Catherine Vaurs‐Barrière

986 citations

26 papers · 734 indexed · h-index 15

Reproductive Medicine top 5%
Obstetrics and Gynecology top 5%
Developmental Neuroscience top 10%
Endocrinology, Diabetes and Metabolism top 10%
- Thyroid Disorders and Treatments 3
Immunology
Molecular Biology
- RNA regulation and disease 6
- RNA modifications and cancer 6
- RNA Research and Splicing 6
- Epigenetics and DNA Methylation 4
Cancer Research
- MicroRNA in disease regulation 3
- Cancer-related molecular mechanisms research 3
Genetics
- Genetics and Neurodevelopmental Disorders 3

Co-authors: Odile Boespflug‐Tanguy B. Dastugue Michel Canis G. Mage Sachiko Matsuzaki Anne Fogli Catherine Sarret Patricia Combes
Cited by: Reproductive Medicine Obstetrics and Gynecology Developmental Neuroscience
Journals: Bioinformatics (1 paper)Annals of Neurology (2 papers)Nature Protocols (1 paper)
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

The 25 scholars most cited alongside Catherine Vaurs‐Barrière, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Catherine Vaurs‐Barrière Line = papers co-authored together Catherine Vaurs‐Barrière links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The Long Non-Coding RNA HOXA-AS2 Promotes Proliferation of Glioma Stem Cells and Modulates Their Inflammation Pathway Mainly through Post-Transcriptional Regulation International Journal of Molecular Sciences ·Elisa Le Boiteux,Pierre‐Olivier Guichet,Konstantin Masliantsev,Bertille Montibus,Catherine Vaurs‐Barrière,Céline Gonthier‐Guéret,Emmanuel Chautard,Pierre Verrelle,Lucie Karayan‐Tapon,Anne Fogli,Franck Court,Philippe Arnaúd	2022	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 Molecular Oncology ·Elisa Le Boiteux,Franck Court,Pierre‐Olivier Guichet,Catherine Vaurs‐Barrière,Isabelle Vaillant,Emmanuel Chautard,Pierre Verrelle,Bruno M. Costa,Lucie Karayan‐Tapon,Anne Fogli,Philippe Arnaúd	2021	17
3	Transcriptional alterations in glioma result primarily from DNA methylation–independent mechanisms Genome Research ·Franck Court,Elisa Le Boiteux,Anne Fogli,Mélanie Müller-Barthélémy,Catherine Vaurs‐Barrière,Emmanuel Chautard,Bruno Pereira,J. Biau,Jean-Louis Kémény,Toufic Khalil,Lucie Karayan‐Tapon,Pierre Verrelle,Philippe Arnaúd	2019	35
4	Detection of the alternative lengthening of telomeres pathway in malignant gliomas for improved molecular diagnosis 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,Toufik Khalil,Nathalie Grandin,Philippe Arnaúd,Michel Charbonneau,Pierre Verrelle	2017	21
5	The tumoral A genotype of the MGMT rs34180180 single-nucleotide polymorphism in aggressive gliomas is associated with shorter patients’ survival Carcinogenesis ·Anne Fogli,Emmanuel Chautard,Catherine Vaurs‐Barrière,Bruno Pereira,Mélanie Müller-Barthélémy,Franck Court,J. Biau,Afonso A. Pinto,Jean-Louis Kémény,Toufic Khalil,Lucie Karayan‐Tapon,Pierre Verrelle,Bruno M. Costa,Philippe Arnaúd	2015	12
6	In Vitro and Mouse Studies Supporting Therapeutic Utility of Triiodothyroacetic Acid in MCT8 Deficiency 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	2014	73
7	Fluorescent mRNA labeling through cytoplasmic FISH Nature Protocols ·Maxime Gasnier,Cynthia Dennis,Catherine Vaurs‐Barrière,Claire Chazaud	2013	8
8	Relevance of SOX17 Variants for Hypomyelinating Leukodystrophies and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) Annals of Human Genetics ·Patricia Combes,Vincent Planche,Éléonore Eymard-Pierre,Catherine Sarret,Diana Rodriguez,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	2012	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 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	2011	32
