Cindy Colson

782 citations
37 papers · 501 · h-index 12

Impact in

  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genomics and Rare Diseases 16
    • Genomic variations and chromosomal abnormalities 8
    • Genetics and Neurodevelopmental Disorders 6
    • Connective tissue disorders research 3
    • Epigenetics and DNA Methylation 4
    • Genomics and Chromatin Dynamics 3
    • RNA modifications and cancer 3

Cindy Colson

32 papers receiving 493 citations

Peers

Cindy Colson
Comparison fields: 5 of 62
  • Genetics 219
  • Developmental Biology 10
  • Molecular Biology 286
  • Aging 5
  • Immunology 49
Replace Stéphanie Moortgat with:
Stéphanie Moortgat Belgium
Maisoon Almugbel Saudi Arabia
Sameena Khan Saudi Arabia
Khalid S. Alqadi Saudi Arabia
Saeed M. Hassan Saudi Arabia
Hakan Ulucan Türkiye
Juliane Eckhold Germany
Anne Dieux‐Coëslier France
Leah R. Fleming United States
Sadegheh Haghshenas Canada
Cindy Colson relative to Stéphanie Moortgat Belgium Stéphanie Moortgat's profile →
Citations per field
00.5×1.5×2.1×
Stéphanie Moortgat · 1×
Citations per year

Countries citing papers authored by Cindy Colson

Since Specialization
Citations

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

Fields of papers citing papers by Cindy Colson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201770
2 201865
3 201949
4 201827
5 202027
6 201526
7 201526
8 202224
9 201921
10 202520
11 201918
12 202317
13 201912
14 202012
15 202312
16 201911
17 202010
18 20238
19 20246
20 20195

About Cindy Colson

Cindy Colson is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Biochemistry, having authored 37 papers that have together received 501 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Prenatal Screening and Diagnostics (4 papers), Epigenetics and DNA Methylation (4 papers), Connective tissue disorders research (3 papers), Genomics and Chromatin Dynamics (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (219 citations), Developmental Biology (10 citations), Molecular Biology (286 citations), Aging (5 citations) and Immunology (49 citations). Cindy Colson has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Marie‐Laure Kottler, Nicolas Richard, Hervé Mittre, Marion Gérard, Daniel Rabier, Agnès Linglart, Arnaud Molin, Nicolas Gruchy, Thierry Billette de Villemeur and H. Ogier de Baulny. Their work appears in journals such as Clinical Genetics, Nature Communications, European Journal of Medical Genetics, Nature Genetics and Neuropediatrics.

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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