Charles Coutton

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 36

Top Venues

International journal of molecular sciences

Clinical genetics

eLife

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Vuthy Ea, Claudine Berthozat, Hélène Dreyfus, Clémentine Legrand, Estelle Rousselet, Magalie Peysselon, Laura Baudet, Guillaume Martinez, Charles Coutton, Marie Bidart
BRCA1 Intragenic Duplication Combined with a Likely Pathogenic TP53 Variant in a Patient with Triple-Negative Breast Cancer: Clinical Risk and Management. International journal of molecular sciences 25 (11) (2024)
Vuthy Ea, Claudine Berthozat, Hélène Dreyfus, Clémentine Legrand, Estelle Rousselet, Magalie Peysselon, Laura Baudet, Guillaume Martinez, Charles Coutton, Marie Bidart
BRCA1 Intragenic Duplication Combined with a Likely Pathogenic TP53 Variant in a Patient with Triple-Negative Breast Cancer: Clinical Risk and Management. International journal of molecular sciences 25 (11) (2024)
Alexis Billes, Mathilde Pujalte, Guillaume Jedraszak, Daniel Amsallem, Elise Boudry-Labis, Odile Boute, Sonia Bouquillon, Elise Brischoux-Boucher, Patrick Callier, Charles Coutton, Anne-Laude Avice Denizet, Klaus Dieterich, Paul Kuentz, James Lespinasse, Benoît Mazel, Gilles Morin, Florence Amram, Perrine Pennamen, Marlène Rio, Juliette Piard, Audrey Putoux, Mélanie Rama, Virginie Roze-Guillaumey, Caroline Schluth-Bolard, Marianne Till, Chloé Trouvé, Gaëlle Vieville, Caroline Rooryck, Damien Sanlaville, Nicolas Chatron
Possible incomplete penetrance of Xq28 int22h-1/int22h-2 duplication. Clinical genetics (2024)
Alexis Billes, Mathilde Pujalte, Guillaume Jedraszak, Daniel Amsallem, Elise Boudry-Labis, Odile Boute, Sonia Bouquillon, Elise Brischoux-Boucher, Patrick Callier, Charles Coutton, Anne-Laude Avice Denizet, Klaus Dieterich, Paul Kuentz, James Lespinasse, Benoît Mazel, Gilles Morin, Florence Amram, Perrine Pennamen, Marlène Rio, Juliette Piard, Audrey Putoux, Mélanie Rama, Virginie Roze-Guillaumey, Caroline Schluth-Bolard, Marianne Till, Chloé Trouvé, Gaëlle Vieville, Caroline Rooryck, Damien Sanlaville, Nicolas Chatron
Possible incomplete penetrance of Xq28 int22h-1/int22h-2 duplication. Clinical genetics 106 (3) (2024)
Jana Muroňová, Zine Eddine Kherraf, Elsa Giordani, Emeline Lambert, Simon Eckert, Caroline Cazin, Amir Amiri-Yekta, Magali Court, Geneviève Chevalier, Guillaume Martinez, Yasmine Neirijnck, Francoise Kühne, Lydia Wehrli, Nikolai Klena, Virginie Hamel, Lisa De Macedo, Jessica Escoffier, Paul Guichard, Charles Coutton, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Anne-Pacale Bouin, Raoudha Zouari, Nicolas Thierry-Mieg, Serge Nef, Stefan Geimer, Corinne Loeuillet, Pierre F Ray, Christophe Arnoult
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse. eLife 12 (2024)
Vuthy Ea, Claudine Berthozat, Hélène Dreyfus, Clémentine Legrand, Estelle Rousselet, Magalie Peysselon, Laura Baudet, Guillaume Martinez, Charles Coutton, Marie Bidart
BRCA1 Intragenic Duplication Combined with a Likely Pathogenic TP53 Variant in a Patient with Triple-Negative Breast Cancer: Clinical Risk and Management. International journal of molecular sciences 25 (11) (2024)
