Isabel Vallcorba

870 total citations
17 papers, 566 citations indexed

About

Isabel Vallcorba is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Isabel Vallcorba has authored 17 papers receiving a total of 566 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Isabel Vallcorba's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (3 papers) and Carcinogens and Genotoxicity Assessment (2 papers). Isabel Vallcorba is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (3 papers) and Carcinogens and Genotoxicity Assessment (2 papers). Isabel Vallcorba collaborates with scholars based in Spain, United States and Netherlands. Isabel Vallcorba's co-authors include Carlos Ortíz-de-Solórzano, A. Santos, Francisco del Pozo, José Miguel García‐Sagredo, Norberto Malpica, J.J. Vaquero, Lucía Fernández, Juan Manuel Torres, Adela Escudero and María Vela and has published in prestigious journals such as Clinical Cancer Research, Environmental Health Perspectives and American Journal of Medical Genetics.

In The Last Decade

Isabel Vallcorba

16 papers receiving 535 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabel Vallcorba Spain 8 227 172 143 130 96 17 566
José Miguel García‐Sagredo Spain 10 235 1.0× 165 1.0× 201 1.4× 117 0.9× 71 0.7× 29 692
Petter Ranefall Sweden 15 154 0.7× 82 0.5× 275 1.9× 82 0.6× 92 1.0× 32 665
Petr Matula Czechia 14 149 0.7× 77 0.4× 219 1.5× 26 0.2× 22 0.2× 43 476
Henrik Failmezger Germany 9 116 0.5× 68 0.4× 337 2.4× 211 1.6× 122 1.3× 15 671
Michael Schwarzfischer Germany 11 223 1.0× 60 0.3× 299 2.1× 54 0.4× 26 0.3× 11 511
Pavel Matula Czechia 18 174 0.8× 82 0.5× 497 3.5× 38 0.3× 47 0.5× 41 716
Mialy DeFelice United States 4 243 1.1× 61 0.4× 251 1.8× 62 0.5× 32 0.3× 5 496
Oliver Hilsenbeck Switzerland 11 294 1.3× 67 0.4× 410 2.9× 50 0.4× 67 0.7× 13 816
Nathalie Harder Germany 15 154 0.7× 73 0.4× 206 1.4× 70 0.5× 79 0.8× 31 525
Marcial García‐Rojo Spain 15 153 0.7× 155 0.9× 109 0.8× 349 2.7× 114 1.2× 57 682

Countries citing papers authored by Isabel Vallcorba

Since Specialization
Citations

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

Fields of papers citing papers by Isabel Vallcorba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabel Vallcorba

This figure shows the co-authorship network connecting the top 25 collaborators of Isabel Vallcorba. A scholar is included among the top collaborators of Isabel Vallcorba 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 Isabel Vallcorba. Isabel Vallcorba is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Nevado, Julián, Raquel Blanco-Lago, Adolfo Hernández, et al.. (2025). Clinician-Based Functional Scoring and Genomic Insights for Prognostic Stratification in Wolf–Hirschhorn Syndrome. Genes. 16(7). 820–820.
2.
García‐Santiago, Fe Amalia, Elena Mansilla, Fernando Santos‐Simarro, et al.. (2021). Prenatal ultrasound findings in Koolen‐de Vries foetuses: Central nervous system anomalies are frequent markers of this syndrome. Molecular Genetics & Genomic Medicine. 9(5). e1649–e1649. 1 indexed citations
3.
Fernández, Lucía, Adela Escudero, María Vela, et al.. (2017). Memory T Cells Expressing an NKG2D-CAR Efficiently Target Osteosarcoma Cells. Clinical Cancer Research. 23(19). 5824–5835. 83 indexed citations
4.
Vallcorba, Isabel, et al.. (2013). Celiac disease and HLA-DQ genotype: diagnosis of different genetic risk profiles related to the age in Badajoz, southwestern Spain. Revista Española de Enfermedades Digestivas. 105(8). 469–476. 14 indexed citations
5.
Pàmpols, Teresa, Joaquı́n Rueda, Montserrat Milà, et al.. (2013). El documento de consentimiento informado para la realización de pruebas genéticas en el ámbito asistencial y en proyectos de investigación. 24(2). 46–56. 2 indexed citations
6.
Pajares, I. López, Olaya Villa, Marta Salido, et al.. (2006). Euchromatic variant 16p+. Implications in prenatal diagnosis. Prenatal Diagnosis. 26(6). 535–538. 15 indexed citations
7.
Vallcorba, Isabel, et al.. (2005). Hemocromatosis hereditaria: estudio fenotípico de una población española. Medicina Clínica. 125(19). 721–726. 3 indexed citations
8.
Vallcorba, Isabel, et al.. (1999). [The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].. PubMed. 199(10). 632–6. 8 indexed citations
9.
Malpica, Norberto, Carlos Ortíz-de-Solórzano, J.J. Vaquero, et al.. (1998). Applying watershed algorithms to the segmentation of clustered nuclei. Cytometry. 28(4). 289–297. 351 indexed citations
10.
Ortíz-de-Solórzano, Carlos, et al.. (1998). Automated FISH spot counting in interphase nuclei: Statistical validation and data correction. Cytometry. 31(2). 93–99. 40 indexed citations
11.
Vallcorba, Isabel, et al.. (1997). Delineation of a duplication map of chromosome 3q: A new case confirms the exclusion of 3q25‐q26.2 from the duplication 3q syndrome critical region. American Journal of Medical Genetics. 68(4). 428–432. 1 indexed citations
12.
Rizzu, Patrizia, Bassem R. Haddad, Isabel Vallcorba, et al.. (1997). Delineation of a duplication map of chromosome 3q: A new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region. American Journal of Medical Genetics. 68(4). 428–432. 28 indexed citations
13.
Vallcorba, Isabel, et al.. (1996). Chromosome painting in biological dosimetry: assessment of the ability to score stable chromosome aberrations using different pairs of paint probes.. Environmental Health Perspectives. 104(suppl 3). 475–477. 2 indexed citations
14.
Vallcorba, Isabel, et al.. (1996). Cytogenetic study of neuroendocrine carcinoma of Merkel cells. Cancer Genetics and Cytogenetics. 92(1). 79–81. 8 indexed citations
15.
García‐Sagredo, José Miguel, et al.. (1996). Chromosome Painting in Biological Dosimetry: Assessment of the Ability to Score Stable Chromosome Aberrations Using Different Pairs of Paint Probes. Environmental Health Perspectives. 104. 475–475. 1 indexed citations
16.
Darnaude, M. Teresa, et al.. (1996). Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.. PubMed. 39(2). 61–3. 5 indexed citations
17.
Paz, P. de, José Miguel García‐Sagredo, Isabel Vallcorba, et al.. (1994). Burkitt lymphoma with a duplication of der(8)t(2;8). Cancer Genetics and Cytogenetics. 76(2). 136–139. 4 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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