Gea Beunders

886 citations
5 papers · 66 · h-index 4

Impact in

    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Autism Spectrum Disorder Research

Papers in

    • Genomics and Rare Diseases 5
    • Genetics and Neurodevelopmental Disorders 3
    • Genomic variations and chromosomal abnormalities 2
    • Congenital heart defects research 1

Gea Beunders

5 papers receiving 66 citations

Peers

Gea Beunders
Comparison fields: 5 of 25
  • Genetics 52
  • Cognitive Neuroscience 10
  • Molecular Biology 34
  • Pediatrics, Perinatology and Child Health 9
  • Cell Biology 5
Replace Julie McCarrier with:
Julie McCarrier United States
Shelagh Joss United Kingdom
Nurit Assia Batzir Israel
Virginia Clowes United Kingdom
Tammy Kammin United Kingdom
Abeer Al‐Saegh Oman
Nobuhiko Okamoto Japan
Mathijs Kattenberg Netherlands
Emily Palen United States
Marco Brumat Italy
Gea Beunders relative to Julie McCarrier United States Julie McCarrier's profile →
Citations per field
00.5×
Julie McCarrier · 1×
Citations per year

Countries citing papers authored by Gea Beunders

Since Specialization
Citations

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

Fields of papers citing papers by Gea Beunders

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gea Beunders, 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 Gea Beunders Line = papers co-authored together Gea Beunders links everyone, so they are left out of the graph.

All Works

5 of 5 papers shown
#Work
1 201422
2 201021
3 201714
4 20127
5 20212

About Gea Beunders

Gea Beunders is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cognitive Neuroscience and Cell Biology, having authored 5 papers that have together received 66 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Congenital heart defects research (1 paper), Cystic Fibrosis Research Advances (1 paper), Neonatal Respiratory Health Research (1 paper), Cellular transport and secretion (1 paper) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Genetics (52 citations), Cognitive Neuroscience (10 citations), Molecular Biology (34 citations), Pediatrics, Perinatology and Child Health (9 citations) and Cell Biology (5 citations). Gea Beunders has collaborated with scholars based in Netherlands, United Kingdom and Belgium. Frequent co-authors include Erik A. Sistermans, Lidewij Henneman, R. Frank Kooy, John Tolmie, Els Voorhoeve, Tjitske Kleefstra, Alexander J. Groffen, Helger G. Yntema, Berten Ceulemans and Martin Callaghan. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, Frontiers in Pediatrics, Genes Brain & Behavior and European Journal of Human Genetics.

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.

Explore authors with similar magnitude of impact