Florence Démurger

1.4k total citations
7 papers, 78 citations indexed

About

Florence Démurger is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Florence Démurger has authored 7 papers receiving a total of 78 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Florence Démurger's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital heart defects research (2 papers). Florence Démurger is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital heart defects research (2 papers). Florence Démurger collaborates with scholars based in France. Florence Démurger's co-authors include Sylvie Odent, Mélanie Fradin, Chloé Quēlin, Sylvie Jaillard, Laurent Pasquier, Marc‐Antoine Belaud‐Rotureau, Dominique Martin‐Coignard, Linda Akloul, Hubert Journel and Josette Lucas and has published in prestigious journals such as Clinical Genetics, American Journal of Medical Genetics Part A and European Journal of Medical Genetics.

In The Last Decade

Florence Démurger

7 papers receiving 66 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Démurger France 5 50 40 33 8 6 7 78
Rosa Baldinger Switzerland 5 54 1.1× 41 1.0× 36 1.1× 4 0.5× 4 0.7× 5 90
Melissa A Dempsey United States 5 47 0.9× 63 1.6× 11 0.3× 7 0.9× 6 1.0× 8 86
Anna Wilsdon United Kingdom 3 40 0.8× 42 1.1× 10 0.3× 10 1.3× 5 0.8× 6 76
Ximena Bonilla United Kingdom 3 22 0.4× 48 1.2× 13 0.4× 4 0.5× 7 1.2× 4 71
Catherine L. Mercer United Kingdom 5 49 1.0× 41 1.0× 13 0.4× 15 1.9× 9 1.5× 6 72
Jin Fang Chai China 5 27 0.5× 32 0.8× 7 0.2× 10 1.3× 3 0.5× 13 72
Valerie Banks United States 3 56 1.1× 56 1.4× 10 0.3× 9 1.1× 9 1.5× 3 77
Isolde Schreyer Germany 5 69 1.4× 30 0.8× 32 1.0× 28 3.5× 2 0.3× 10 87
Luis Daniel Campos-Acevedo Mexico 6 37 0.7× 44 1.1× 13 0.4× 2 0.3× 11 1.8× 16 80
Marine Lebrun France 5 46 0.9× 39 1.0× 14 0.4× 12 1.5× 5 0.8× 9 78

Countries citing papers authored by Florence Démurger

Since Specialization
Citations

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

Fields of papers citing papers by Florence Démurger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Démurger

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Démurger. A scholar is included among the top collaborators of Florence Démurger 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 Florence Démurger. Florence Démurger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

7 of 7 papers shown
1.
Lavillaureix, Alinoë, Philippe Loget, Erika Launay, et al.. (2022). Prenatal phenotype of 22q11 micro-duplications: A systematic review and report on 12 new cases. European Journal of Medical Genetics. 65(2). 104422–104422. 7 indexed citations
2.
Schaefer, Élise, Christèle Dubourg, Wilfrid Carré, et al.. (2021). Skraban‐Deardorff syndrome: Six new cases of WDR 26 ‐related disease and expansion of the clinical phenotype. Clinical Genetics. 99(5). 732–739. 4 indexed citations
3.
Démurger, Florence, Kamran Moradkhani, Olivier Pichon, et al.. (2019). 11q24.2q24.3 microdeletion in two families presenting features of Jacobsen syndrome, without intellectual disability: Role of FLI1, ETS1, and SENCR long noncoding RNA. American Journal of Medical Genetics Part A. 179(6). 993–1000. 12 indexed citations
4.
Quēlin, Chloé, Philippe Loget, Lucile Boutaud, et al.. (2018). Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis. American Journal of Medical Genetics Part A. 176(7). 1610–1613. 11 indexed citations
5.
Pasquier, Laurent, Mélanie Fradin, Dominique Martin‐Coignard, et al.. (2015). Karyotype is not dead (yet)!. European Journal of Medical Genetics. 59(1). 11–15. 31 indexed citations
6.
Démurger, Florence, Laurent Pasquier, Christèle Dubourg, et al.. (2013). Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis. Molecular Syndromology. 4(6). 267–272. 11 indexed citations
7.
Jaillard, Sylvie, Philippe Loget, Josette Lucas, et al.. (2010). Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect. European Journal of Medical Genetics. 54(2). 186–188. 2 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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