterovirus fulminant myocarditis as cause of acute heart failure in a newborn. IJC Heart & Vasculature. 42. 101093–101093. 2 indexed citations
5.
Pezzani, Lidia, Lucia Mauri, Angelo Selicorni, et al.. (2020). Aortic dilation in Sotos syndrome: An underestimated feature?. American Journal of Medical Genetics Part A. 182(7). 1819–1823. 6 indexed citations
6.
7.
Jalal, Zakaria, Sébastien Hascoët, François Godart, et al.. (2018). Long-Term Outcomes After Percutaneous Closure of Ostium Secundum Atrial Septal Defect in the Young. JACC: Cardiovascular Interventions. 11(8). 795–804. 40 indexed citations
8.
Hascoët, Sébastien, Lucia Mauri, Caroline Claude, et al.. (2017). Infective Endocarditis Risk After Percutaneous Pulmonary Valve Implantation With the Melody and Sapien Valves. JACC: Cardiovascular Interventions. 10(5). 510–517. 69 indexed citations
9.
Mauri, Lucia, Emanuela Manfredini, Alessandra Longo, et al.. (2016). Clinical evaluation and molecular screening of a large consecutive series of albino patients. Journal of Human Genetics. 62(2). 277–290. 16 indexed citations
10.
Mauri, Lucia, Steffen Uebe, Heinrich Sticht, et al.. (2016). Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma. Orphanet Journal of Rare Diseases. 11(1). 108–108. 28 indexed citations
11.
Jalal, Zakaria, Lucia Mauri, Claire Dauphin, et al.. (2016). Abstract 17866: Long-Term Outcome Following Percutaneous Closure of Isolated Secundum Atrial Septal Defects in Children: A French Nationwide Series of 1000 Consecutive Patients. 134. 1 indexed citations
12.
Pasutto, Francesca, Lucia Mauri, Bernt Popp, et al.. (2015). Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma. Gene. 568(1). 76–80. 7 indexed citations
13.
Hascoët, Sébastien, Zakaria Jalal, Alban‐Elouen Baruteau, et al.. (2015). Stenting in paediatric and adult congenital heart diseases: A French multicentre study in the current era. Archives of cardiovascular diseases. 108(12). 650–660. 13 indexed citations
14.
Straniero, Letizia, Valeria Rimoldi, Giulia Soldà, et al.. (2015). Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites. Journal of Human Genetics. 60(9). 467–471. 5 indexed citations
15.
Hascoët, Sébastien, Alban‐Elouen Baruteau, Zakaria Jalal, et al.. (2014). Stents in paediatric and adult congenital interventional cardiac catheterization. Archives of cardiovascular diseases. 107(8-9). 462–475. 33 indexed citations
16.
Mauri, Lucia, Philippe Aldebert, Thomas Cuisset, Jacques Quilici, & Alain Fraisse. (2014). Percutaneous Closure of a Poorly Tolerated Post–Transcatheter Aortic Valve Implantation Ventricular Septal Defect. The Annals of Thoracic Surgery. 98(5). 1823–1826. 5 indexed citations
17.
Mauri, Lucia, et al.. (2014). Transcatheter closure of complex atrial septal defects is efficient under intracardiac echocardiographic guidance. Archives of cardiovascular diseases. 107(12). 646–653. 15 indexed citations
18.
Rimoldi, Valeria, Letizia Straniero, Rosanna Asselta, et al.. (2013). Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II. Gene. 537(1). 79–84. 15 indexed citations
19.
Pomé, Giuseppe, et al.. (1995). Isolated congenital left ventricular diverticulum. European Journal of Cardio-Thoracic Surgery. 9(12). 709–712. 14 indexed citations
20.
Vignati, Gabriele, et al.. (1993). The use of propafenone in the treatment of tachyarrhythmias in children. European Heart Journal. 14(4). 546–550. 16 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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