Éléonore Eymard-Pierre

1.7k total citations
38 papers, 1.1k citations indexed

About

Éléonore Eymard-Pierre is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Éléonore Eymard-Pierre has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Genetics. Recurrent topics in Éléonore Eymard-Pierre's work include Genomic variations and chromosomal abnormalities (11 papers), RNA regulation and disease (9 papers) and Prenatal Screening and Diagnostics (6 papers). Éléonore Eymard-Pierre is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), RNA regulation and disease (9 papers) and Prenatal Screening and Diagnostics (6 papers). Éléonore Eymard-Pierre collaborates with scholars based in France, United States and Italy. Éléonore Eymard-Pierre's co-authors include Odile Boespflug‐Tanguy, Enrico Bertini, Filippo M. Santorelli, Raphael Schiffmann, Anne Fogli, M. Di Capua, Gaëtan Lesca, Diana Rodriguez, Sandra Dollet and Christine R. Kaneski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Annals of Neurology.

In The Last Decade

Éléonore Eymard-Pierre

36 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Éléonore Eymard-Pierre France 16 685 272 215 199 184 38 1.1k
Helen Griffin United Kingdom 23 1.0k 1.5× 174 0.6× 117 0.5× 160 0.8× 155 0.8× 49 1.5k
Paul R. Kasher United Kingdom 12 384 0.6× 305 1.1× 192 0.9× 96 0.5× 153 0.8× 29 847
Wojciech Wiszniewski United States 18 509 0.7× 119 0.4× 77 0.4× 144 0.7× 102 0.6× 42 1.1k
Winnie Xin United States 18 493 0.7× 430 1.6× 233 1.1× 235 1.2× 107 0.6× 29 1.2k
Shamir Zenvirt Israel 16 618 0.9× 203 0.7× 46 0.2× 173 0.9× 114 0.6× 22 1.2k
Pascale Bomont France 19 627 0.9× 242 0.9× 89 0.4× 532 2.7× 231 1.3× 26 1.3k
A. Löfgren Belgium 18 1.1k 1.6× 304 1.1× 82 0.4× 164 0.8× 308 1.7× 37 1.8k
Julian Blake United Kingdom 20 603 0.9× 357 1.3× 87 0.4× 238 1.2× 259 1.4× 39 1.3k
Wei‐Ming Duan China 17 421 0.6× 122 0.4× 62 0.3× 54 0.3× 154 0.8× 32 871
Sabina Barresi Italy 19 490 0.7× 66 0.2× 95 0.4× 128 0.6× 62 0.3× 68 842

Countries citing papers authored by Éléonore Eymard-Pierre

Since Specialization
Citations

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

Fields of papers citing papers by Éléonore Eymard-Pierre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Éléonore Eymard-Pierre. 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 Éléonore Eymard-Pierre. The network helps show where Éléonore Eymard-Pierre may publish in the future.

