Les publications :

Oligogenic heterozygous inheritance of sperm abnormalities in mouse

Martinez G, Coutton C, Loeuillet C, Cazin C, Muroňová J, Boguenet M, Lambert E, Dhellemmes…

Elife 2022 Apr 22;11:e75373. doi: 10.7554/eLife.75373.

Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia

Kherraf ZE, Cazin C, Bouker A, Fourati Ben Mustapha S, Hennebicq S, Septier A, Coutton…

Am J Hum Genet 2022 Mar 3;109(3):508-517. doi: 10.1016/j.ajhg.2022.01.011. Epub 2022 Feb 15

Biallelic mutations in ARMC2 lead to severe astheno-teratozoospermia due to sperm flagellum malformations (MMAF) in human and mouse

Coutton C., Martinez G., …Thierry-Mieg N., Arnoult C. * and Ray P.F.

American Journal of Human genetics 2019 104(2):331-340 IF 8.85 *co dernier auteur

CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.

Beurois J, Martinez G, …, Arnoult C, Ray PF, Coutton C.

Hum Reprod 2019 34(10): 2071-2079. IF 5.72

A homozygous ancestral SVA-insertion mediated deletion in WDR66 induces multiple morphological abnormalities of the sperm flagellum and male infertility

Kherraf Z.E., Amiri-Yekta A., …, Arnoult C., Bonhivers M. and Ray P.F.

American Journal of Human genetics 2018 103(3):400-412. doi: 10.1016/j.ajhg.2018.07.014 IF 10.36

Absence of cilia- and flagella-associated protein 69 (CFAP69) causes male infertility due to multiple morphological abnormalities of the flagella (MMAF) in human and mouse

Dong F.N., Amiri-Yekta A., …. Arnoult C., Touré A. , Ray P.F., Zhao H., Coutton…

American Journal of Human genetics 2018 102: 636-648. doi: 10.1016/j.ajhg.2018.03.007 IF IF 8.85

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

Coutton C, Vargas AS, …., Arnoult C, Ray PF.

Nature Comm 2018 9: 686-96. doi: 10.1038/s41467-017-02792-7* co dernier auteur IF 12.12

PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice

Christou-Kent M. , Zine-Eddine Kherraf Z-E, …. and Arnoult C.

EMBO Molecular Medicine 2018 10(5). pii: e8515. doi: 10.15252/emmm.201708515 IF 9.50

Whole-exome sequencing identifies mutations in the Fibrous Sheath Interaction Protein 2 (FSIP2) as a recurrent cause of multiple morphological abnormalities of the sperm flagella (MMAF)

Martinez G., Raoudha Zouari R., …., Arnoult C., Ray P.F., Coutton C.

Human reproduction 2018 33(10):1973-1984. doi: 10.1093/humrep/dey264 IF 5.00

SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes

Kherraf Z., Christou-Kent M., ….. and Arnoult C.

EMBO Molecular Medicine 2017 9:1132-1149. doi: 10.15252/emmm.201607461 IF 9.24