Les publications :

Treatment of Mouse Sperm with a Non-Catalytic Mutant of PLA2G10 Reveals That PLA2G10 Improves In Vitro Fertilization through Both Its Enzymatic Activity and as Ligand of PLA2R1.

Abi Nahed R, Dhellemmes M, Payré C, Le Blévec E, Perrier JP, Hennebicq S, Escoffier…

Int J Mol Sci. 2022

When idiopathic male infertility is rooted in maternal malnutrition during the perinatal period in mice.

Muranishi Y, Parry L, Vachette-Dit-Martin M, Saez F, Coudy-Gandilhon C, Sauvanet P, Volle DH, Tournayre…

Biol Reprod 2022

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

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

Lorès P, Kherraf ZE, Amiri-Yekta A, Whitfield M, Daneshipour A, Stouvenel L, Cazin C, Cavarocchi…

Hum Genet. 2021

A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females

Corinne Loeuillet, Magali Dhellemmes, Caroline Cazin, Zine-Eddine Kherraf, Selima Fourati Ben Mustapha, Raoudha Zouari, Nicolas…

Clinical Genetics 2021

AFU and SALF recommendations for the evaluation of male infertility.

Huyghe E, Boitrelle F, Methorst C, Mieusset R, Ray PF, Akakpo W, Koscinski I, Chalas…

Prog Urol. 2021

Ankrd31 in Sperm and Epididymal Integrity.

Manfrevola F, Martinez G, Coutton C, Rocco D, Reynaud K, Le Vern Y, Froment P,…

Front Cell Dev Biol 2021

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.

Shen Q, Martinez G, Liu H, Beurois J, Wu H, Amiri-Yekta A, Liang D, Kherraf…

Hum Genet 2021

Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy.

Fatemi N, Salehi N, Pignata L, Palumbo P, Cubellis MV, Ramazanali F, Ray P, Varkiani…

J Med Genet 2021

CFAP61 is required for sperm flagellum formation and male fertility in human and mouse.

Liu S, Zhang J, Kherraf ZE, Sun S, Zhang X, Cazin C, Coutton C, Zouari…

Development 2021

Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B.

Cazin C, Neirijnck Y, Loeuillet C, Wehrli L, Kühne F, Lordey I, Mustapha SFB, Bouker…

Cells 2021

Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

Lorès P, Kherraf ZE, Amiri-Yekta A, Whitfield M, Daneshipour A, Stouvenel L, Cazin C, Cavarocchi…

Hum Genet. 2021