Catherine Vaurs‐Barrière

986 citations

26 papers · 734 indexed · h-index 15

Co-authors: Odile Boespflug‐Tanguy B. Dastugue Michel Canis G. Mage Sachiko Matsuzaki Anne Fogli Catherine Sarret Patricia Combes
Topics: RNA regulation and disease (6 papers)RNA modifications and cancer (6 papers)RNA Research and Splicing (6 papers)
Cited by: Reproductive Medicine Obstetrics and Gynecology Developmental Neuroscience
Journals: Bioinformatics Annals of Neurology Nature Protocols
Partner nations: France Italy United Kingdom

In The Last Decade

Catherine Vaurs‐Barrière

26 papers receiving 717 citations

Peers

Countries citing papers authored by Catherine Vaurs‐Barrière

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Vaurs‐Barrière

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine Vaurs‐Barrière. 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 Catherine Vaurs‐Barrière. The network helps show where Catherine Vaurs‐Barrière may publish in the future.

Co-authorship network of co-authors of Catherine Vaurs‐Barrière

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Vaurs‐Barrière. A scholar is included among the top collaborators of Catherine Vaurs‐Barrière 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 Catherine Vaurs‐Barrière. Catherine Vaurs‐Barrière 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:

20 of 20 papers shown

#	Work	Indexed citations
1	The Long Non-Coding RNA HOXA-AS2 Promotes Proliferation of Glioma Stem Cells and Modulates Their Inflammation Pathway Mainly through Post-Transcriptional Regulation 2022 ·International Journal of Molecular Sciences ·(unknown),Pierre‐Olivier Guichet,(unknown),(unknown),Catherine Vaurs‐Barrière,Céline Gonthier‐Guéret,Emmanuel Chautard,Pierre Verrelle,Lucie Karayan‐Tapon,Anne Fogli,Franck Court,Philippe Arnaúd	9
2	Widespread overexpression from the four DNA hypermethylated HOX clusters in aggressive ( IDH wt) glioma is associated with H3K27me3 depletion and alternative promoter usage 2021 ·Molecular Oncology ·(unknown),Franck Court,Pierre‐Olivier Guichet,Catherine Vaurs‐Barrière,Isabelle Vaillant,Emmanuel Chautard,Pierre Verrelle,Bruno M. Costa,Lucie Karayan‐Tapon,Anne Fogli,Philippe Arnaúd	17
3	Transcriptional alterations in glioma result primarily from DNA methylation–independent mechanisms 2019 ·Genome Research ·Franck Court,(unknown),Anne Fogli,(unknown),Catherine Vaurs‐Barrière,Emmanuel Chautard,Bruno Pereira,J. Biau,Jean-Louis Kémény,Toufic Khalil,Lucie Karayan‐Tapon,Pierre Verrelle,Philippe Arnaúd	35
4	Detection of the alternative lengthening of telomeres pathway in malignant gliomas for improved molecular diagnosis 2017 ·Journal of Neuro-Oncology ·Anne Fogli,Marie-Véronique Demattei,Laetitia Corset,Catherine Vaurs‐Barrière,Emmanuel Chautard,J. Biau,Jean‐Louis Kémény,Catherine Godfraind,Bruno Pereira,(unknown),Nathalie Grandin,Philippe Arnaúd,Michel Charbonneau,Pierre Verrelle	21
5	The tumoral A genotype of the MGMT rs34180180 single-nucleotide polymorphism in aggressive gliomas is associated with shorter patients’ survival 2015 ·Carcinogenesis ·Anne Fogli,Emmanuel Chautard,Catherine Vaurs‐Barrière,Bruno Pereira,(unknown),Franck Court,J. Biau,(unknown),Jean-Louis Kémény,Toufic Khalil,Lucie Karayan‐Tapon,Pierre Verrelle,Bruno M. Costa,Philippe Arnaúd	12
6	In Vitro and Mouse Studies Supporting Therapeutic Utility of Triiodothyroacetic Acid in MCT8 Deficiency 2014 ·Molecular Endocrinology ·Simone Kersseboom,Sigrun Horn,W. Edward Visser,Jiesi Chen,Edith C. H. Friesema,Catherine Vaurs‐Barrière,Robin P. Peeters,Heike Heuer,Theo J. Visser	73
7	Fluorescent mRNA labeling through cytoplasmic FISH 2013 ·Nature Protocols ·(unknown),Cynthia Dennis,Catherine Vaurs‐Barrière,Claire Chazaud	8
8	Relevance of SOX17 Variants for Hypomyelinating Leukodystrophies and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) 2012 ·Annals of Human Genetics ·Patricia Combes,Vincent Planche,Éléonore Eymard-Pierre,Catherine Sarret,Diana Rodriguez,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	5
9	Molecular Genetic Analysis of the PLP1 Gene in 38 Families with PLP1-related disorders: Identification and Functional Characterization of 11 Novel PLP1 Mutations 2011 ·Orphanet Journal of Rare Diseases ·Serena Grossi,Stefano Regis,Roberta Biancheri,Matthew Mort,Susanna Lualdi,Enrico Bertini,Graziella Uziel,Odile Boespflug‐Tanguy,Alessandro Simonati,Fabio Corsolini,Ercan Demir,Valentina Marchiani,Antonio Percesepe,Franco Stanzial,Andrea Rossi,Catherine Vaurs‐Barrière,D.N. Cooper,Mirella Filocamo	32
