Matthieu Décamp

422 total citations
9 papers, 132 citations indexed

About

Matthieu Décamp is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Matthieu Décamp has authored 9 papers receiving a total of 132 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Matthieu Décamp's work include Genetic Syndromes and Imprinting (2 papers), Genomics and Rare Diseases (2 papers) and Acute Myeloid Leukemia Research (2 papers). Matthieu Décamp is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Genomics and Rare Diseases (2 papers) and Acute Myeloid Leukemia Research (2 papers). Matthieu Décamp collaborates with scholars based in France, Japan and United Kingdom. Matthieu Décamp's co-authors include Nicolas Gruchy, Nathalie Leporrier, Joris Andrieux, Hervé Mittre, Nicolas Richard, Ghislaine Plessis, G. Benoist, Corinne Jeanne‐Pasquier, Florence Petit and Jean‐Marie Cuisset and has published in prestigious journals such as Human Reproduction, Bone and Prenatal Diagnosis.

In The Last Decade

Matthieu Décamp

8 papers receiving 120 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Matthieu Décamp France 7 89 60 55 12 8 9 132
Hannaleena Kokkonen Finland 8 173 1.9× 152 2.5× 83 1.5× 12 1.0× 10 1.3× 20 238
Liliana Fernández United States 6 87 1.0× 49 0.8× 41 0.7× 7 0.6× 10 1.3× 8 151
Mylène Béri France 7 150 1.7× 79 1.3× 65 1.2× 8 0.7× 13 1.6× 8 175
Brooke Tata France 5 58 0.7× 94 1.6× 36 0.7× 3 0.3× 7 0.9× 5 410
Gyri Aasland Gradek Norway 5 76 0.9× 58 1.0× 32 0.6× 11 0.9× 13 1.6× 5 151
Sonia Bouquillon France 6 78 0.9× 69 1.1× 23 0.4× 11 0.9× 9 1.1× 8 121
Dana Knutzen United States 7 39 0.4× 48 0.8× 63 1.1× 32 2.7× 30 3.8× 9 174
Marie‐Laure Vuillaume France 10 90 1.0× 74 1.2× 29 0.5× 6 0.5× 3 0.4× 16 138
Angharad M. Roberts United Kingdom 7 99 1.1× 69 1.1× 57 1.0× 13 1.1× 4 0.5× 15 199
Renchao Liu China 6 84 0.9× 62 1.0× 16 0.3× 20 1.7× 3 0.4× 16 152

Countries citing papers authored by Matthieu Décamp

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Matthieu Décamp

This figure shows the co-authorship network connecting the top 25 collaborators of Matthieu Décamp. A scholar is included among the top collaborators of Matthieu Décamp based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Matthieu Décamp. Matthieu Décamp is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

9 of 9 papers shown
1.
Bidet, Audrey, Wendy Cuccuini, Matthieu Décamp, et al.. (2023). Cytogenetics in the management of acute myeloid leukemia and histiocytic/dendritic cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH). Current Research in Translational Medicine. 71(4). 103421–103421. 2 indexed citations
2.
Décamp, Matthieu, Catherine Godon, Olivier Theisen, et al.. (2023). Cytogenetics in the management of myeloproliferative neoplasms, mastocytosis and myelodysplastic/myeloproliferative neoplasms: Guidelines from the Group Francophone de Cytogénétique Hématologique (GFCH). Current Research in Translational Medicine. 71(4). 103424–103424.
3.
Colson, Cindy, Matthieu Décamp, Nicolas Gruchy, et al.. (2019). High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B. Bone. 123. 145–152. 18 indexed citations
4.
Jedraszak, Guillaume, Aline Receveur, Matthieu Décamp, et al.. (2015). Growth hormone deficiency and pituitary malformation in a recurrent Cat-Eye syndrome: A family report. Annales d Endocrinologie. 76(5). 629–634. 17 indexed citations
5.
Petit, Florence, Ghislaine Plessis, Matthieu Décamp, et al.. (2014). 21q21 deletion involving NCAM2: Report of 3 cases with neurodevelopmental disorders. European Journal of Medical Genetics. 58(1). 44–46. 27 indexed citations
6.
Jean‐Marçais, Nolwenn, Matthieu Décamp, Marion Gérard, et al.. (2014). The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature. American Journal of Medical Genetics Part A. 167(1). 185–189. 9 indexed citations
7.
Molin, Arnaud, G. Benoist, Corinne Jeanne‐Pasquier, et al.. (2013). 12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4. European Journal of Medical Genetics. 56(10). 580–583. 11 indexed citations
8.
Gruchy, Nicolas, Matthieu Décamp, Nicolas Richard, et al.. (2011). Array CGH analysis in high‐risk pregnancies: comparing DNA from cultured cells and cell‐free fetal DNA. Prenatal Diagnosis. 32(4). 383–388. 29 indexed citations
9.
Gruchy, Nicolas, François Vialard, Matthieu Décamp, et al.. (2011). Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome. Human Reproduction. 26(9). 2570–2575. 19 indexed citations

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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