Agnès Choiset

675 total citations
20 papers, 390 citations indexed

About

Agnès Choiset is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Agnès Choiset has authored 20 papers receiving a total of 390 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pediatrics, Perinatology and Child Health, 11 papers in Genetics and 8 papers in Surgery. Recurrent topics in Agnès Choiset's work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital Anomalies and Fetal Surgery (8 papers). Agnès Choiset is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital Anomalies and Fetal Surgery (8 papers). Agnès Choiset collaborates with scholars based in France and Japan. Agnès Choiset's co-authors include F. Thépot, Sylvie Girard, Marguerite Prieur, J Boué, Patrice Eydoux, Jean‐François Viel, Sylvie Ramond, E Gautier, Nicole Morichon and Marianne Till and has published in prestigious journals such as The American Journal of Human Genetics, Human Reproduction and Human Genetics.

In The Last Decade

Agnès Choiset

20 papers receiving 353 citations

Peers

Agnès Choiset

PPCH

GENET

SURGE

PHYSI

Debra Day‐Salvatore United States

Ivana Joksić Serbia

C. A. Clarke United Kingdom

Kohzo Aisaka Japan

Michiko Ohno Japan

R. Palmarino Italy

Koumudi Godbole India

George Rebello South Africa

A. Bou� France

C. Méndez Mexico

Debra Day‐Salvatore United States

Agnès Choiset

166 ×0.9

PPCH

82 ×0.5

GENET

52 ×0.5

SURGE

51 ×0.5

97 ×2.2

PHYSI

Citations per year, relative to Agnès Choiset Agnès Choiset (= 1×) peers Debra Day‐Salvatore

Countries citing papers authored by Agnès Choiset

Since Specialization

Citations

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

Fields of papers citing papers by Agnès Choiset

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Agnès Choiset

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

All Works

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20 of 20 papers shown

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

Brun, S., Guillaume Pidoux, Agnès Choiset, et al.. (2014). Pattern of secretion of pregnancy-associated plasma protein-A (PAPP-A) during pregnancies complicated by fetal aneuploidy, in vivo and in vitro. Reproductive Biology and Endocrinology. 12(1). 129–129. 15 indexed citations

Esvan, Maxime, Jean-Baptiste Meynard, Aziza Lebbar, et al.. (2011). Amniocentesis Performed for Karyotyping after Identified Ultrasonographic Abnormalities: What to Expect?. Fetal Diagnosis and Therapy. 31(1). 55–62. 4 indexed citations

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

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

Lebbar, Aziza, Agnès Choiset, Sylvie Girard, et al.. (2009). Is Rapid Aneuploidy Screening Used Alone Acceptable in Prenatal Diagnosis? An Evaluation of the Possible Role of Ultrasound Examination. Fetal Diagnosis and Therapy. 25(2). 285–290. 8 indexed citations

Grangé, G., Aziza Lebbar, Agnès Choiset, et al.. (2008). Fetal Loss after Amniocentesis in a Series of 5,780 Procedures. Fetal Diagnosis and Therapy. 23(3). 217–221. 15 indexed citations

Prieur, Marguerite, et al.. (2005). Intrachromosomal insertion mimicking a pericentric inversion: Molecular cytogenetic characterization of a three break rearrangement of chromosome 20. American Journal of Medical Genetics Part A. 138A(3). 288–293. 31 indexed citations

Amiel, Jeanne, Yolanda Espinosa‐Parrilla, Julie Steffann, et al.. (2001). Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures. The American Journal of Human Genetics. 69(6). 1370–1377. 79 indexed citations

10.

Vanier, M. T., Claire Rodriguez‐Lafrasse, Robert Rousson, et al.. (1992). Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk.. PubMed. 51(1). 111–22. 45 indexed citations

11.

Labbé, Sébastien M., et al.. (1989). [The placenta and trisomies 13, 18, 21].. PubMed. 18(8). 989–96. 9 indexed citations

12.

Eydoux, Patrice, Agnès Choiset, F. Thépot, et al.. (1989). Chromosomal prenatal diagnosis: Study of 936 cases of intrauterine abnormalities after ultrasound assessment. Prenatal Diagnosis. 9(4). 255–269. 81 indexed citations

13.

Choiset, Agnès, et al.. (1989). [Chorionic villi sampling. Results with the first 500 samples].. PubMed. 18(3). 313–9. 1 indexed citations

14.

Girard, Sylvie, et al.. (1988). Agyria ? pachygyria and Miller-Dieker syndrome: clinical, genetic and chromosome studies. Human Genetics. 79(2). 163–167. 5 indexed citations

15.

Choiset, Agnès, et al.. (1988). Interstitial dup(1p) and severe intrauterine growth retardation.. PubMed. 31(2). 129–31. 11 indexed citations

16.

Rocchiccioli, F., Patrick Aubourg, & Agnès Choiset. (1987). Immediate prenatal diagnosis of Zellweger syndrome by direct measurement of very long chain fatty acids in chorionic villus cells. Prenatal Diagnosis. 7(5). 349–354. 10 indexed citations

17.

Serville, F, Robert Saura, Claude Billeaud, et al.. (1987). De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome.. PubMed. 30(3). 170–4. 1 indexed citations

18.

Poënaru, Livia, et al.. (1985). Lysosomal hydrolase activity in chorionic villi and embryonic cells in culture. Human Genetics. 69(4). 378–379. 10 indexed citations

19.

Choiset, Agnès, et al.. (1984). [Sampling, culturing and karyotyping of chorionic villi].. PubMed. 13(4). 403–7. 1 indexed citations

20.

Boué, J, Sylvie Girard, F. Thépot, Agnès Choiset, & A Boué. (1982). Unexpected structural chromosome rearrangements in prenatal diagnosis. Prenatal Diagnosis. 2(3). 163–168. 18 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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