Céline Poirsier

488 total citations
6 papers, 125 citations indexed

About

Céline Poirsier is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Oncology. According to data from OpenAlex, Céline Poirsier has authored 6 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Oncology. Recurrent topics in Céline Poirsier's work include Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Pancreatic and Hepatic Oncology Research (1 paper). Céline Poirsier is often cited by papers focused on Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Pancreatic and Hepatic Oncology Research (1 paper). Céline Poirsier collaborates with scholars based in France, Canada and United Kingdom. Céline Poirsier's co-authors include Marta Spodenkiewicz, Martine Doco‐Fenzy, Anne-Sophie Lèbre, Dominique Gaillard, Marc Labrousse, Carl Arndt, Vincent Cottin, Michel Spodenkiewicz, Maureen Cleary and Nathalie Bednarek and has published in prestigious journals such as Journal of Medical Genetics, Otology & Neurotology and Biology.

In The Last Decade

Céline Poirsier

5 papers receiving 111 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Céline Poirsier France	5	64	36	29	27	16	6	125
Barbara Knapp Germany	7	114 1.8×	39 1.1×	35 1.2×	7 0.3×	6 0.4×	10	145
Victor Murcia Pienkowski Poland	8	103 1.6×	12 0.3×	41 1.4×	12 0.4×	10 0.6×	19	150
Nicola Horn Germany	8	109 1.7×	11 0.3×	58 2.0×	13 0.5×	4 0.3×	11	151
Stephanie Cox United States	6	156 2.4×	33 0.9×	51 1.8×	33 1.2×	36 2.3×	6	240
Manuela Oppo Italy	8	90 1.4×	13 0.4×	52 1.8×	22 0.8×	6 0.4×	8	129
Alka V. Ekbote India	7	136 2.1×	8 0.2×	102 3.5×	17 0.6×	26 1.6×	13	216
Annick Cabot France	5	167 2.6×	35 1.0×	52 1.8×	26 1.0×	18 1.1×	5	240
Amit Kawalia Germany	6	59 0.9×	23 0.6×	23 0.8×	3 0.1×	6 0.4×	7	112
Mariet W. Elting Netherlands	3	44 0.7×	12 0.3×	26 0.9×	6 0.2×	5 0.3×	3	94
Charles Van Goethem France	7	74 1.2×	5 0.1×	47 1.6×	9 0.3×	21 1.3×	13	121

Countries citing papers authored by Céline Poirsier

Since Specialization

Citations

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

Fields of papers citing papers by Céline Poirsier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Poirsier

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Mercier, Sandra, Céline Poirsier, Nathalie Bednarek, et al.. (2025). Commentary on UBTF haploinsufficiency associated with UBTF-related global developmental delay and distinctive facial features without neuroregression. Journal of Medical Genetics. 62(10). 653–655.

2.

Barraud, Sara, Lucie Coppin, D. Zachar, et al.. (2021). A large extended family with hyperparathyroidism-jaw tumor syndrome due to deletion of the third exon of CDC73: clinical and molecular features. Endocrine. 73(3). 693–701. 4 indexed citations

3.

Spodenkiewicz, Marta, et al.. (2021). Adult diagnosis of Townes–Brocks syndrome with renal failure: Two related cases and review of literature. American Journal of Medical Genetics Part A. 185(3). 937–944. 10 indexed citations

4.

Spodenkiewicz, Marta, Michel Spodenkiewicz, Maureen Cleary, et al.. (2020). Clinical Genetics of Prolidase Deficiency: An Updated Review. Biology. 9(5). 108–108. 34 indexed citations

5.

Poirsier, Céline, Marta Spodenkiewicz, Carl Arndt, et al.. (2018). Genetics of Usher Syndrome: New Insights From a Meta-analysis. Otology & Neurotology. 40(1). 121–129. 61 indexed citations

6.

Poirsier, Céline, Emilie Landais, Nathalie Bednarek, et al.. (2014). Report on 3 patients with 12p duplication including GRIN2B. European Journal of Medical Genetics. 57(5). 185–194. 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.

Explore authors with similar magnitude of impact