Jana Muroňová, Zine Eddine Kherraf, Elsa Giordani, Emeline Lambert, Simon Eckert, Caroline Cazin, Amir Amiri-Yekta, Magali Court, Geneviève Chevalier, Guillaume Martinez, Yasmine Neirijnck, Francoise Kühne, Lydia Wehrli, Nikolai Klena, Virginie Hamel, Lisa De Macedo, Jessica Escoffier, Paul Guichard, Charles Coutton, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Anne-Pacale Bouin, Raoudha Zouari, Nicolas Thierry-Mieg, Serge Nef, Stefan Geimer, Corinne Loeuillet, Pierre F Ray, Christophe Arnoult
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse. eLife 12 (2024)
Jana Muroňová, Zine Eddine Kherraf, Elsa Giordani, Emeline Lambert, Simon Eckert, Caroline Cazin, Amir Amiri-Yekta, Magali Court, Geneviève Chevalier, Guillaume Martinez, Yasmine Neirijnck, Francoise Kühne, Lydia Wehrli, Nikolai Klena, Virginie Hamel, Lisa De Macedo, Jessica Escoffier, Paul Guichard, Charles Coutton, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Anne-Pacale Bouin, Raoudha Zouari, Nicolas Thierry-Mieg, Serge Nef, Stefan Geimer, Corinne Loeuillet, Pierre F Ray, Christophe Arnoult
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse. eLife 12 (2024)
Jana Muroňová, Zine Eddine Kherraf, Elsa Giordani, Emeline Lambert, Simon Eckert, Caroline Cazin, Amir Amiri-Yekta, Magali Court, Geneviève Chevalier, Guillaume Martinez, Yasmine Neirijnck, Francoise Kühne, Lydia Wehrli, Nikolai Klena, Virginie Hamel, Lisa De Macedo, Jessica Escoffier, Paul Guichard, Charles Coutton, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Anne-Pacale Bouin, Raoudha Zouari, Nicolas Thierry-Mieg, Serge Nef, Stefan Geimer, Corinne Loeuillet, Pierre F Ray, Christophe Arnoult
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse. eLife 12 (2024)
Guillaume Martinez, Anne-Laure Barbotin, Caroline Cazin, Zeina Wehbe, Angèle Boursier, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh-Hanieh Hosseini, Nathalie Rives, Aurélie Feraille, Nicolas Thierry-Mieg, Marie Bidart, Véronique Satre, Christophe Arnoult, Pierre F Ray, Zine-Eddine Kherraf, Charles Coutton
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. International journal of molecular sciences 24 (3) (2023)
Edgar Del Llano, Aurore Perrin, Frédéric Morel, Françoise Devillard, Radu Harbuz, Véronique Satre, Florence Amblard, Marie Bidart, Sylviane Hennebicq, Sophie Brouillet, Pierre F Ray, Charles Coutton, Guillaume Martinez
Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry. International journal of molecular sciences 24 (4) (2023)
Edgar Del Llano, Aurore Perrin, Frédéric Morel, Françoise Devillard, Radu Harbuz, Véronique Satre, Florence Amblard, Marie Bidart, Sylviane Hennebicq, Sophie Brouillet, Pierre F Ray, Charles Coutton, Guillaume Martinez
Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry. International journal of molecular sciences 24 (4) (2023)
Edgar Del Llano, Aurore Perrin, Frédéric Morel, Françoise Devillard, Radu Harbuz, Véronique Satre, Florence Amblard, Marie Bidart, Sylviane Hennebicq, Sophie Brouillet, Pierre F Ray, Charles Coutton, Guillaume Martinez
Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry. International journal of molecular sciences 24 (4) (2023)
Zine-Eddine Kherraf, Anne-Laure Barbotin, Guillaume Martinez, Aurélien Mazet, Caroline Cazin, Charles Coutton, Christophe Arnoult, Nicolas Thierry-Mieg, Nathalie Rives, Aurélie Rives-Feraille, Pierre F Ray
