Corinne Métay

1.5k total citations
31 papers, 376 citations indexed

About

Corinne Métay is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Corinne Métay has authored 31 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Corinne Métay's work include Cardiomyopathy and Myosin Studies (9 papers), Muscle Physiology and Disorders (6 papers) and Immune Cell Function and Interaction (5 papers). Corinne Métay is often cited by papers focused on Cardiomyopathy and Myosin Studies (9 papers), Muscle Physiology and Disorders (6 papers) and Immune Cell Function and Interaction (5 papers). Corinne Métay collaborates with scholars based in France, Netherlands and Vietnam. Corinne Métay's co-authors include Gérard Tachdjian, Sophie Brisset, Lucie Tosca, Michel Goossens, Françoise Barré‐Sinoussi, Audrey Briand‐Suleau, Gianfranco Pancino, Daniel Scott‐Algara, Pierre Versmisse and Évelyne Bégaud and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Human Reproduction.

In The Last Decade

Corinne Métay

29 papers receiving 347 citations

Peers

Countries citing papers authored by Corinne Métay

Since Specialization

Citations

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

Fields of papers citing papers by Corinne Métay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Métay

This figure shows the co-authorship network connecting the top 25 collaborators of Corinne Métay. A scholar is included among the top collaborators of Corinne Métay 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 Corinne Métay. Corinne Métay is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure 2025 ·Revue Neurologique ·Diana Maria Chiţimuș, Clovis Adam, Cécile Cauquil, Boris Keren, Nicholas Heming, (unknown), Djillali Annane, Guillaume Nicolas, Pascal Laforêt, Corinne Métay, (unknown)	0
2	Myotilin gene duplication causing late‐onset myotilinopathy 2025 ·European Journal of Neurology ·Marco Spinazzi, Marco Savarese, Franck Letournel, (unknown), Florence Manero, (unknown), (unknown), Corinne Métay, (unknown), Bjarne Udd	1
3	Phenotype variability and natural history of X-linked myopathy with excessive autophagy 2024 ·Journal of Neurology ·Gorka Fernández‐Eulate, Girolamo Alfieri, Marco Spinazzi, (unknown), Fanny Duval, Guilhem Solé, Florence Caillon, Sandra Mercier, Yann Péréon, Armelle Magot, Antoine Pégat, Emmanuelle Salort‐Campana, B. Chabrol, Svetlana Gorokhova, Martin Krahn, Valérie Biancalana, Teresinha Evangelista, Anthony Béhin, Corinne Métay, Tanya Stojkovic	1
4	Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variant 2023 ·Acta Neuropathologica Communications ·(unknown), (unknown), (unknown), (unknown), Marcello Villanova, Corinne Métay, Chiara Fiorillo, (unknown), Luciano Merlini, Patrizia Sabatelli, Norma B. Romero, Frédéric Relaix, François‐Jérôme Authier, Valentina Taglietti, Marco Savarese, (unknown), Coen A. C. Ottenheijm, Isabelle Richard, Edoardo Malfatti	3
5	A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report 2023 ·SHILAP Revista de lepidopterología ·(unknown), Corinne Métay, Michael Frank, Nicolas Denarié, Salma Adham, Clarisse Billon, Anne Debost‐Legrand, Xavier Jeunemaı̂tre, (unknown), Karen Gaudon, Philippe de Mazancourt, Ahmed Mekki, Robert Carlier, Karelle Bénistan	2
6	Deep Characterization of a Greek Patient with Desmin-Related Myofibrillar Myopathy and Cardiomyopathy 2023 ·International Journal of Molecular Sciences ·Constantinos Papadopoulos, Edoardo Malfatti, Corinne Métay, Boris Keren, (unknown), Julien Buratti, Sophia Xirou, (unknown), George K. Papadimas	2
7	A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder 2021 ·SHILAP Revista de lepidopterología ·(unknown), Philippe de Mazancourt, Corinne Métay, Robert Carlier, Valérie Allamand, Corine Gartioux, (unknown), (unknown), (unknown), Ahmed Mekki, Pascale Richard, Caroline Michot, Karelle Bénistan	6
8	A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency 2020 ·Annals of Clinical and Translational Neurology ·Aurélien Perrin, Corinne Métay, Marcello Villanova, Robert‐Yves Carlier, Elena Pegoraro, Raúl Juntas‐Morales, Tanya Stojkovic, Isabelle Richard, Pascale Richard, Norma B. Romero, Henk Granzier, M. Kœnig, Edoardo Malfatti, Mireille Cossée	9
