Víctor Raggio

653 total citations
29 papers, 207 citations indexed

About

Víctor Raggio is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Víctor Raggio has authored 29 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Víctor Raggio's work include Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers) and Lipoproteins and Cardiovascular Health (4 papers). Víctor Raggio is often cited by papers focused on Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers) and Lipoproteins and Cardiovascular Health (4 papers). Víctor Raggio collaborates with scholars based in Uruguay, Poland and Portugal. Víctor Raggio's co-authors include Martín Graña, Hugo Naya, Sanaa Muheisen, Linda M. Reis, Hagith Yonath, Leonardo Salviati, Dennis P. Han, Deborah M. Costakos, Elena V. Semina and Rebecca C. Tyler and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Human Genetics.

In The Last Decade

Víctor Raggio

26 papers receiving 204 citations

Peers

Countries citing papers authored by Víctor Raggio

Since Specialization

Citations

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

Fields of papers citing papers by Víctor Raggio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Víctor Raggio

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

#	Work	Indexed citations
1	A labeled medical records corpus for the timely detection of rare diseases using machine learning approaches 2025 ·Scientific Reports ·(unknown), Víctor Raggio, Hugo Naya, Lucía Spangenberg, Leticia Cagnina	1
2	Exome Sequencing Reveals Biallelic Mutations in MBTPS1 Gene in a Girl with a Very Rare Skeletal Dysplasia 2024 ·Diagnostics ·Víctor Raggio, (unknown), (unknown), (unknown), Lucía Spangenberg	1
3	Case Report: Mycosis fungoides as an exclusive manifestation of common variable immunodeficiency in a family with a NFKB2 gene mutation 2023 ·Frontiers in Oncology ·(unknown), Sofía Grille, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Daniela Lens, Víctor Raggio, Lucía Spangenberg	2
4	Two mutations in theSBDSgene reveal a diagnosis of Shwachman–Diamond syndrome in a patient with atypical symptoms 2022 ·Molecular Case Studies ·(unknown), Sofía Grille, (unknown), (unknown), (unknown), Cecilia Guillermo, Víctor Raggio, Lucía Spangenberg	3
5	Blood cell respiration rates and mtDNA copy number: A promising tool for the diagnosis of mitochondrial disease 2021 ·Mitochondrion ·Martina Alonso, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Daniela Lens, (unknown), Martín Graña, Hugo Naya, (unknown), Lucía Spangenberg, Víctor Raggio, Aída Lemes, Laura Castro, Celia Quijano	7
6	Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease 2021 ·Human Genomics ·Víctor Raggio, (unknown), (unknown), (unknown), (unknown), Gonzalo Costa, (unknown), Gonzalo Greif, (unknown), (unknown), (unknown), (unknown), Gabriel González, Jong-Yeon Shin, (unknown), Changhoon Kim, Jeong‐Sun Seo, Martín Graña, Hugo Naya, Lucía Spangenberg	5
7	CBG Montevideo: A Clinically Novel SERPINA6 Mutation Leading to Haploinsufficiency of Corticosteroid-binding Globulin 2021 ·Journal of the Endocrine Society ·Emily J. Meyer, Lucía Spangenberg, María José Ramírez-Bajo, Sunita M C De Sousa, Víctor Raggio, David J. Torpy	7
8	Deep sequencing discovery of causal mtDNA mutations in a patient with unspecific neurological disease 2018 ·Mitochondrion ·Lucía Spangenberg, Martín Graña, (unknown), (unknown), (unknown), Gonzalo Greif, (unknown), Alicia Vaglio, (unknown), Carlos Robello, Laura Castro, Celia Quijano, Víctor Raggio, Hugo Naya	4
9	A novel mutation in the OAR domain of the ARX gene 2017 ·Clinical Case Reports ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Martı́n Ciganda, (unknown), Víctor Raggio, Leda Roche, (unknown)	4
10	3697G>A in MT-ND1 is a causative mutation in mitochondrial disease 2016 ·Mitochondrion ·Lucía Spangenberg, Martín Graña, Gonzalo Greif, Juan M. Suárez-Rivero, (unknown), (unknown), (unknown), (unknown), Aída Lemes, (unknown), (unknown), José A. Sánchez‐Alcázar, Carlos Robello, Víctor Raggio, Hugo Naya	11
11	Molecular characterization of genes modifying the age at onset in Huntington's disease in Uruguayan patients 2015 ·International Journal of Neuroscience ·(unknown), (unknown), Víctor Raggio, Patricia Esperón	6
12	Análisis molecular de familias uruguayas con Enfermedad de Huntington 2014 ·Víctor Raggio, (unknown), (unknown), (unknown), Andrés G. Lescano, (unknown), (unknown), (unknown), Roberto Ventura, (unknown), Patricia Esperón	1
13	Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes 2013 ·Human Genetics ·Linda M. Reis, Rebecca C. Tyler, Sanaa Muheisen, Víctor Raggio, Leonardo Salviati, Dennis P. Han, Deborah M. Costakos, Hagith Yonath, (unknown), (unknown), Elena V. Semina	70
14	[Advances in the identification of the aetiology of mental retardation]. 2013 ·PubMed ·Gabriel González, Víctor Raggio, (unknown), (unknown), Leda Roche	2
15	Identification of relations between risk factors and their pathologies or health conditions by mining scientific literature 2010 ·Studies in health technology and informatics ·Thierry Hamon, Martín Graña, Víctor Raggio, Natalia Grabar, Hugo Naya	22
16	Perfil genómico de riesgo en la práctica clínica 2009 ·SHILAP Revista de lepidopterología ·Víctor Raggio, Leda Roche	3
17	Genotipo de los genes VKORC1 y CYP2C9 en la respuesta individual a la warfarina 2008 ·SHILAP Revista de lepidopterología ·Patricia Esperón, Víctor Raggio, (unknown), (unknown), (unknown), Mario Stoll	3
18	LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay 2008 ·Parkinsonism & Related Disorders ·Ignácio F. Mata, Carlos Cosentino, (unknown), Luis Torres, Pilar Mazzetti, (unknown), Víctor Raggio, (unknown), (unknown), Dora Yearout, (unknown), Cyrus P. Zabetian	29
19	Maldición de Ondina: presentación de un caso clínico 2007 ·(unknown), Víctor Raggio	0
20	Respuesta terapéutica inadecuada a la warfarina en un paciente genéticamente susceptible 2005 ·SHILAP Revista de lepidopterología ·Víctor Raggio, Pablo Neira, Patricia Esperón, (unknown), Mario Stoll	3

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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