Coutton, Charles

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

Ben Khelifa, M., Coutton, C., Zouari, R., Karaouzène, T., Rendu, J., Bidart, M., Yassine, S., Pierre, V., Delaroche, J., Hennebicq, S., et al. (2014) · The American Journal of Human Genetics

Sperm and Testicular FunctionCystic Fibrosis Research Advances

Cited by 474

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Jacquemont, S., Reymond, A., Zufferey, F., Harewood, L., Walters, R. G., Kutalik, Z., Martinet, D., Shen, Y., Valsesia, A., Beckmann, N. D., et al. (2011) · Nature

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 462

Teratozoospermia: spotlight on the main genetic actors in the human

Coutton, C., Escoffier, J., Martinez, G., Arnoult, C., & Ray, P. F. (2015) · Human Reproduction Update

Sperm and Testicular FunctionReproductive Biology and Fertility

Cited by 352

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

Coutton, C., Vargas, A. S., Amiri-Yekta, A., Kherraf, Z.-E., Ben Mustapha, S. F., Le Tanno, P., Wambergue-Legrand, C., Karaouzène, T., Martinez, G., Crouzy, S., et al. (2018) · Nature Communications

Sperm and Testicular FunctionCystic Fibrosis Research Advances

Cited by 245

Genetic abnormalities leading to qualitative defects of sperm morphology or function

Ray, P. F., Toure, A., Metzler‐Guillemain, C., Mitchell, M. J., Arnoult, C., & Coutton, C. (2017) · Clinical Genetics

Sperm and Testicular FunctionReproductive Biology and Fertility

Cited by 179

Genetics of teratozoospermia: Back to the head

Beurois, J., Cazin, C., Kherraf, Z.-E., Martinez, G., Celse, T., Touré, A., Arnoult, C., Ray, P. F., & Coutton, C. (2020) · Best Practice & Research Clinical Endocrinology & Metabolism

Sperm and Testicular FunctionReproductive biology and impacts on aquatic species

Cited by 71

Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men

Ray, P., Ounis, L., Zoghmar, A., Coutton, C., Rouabah, L., Hachemi, M., Martinez, D., Martinez, G., Bellil, I., Khelifi, D., et al. (2015) · Asian Journal of Andrology

Sperm and Testicular FunctionGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 55

Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player

Celse, T., Cazin, C., Mietton, F., Martinez, G., Martinez, D., Thierry-Mieg, N., Septier, A., Guillemain, C., Beurois, J., Clergeau, A., et al. (2021) · Human Genetics

Sperm and Testicular FunctionGenomics and Rare Diseases

Cited by 42

Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa

Cazin, C., Boumerdassi, Y., Martinez, G., Fourati Ben Mustapha, S., Whitfield, M., Coutton, C., Thierry-Mieg, N., Di Pizio, P., Rives, N., Arnoult, C., et al. (2021) · International Journal of Molecular Sciences

Sperm and Testicular FunctionGenomics and Rare Diseases

Cited by 16