Co-authorship network of co-authors of Éléonore Eymard-Pierre

This figure shows the co-authorship network connecting the top 25 collaborators of Éléonore Eymard-Pierre. A scholar is included among the top collaborators of Éléonore Eymard-Pierre 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 Éléonore Eymard-Pierre. Éléonore Eymard-Pierre 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.
Dollet, Sandra, Éléonore Eymard-Pierre, Bruno Pereira, et al.. (2025). Analysis of maturation dynamics and oocyte nuclear quality after rescue-IVM and semi-automated vitrification. Human Reproduction. 40(7). 1344–1356.
2.
Sarret, Catherine, Zahra Ashkavand, Imen Dorboz, et al.. (2019). Deleterious mutations in ALDH1L2 suggest a novel cause for neuro-ichthyotic syndrome. npj Genomic Medicine. 4(1). 17–17. 15 indexed citations
3.
Dorboz, Imen, Hélène Dumay‐Odelot, Yosra Bouyacoub, et al.. (2018). Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation. Neurology Genetics. 4(6). e289–e289. 55 indexed citations
4.
Halim, Nizar Ben, Imen Dorboz, Rym Kéfi, et al.. (2015). Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population. Neurological Sciences. 37(3). 403–409. 9 indexed citations
5.
Goumy, Carole, Fanny Laffargue, Éléonore Eymard-Pierre, et al.. (2014). Congenital diaphragmatic hernia may be associated with 17q12 microdeletion syndrome. American Journal of Medical Genetics Part A. 167(1). 250–253. 19 indexed citations
6.
Pebrel‐Richard, Céline, Éléonore Eymard-Pierre, Laëtitia Gouas, et al.. (2014). Clinical and molecular description of a 17q21.33 microduplication in a girl with severe kyphoscoliosis and developmental delay. European Journal of Medical Genetics. 57(10). 552–557. 2 indexed citations
7.
Debost‐Legrand, Anne, Éléonore Eymard-Pierre, Céline Pebrel‐Richard, et al.. (2012). A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask‐like facial syndrome. American Journal of Medical Genetics Part A. 161(1). 162–165. 7 indexed citations
8.
Pebrel‐Richard, Céline, Laëtitia Gouas, Éléonore Eymard-Pierre, et al.. (2012). An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairment. European Journal of Medical Genetics. 55(11). 650–655. 14 indexed citations
9.
Sarret, Catherine, Catherine Vaurs‐Barrière, Imen Dorboz, et al.. (2011). Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort. Journal of the Neurological Sciences. 312(1-2). 123–126. 8 indexed citations
10.
Goumy, Carole, Éléonore Eymard-Pierre, Charles W. Richard, et al.. (2011). Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant. Gene. 490(1-2). 15–17. 1 indexed citations
11.
Goumy, Carole, Laëtitia Gouas, Céline Pebrel‐Richard, et al.. (2010). Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities. Genetics in Medicine. 12(6). 376–380. 6 indexed citations
12.
Mochel, Fanny, Catherine Sarret, Éléonore Eymard-Pierre, et al.. (2010). Elevated CSF N-acetylaspartylglutamate suggests specific molecular diagnostic abnormalities in patients with white matter diseases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(11). 1112–1117. 15 indexed citations
13.
Brugman, F., et al.. (2007). ADULT-ONSET PRIMARY LATERAL SCLEROSIS IS NOT ASSOCIATED WITH MUTATIONS IN THE ALS2 GENE. Neurology. 69(7). 702–704. 9 indexed citations
14.
Teijido, Óscar, Éléonore Eymard-Pierre, Bruce H. Cohen, et al.. (2006). Vacuolating megalencephalic leukoencephalopathy with subcortical cysts: functional studies of novel variants inMLC1. Human Mutation. 27(3). 292–292. 26 indexed citations
15.
Fogli, Anne, Raphael Schiffmann, Enrico Bertini, et al.. (2004). The effect of genotype on the natural history of eIF2B-related leukodystrophies. Neurology. 62(9). 1509–1517. 117 indexed citations
16.
Fogli, Anne, Diana Rodriguez, Éléonore Eymard-Pierre, & Odile Boespflug‐Tanguy. (2003). eIF2B et la leucodystrophie des Indiens Cree. médecine/sciences. 19(3). 283–285. 1 indexed citations
17.
Fogli, Anne, Diana Rodriguez, Éléonore Eymard-Pierre, & Odile Boespflug‐Tanguy. (2003). eIF2B et la leucodystrophie des IndiensCree. médecine/sciences. 19(3). 283–285. 1 indexed citations
18.
Fogli, Anne, Diana Rodriguez, Éléonore Eymard-Pierre, et al.. (2003). Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations. The American Journal of Human Genetics. 72(6). 1544–1550. 133 indexed citations
19.
Patrono, Carlo, Éléonore Eymard-Pierre, Filippo M. Santorelli, et al.. (2003). Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cysts. Neurology. 61(4). 534–537. 52 indexed citations
20.
Eymard-Pierre, Éléonore, Gaëtan Lesca, Sandra Dollet, et al.. (2002). Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin Gene. The American Journal of Human Genetics. 71(3). 518–527. 175 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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