Publications :

Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters.

Coudert A, Cazin C, Amiri-Yekta A, Fourati Ben Mustapha S, Zouari R, Bessonat J, Zoghmar…

J Genet Genomics. 2023

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans.

Cavarocchi E, Sayou C, Lorès P, Cazin C, Stouvenel L, El Khouri E, Coutton C,…

iScience 2023

New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.

Martinez G, Barbotin AL, Cazin C, Wehbe Z, Boursier A, Amiri-Yekta A, Daneshipour A, Hosseini…

Int J Mol Sci 2023

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function.

Dacheux D, Martinez G, Broster Reix C, Beurois J, Lores P, Tounkara M, Dupuy J,…

Elife 2023

OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum.

Celse T, Tingaud-Sequeira A, Dieterich K, Siegfried G, Lecaignec C, Bouneau L, Fannemel M, Salaun…

J Med Genet. 2023

Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy.

Boursier A, Boudry A, Mitchell V, Loyens A, Rives N, Moerman A, Thomas L, Escudier…

Reprod Biomed Online 2023

Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry.

Del Llano E, Perrin A, Morel F, Devillard F, Harbuz R, Satre V, Amblard F,…

Int J Mol Sci 2023

Understanding the genetics of human infertility.

Sang Q, Ray PF, Wang L.

Science 2023

3D time-lapse imaging of a mouse embryo using intensity diffraction tomography embedded inside a deep learning framework

Pierré W, Hervé L, Paviolo C, Mandula O, Remondiere V, Morales S, Grudinin S, Ray…

Appl Opt 2022

From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene.

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

Am J Hum Genet 2022

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice.

Cong J, Wang X, Amiri-Yekta A, Wang L, Kherraf ZE, Liu C, Cazin C, Tang…

J Med Genet. 2022

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.