Alice Masurel

1.1k total citations
5 papers, 99 citations indexed

About

Alice Masurel is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Alice Masurel has authored 5 papers receiving a total of 99 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Alice Masurel's work include Epigenetics and DNA Methylation (2 papers), Vascular Malformations and Hemangiomas (2 papers) and Genital Health and Disease (1 paper). Alice Masurel is often cited by papers focused on Epigenetics and DNA Methylation (2 papers), Vascular Malformations and Hemangiomas (2 papers) and Genital Health and Disease (1 paper). Alice Masurel collaborates with scholars based in France and Denmark. Alice Masurel's co-authors include Laurence Olivier-Faivre, P. Vabres, Laurence Faivre, Mondher Chouchane, Anne‐Laure Mosca‐Boidron, Maria Kirchhoff, Christel Thauvin‐Robinet, Patrick Callier, Francine Mugneret and Nathalie Marle and has published in prestigious journals such as Clinical Genetics, JAMA Dermatology and American Journal of Medical Genetics Part A.

In The Last Decade

Alice Masurel

5 papers receiving 87 citations

Peers

Alice Masurel

GENET

NEURO

MB

RHEUM

PHYSI

Andrea Dieckmann Germany

Ruth Armstrong United Kingdom

Martim Bartels Netherlands

Cécile Zordan France

Dilek Aktaş Türkiye

Florian Thibord United States

Fiorenza Soli Italy

Ella Wilkins Australia

Ágnes Sallai Hungary

Leila Sozaeva Russia

Andrea Dieckmann Germany

Alice Masurel

14 ×0.3

GENET

25 ×0.8

NEURO

28 ×1.0

MB

4 ×0.2

RHEUM

32 ×1.5

PHYSI

Citations per year, relative to Alice Masurel Alice Masurel (= 1×) peers Andrea Dieckmann

Countries citing papers authored by Alice Masurel

Since Specialization

Citations

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

Fields of papers citing papers by Alice Masurel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alice Masurel

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

All Works

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5 of 5 papers shown

1.

Messaoudi, Kahia, et al.. (2024). Prenatal Diagnosis of Proteus Syndrome: About a Case. American Journal of Medical Genetics Part A. 197(5). e63968–e63968. 1 indexed citations

2.

Thauvin‐Robinet, Christel, Laurence Duplomb, Alice Masurel, et al.. (2015). Homozygous FIBP nonsense variant responsible of syndromic overgrowth, with overgrowth, macrocephaly, retinal coloboma and learning disabilities. Clinical Genetics. 89(5). e1–4. 16 indexed citations

3.

Giroud, M, Benoît Daubail, Mondher Chouchane, et al.. (2014). Angelman Syndrome: A Case Series Assessing Neurological Issues in Adulthood. European Neurology. 73(1-2). 119–125. 10 indexed citations

4.

Masurel, Alice, et al.. (2013). Juvenile Xanthogranuloma and Nevus Anemicus in the Diagnosis of Neurofibromatosis Type 1. JAMA Dermatology. 150(1). 42–42. 48 indexed citations

5.

Kirchhoff, Maria, Nathalie Marle, Mondher Chouchane, et al.. (2013). Delineation of a new chromosome 20q11.2 duplication syndrome including the ASXL1 gene. American Journal of Medical Genetics Part A. 161(7). 1594–1598. 24 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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