| Teratozoospermia: spotlight on the main genetic actors in the human C Coutton, J Escoffier, G Martinez, C Arnoult, PF Ray Human reproduction update 21 (4), 455-485, 2015 | 327 | 2015 |
| Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human C Coutton, AS Vargas, A Amiri-Yekta, ZE Kherraf, SF Ben Mustapha, ... Nature communications 9 (1), 686, 2018 | 196 | 2018 |
| Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus V Pierre, G Martinez, C Coutton, J Delaroche, S Yassine, C Novella, ... Development 139 (16), 2955-2965, 2012 | 189 | 2012 |
| The genetic architecture of morphological abnormalities of the sperm tail A Touré, G Martinez, ZE Kherraf, C Cazin, J Beurois, C Arnoult, PF Ray, ... Human Genetics 140 (1), 21-42, 2021 | 151 | 2021 |
| Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP J Escoffier, HC Lee, S Yassine, R Zouari, G Martinez, T Karaouzène, ... Human molecular genetics 25 (5), 878-891, 2016 | 150 | 2016 |
| Absence of CFAP69 causes male infertility due to multiple morphological abnormalities of the flagella in human and mouse FN Dong, A Amiri-Yekta, G Martinez, A Saut, J Tek, L Stouvenel, P Lorès, ... The American Journal of Human Genetics 102 (4), 636-648, 2018 | 135 | 2018 |
| Bi-allelic mutations in ARMC2 lead to severe astheno-teratozoospermia due to sperm flagellum malformations in humans and mice C Coutton, G Martinez, ZE Kherraf, A Amiri-Yekta, M Boguenet, A Saut, ... The American Journal of Human Genetics 104 (2), 331-340, 2019 | 132 | 2019 |
| Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injection C Wambergue, R Zouari, S Fourati Ben Mustapha, G Martinez, F Devillard, ... Human reproduction 31 (6), 1164-1172, 2016 | 115 | 2016 |
| Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella G Martinez, ZE Kherraf, R Zouari, S Fourati Ben Mustapha, A Saut, ... Human Reproduction 33 (10), 1973-1984, 2018 | 109 | 2018 |
| SPINK 2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes ZE Kherraf, M Christou‐Kent, T Karaouzene, A Amiri‐Yekta, G Martinez, ... EMBO Molecular Medicine 9 (8), 1132-1149, 2017 | 108 | 2017 |
| Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation J Escoffier, S Yassine, HC Lee, G Martinez, J Delaroche, C Coutton, ... MHR: Basic science of reproductive medicine 21 (2), 157-168, 2015 | 99 | 2015 |
| A homozygous ancestral SVA-insertion-mediated deletion in WDR66 induces multiple morphological abnormalities of the sperm flagellum and male infertility ZE Kherraf, A Amiri-Yekta, D Dacheux, T Karaouzène, C Coutton, ... The American Journal of Human Genetics 103 (3), 400-412, 2018 | 91 | 2018 |
| Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development S Yassine, J Escoffier, G Martinez, C Coutton, T Karaouzene, R Zouari, ... Mhr: Basic science of reproductive medicine 21 (2), 169-185, 2015 | 71 | 2015 |
| PATL 2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice M Christou‐Kent, ZE Kherraf, A Amiri‐Yekta, E Le Blévec, T Karaouzène, ... EMBO Molecular Medicine 10 (5), e8515, 2018 | 63 | 2018 |
| Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men L Ounis, A Zoghmar, C Coutton, L Rouabah, M Hachemi, D Martinez, ... Asian Journal of Andrology 17 (1), 68-73, 2015 | 56 | 2015 |
| Impact of Hodgkin or non-Hodgkin lymphoma and their treatments on sperm aneuploidy: a prospective study by the French CECOS network G Martinez, M Walschaerts, M Le Mitouard, R Borye, C Thomas, J Auger, ... Fertility and sterility 107 (2), 341-350. e5, 2017 | 53 | 2017 |
| Is cell-free DNA in spent embryo culture medium an alternative to embryo biopsy for preimplantation genetic testing? A systematic review S Brouillet, G Martinez, C Coutton, S Hamamah Reproductive biomedicine online 40 (6), 779-796, 2020 | 51 | 2020 |
| CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report J Beurois, G Martinez, C Cazin, ZE Kherraf, A Amiri-Yekta, N Thierry-Mieg, ... Human Reproduction 34 (10), 2071-2079, 2019 | 46 | 2019 |
| Genetics of teratozoospermia: Back to the head J Beurois, C Cazin, ZE Kherraf, G Martinez, T Celse, A Touré, C Arnoult, ... Best practice & research Clinical endocrinology & metabolism 34 (6), 101473, 2020 | 43 | 2020 |
| