Aurélie Coussement

567 total citations
16 papers, 141 citations indexed

About

Aurélie Coussement is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Aurélie Coussement has authored 16 papers receiving a total of 141 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Aurélie Coussement's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Congenital heart defects research (2 papers). Aurélie Coussement is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Congenital heart defects research (2 papers). Aurélie Coussement collaborates with scholars based in France, Spain and Italy. Aurélie Coussement's co-authors include Jean‐Michel Dupont, Agnès Choiset, Céline Dupont, Martin Buckley, Brigitte Benzacken, François Vialard, P Fabiani, Anne‐Claude Tabet, Philippe Chevallier and Jérôme Toutain and has published in prestigious journals such as Gastroenterology, BMC Health Services Research and Clinical Genetics.

In The Last Decade

Aurélie Coussement

13 papers receiving 116 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aurélie Coussement France	7	67	40	38	33	26	16	141
Michelle Steinraths Canada	8	104 1.6×	60 1.5×	60 1.6×	12 0.4×	23 0.9×	12	168
Lisa D.S. Bloomer United Kingdom	6	53 0.8×	44 1.1×	11 0.3×	25 0.8×	21 0.8×	7	131
Odile Boute‐Bénéjean France	7	64 1.0×	75 1.9×	22 0.6×	35 1.1×	26 1.0×	13	147
Joanna Lazier Canada	8	67 1.0×	46 1.1×	55 1.4×	21 0.6×	10 0.4×	19	126
Paulette Barahona Australia	6	88 1.3×	36 0.9×	74 1.9×	21 0.6×	12 0.5×	14	148
Elizabeth Lemos Silveira Brazil	5	62 0.9×	122 3.0×	13 0.3×	18 0.5×	6 0.2×	7	183
Jean-François Subra France	4	157 2.3×	120 3.0×	24 0.6×	149 4.5×	24 0.9×	7	240
Alice Masurel France	4	40 0.6×	29 0.7×	11 0.3×	19 0.6×	8 0.3×	5	99
Eileen Roberts United Kingdom	4	54 0.8×	30 0.8×	46 1.2×	64 1.9×	35 1.3×	5	131
Saray Rodríguez-Diaz Spain	7	39 0.6×	112 2.8×	11 0.3×	30 0.9×	40 1.5×	14	160

Countries citing papers authored by Aurélie Coussement

Since Specialization

Citations

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

Fields of papers citing papers by Aurélie Coussement

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurélie Coussement

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

All Works

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16 of 16 papers shown

Coussement, Aurélie, et al.. (2024). Generation of IPi001-A/B/C human induced pluripotent stem cell lines from healthy amniotic fluid cells. Stem Cell Research. 76. 103350–103350.

Lœuillet, Laurence, Juliette Nectoux, E. Pannier, et al.. (2022). Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth Defects Research. 115(5). 563–571. 1 indexed citations

Chalus, Aliénor de, Solveig Heide, Nathalie Lédée, et al.. (2019). Double chromosomal translocation in an infertile man: one-step FISH meiotic segregation analysis and reproductive prognosis. Journal of Assisted Reproduction and Genetics. 36(5). 973–978. 3 indexed citations

Hermann, M., Babak Khoshnood, Olivia Anselem, et al.. (2019). Lack of consensus in the choice of termination of pregnancy for Turner syndrome in France. BMC Health Services Research. 19(1). 994–994. 3 indexed citations

Hureaux, Marguerite, Nicolas Chatron, Aurélie Coussement, et al.. (2019). SOX3 duplication: A genetic cause to investigate in fetuses with neural tube defects. Prenatal Diagnosis. 39(11). 1026–1034. 14 indexed citations

Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations

Coussement, Aurélie, M. Thomas P. Gilbert, Florent Dumont, et al.. (2016). Aneuploidy: the impact of chromosome imbalance on nuclear organization and overall genome expression. Clinical Genetics. 90(1). 35–48. 12 indexed citations

Feenstra, Jelena D. Milosevic, Laïla El Khattabi, Anne Roubergue, et al.. (2014). Inverted duplication with deletion: First interstitial case suggesting a novel undescribed mechanism of formation. American Journal of Medical Genetics Part A. 164(12). 3180–3186. 6 indexed citations

Dupont, Céline, Francesca Romana Grati, Kwong Wai Choy, et al.. (2014). Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations. Prenatal Diagnosis. 35(1). 35–43. 33 indexed citations

10.

Coussement, Aurélie, et al.. (2011). Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: An array‐CGH study. American Journal of Medical Genetics Part A. 155(10). 2597–2600. 15 indexed citations

11.

Perelman, Sergio, et al.. (2006). NRP1 Traumatisme cerebral non accidentel de l’enfant : quelle terminologie utiliser. Journal de Radiologie. 87(10). 1499–1499.

12.

Chevallier, Philippe, et al.. (1999). [Radiologic aspects of the complications of duodenal diverticula].. PubMed. 80(2). 134–40. 23 indexed citations

13.

Mariani, R, et al.. (1996). Hypopituitarisme post-traumatisme crânien: à propos de trois cas. Archives de Pédiatrie. 3(8). 796–801. 12 indexed citations

14.

Duvauferrier, R, et al.. (1995). [Image data bases and multimedia works on server and CD-ROM in medical imaging. A French experience].. PubMed. 76(12). 1079–85. 3 indexed citations

15.

Caroli‐Bosc, François‐Xavier, P Hastier, Christiane Deveau, et al.. (1995). Prevalence of gallstone disease in a village of South of France (Vidauban). Gastroenterology. 108(4). A7–A7. 1 indexed citations

16.

Mariani, R, et al.. (1993). [Sertoli-Leydig tumors in children. 2 case reports].. PubMed. 40(7). 438–43.

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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