Myriam Vézain

903 total citations
13 papers, 462 citations indexed

About

Myriam Vézain is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Myriam Vézain has authored 13 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Myriam Vézain's work include RNA Research and Splicing (6 papers), RNA modifications and cancer (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Myriam Vézain is often cited by papers focused on RNA Research and Splicing (6 papers), RNA modifications and cancer (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Myriam Vézain collaborates with scholars based in France, Italy and United States. Myriam Vézain's co-authors include Mario Tosi, Alexandra Martins, Thierry Frébourg, Isabelle Tournier, Pascale Saugier-Véber, Françoise Charbonnier, Jamal Tazi, Johann Soret, Stéphanie Baert‐Desurmont and Annick Toutain and has published in prestigious journals such as Molecular Cell, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Myriam Vézain

13 papers receiving 461 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Myriam Vézain France	9	352	123	109	81	76	13	462
Katsumi Harada Japan	10	178 0.5×	175 1.4×	85 0.8×	95 1.2×	58 0.8×	21	369
Lauren A. Solomon Canada	14	260 0.7×	91 0.7×	65 0.6×	59 0.7×	21 0.3×	22	483
Rossella Tricarico Italy	12	275 0.8×	32 0.3×	82 0.8×	110 1.4×	116 1.5×	19	426
Wendy J. Ingram Australia	7	267 0.8×	61 0.5×	44 0.4×	41 0.5×	23 0.3×	10	346
Mahmoud Mansouri Sweden	12	211 0.6×	159 1.3×	174 1.6×	86 1.1×	106 1.4×	21	522
Laura A. New Canada	10	242 0.7×	50 0.4×	75 0.7×	26 0.3×	42 0.6×	16	431
Manfred Schwab Germany	8	336 1.0×	103 0.8×	87 0.8×	142 1.8×	58 0.8×	8	573
Rachel Soemedi United States	9	405 1.2×	61 0.5×	108 1.0×	48 0.6×	25 0.3×	11	523
Erin R. Okawa United States	8	338 1.0×	36 0.3×	87 0.8×	134 1.7×	19 0.3×	13	492
Jennifer B. Edwards United States	8	284 0.8×	113 0.9×	33 0.3×	115 1.4×	29 0.4×	9	444

Countries citing papers authored by Myriam Vézain

Since Specialization

Citations

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

Fields of papers citing papers by Myriam Vézain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Myriam Vézain

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

All Works

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13 of 13 papers shown

Lecoquierre, François, Olivier Quenez, Sophie Coutant, et al.. (2023). High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disorders. Human Genetics. 142(6). 773–783. 4 indexed citations

Vézain, Myriam, Yoann Vial, Sophie Coutant, et al.. (2022). Retrotransposon insertion as a novel mutational cause of spinal muscular atrophy. Human Genetics. 142(1). 125–138. 2 indexed citations

Dabaj, Ivana, Lénaïg Abily-Donval, Axel Lebas, et al.. (2021). Next-Generation Molecular Investigations in Lysosomal Diseases: Clinical Integration of a Comprehensive Targeted Panel. Diagnostics. 11(2). 294–294. 2 indexed citations

Marguet, Florent, Myriam Vézain, Pascale Marcorelles, et al.. (2021). Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants. Acta Neuropathologica Communications. 9(1). 104–104. 15 indexed citations

Vézain, Myriam, Marina Rubio, Valérie Dupé, et al.. (2018). A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis. Acta Neuropathologica Communications. 6(1). 109–109. 16 indexed citations

Coutant, Sophie, Émilie Angot, Jean‐Christophe Sabourin, et al.. (2016). Familial solitary chondrosarcoma resulting from germline EXT2 mutation. Genes Chromosomes and Cancer. 56(2). 128–134. 5 indexed citations

Marguet, Florent, Annie Laquerrière, Alice Goldenberg, et al.. (2016). Clinical and pathologic features of Aicardi–Goutières syndrome due to an IFIH1 mutation: A pediatric case report. American Journal of Medical Genetics Part A. 170(5). 1317–1324. 14 indexed citations

Mungamuri, Sathish Kumar, Dorthe Cartier, Ravi Sachidanandam, et al.. (2016). CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations. Molecular Cell. 63(3). 526–538. 51 indexed citations

Vézain, Myriam, Bénédicte Gérard, Séverine Drunat, et al.. (2011). A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy. Human Mutation. 32(9). 989–994. 17 indexed citations

10.

Vézain, Myriam, Pascale Saugier-Véber, Renaud Touraine, et al.. (2009). A rareSMN2variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy. Human Mutation. 31(1). E1110–E1125. 89 indexed citations

11.

Bonnet, Céline, Sophie Krieger, Myriam Vézain, et al.. (2008). Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene. Journal of Medical Genetics. 45(7). 438–446. 89 indexed citations

12.

Tournier, Isabelle, Myriam Vézain, Alexandra Martins, et al.. (2008). A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects. Human Mutation. 29(12). 1412–1424. 126 indexed citations

13.

Vézain, Myriam, Pascale Saugier-Véber, Judith Melki, et al.. (2007). A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy. European Journal of Human Genetics. 15(10). 1054–1062. 32 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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