Filippo Pinto e Vairo

2.9k total citations
111 papers, 1.4k citations indexed

About

Filippo Pinto e Vairo is a scholar working on Physiology, Molecular Biology and Rheumatology. According to data from OpenAlex, Filippo Pinto e Vairo has authored 111 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Physiology, 35 papers in Molecular Biology and 23 papers in Rheumatology. Recurrent topics in Filippo Pinto e Vairo's work include Lysosomal Storage Disorders Research (54 papers), Cellular transport and secretion (17 papers) and Glycogen Storage Diseases and Myoclonus (16 papers). Filippo Pinto e Vairo is often cited by papers focused on Lysosomal Storage Disorders Research (54 papers), Cellular transport and secretion (17 papers) and Glycogen Storage Diseases and Myoclonus (16 papers). Filippo Pinto e Vairo collaborates with scholars based in Brazil, United States and Germany. Filippo Pinto e Vairo's co-authors include Ida Vanessa Döederlein Schwartz, Roberto Giugliani, Eric W. Klee, Guilherme Baldo, Carolina Fischinger Moura de Souza, Paldeep S. Atwal, Jennifer Gass, Sarah Macklin, Fabiano de Oliveira Poswar and Francyne Kubaski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Filippo Pinto e Vairo

98 papers receiving 1.4k citations

Peers

Filippo Pinto e Vairo
Tarekegn Geberhiwot United Kingdom
Anaïs Brassier France
Carolina Fischinger Moura de Souza Brazil
Amel Karaa United States
Julian Raiman Canada
Diana Ballhausen Switzerland
Wenjuan Qiu China
Federica Deodato Italy
Caroline Sevin France
György Fekete Hungary
Tarekegn Geberhiwot United Kingdom
Filippo Pinto e Vairo
Citations per year, relative to Filippo Pinto e Vairo Filippo Pinto e Vairo (= 1×) peers Tarekegn Geberhiwot

Countries citing papers authored by Filippo Pinto e Vairo

Since Specialization
Citations

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

Fields of papers citing papers by Filippo Pinto e Vairo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Filippo Pinto e Vairo. 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 Filippo Pinto e Vairo. The network helps show where Filippo Pinto e Vairo may publish in the future.

Co-authorship network of co-authors of Filippo Pinto e Vairo

This figure shows the co-authorship network connecting the top 25 collaborators of Filippo Pinto e Vairo. A scholar is included among the top collaborators of Filippo Pinto e Vairo 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 Filippo Pinto e Vairo. Filippo Pinto e Vairo 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.
Vairo, Filippo Pinto e, Michael T. Zimmermann, Salomão Dória Jorge, et al.. (2025). Discovery of a MET-driven monogenic cause of steatotic liver disease. Hepatology. 82(6). 1512–1522.
2.
Goldstein, Jennifer, Emily Groopman, Shruthi Mohan, et al.. (2024). Developing a scoring system for gene curation prioritization in lysosomal diseases. Molecular Genetics and Metabolism. 143(1-2). 108572–108572.
3.
Guicciardi, Maria Eugenia, Erik Jessen, Jingchun Yang, et al.. (2024). IL-17 signaling in primary sclerosing cholangitis patient-derived organoids. Hepatology Communications. 8(6). 7 indexed citations
4.
Warren, Christopher J., Laura Duncan, C. A. Gill, et al.. (2024). EMBEDDING GENOME SEQUENCING AND GENETIC COUNSELLING INTO THE MALE INFERTILITY PRACTICE. Fertility and Sterility. 122(4). e264–e264.
5.
Byeon, Seul Kee, Jin Yong Kim, Roman M. Zenka, et al.. (2024). Development of a Multiplexed Sphingolipids Method for Diagnosis of Inborn Errors of Ceramide Metabolism. Clinical Chemistry. 70(11). 1366–1374. 2 indexed citations
6.
Kubaski, Francyne, Inês Sousa, Camilo Silva, et al.. (2023). Pilot Study of Newborn Screening for Six Lysosomal Diseases in Brazil. SSRN Electronic Journal. 1 indexed citations
7.
Almeida, Hiram Larangeira de, et al.. (2021). Biallelic splicing variants in the nucleolar 60S assembly factor RBM28 cause the ribosomopathy ANE syndrome. Proceedings of the National Academy of Sciences. 118(19). 12 indexed citations
8.
Miao, Jing, Filippo Pinto e Vairo, Marie C. Hogan, et al.. (2021). Identification of Genetic Causes of Focal Segmental Glomerulosclerosis Increases With Proper Patient Selection. Mayo Clinic Proceedings. 96(9). 2342–2353. 27 indexed citations
9.
Smith, Richard S., Marta Florio, Shyam K. Akula, et al.. (2021). Early role for a Na + ,K + -ATPase ( ATP1A3 ) in brain development. Proceedings of the National Academy of Sciences. 118(25). 28 indexed citations
10.
Vairo, Filippo Pinto e, Jennifer L. Kemppainen, John C. Lieske, Peter C. Harris, & Marie C. Hogan. (2021). Establishing a nephrology genetic clinic. Kidney International. 100(2). 254–259. 14 indexed citations
11.
Vairo, Filippo Pinto e, et al.. (2021). Bone marrow burden score is not useful as a follow-up parameter in stable patients with type 1 Gaucher disease after 5 years of treatment. Blood Cells Molecules and Diseases. 90. 102591–102591. 6 indexed citations
12.
Santiago, Karina Miranda, João Pedreira Duprat Neto, Patrícia Ashton‐Prolla, et al.. (2020). Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients. Journal of the European Academy of Dermatology and Venereology. 34(10). 2392–2401. 15 indexed citations
13.
Schultz‐Rogers, Laura, Karthik Muthusamy, Filippo Pinto e Vairo, Eric W. Klee, & Brendan C. Lanpher. (2020). Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report. BMC Medical Genetics. 21(1). 219–219. 7 indexed citations
14.
Mangaonkar, Abhishek A., Alejandro Ferrer, Filippo Pinto e Vairo, et al.. (2019). Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained Cytopenias. Mayo Clinic Proceedings. 94(9). 1753–1768. 12 indexed citations
15.
16.
Schuh, Artur Francisco Schumacher, Filippo Pinto e Vairo, Marina Siebert, et al.. (2019). Evaluation of the frequency of non-motor symptoms of Parkinson’s disease in adult patients with Gaucher disease type 1. Orphanet Journal of Rare Diseases. 14(1). 103–103. 14 indexed citations
17.
Giugliani, Roberto, Fabiano de Oliveira Poswar, Cláudia Vanzella, et al.. (2018). Intrathecal/Intracerebroventricular enzyme replacement therapy for the mucopolysaccharidoses: efficacy, safety, and prospects. Expert Opinion on Orphan Drugs. 6(7). 403–411. 12 indexed citations
18.
Conboy, Erin, Filippo Pinto e Vairo, Darrel Waggoner, et al.. (2017). Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation. SHILAP Revista de lepidopterología. 2017. 1–4. 13 indexed citations
19.
Ashton‐Prolla, Patrícia, José Roberto Goldim, Filippo Pinto e Vairo, Úrsula da Silveira Matte, & Jorge Sequeiros. (2015). Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil. Journal of Community Genetics. 6(3). 275–283. 17 indexed citations
20.
Vairo, Filippo Pinto e, et al.. (2012). Genotypic and phenotypic characterization of Brazilian patients with GM1 gangliosidosis. Gene. 512(1). 113–116. 20 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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