Mireille Claustres

18.2k citations

221 papers · 8.2k indexed · 1 hit paper · h-index 46

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Genetics top 1%
- Genomics and Rare Diseases

Papers in

Genetics 31
- Congenital Ear and Nasal Anomalies 20
- Genomics and Rare Diseases 19
Sensory Systems 14

Co-authors: Christophe Béroud Dalil Hamroun Gwenaëlle Collod‐Béroud Sylvie Tuffery‐Giraud Anne‐Françoise Roux Jacques Demaille Marie Desgeorges Caroline Guittard
Journals: Human Mutation (41 papers)European Journal of Human Genetics (20 papers)Human Genetics (19 papers)Human Molecular Genetics (8 papers)Journal of Cystic Fibrosis (7 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Mireille Claustres

217 papers receiving 8.0k citations

Hit Papers

align trajectories log scale

Human Splicing Finder: an online bioinformatics tool to predict splicing signals 2009 · 1.9k citations

Peers

Countries citing papers authored by Mireille Claustres

Since Specialization

Citations

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

Fields of papers citing papers by Mireille Claustres

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR‐101 that regulate WISP1 expression The Journal of Pathology ·A. Pommier, Jessica Varilh, Solenne Bleuse, Karine Delétang, Jennifer Bonini, Anne Bergougnoux, Emmanuelle Brochiero, M. Kœnig, Mireille Claustres, Magali Taulan‐Cadars	2020	8
2	Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2) European Journal of Human Genetics ·Claire Guissart, Nathalie Drouot, İbrahim Öncel, Bruno Leheup, Ruth Gershoni-Barush, Jean Muller, Sacha Ferdinandusse, Lise Larrieu, Mathieu Anheim, Elif Acar Arslan, Mireille Claustres, Christine Tranchant, Haluk Topaloğlu, Michel Kœnig	2015	15
3	Towards a European consensus for reporting incidental findings during clinical NGS testing European Journal of Human Genetics ·Jayne Y. Hehir‐Kwa, Mireille Claustres, Ros Hastings, Conny M.A. van Ravenswaaij‐Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon‐Thomsen, Philippos C. Patsalis, Joris Vermeesch, Martina C. Cornel, Beverly Searle, Aarno Palotie, Ettore Capoluongo, Borut Peterlin, Xavier Estivill, Peter N. Robinson	2015	56
4	FUBP1: a new protagonist in splicing regulation of the DMD gene Nucleic Acids Research ·Julie Miro, Abdelhamid Mahdi Laaref, Valérie Rofidal, Rosyne Lagrafeuille, Sonia Hem, Delphine Thorel, Déborah Méchin, Kamel Mamchaoui, Vincent Mouly, Mireille Claustres, Sylvie Tuffery‐Giraud	2015	28
5	Should diffuse bronchiectasis still be considered a CFTR-related disorder? Journal of Cystic Fibrosis ·Anne Bergougnoux, Victoria Viart, Julie Miro, Sébastien Bommart, Nicolas Molinari, Marie des Georges, Mireille Claustres, R. Chiron, Magali Taulan‐Cadars	2015	16
6	Mutation of SLC9A1, encoding the major Na+/H+ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome Human Molecular Genetics ·Claire Guissart, Xinrui Li, Bruno Leheup, Nathalie Drouot, B. Montaut-Verient, Emmanuel Raffo, P. Jonveaux, Anne‐Françoise Roux, Mireille Claustres, Larry Fliegel, M. Kœnig	2014	37
7	A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice Journal of Cystic Fibrosis ·Cathérine Costa, V. Prulière‐Escabasse, Alix de Becdelièvre, Christine Gameiro, Lisa Golmard, Caroline Guittard, Laurence Bassinet, Thierry Bienvenu, Marie des Georges, Ralph Epaud, Éric Bieth, Irina Giurgea, Abdel Aissat, Alexandre Hinzpeter, Bruno Costes, Pascale Fanen, Michel Goossens, Mireille Claustres, A. Coste, Emmanuelle Girodon	2011	17
8	DYT6 dystonia: Review of the literature and creation of the UMD locus-specific database (LSDB) for mutations in the THAP1 gene Human Mutation ·Arnaud Blanchard, Vuthy Ea, Agathe Roubertie, Mélanie Martin, Coline Coquart, Mireille Claustres, Christophe Béroud, Gwenaëlle Collod‐Béroud	2011	39
9	Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency, Centromeric Instability, Facial Anomalies (ICF) Syndrome PLoS ONE ·Marie-Elisabeth Brun, Erica Lana, Isabelle Rivals, Marie‐Paule Lefranc, Pierre Sarda, Mireille Claustres, André Mégarbané, Albertina De Sario	2011	25