9	Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: A two-hit case with more severe clinical manifestations 2015 ·European Journal of Medical Genetics ·Sophie Brisset, Yline Capri, Audrey Briand‐Suleau, Lucie Tosca, Domitille Gras, (unknown), (unknown), Julien Saada, (unknown), Alain Verloès, Michel Goossens, Gérard Tachdjian, Corinne Métay	19
10	Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts 2015 ·European Journal of Medical Genetics ·Laure Raymond, Bruno Francou, François Petit, Lucie Tosca, Audrey Briand‐Suleau, Corinne Métay, Jelena Martinović, Anne‐Gaël Cordier, Alexandra Benachi, (unknown), Anne Guiochon‐Mantel, Michel Goossens, Gérard Tachdjian, Sophie Brisset	3
11	Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease 2015 ·Molecular Cytogenetics ·(unknown), Corinne Métay, Sophie Brisset, Georges Deschênes, (unknown), François Petit, Federico Di Rocco, Michel Goossens, Gérard Tachdjian, Philippe Labrune, Lucie Tosca	11
12	SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication 2014 ·European Journal of Medical Genetics ·Audrey Briand‐Suleau, Jelena Martinović, Lucie Tosca, (unknown), Sophie Brisset, Jérôme Bouligand, (unknown), Irina Giurgea, (unknown), (unknown), Carole Goumy, Christine Francannet, Anne Guiochon‐Mantel, Alexandra Benachi, Joris Vermeesch, Gérard Tachdjian, Philippe Vago, Michel Goossens, Corinne Métay	2
13	Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23 2014 ·Molecular Cytogenetics ·Sophie Brisset, (unknown), Petra Dušátková, Audrey Briand‐Suleau, Karen Milcent, Corinne Métay, (unknown), Zdenĕk Šumnı́k, Lucie Tosca, Michel Goossens, Philippe Labrune, (unknown), Jan Lebl, Gérard Tachdjian, Zdeněk Sedláček	11
14	SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development 2012 ·Human Reproduction ·Jacques Young, Corinne Métay, Jérôme Bouligand, (unknown), Bruno Francou, Luigi Maione, Lucie Tosca, Julie Sarfati, Frédéric Brioude, Blandine Esteva, Audrey Briand‐Suleau, Sophie Brisset, Michel Goossens, Gérard Tachdjian, Anne Guiochon‐Mantel	99
15	Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11 2011 ·European Journal of Human Genetics ·Christian Wentzel, Evica Rajcan‐Separovic, Claudia Ruivenkamp, Sandra Chantot‐Bastaraud, Corinne Métay, Joris Andrieux, Göran Annerén, Antoinet C.J. Gijsbers, (unknown), Capucine Hyon, Marie‐France Portnoï, Eva‐Lena Stattin, (unknown), Sarina G. Kant, Michelle Steinraths, Sandrine Marlin, Irina Giurgea, Ann‐Charlotte Thuresson	27
16	Genotype–phenotype correlation in 13q13.3–q21.3 deletion 2011 ·European Journal of Medical Genetics ·Lucie Tosca, Sophie Brisset, François Petit, Corinne Métay, (unknown), (unknown), Axel Lebas, (unknown), Olivier Picone, (unknown), Sophie Prévôt, Marc Tardieu, Michel Goossens, Gérard Tachdjian	15
17	Reduced CD4 T cell activation and in vitro susceptibility to HIV-1 infection in exposed uninfected Central Africans 2006 ·Retrovirology ·Évelyne Bégaud, Loïc Chartier, (unknown), (unknown), (unknown), Pierre Versmisse, Guillaume Breton, Arnaud Fontanet, Corinne Métay, Hervé Fleury, Françoise Barré‐Sinoussi, Daniel Scott‐Algara, Gianfranco Pancino	90
18	A natural CCL5/RANTES variant antagonist for CCR1 and CCR3 2006 ·Immunogenetics ·Corinne Métay, Ahidjo Ayouba, Anfumbom Kfutwah, Kavita S. Lole, Stéphane Pêtres, Yasmine Dudoit, Philippe Déterre, Elisabeth Menu, Françoise Barré‐Sinoussi, Patrice Debré, Ioannis Théodorou	9
19	Influence of the R22H variant of macrophage inflammatory protein 1β/Lag-1 in HIV-1 survival 2005 ·AIDS ·Corinne Métay, Laurence Meyer, (unknown), Anne Persoz, A Bourdais, Yasmine Dudoit, Jean‐François Delfraissy, Patrice Debré, Ioannis Théodorou	4
20	New CCR5 variants associated with reduced HIV coreceptor function in southeast Asia 2004 ·AIDS ·Corinne Métay, Liying Ma, Lien X Truong, Yasmine Dudoit, Pierre Versmisse, (unknown), Marie Nguyen, Daniel Scott‐Algara, Françoise Barré‐Sinoussi, Patrice Debré, Georges Bismuth, Gianfranco Pancino, Ioannis Théodorou	20

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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