Isabel Vallcorba

870 citations
17 papers · 566 · h-index 8

Impact in

Papers in

    • Genomic variations and chromosomal abnormalities 8
    • Congenital Ear and Nasal Anomalies 2
    • Hemoglobinopathies and Related Disorders 1
    • Molecular Biology Techniques and Applications 2
    • Single-cell and spatial transcriptomics 1

Isabel Vallcorba

16 papers receiving 535 citations

Peers

Isabel Vallcorba
Comparison fields: 5 of 96
  • Biophysics 227
  • Media Technology 96
  • Computer Vision and Pattern Recognition 172
  • Artificial Intelligence 130
  • Oncology 96
Replace José Miguel García‐Sagredo with:
José Miguel García‐Sagredo Spain
Petter Ranefall Sweden
Nathalie Harder Germany
Oliver Hilsenbeck Switzerland
Michael Schwarzfischer Germany
Mialy DeFelice United States
Marcial García‐Rojo Spain
Henrik Failmezger Germany
Daniel Heim Germany
Petr Matula Czechia
Isabel Vallcorba relative to José Miguel García‐Sagredo Spain José Miguel García‐Sagredo's profile →
Citations per field
00.5×1.5×1.9×
José Miguel García‐Sagredo · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Isabel Vallcorba, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Isabel Vallcorba Line = papers co-authored together Isabel Vallcorba links everyone, so they are left out of the graph.

All Works

17 of 17 papers shown
#Work
1 1998351
2 201783
3 199840
4 199728
5 200615
6 201314
7
[The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].
19998
8 19968
9
Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
19965
10 19944
11 20053
12 19962
13 20132
14 19971
15 20211
16 19961
17 20250

About Isabel Vallcorba

Isabel Vallcorba is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Hematology, having authored 17 papers that have together received 566 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (3 papers), Iron Metabolism and Disorders (2 papers), Molecular Biology Techniques and Applications (2 papers), Carcinogens and Genotoxicity Assessment (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Single-cell and spatial transcriptomics (1 paper) and Hemoglobinopathies and Related Disorders (1 paper). The work is most often cited by research in Biophysics (227 citations), Media Technology (96 citations), Computer Vision and Pattern Recognition (172 citations), Artificial Intelligence (130 citations) and Oncology (96 citations). Isabel Vallcorba has collaborated with scholars based in Spain, United States and Netherlands. Frequent co-authors include Francisco del Pozo, A. Santos, Carlos Ortíz-de-Solórzano, José Miguel García‐Sagredo, J.J. Vaquero, Norberto Malpica, Adela Escudero, Antonio Valeri, Jaime Valentín and Wing Leung. Their work appears in journals such as Cytometry, Environmental Health Perspectives, Clinical Cancer Research, Prenatal Diagnosis and Genes.

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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