10	Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort 2011 ·Journal of the Neurological Sciences ·Catherine Sarret,(unknown),Catherine Vaurs‐Barrière,Imen Dorboz,Éléonore Eymard-Pierre,Patricia Combes,G Giraud,Ronald J. A. Wanders,Alexandra Afenjar,Christine Francannet,Odile Boespflug‐Tanguy	8
11	Pelizaeus–Merzbacher–Like disease presentation of MCT8 mutated male subjects 2009 ·Annals of Neurology ·Catherine Vaurs‐Barrière,(unknown),Catherine Sarret,G Giraud,Vincent des Portes,(unknown),Giuseppe De Michele,Bernard Dan,Angela F. Brady,Odile Boespflug‐Tanguy,Renaud Touraine	84
12	Novel neuronal proteolipid protein isoforms encoded by the human myelin proteolipid protein 1 gene 2009 ·Neuroscience ·Catherine Sarret,Patricia Combes,(unknown),A. Gélot,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	23
13	PLP1splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations 2008 ·Human Mutation ·Marie‐Noëlle Bonnet‐Dupeyron,Patricia Combes,(unknown),(unknown),Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	18
14	Genes involved in leukodystrophies: A glance at glial functions 2008 ·Current Neurology and Neuroscience Reports ·Odile Boespflug‐Tanguy,Pierre Labauge,Anne Fogli,Catherine Vaurs‐Barrière	38
15	PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: identification of one partial triplication and two partial deletions of PLP1 2006 ·Neurogenetics ·Patricia Combes,(unknown),(unknown),Raphael Schiffmann,Enrico Bertini,Diana Rodriguez,John A.L. Armour,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	21
16	DNA microarray analysis of gene expression in eutopic endometrium from patients with deep endometriosis using laser capture microdissection 2005 ·Fertility and Sterility ·Sachiko Matsuzaki,Michel Canis,Catherine Vaurs‐Barrière,Odile Boespflug‐Tanguy,B. Dastugue,G. Mage	126
17	Golli‐MBP Copy Number Analysis by FISH, QMPSF and MAPH in 195 Patients with Hypomyelinating Leukodystrophies 2005 ·Annals of Human Genetics ·Catherine Vaurs‐Barrière,(unknown),Patricia Combes,(unknown),(unknown),Raphael Schiffmann,Enrico Bertini,Diana Rodriguez,Philippe Vago,John A.L. Armour,Pascale Saugier-Véber,Thierry Frébourg,Robin J. Leach,Odile Boespflug‐Tanguy	14
18	DNA microarray analysis of gene expression profiles in deep endometriosis using laser capture microdissection 2004 ·Molecular Human Reproduction ·Sachiko Matsuzaki,Michel Canis,Catherine Vaurs‐Barrière,J.-L. Pouly,Odile Boespflug‐Tanguy,(unknown),Pierre Déchelotte,B. Dastugue,K. Okamura,G. Mage	90
19	Insertion of mutant proteolipid protein results in missorting of myelin proteins 2003 ·Annals of Neurology ·Catherine Vaurs‐Barrière,Kondi Wong,(unknown),Mones Abu‐Asab,Michael D. Weiss,Christine R. Kaneski,(unknown),Simona Bonavita,Isabelle Creveaux,John D. Heiss,Maria Tsokos,Ehud Goldin,Richard H. Quarles,Odile Boespflug‐Tanguy,Raphael Schiffmann	19
20	Pathology of sporadic breast tumors with LOH at the BRCA1 locus: correlation with histopathological features specific to familial BRCA1 tumors and absence of microsatellite instability. 1998 ·International Journal of Oncology ·Catherine Vaurs‐Barrière,Valérie Vidal,Frédérique Penault‐Llorca,Fabrice Kwiatkowski,Christine Maugard,Y.-J. Bignon	7

About Catherine Vaurs‐Barrière

Catherine Vaurs‐Barrière is a scholar working on Molecular Biology, Cancer Research and Obstetrics and Gynecology, having authored 26 papers that have together received 734 indexed citations. Recurring topics across this work include RNA regulation and disease (6 papers), RNA modifications and cancer (6 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Reproductive Medicine (206 citations), Obstetrics and Gynecology (149 citations) and Developmental Neuroscience (37 citations). Catherine Vaurs‐Barrière has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include Odile Boespflug‐Tanguy, B. Dastugue, Michel Canis, G. Mage, Sachiko Matsuzaki, Anne Fogli, Catherine Sarret, Patricia Combes, Edith C. H. Friesema and Theo J. Visser. Their work appears in journals such as Bioinformatics, Annals of Neurology and Nature Protocols.

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