Matthieu Décamp
Impact in
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- Prenatal Screening and Diagnostics
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- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Kidney Cyst Diseases
Papers in
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- Epigenetics and DNA Methylation 1
- Genetics 6
- Genetics and Neurodevelopmental Disorders 2
- Genomics and Rare Diseases 2
- Genetic Syndromes and Imprinting 2
- Myeloproliferative Neoplasms: Diagnosis and Treatment 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Nicolas Gruchy (4 shared papers)Nathalie Leporrier (3 shared papers)Joris Andrieux (3 shared papers)Nicolas Richard (2 shared papers)Hervé Mittre (2 shared papers)G. Benoist (2 shared papers)Ghislaine Plessis (2 shared papers)Corinne Jeanne‐Pasquier (2 shared papers)
- Journals
- European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (1 paper)Bone (1 paper)Human Reproduction (1 paper)Current Research in Translational Medicine (2 papers)
- Partner nations
- FranceJapanUnited States
In The Last Decade
Matthieu Décamp
8 papers receiving 123 citations
Peers
Comparison fields: 5 of 34
- Pediatrics, Perinatology and Child Health 44
- Genetics 63
- Developmental Neuroscience 6
- Developmental Biology 2
- Molecular Biology 45
Countries citing papers authored by Matthieu Décamp
This map shows the geographic impact of Matthieu Décamp'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 Matthieu Décamp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthieu Décamp more than expected).
Fields of papers citing papers by Matthieu Décamp
This network shows the impact of papers produced by Matthieu Décamp. 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 Matthieu Décamp. The network helps show where Matthieu Décamp may publish in the future.
Co-authors
The 25 scholars most cited alongside Matthieu Décamp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 30 | |
| 2 | 2014 | 27 | |
| 3 | 2011 | 19 | |
| 4 | 2019 | 18 | |
| 5 | 2015 | 17 | |
| 6 | 2013 | 11 | |
| 7 | 2014 | 9 | |
| 8 | 2023 | 4 | |
| 9 | 2023 | 0 |
About Matthieu Décamp
Matthieu Décamp is a scholar working on Molecular Biology, Genetics, Genetics, Pediatrics, Perinatology and Child Health and Hematology, having authored 9 papers that have together received 135 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Genomics and Rare Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers), Acute Myeloid Leukemia Research (2 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers), Prenatal Screening and Diagnostics (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (44 citations), Genetics (63 citations), Developmental Neuroscience (6 citations), Developmental Biology (2 citations) and Molecular Biology (45 citations). Matthieu Décamp has collaborated with scholars based in France, Japan and United States. Frequent co-authors include Nicolas Gruchy, Nathalie Leporrier, Joris Andrieux, Nicolas Richard, Hervé Mittre, G. Benoist, Ghislaine Plessis, Corinne Jeanne‐Pasquier, Jean‐Marie Cuisset and Moira Blyth. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, Bone, Human Reproduction and Current Research in Translational Medicine.
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.