A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility. Clinical genetics (2023)
Gaëlle Friocourt, Aurore Perrin, Paul A Saunders, Elvira Nikalayevich, Cécile Voisset, Charles Coutton, Guillaume Martinez, Frédéric Morel
Bypassing Mendel's First Law: Transmission Ratio Distortion in Mammals. International journal of molecular sciences 24 (2) (2023)
Guillaume Martinez, Anne-Laure Barbotin, Caroline Cazin, Zeina Wehbe, Angèle Boursier, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh-Hanieh Hosseini, Nathalie Rives, Aurélie Feraille, Nicolas Thierry-Mieg, Marie Bidart, Véronique Satre, Christophe Arnoult, Pierre F Ray, Zine-Eddine Kherraf, Charles Coutton
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. International journal of molecular sciences 24 (3) (2023)
Edgar Del Llano, Aurore Perrin, Frédéric Morel, Françoise Devillard, Radu Harbuz, Véronique Satre, Florence Amblard, Marie Bidart, Sylviane Hennebicq, Sophie Brouillet, Pierre F Ray, Charles Coutton, Guillaume Martinez
Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry. International journal of molecular sciences 24 (4) (2023)
Denis Dacheux, Guillaume Martinez, Christine E Broster Reix, Julie Beurois, Patrick Lores, Magamba Tounkara, Jean-William Dupuy, Derrick Roy Robinson, Corinne Loeuillet, Emeline Lambert, Zeina Wehbe, Jessica Escoffier, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh-Hanieh Hosseini, Raoudha Zouari, Selima Fourati Ben Mustapha, Lazhar Halouani, Xiaohui Jiang, Ying Shen, Chunyu Liu, Nicolas Thierry-Mieg, Amandine Septier, Marie Bidart, Véronique Satre, Caroline Cazin, Zine Eddine Kherraf, Christophe Arnoult, Pierre F Ray, Aminata Toure, Mélanie Bonhivers, Charles Coutton
Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function. eLife 12 (2023)
Edgar Del Llano, Aurore Perrin, Frédéric Morel, Françoise Devillard, Radu Harbuz, Véronique Satre, Florence Amblard, Marie Bidart, Sylviane Hennebicq, Sophie Brouillet, Pierre F Ray, Charles Coutton, Guillaume Martinez
Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry. International journal of molecular sciences 24 (4) (2023)
Gaëlle Friocourt, Aurore Perrin, Paul A Saunders, Elvira Nikalayevich, Cécile Voisset, Charles Coutton, Guillaume Martinez, Frédéric Morel
Bypassing Mendel's First Law: Transmission Ratio Distortion in Mammals. International journal of molecular sciences 24 (2) (2023)
Guillaume Martinez, Anne-Laure Barbotin, Caroline Cazin, Zeina Wehbe, Angèle Boursier, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh-Hanieh Hosseini, Nathalie Rives, Aurélie Feraille, Nicolas Thierry-Mieg, Marie Bidart, Véronique Satre, Christophe Arnoult, Pierre F Ray, Zine-Eddine Kherraf, Charles Coutton
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. International journal of molecular sciences 24 (3) (2023)
Gaëlle Friocourt, Aurore Perrin, Paul A Saunders, Elvira Nikalayevich, Cécile Voisset, Charles Coutton, Guillaume Martinez, Frédéric Morel
Bypassing Mendel's First Law: Transmission Ratio Distortion in Mammals. International journal of molecular sciences 24 (2) (2023)
Gaëlle Friocourt, Aurore Perrin, Paul A Saunders, Elvira Nikalayevich, Cécile Voisset, Charles Coutton, Guillaume Martinez, Frédéric Morel