10	Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort Journal of the Neurological Sciences ·Catherine Sarret,Mélanie Rigal,Catherine Vaurs‐Barrière,Imen Dorboz,Éléonore Eymard-Pierre,Patricia Combes,G Giraud,Ronald J. A. Wanders,Alexandra Afenjar,Christine Francannet,Odile Boespflug‐Tanguy	2011	8
11	Pelizaeus–Merzbacher–Like disease presentation of MCT8 mutated male subjects Annals of Neurology ·Catherine Vaurs‐Barrière,Marlène Deville,Catherine Sarret,G Giraud,Vincent des Portes,José‐Maria Prats‐Viñas,Giuseppe De Michele,Bernard Dan,Angela F. Brady,Odile Boespflug‐Tanguy,Renaud Touraine	2009	84
12	Novel neuronal proteolipid protein isoforms encoded by the human myelin proteolipid protein 1 gene Neuroscience ·Catherine Sarret,Patricia Combes,Pierre Micheau,A. Gélot,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	2009	23
13	PLP1splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations Human Mutation ·Marie‐Noëlle Bonnet‐Dupeyron,Patricia Combes,Paola Santander,Fabrice Cailloux,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	2008	18
14	Genes involved in leukodystrophies: A glance at glial functions Current Neurology and Neuroscience Reports ·Odile Boespflug‐Tanguy,Pierre Labauge,Anne Fogli,Catherine Vaurs‐Barrière	2008	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 Neurogenetics ·Patricia Combes,Marie-Noelle Bonnet-Dupeyron,Fernande Gauthier‐Barichard,Raphael Schiffmann,Enrico Bertini,Diana Rodriguez,John A.L. Armour,Odile Boespflug‐Tanguy,Catherine Vaurs‐Barrière	2006	21
16	DNA microarray analysis of gene expression in eutopic endometrium from patients with deep endometriosis using laser capture microdissection Fertility and Sterility ·Sachiko Matsuzaki,Michel Canis,Catherine Vaurs‐Barrière,Odile Boespflug‐Tanguy,B. Dastugue,G. Mage	2005	126
17	Golli‐MBP Copy Number Analysis by FISH, QMPSF and MAPH in 195 Patients with Hypomyelinating Leukodystrophies Annals of Human Genetics ·Catherine Vaurs‐Barrière,M‐N. Bonnet‐Dupeyron,Patricia Combes,Fernande Gauthier‐Barichard,Xavier T. Reveles,Raphael Schiffmann,Enrico Bertini,Diana Rodriguez,Philippe Vago,John A.L. Armour,Pascale Saugier-Véber,Thierry Frébourg,Robin J. Leach,Odile Boespflug‐Tanguy	2005	14
18	DNA microarray analysis of gene expression profiles in deep endometriosis using laser capture microdissection Molecular Human Reproduction ·Sachiko Matsuzaki,Michel Canis,Catherine Vaurs‐Barrière,J.-L. Pouly,Odile Boespflug‐Tanguy,F. Penault-Llorca,Pierre Déchelotte,B. Dastugue,K. Okamura,G. Mage	2004	90
19	Insertion of mutant proteolipid protein results in missorting of myelin proteins Annals of Neurology ·Catherine Vaurs‐Barrière,Kondi Wong,Thaïs D. Weibel,Mones Abu‐Asab,Michael D. Weiss,Christine R. Kaneski,Tong‐Hui Mixon,Simona Bonavita,Isabelle Creveaux,John D. Heiss,Maria Tsokos,Ehud Goldin,Richard H. Quarles,Odile Boespflug‐Tanguy,Raphael Schiffmann	2003	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. International Journal of Oncology ·Catherine Vaurs‐Barrière,Valérie Vidal,Frédérique Penault‐Llorca,Fabrice Kwiatkowski,Christine Maugard,Y.-J. Bignon	1998	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), RNA Research and Splicing (6 papers), Epigenetics and DNA Methylation (4 papers), MicroRNA in disease regulation (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Cancer-related molecular mechanisms research (3 papers) and Thyroid Disorders and Treatments (3 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.

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