Víctor Martínez‐Glez

3.1k total citations
61 papers, 1.4k citations indexed

About

Víctor Martínez‐Glez is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Víctor Martínez‐Glez has authored 61 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 23 papers in Molecular Biology and 17 papers in Surgery. Recurrent topics in Víctor Martínez‐Glez's work include Vascular Malformations and Hemangiomas (14 papers), Tumors and Oncological Cases (10 papers) and Neurofibromatosis and Schwannoma Cases (8 papers). Víctor Martínez‐Glez is often cited by papers focused on Vascular Malformations and Hemangiomas (14 papers), Tumors and Oncological Cases (10 papers) and Neurofibromatosis and Schwannoma Cases (8 papers). Víctor Martínez‐Glez collaborates with scholars based in Spain, Brazil and Egypt. Víctor Martínez‐Glez's co-authors include Pablo Lapunzina, Víctor L. Ruiz‐Pérez, Eulalia Valencia, José A. Caparrós‐Martín, Samia A. Temtamy, Mona Aglan, Khalda Amr, Julián Nevado, Jair Tenorio and Sixto García‐Miñáur and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Víctor Martínez‐Glez

57 papers receiving 1.4k citations

Peers

Víctor Martínez‐Glez
Jeroen Knijnenburg Netherlands
Jan M. Cobben Netherlands
Marjolijn C.J. Jongmans Netherlands
James O’Sullivan United Kingdom
Sanjeev S. Bhaskar United Kingdom
Lesley C. Adès Australia
Luitgard M. Neumann Germany
Astrid S. Plomp Netherlands
Nina Horelli‐Kuitunen Finland
Trijnie Dijkhuizen Netherlands
Jeroen Knijnenburg Netherlands
Víctor Martínez‐Glez
Citations per year, relative to Víctor Martínez‐Glez Víctor Martínez‐Glez (= 1×) peers Jeroen Knijnenburg

Countries citing papers authored by Víctor Martínez‐Glez

Since Specialization
Citations

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

Fields of papers citing papers by Víctor Martínez‐Glez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Víctor Martínez‐Glez

This figure shows the co-authorship network connecting the top 25 collaborators of Víctor Martínez‐Glez. A scholar is included among the top collaborators of Víctor Martínez‐Glez 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 Martínez‐Glez. Víctor Martínez‐Glez 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.
Rodríguez‐Laguna, Lara, et al.. (2025). Association of Somatic KRAS Variants with Osteolysis in Arteriovenous Malformations. European Journal of Pediatric Surgery. 35(5). 362–368.
2.
Spataro, Nino, Juan Pablo Trujillo‐Quintero, Elisabeth Gabau, et al.. (2023). High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders. Genes. 14(3). 708–708. 3 indexed citations
3.
Rodríguez‐Laguna, Lara, et al.. (2023). Lymphatic Malformations in Parkes Weber's Syndrome: Retrospective Review of 16 Cases in a Vascular Anomalies Center. European Journal of Pediatric Surgery. 34(1). 78–83.
4.
Triana, Paloma, et al.. (2022). Larotrectinib as an Effective Therapy in Congenital Infantile Fibrosarcoma: Report of Two Cases. SHILAP Revista de lepidopterología. 10(1). e76–e79. 6 indexed citations
5.
Martínez‐Glez, Víctor, Lara Rodríguez‐Laguna, Vanesa Viana‐Huete, et al.. (2021). Segmental undergrowth is associated with pathogenic variants in vascular malformation genes: A retrospective case‐series study. Clinical Genetics. 101(3). 296–306. 9 indexed citations
6.
Rodríguez‐Laguna, Lara, et al.. (2021). Mixed vascular naevus syndrome: report of three children with somatic GNA11 mutation and new systemic associations. Clinical and Experimental Dermatology. 47(1). 129–135. 2 indexed citations
7.
Douzgou, Sofia, Eulàlia Baselga, Moise Danielpour, et al.. (2021). A standard of care for individuals with PIK3CA ‐related disorders: An international expert consensus statement. Clinical Genetics. 101(1). 32–47. 20 indexed citations
8.
Martínez‐Glez, Víctor, Jair Tenorio, Julián Nevado, et al.. (2020). A six-attribute classification of geneticmosaicism. Genetics in Medicine. 22(11). 1743–1757. 42 indexed citations
9.
Gordo, Gema, Lara Rodríguez‐Laguna, Noelia Agrá, et al.. (2019). Constitutional mosaicism in RASA1 ‐related capillary malformation‐arteriovenous malformation. Clinical Genetics. 95(4). 516–519. 9 indexed citations
10.
Gordo, Gema, Jair Tenorio, Pedro Arias, et al.. (2017). mTOR mutations in Smith‐Kingsmore syndrome: Four additional patients and a review. Clinical Genetics. 93(4). 762–775. 29 indexed citations
11.
Valencia, Eulalia, José A. Caparrós‐Martín, Ma Salomé Sirerol-Piquer, et al.. (2014). Report of a newly indentified patient with mutations in BMP1 and underlying pathogenetic aspects. American Journal of Medical Genetics Part A. 164(5). 1143–1150. 24 indexed citations
12.
Caparrós‐Martín, José A., Eulalia Valencia, Verónica Pulido, et al.. (2013). Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations. American Journal of Medical Genetics Part A. 161(6). 1354–1369. 46 indexed citations
13.
Vallespín, Elena, María Palomares‐Bralo, M. A. Mori, et al.. (2013). Customized high resolution CGH‐array for clinical diagnosis reveals additional genomic imbalances in previous well‐defined pathological samples. American Journal of Medical Genetics Part A. 161(8). 1950–1960. 27 indexed citations
14.
Torres‐Martín, Miguel, Víctor Martínez‐Glez, Luis Lassaletta, et al.. (2012). Expression analysis of tumor-related genes involved in critical regulatory pathways in schwannomas. Clinical & Translational Oncology. 15(5). 409–411. 7 indexed citations
15.
Romanelli, Valeria, Víctor Martínez‐Glez, Mario F. Fraga, et al.. (2011). Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. European Journal of Human Genetics. 19(4). 416–421. 36 indexed citations
16.
Martínez‐Glez, Víctor, Eulalia Valencia, José A. Caparrós‐Martín, et al.. (2011). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation. 33(2). 343–350. 155 indexed citations
17.
Lapunzina, Pablo, Mona Aglan, Samia A. Temtamy, et al.. (2010). Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 87(1). 110–114. 205 indexed citations
18.
Romanelli, Valeria, Julián Nevado, Mario F. Fraga, et al.. (2010). Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism. Journal of Medical Genetics. 48(3). 212–216. 28 indexed citations
19.
Martínez‐Glez, Víctor, et al.. (2008). Microarray Gene Expression Profiling in Meningiomas and Schwannomas. Current Medicinal Chemistry. 15(8). 826–833. 9 indexed citations
20.
Alonso, M. Eva, M. Josefa Bello, Dolores Arjona, et al.. (2005). Real-Time Quantitative PCR Analysis of Gene Dosages Reveals Gene Amplification in Low-Grade Oligodendrogliomas. American Journal of Clinical Pathology. 123(6). 900–906. 11 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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