Bypassing Mendel's First Law: Transmission Ratio Distortion in Mammals. International journal of molecular sciences 24 (2) (2023)
Guillaume Martinez, Anne-Laure Barbotin, Caroline Cazin, Zeina Wehbe, Angèle Boursier, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh-Hanieh Hosseini, Nathalie Rives, Aurélie Feraille, Nicolas Thierry-Mieg, Marie Bidart, Véronique Satre, Christophe Arnoult, Pierre F Ray, Zine-Eddine Kherraf, Charles Coutton
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. International journal of molecular sciences 24 (3) (2023)
Guillaume Jouret, Solveig Heide, Arthur Sorlin, Laurence Faivre, Sandra Chantot-Bastaraud, Claire Beneteau, Marie Denis-Musquer, Peter D Turnpenny, Charles Coutton, Gaëlle Vieville, Julien Thevenon, Austin Larson, Florence Petit, Elise Boudry, Thomas Smol, Bruno Delobel, Bénédicte Duban-Bedu, Chiara Fallerini, Francesca Mari, Caterina Lo Rizzo, Alessandra Renieri, Jean-Hubert Caberg, Anne Sophie Denommé-Pichon, Frédéric Tran Mau-Them, Isabelle Maystadt, Thomas Courtin, Boris Keren, Linda Mouthon, Perrine Charles, Silvestre Cuinat, Bertrand Isidor, Philippe Theis, Christian Müller, Marizela Kulisic, Seval Türkmen, Daniel Stieber, Dominique Bourgeois, Emmanuel Scalais, Barbara Klink
Understanding the new BRD4-related syndrome: Clinical and genomic delineation with an international cohort study. Clinical genetics 102 (2) (2022)
Quentin Testard, Xavier Vanhoye, Kevin Yauy, Marie-Emmanuelle Naud, Gaelle Vieville, Francis Rousseau, Benjamin Dauriat, Valentine Marquet, Sylvie Bourthoumieu, David Geneviève, Vincent Gatinois, Constance Wells, Marjolaine Willems, Christine Coubes, Lucile Pinson, Rodolphe Dard, Aude Tessier, Bérénice Hervé, François Vialard, Ines Harzallah, Renaud Touraine, Benjamin Cogné, Wallid Deb, Thomas Besnard, Olivier Pichon, Béatrice Laudier, Laurent Mesnard, Alice Doreille, Tiffany Busa, Chantal Missirian, Véronique Satre, Charles Coutton, Tristan Celse, Radu Harbuz, Laure Raymond, Jean-François Taly, Julien Thevenon
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases. Journal of medical genetics 59 (12) (2022)
Tristan Celse, Angèle Tingaud-Sequeira, Klaus Dieterich, Geraldine Siegfried, Cédric Lecaignec, Laurence Bouneau, Madeleine Fannemel, Gaelle Salaun, Fanny Laffargue, Guillaume Martinez, Véronique Satre, Gaelle Vieville, Marie Bidart, Cecilia Soussi Zander, Ann-Charlotte Turesson, Miranda Splitt, Dorothee Reboul, Jean Chiesa, Philippe Khau Van Kien, Manon Godin, Nicolas Gruchy, Himanshu Goel, Elizabeth Palmer, Kalliope Demetriou, Carolyn Shalhoub, Caroline Rooryck, Charles Coutton
OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum. Journal of medical genetics (2022)
Guillaume Martinez, Catherine Metzler-Guillemain, Caroline Cazin, Zine-Eddine Kherraf, Odile Paulmyer-Lacroix, Christophe Arnoult, Pierre F Ray, Charles Coutton
Expanding the sperm phenotype caused by mutations in SPATA20: A novel splicing mutation in an infertile patient with partial globozoospermia. Clinical genetics (2022)
Guillaume Martinez, Catherine Metzler-Guillemain, Caroline Cazin, Zine-Eddine Kherraf, Odile Paulmyer-Lacroix, Christophe Arnoult, Pierre F Ray, Charles Coutton
