Christel Vaché

1.2k citations

24 papers · 799 · h-index 14

Impact in

Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
Molecular Biology
- Retinal Development and Disorders
- RNA regulation and disease
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- CRISPR and Genetic Engineering
- RNA modifications and cancer

Papers in

Molecular Biology 19
- RNA and protein synthesis mechanisms 10
- RNA Research and Splicing 5
- Retinal Development and Disorders 4
- RNA regulation and disease 3
- RNA modifications and cancer 3
- Advanced biosensing and bioanalysis techniques 2
Sensory Systems 6
- Hearing, Cochlea, Tinnitus, Genetics 6

Co-authors: Anne‐Françoise Roux (18 shared papers)Eric Clottes (1 shared paper)Fabrice Rossignol (1 shared paper)Mireille Claustres (9 shared papers)David Baux (16 shared papers)Sue Malcolm (7 shared papers)Catherine Blanchet (10 shared papers)Lise Larrieu (6 shared papers)
Journals: Human Mutation (7 papers)European Journal of Human Genetics (4 papers)Environmental Toxicology and Chemistry (2 papers)Gene (1 paper)Frontiers in Genetics (1 paper)
Partner nations: France United Kingdom United States

In The Last Decade

Christel Vaché

23 papers receiving 790 citations

Peers

Countries citing papers authored by Christel Vaché

Since Specialization

Citations

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

Fields of papers citing papers by Christel Vaché

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Christel Vaché, 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 Christel Vaché Line = papers co-authored together Christel Vaché links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Natural antisense transcripts of hypoxia-inducible factor 1alpha are detected in different normal and tumour human tissues Gene ·Fabrice Rossignol, Christel Vaché, Eric Clottes	2002	121
2	Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation Molecular Therapy — Nucleic Acids ·Radulfus WN Slijkerman, Christel Vaché, Margo Dona, Gema García‐García, Mireille Claustres, Lisette Hetterschijt, Theo Peters, Bas P. Hartel, Ronald J. E. Pennings, José M Millan, Elena Aller, Alejandro Garanto, Rob W.J. Collin, Hannie Kremer, Anne‐Françoise Roux, Erwin van Wijk	2016	104
3	Usher syndrome type 2 caused by activation of an USH2A pseudoexon: Implications for diagnosis and therapy Human Mutation ·Christel Vaché, Thomas Besnard, Pauline Le Berre, Gema García‐García, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Hanno J. Bolz, José del R. Millán, Christian Hamel, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux	2011	82
4	Bioelectrical impedance analysis measurements of total body water and extracellular water in healthy elderly subjects International Journal of Obesity ·Christel Vaché, Paulette Rousset, Pierre Gachon, AM Gachon, Béatrice Morio, A Boulier, J Coudert, B. Beaufrère, Patrick Ritz	1998	64
5	WholeUSH2AGene Sequencing Identifies Several New Deep Intronic Mutations Human Mutation ·Alessandro Liquori, Christel Vaché, David Baux, Catherine Blanchet, Christian Hamel, Sue Malcolm, M. Kœnig, Mireille Claustres, Anne‐Françoise Roux	2015	61
6	Non-USH2A mutations in USH2 patients Human Mutation ·Thomas Besnard, Christel Vaché, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Sylvie Odent, Patricia Blanchet, Patrick Calvas, Christian Hamel, Hélène Dollfus, Geneviève Lina‐Granade, James Lespinasse, Albert David, Bertrand Isidor, G Morin, Sue Malcolm, Sylvie Tuffery‐Giraud, Mireille Claustres, Anne‐Françoise Roux	2011	51
7	Enrichment of LOVD-USHbases with 152USH2AGenotypes Defines an Extensive Mutational Spectrum and Highlights Missense Hotspots Human Mutation ·David Baux, Catherine Blanchet, Christian Hamel, Isabelle Meunier, Lise Larrieu, Valérie Faugère, Christel Vaché, Pierangela Castorina, Bernard Puech, Dominique Bonneau, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux	2014	51
8	Experience of targeted Usher exome sequencing as a clinical test Molecular Genetics & Genomic Medicine ·Thomas Besnard, Gema García‐García, David Baux, Christel Vaché, Valérie Faugère, Lise Larrieu, Susana Léonard, José M. Millán, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux	2013	47
9	Four-Year Follow-up of Diagnostic Service in USH1 Patients Investigative Ophthalmology & Visual Science ·Anne‐Françoise Roux, Valérie Faugère, Christel Vaché, David Baux, Thomas Besnard, Susana Léonard, Catherine Blanchet, Christian Hamel, Michel Mondain, Brigitte Gilbert‐Dussardier, Patrick Edery, Didier Lacombe, Dominique Bonneau, Muriel Holder‐Espinasse, Umberto Ambrosetti, Hubert Journel, Albert David, Geneviève Lina‐Granade, Sue Malcolm, Mireille Claustres	2011	42