10	UMD-CFTR: A database dedicated to CF and CFTR-related disorders Human Mutation ·Corinne Bareil, C. Thèze, Christophe Béroud, Dalil Hamroun, Caroline Guittard, Céline René, Damien Paulet, Marie des Georges, Mireille Claustres	2010	22
11	Human Splicing Finder: an online bioinformatics tool to predict splicing signals Nucleic Acids Research ·François-Olivier Desmet, Dalil Hamroun, Marine Lalande, Gwenaëlle Collod‐Béroud, Mireille Claustres, Christophe Béroud Hit paper breakdown →	2009	1864
12	Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines Pathologie Biologie ·Véronique Humbertclaude, Sylvie Tuffery‐Giraud, Corinne Bareil, C. Thèze, Damien Paulet, François-Olivier Desmet, Dalil Hamroun, David Baux, Anne Girardet, Gwenaëlle Collod‐Béroud, Philippe Khau Van Kien, Anne‐Françoise Roux, M. des Georges, Christophe Béroud, Mireille Claustres	2009	0
13	TheFBN2gene: new mutations, locus-specific database (Universal Mutation DatabaseFBN2), and genotype-phenotype correlations Human Mutation ·Melissa Yana Frédéric, Christine Monino, Christoph Marschall, Dalil Hamroun, Laurence Faivre, Guillaume Jondeau, Hanns-Georg Klein, Luitgard M. Neumann, Élodie Gautier, Christine Binquet, Cheryl L. Maslen, Maurice Godfrey, Prateek Gupta, Dianna M. Milewicz, Cathérine Boileau, Mireille Claustres, Christophe Béroud, Gwenaëlle Collod‐Béroud	2008	46
14	Efficient strategies for preimplantation genetic diagnosis of spinal muscular atrophy Fertility and Sterility ·Anne Girardet, C. Mata Fernández, Mireille Claustres	2008	17
15	First determination of the incidence of the unique TOR1A gene mutation, c.907delGAG, in a Mediterranean population Movement Disorders ·Melissa Yana Frédéric, Estelle Lucarz, Christine Monino, Céline Saquet, Delphine Thorel, Mireille Claustres, Sylvie Tuffery‐Giraud, Gwenaëlle Collod‐Béroud	2007	19
16	Meta-analysis of the p53 Mutation Database for Mutant p53 Biological Activity Reveals a Methodologic Bias in Mutation Detection Clinical Cancer Research ·Thierry Soussi, Bernard Asselain, Dalil Hamroun, Shunsuke Kato, Chikashi Ishioka, Mireille Claustres, Christophe Béroud	2006	58
17	Evaluation of dHPLC for CX26 Mutation Screening in Patients from Southern France with Sensorineural Deafness Genetic Testing ·Nathalie Pallarès-Ruiz, Patricia Blanchet, Michel Mondain, Sabine Low-Hong, Jacques Demaille, Mireille Claustres, Anne‐Françoise Roux	2001	6
18	Génétique, dépistage et épidémiologie de la mucoviscidose MTP. Médecine thérapeutique pédiatrie ·Mireille Claustres	1998	2
19	Cystic fibrosis typing with DNA probes and screening for ΔF508 deletion in families from Southern France Human Genetics ·Mireille Claustres, Marie Desgeorges, Paule Kjellherg, H. Bellet, Jacques Demaille, Michèle Ramsay	1990	3
20	Androgen and Erythropoiesis: Evidence for an Androgen Receptor in Erythroblasts from Human Bone Marrow Cultures Hormone Research ·Mireille Claustres, Charles Sultan	1988	41

About Mireille Claustres

Mireille Claustres is a scholar working on Genetics, Sensory Systems, Pulmonary and Respiratory Medicine, Genetics and Molecular Biology, having authored 221 papers that have together received 8.2k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (75 papers), Neonatal Respiratory Health Research (35 papers), Muscle Physiology and Disorders (25 papers), RNA Research and Splicing (23 papers), Tracheal and airway disorders (22 papers), Congenital Ear and Nasal Anomalies (20 papers), Genomics and Rare Diseases (19 papers) and RNA and protein synthesis mechanisms (16 papers). The work is most often cited by research in Sensory Systems (841 citations), Genetics (722 citations), Genetics (1.8k citations), Molecular Biology (4.3k citations) and Pulmonary and Respiratory Medicine (1.7k citations). Mireille Claustres has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Christophe Béroud, Dalil Hamroun, Gwenaëlle Collod‐Béroud, Sylvie Tuffery‐Giraud, Anne‐Françoise Roux, Jacques Demaille, Marie Desgeorges, Caroline Guittard, David Baux and Nathalie Pallarès-Ruiz. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Human Genetics, Human Molecular Genetics and Journal of Cystic Fibrosis.

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