Expanding the sperm phenotype caused by mutations in SPATA20: a novel splicing mutation in an infertile patient with partial globozoospermia. Clinical genetics (2022)
Qunshan Shen, Guillaume Martinez, Hongbin Liu, Julie Beurois, Huan Wu, Amir Amiri-Yekta, Dan Liang, Zine-Eddine Kherraf, Marie Bidart, Caroline Cazin, Tristan Celse, Véronique Satre, Nicolas Thierry-Mieg, Marjorie Whitfield, Aminata Touré, Bing Song, Mingrong Lv, Kuokuo Li, Chunyu Liu, Fangbiao Tao, Xiaojin He, Feng Zhang, Christophe Arnoult, Pierre F Ray, Yunxia Cao, Charles Coutton
Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse. Human genetics 140 (9) (2021)
Roseline Vibert, Cyril Mignot, Boris Keren, Sandra Chantot-Bastaraud, Marie-France Portnoï, Marie-Christine Nouguès, Marie-Laure Moutard, Anne Faudet, Sandra Whalen, Damien Haye, Catherine Garel, Nicolas Chatron, Massimiliano Rossi, Catherine Vincent-Delorme, Odile Boute, Bruno Delobel, Joris Andrieux, Françoise Devillard, Charles Coutton, Jacques Puechberty, Céline Pebrel-Richard, Cindy Colson, Marion Gerard, Chantal Missirian, Sabine Sigaudy, Tiffany Busa, Martine Doco-Fenzy, Valérie Malan, Marlène Rio, Bérénice Doray, Damien Sanlaville, Jean-Pierre Siffroi, Delphine Héron, Solveig Heide
Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: genotype-phenotype correlation for anomalies of the corpus callosum. Clinical genetics (2021)
Emma Cavarocchi, Marjorie Whitfield, Ahmed Chargui, Laurence Stouvenel, Patrick Lorès, Charles Coutton, Christophe Arnoult, Pietro Santulli, Catherine Patrat, Nicolas Thierry-Mieg, Pierre F Ray, Emmanuel Dulioust, Aminata Toure
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility. Clinical genetics 99 (5) (2021)
Aminata Touré, Guillaume Martinez, Zine-Eddine Kherraf, Caroline Cazin, Julie Beurois, Christophe Arnoult, Pierre F Ray, Charles Coutton
The genetic architecture of morphological abnormalities of the sperm tail. Human genetics 140 (1) (2020)
Guillaume Martinez, Julie Beurois, Denis Dacheux, Caroline Cazin, Marie Bidart, Zine-Eddine Kherraf, Derrick R Robinson, Véronique Satre, Gerald Le Gac, Chandran Ka, Isabelle Gourlaouen, Yann Fichou, Graciane Petre, Emmanuel Dulioust, Raoudha Zouari, Nicolas Thierry-Mieg, Aminata Touré, Christophe Arnoult, Mélanie Bonhivers, Pierre Ray, Charles Coutton
Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility. Journal of medical genetics 57 (10) (2020)
Zine-Eddine Kherraf, Caroline Cazin, Charles Coutton, Amir Amiri-Yekta, Guillaume Martinez, Magalie Boguenet, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Hamid Gourabi, Seyedeh Hanieh Hosseini, Abbas Daneshipour, Aminata Touré, Nicolas Thierry-Mieg, Raoudha Zouari, Christophe Arnoult, Pierre F Ray
Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Clinical genetics 96 (5) (2019)
Graciane Petre, Patrick Lorès, Hervé Sartelet, Aurélie Truffot, Brice Poreau, Sandrine Brandeis, Guillaume Martinez, Véronique Satre, Radu Harbuz, Pierre F Ray, Florence Amblard, Françoise Devillard, Gaëlle Vieville, Francois Berger, Pierre-Simon Jouk, Daniel Vaiman, Aminata Touré, Charles Coutton, Marie Bidart
Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction. Clinical genetics 94 (6) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Charles Coutton