Myriam Vézain

903 citations

13 papers · 462 indexed · h-index 9

Co-authors: Mario Tosi Alexandra Martins Thierry Frébourg Isabelle Tournier Pascale Saugier-Véber Françoise CharbonnierQing WangJohann Soret
Topics: RNA Research and Splicing (6 papers)RNA modifications and cancer (4 papers)Neurogenetic and Muscular Disorders Research (4 papers)
Cited by: Genetics Cancer Research Molecular Biology
Journals: Molecular Cell Journal of Medical Genetics Human Mutation
Partner nations: France Italy United States

In The Last Decade

Myriam Vézain

13 papers receiving 461 citations

Peers

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

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

13 of 13 papers shown

#	Work	Indexed citations
1	High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disorders 2023 ·Human Genetics ·François Lecoquierre,Olivier Quenez,(unknown),Sophie Coutant,Myriam Vézain,(unknown),Nathalie Drouot,Anne Boland,Robert Olaso,Vincent Meyer,Jean‐François Deleuze,(unknown),(unknown),(unknown),Pascale Saugier-Véber,Alice Goldenberg,Anne‐Marie Guerrot,Gaël Nicolas	4
2	Retrotransposon insertion as a novel mutational cause of spinal muscular atrophy 2022 ·Human Genetics ·Myriam Vézain,(unknown),Yoann Vial,Sophie Coutant,Séverine Drunat,Jon Andoni Urtizberea,Anne‐Sophie Rolland,Agnès Jacquin-Piques,(unknown),Gaël Nicolas,François Lecoquierre,Pascale Saugier-Véber	2
3	Next-Generation Molecular Investigations in Lysosomal Diseases: Clinical Integration of a Comprehensive Targeted Panel 2021 ·Diagnostics ·(unknown),(unknown),Ivana Dabaj,(unknown),Lénaïg Abily-Donval,Axel Lebas,Myriam Vézain,Bénédicte Héron,I. Marie,Marc Duval-Arnould,Stéphane Marret,Abdellah Tebani,Soumeya Bekri	2
4	Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants 2021 ·Acta Neuropathologica Communications ·Florent Marguet,Myriam Vézain,Pascale Marcorelles,Séverine Audebert‐Bellanger,Kévin Cassinari,Nathalie Drouot,Pascal Chambon,Bruno J. Gonzalez,Arie Horowitz,Annie Laquerrière,Pascale Saugier-Véber	15
5	A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis 2018 ·Acta Neuropathologica Communications ·Myriam Vézain,(unknown),Marina Rubio,Valérie Dupé,Leslie Ratié,Véronique David,Laurent Pasquier,Sylvie Odent,Sophie Coutant,Isabelle Tournier,(unknown),Homa Adle‐Biassette,Denis Vivien,Thierry Frébourg,Bruno J. Gonzalez,Annie Laquerrière,Pascale Saugier-Véber	16
6	Familial solitary chondrosarcoma resulting from germline EXT2 mutation 2016 ·Genes Chromosomes and Cancer ·(unknown),(unknown),Sophie Coutant,Émilie Angot,Jean‐Christophe Sabourin,Paul Michelin,(unknown),Françoise Charbonnier,Myriam Vézain,Gaëlle Bougeard,Stéphanie Baert‐Desurmont,Thierry Frébourg,Isabelle Tournier	5
7	Clinical and pathologic features of Aicardi–Goutières syndrome due to an IFIH1 mutation: A pediatric case report 2016 ·American Journal of Medical Genetics Part A ·Florent Marguet,Annie Laquerrière,Alice Goldenberg,Anne‐Marie Guerrot,Olivier Quenez,(unknown),Catherine Vanhulle,(unknown),Françoise Charbonnier,Myriam Vézain,Soumeya Bekri,Isabelle Tournier,Thierry Frébourg,Gaël Nicolas	14
8	CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations 2016 ·Molecular Cell ·(unknown),Sathish Kumar Mungamuri,Dorthe Cartier,Ravi Sachidanandam,Anitha D. Jayaprakash,Sahil Adriouch,Myriam Vézain,Françoise Charbonnier,(unknown),Sophie Coutant,Shen Yao,(unknown),David Alexandre,Isabelle Tournier,Olivier Boyer,Stuart A. Aaronson,Youssef Anouar,Luca Grumolato	51
9	A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy 2011 ·Human Mutation ·Myriam Vézain,Bénédicte Gérard,Séverine Drunat,Benoît Funalot,(unknown),(unknown),Jean‐Michel Vallat,Thierry Frébourg,Mario Tosi,Alexandra Martins,Pascale Saugier-Véber	17
10	A rareSMN2variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy 2009 ·Human Mutation ·Myriam Vézain,Pascale Saugier-Véber,(unknown),Renaud Touraine,(unknown),Annick Toutain,(unknown),(unknown),(unknown),Mario Tosi,Alexandra Martins	89
11	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 2008 ·Journal of Medical Genetics ·Céline Bonnet,Sophie Krieger,Myriam Vézain,Antoine Rousselin,Isabelle Tournier,Alexandra Martins,Pascaline Berthet,Annie Chevrier,Catherine Dugast,Valérie Layet,Anita De Rossi,Rosette Lidereau,Thierry Frébourg,Agnès Hardouin,Mario Tosi	89
12	A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects 2008 ·Human Mutation ·Isabelle Tournier,Myriam Vézain,Alexandra Martins,Françoise Charbonnier,Stéphanie Baert‐Desurmont,Sylviane Olschwang,Qing Wang,(unknown),Johann Soret,Jamal Tazi,Thierry Frébourg,Mario Tosi	126
13	A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy 2007 ·European Journal of Human Genetics ·Myriam Vézain,Pascale Saugier-Véber,Judith Melki,Annick Toutain,Éric Bieth,Marie Husson,Jean‐Michel Pedespan,Louis Viollet,I. Pénisson-Besnier,(unknown),Jacqueline Bou,Thierry Frébourg,Mario Tosi	32

About Myriam Vézain

Myriam Vézain is a scholar working on Genetics, Cancer Research and Urology, having authored 13 papers that have together received 462 indexed citations. Recurring topics across this work include RNA Research and Splicing (6 papers), RNA modifications and cancer (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). The work is most often cited by research in Genetics (123 citations), Cancer Research (81 citations) and Molecular Biology (352 citations). Myriam Vézain has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Mario Tosi, Alexandra Martins, Thierry Frébourg, Isabelle Tournier, Pascale Saugier-Véber, Françoise Charbonnier, Qing Wang, Johann Soret, Jamal Tazi and Sylviane Olschwang. Their work appears in journals such as Molecular Cell, Journal of Medical Genetics and Human Mutation.

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