10	SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect Brain ·Alisdair McNeill, Emanuela Iovino, Luke Mansard, Christel Vaché, David Baux, Emma Bedoukian, Helen Cox, John Dean, David Goudie, Ajith Kumar, Ruth Newbury‐Ecob, Chiara Fallerini, Alessandra Renieri, Diego Lopergolo, Francesca Mari, Catherine Blanchet, Marjolaine Willems, Anne‐Françoise Roux, Tommaso Pippucci, Eric Delpire	2020	34
11	Ex vivo splicing assays of mutations at noncanonical positions of splice sites in USHER genes Human Mutation ·Sandie Le Guédard-Méreuze, Christel Vaché, David Baux, Valérie Faugère, Lise Larrieu, Caroline Abadie, Andreas Janecke, Mireille Claustres, Anne‐Françoise Roux, Sylvie Tuffery‐Giraud	2010	30
12	A potential genomic biomarker for the detection of polycyclic aromatic hydrocarbon pollutants: Multidrug resistance gene 49 in Drosophila melanogaster Environmental Toxicology and Chemistry ·Christel Vaché, Olivier Camarès, Marie‐Céleste, Cardoso‐Ferreira, B. Dastugue, Isabelle Creveaux, Chantal Vaury, Mahchid Bamdad	2007	28
13	Nasal epithelial cells are a reliable source to study splicing variants in Usher syndrome Human Mutation ·Christel Vaché, Thomas Besnard, Catherine Blanchet, David Baux, Lise Larrieu, Valérie Faugère, Michel Mondain, Christian Hamel, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux	2010	26
14	Drosophila melanogaster P-glycoprotein: A membrane detoxification system toward polycyclic aromatic hydrocarbon pollutants Environmental Toxicology and Chemistry ·Christel Vaché, Olivier Camarès, Fabienne De Graeve, B. Dastugue, Annie Meiniel, Chantal Vaury, Serge Pellier, Eva Leoz-Garziandia, Mahchid Bamdad	2006	17
15	Low-cost measurement of body composition with 18O-enriched water. PubMed ·Christel Vaché, Pierre Gachon, M. Ferry, B. Beaufrère, P. Ritz	1995	11
16	A 4.6 Mb Inversion Leading to PCDH15-LINC00844 and BICC1-PCDH15 Fusion Transcripts as a New Pathogenic Mechanism Implicated in Usher Syndrome Type 1 Frontiers in Genetics ·Christel Vaché, Jacques Puechberty, Valérie Faugère, Floriane Darmaisin, Alessandro Liquori, David Baux, Catherine Blanchet, Gema García‐García, Isabelle Meunier, Franck Pellestor, M. Kœnig, Anne‐Françoise Roux	2020	7
17	Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analyses Human Mutation ·Christel Vaché, Simona Torriano, Valérie Faugère, Nejla Erkilic, David Baux, Gema García‐García, Christian P. Hamel, Isabelle Meunier, Xavier Zanlonghi, M. Kœnig, Vasiliki Kalatzis, Anne‐Françoise Roux	2018	7
18	Identification of the First Single GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss Diagnostics ·Luke Mansard, Christel Vaché, Julie Bianchi, Corinne Baudoin, Isabelle Perthus, Bertrand Isidor, Catherine Blanchet, David Baux, M. Kœnig, Vasiliki Kalatzis, Anne‐Françoise Roux	2022	6
19	Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa Stem Cell Research ·Carla Sanjurjo-Soriano, Nejla Erkilic, Christel Vaché, Grégor Dubois, Anne‐Françoise Roux, Isabelle Meunier, Vasiliki Kalatzis	2022	4
20	Reclassification of a TMC1 synonymous substitution as a variant disrupting splicing regulatory elements associated with recessive hearing loss European Journal of Human Genetics ·Christel Vaché, David Baux, Julie Bianchi, Corinne Baudoin, Valérie Faugère, Christine Francannet, M. Kœnig, Vasiliki Kalatzis, Anne‐Françoise Roux	2021	2

About Christel Vaché

Christel Vaché is a scholar working on Molecular Biology, Sensory Systems, Genetics, Plant Science and Cancer Research, having authored 24 papers that have together received 799 indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (10 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers), RNA Research and Splicing (5 papers), Retinal Development and Disorders (4 papers), RNA regulation and disease (3 papers), RNA modifications and cancer (3 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Body Composition Measurement Techniques (2 papers). The work is most often cited by research in Sensory Systems (213 citations), Molecular Biology (611 citations), Cancer Research (121 citations), Ophthalmology (69 citations) and Otorhinolaryngology (33 citations). Christel Vaché has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Anne‐Françoise Roux, Eric Clottes, Fabrice Rossignol, Mireille Claustres, David Baux, Sue Malcolm, Catherine Blanchet, Lise Larrieu, Gema García‐García and Valérie Faugère. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Environmental Toxicology and Chemistry, Gene and Frontiers in Genetics.

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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Christel Vaché

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Christel Vaché

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About Christel Vaché

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