Barbara D′haene

1.0k citations
11 papers · 670 · h-index 9

Impact in

    • MicroRNA in disease regulation
    • Cancer-related molecular mechanisms research
  • Genetics top 10%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomic variations and chromosomal abnormalities

Papers in

    • Molecular Biology Techniques and Applications 2
    • Kruppel-like factors research 1
    • Genomic variations and chromosomal abnormalities 2
    • Congenital Ear and Nasal Anomalies 1

Barbara D′haene

10 papers receiving 659 citations

Peers

Barbara D′haene
Comparison fields: 5 of 87
  • Cancer Research 196
  • Genetics 186
  • Molecular Biology 410
  • Reproductive Medicine 49
  • Nephrology 33
Replace Mohammed Kanchwala with:
Mohammed Kanchwala United States
Marcela Yamamoto Brazil
Natasha Jansz Australia
Pierre Dehan Belgium
I. Reima Finland
Gloria Arriagada Chile
Marianna Giarrè Germany
Simon Denil Belgium
Mary T. Murray United States
Barbara D′haene relative to Mohammed Kanchwala United States Mohammed Kanchwala's profile →
Citations per field
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Mohammed Kanchwala · 1×
Citations per year

Countries citing papers authored by Barbara D′haene

Since Specialization
Citations

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

Fields of papers citing papers by Barbara D′haene

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara D′haene. 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 Barbara D′haene. The network helps show where Barbara D′haene may publish in the future.

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 2010254
2 2011146
3 201591
4 201064
5 201356
6 201018
7 201414
8 201013
9 200812
10
Molecular analysis in a large cohort of patients with anterior segment malformations: expanding the spectrum of FOXC1/PITX2 mutations and copy number changes
20102
11 20120

About Barbara D′haene

Barbara D′haene is a scholar working on Molecular Biology, Genetics, Cancer Research, Surgery and Pediatrics, Perinatology and Child Health, having authored 11 papers that have together received 670 indexed citations. Recurring topics across this work include Cancer-related molecular mechanisms research (4 papers), MicroRNA in disease regulation (2 papers), Prenatal Screening and Diagnostics (2 papers), Molecular Biology Techniques and Applications (2 papers), Chromosomal and Genetic Variations (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Congenital Ear and Nasal Anomalies (1 paper) and Kruppel-like factors research (1 paper). The work is most often cited by research in Cancer Research (196 citations), Genetics (186 citations), Molecular Biology (410 citations), Reproductive Medicine (49 citations) and Nephrology (33 citations). Barbara D′haene has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Jo Vandesompele, Jan Hellemans, Pieter Mestdagh, Elfride De Baere, Michael A. Rudnicki, Heinz Regele, Paul Perco, Bernd Mayer, Johannes Leierer and Andreas Heinzel. Their work appears in journals such as Human Mutation, The Journal of Clinical Endocrinology & Metabolism, Methods, Cancer Research 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.

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