Aline Receveur

757 total citations
22 papers, 200 citations indexed

About

Aline Receveur is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Aline Receveur has authored 22 papers receiving a total of 200 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Molecular Biology. Recurrent topics in Aline Receveur's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). Aline Receveur is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). Aline Receveur collaborates with scholars based in France, United Kingdom and Australia. Aline Receveur's co-authors include Joris Andrieux, Michèle Mathieu‐Dramard, Henri Copin, Guillaume Jedraszak, G Morin, Bénédicte Demeer, Sophie Julia, Ghislaine Plessis, Gilles Morin and Dominique Martin‐Coignard and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Obstetrics and Gynecology and International Journal of Cancer.

In The Last Decade

Aline Receveur

21 papers receiving 152 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aline Receveur France 9 109 81 50 29 27 22 200
Shun‐Ping Chang Taiwan 10 94 0.9× 96 1.2× 89 1.8× 33 1.1× 16 0.6× 41 278
Julia Kolarova Germany 9 76 0.7× 127 1.6× 55 1.1× 9 0.3× 28 1.0× 20 190
Carole Goumy France 11 185 1.7× 125 1.5× 100 2.0× 51 1.8× 15 0.6× 36 324
Nicholas Hickson United Kingdom 8 54 0.5× 66 0.8× 26 0.5× 22 0.8× 54 2.0× 10 185
Fatih Z Boyar United States 8 169 1.6× 194 2.4× 70 1.4× 69 2.4× 40 1.5× 18 342
Thomas R. W. Oliver United Kingdom 5 70 0.6× 119 1.5× 73 1.5× 14 0.5× 90 3.3× 9 252
Nadja Kokalj Vokač Slovenia 8 62 0.6× 79 1.0× 49 1.0× 11 0.4× 11 0.4× 27 179
Shu Yau United Kingdom 8 90 0.8× 130 1.6× 38 0.8× 8 0.3× 12 0.4× 10 258
Ann‐Leslie Zaslav United States 9 138 1.3× 46 0.6× 99 2.0× 30 1.0× 10 0.4× 24 214
Kristen L. Sund United States 9 171 1.6× 193 2.4× 56 1.1× 7 0.2× 19 0.7× 15 326

Countries citing papers authored by Aline Receveur

Since Specialization
Citations

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

Fields of papers citing papers by Aline Receveur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aline Receveur

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

All Works

20 of 20 papers shown
1.
Benazra, Marion, Pascale Kleinfinger, Mylène Valduga, et al.. (2024). Optical genome mapping identifies a homozygous deletion in the non-coding region of the SCN9A gene in individuals from the same family with congenital insensitivity to pain. Frontiers in Genetics. 15. 1375770–1375770.
2.
Morales, Elisa, Jelena Martinović, Philippe Labrune, et al.. (2022). Management of copy number variants associated with incomplete penetrance and variable expressivity—Results of a French survey. Clinical Genetics. 103(3). 335–340. 1 indexed citations
3.
Monier, Isabelle, Aline Receveur, V. Houfflin‐Debarge, et al.. (2022). Should Prenatal Chromosomal Microarray Analysis Be Offered for Isolated Fetal Growth Restriction? A French Multicenter Study. Obstetrical & Gynecological Survey. 77(6). 336–338. 4 indexed citations
4.
Petit, François, et al.. (2021). Early prenatal diagnosis of alveolar capillary dysplasia with misalignment of pulmonary veins due to a 16q24.1 deletion. American Journal of Medical Genetics Part A. 185(5). 1494–1497. 2 indexed citations
5.
Monier, Isabelle, Aline Receveur, V. Houfflin‐Debarge, et al.. (2021). Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study. American Journal of Obstetrics and Gynecology. 225(6). 676.e1–676.e15. 10 indexed citations
6.
Chalas, Céline, Aline Receveur, Nelly Frydman, et al.. (2020). A case of germline mosaicism for a 7q32.1q33 deletion in a sperm donor: consequences on pregnancy follow-up and recommendations. Basic and Clinical Andrology. 30(1). 14–14. 5 indexed citations
7.
Receveur, Aline, Sophie Brisset, Jelena Martinović, et al.. (2017). Prenatal diagnosis of isochromosome 20q in a fetus with vertebral anomaly and rocker-bottom feet. Taiwanese Journal of Obstetrics and Gynecology. 56(5). 677–680. 3 indexed citations
8.
Jedraszak, Guillaume, et al.. (2015). Azoospermia and trisomy 18p syndrome: a fortuitous association? A patient report and a review of the literature. Molecular Cytogenetics. 8(1). 34–34. 15 indexed citations
9.
Brémond‐Gignac, Dominique, Gilles Morin, Guillaume Jedraszak, et al.. (2015). Cat eye syndrome. Journal Français d Ophtalmologie. 38(4). 368–369. 1 indexed citations
10.
Jedraszak, Guillaume, Bénédicte Demeer, Michèle Mathieu‐Dramard, et al.. (2015). Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients. American Journal of Medical Genetics Part A. 167(3). 504–511. 17 indexed citations
11.
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
12.
Jedraszak, Guillaume, Aline Receveur, Joris Andrieux, et al.. (2015). Severe Psychomotor Delay in a Severe Presentation of Cat-Eye Syndrome. SHILAP Revista de lepidopterología. 2015. 1–4. 3 indexed citations
13.
Jedraszak, Guillaume, Aline Receveur, Joris Andrieux, et al.. (2013). A severe prenatal presentation of Cat Eye Syndrome. Clinical Dysmorphology. 22(4). 175–177. 2 indexed citations
14.
Demeer, Bénédicte, Joris Andrieux, Aline Receveur, et al.. (2012). Duplication 16p13.3 and the CREBBP gene: Confirmation of the phenotype. European Journal of Medical Genetics. 56(1). 26–31. 41 indexed citations
15.
Katzaki, Eleni, Gilles Morin, Marzia Pollazzon, et al.. (2010). Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients. American Journal of Medical Genetics Part A. 152A(7). 1711–1717. 19 indexed citations
16.
Nguyen‐Khac, Florence, Frédéric Davi, Aline Receveur, et al.. (2005). Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin. Cancer Genetics and Cytogenetics. 159(1). 74–78. 4 indexed citations
17.
Receveur, Aline, Jérôme Couturier, Vincent Molinié, et al.. (2005). Characterization of quantitative chromosomal abnormalities in renal cell carcinomas by interphase four-color fluorescence in situ hybridization. Cancer Genetics and Cytogenetics. 158(2). 110–118. 20 indexed citations
18.
Receveur, Aline, et al.. (2004). Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia. Annales de Génétique. 47(4). 423–427. 9 indexed citations
19.
Kahn, Edmond, Aline Receveur, Philippe Coullin, et al.. (2004). Multiple excitation confocal analysis of targets in nuclei of cytogenetic preparations.. PubMed. 26(1). 1–6. 3 indexed citations
20.
Gross‐Goupil, Marine, Philippe Riou, Jean‐François Emile, et al.. (2003). Analysis of chromosomal instability in pulmonary or liver metastases and matched primary hepatocellular carcinoma after orthotopic liver transplantation. International Journal of Cancer. 104(6). 745–751. 16 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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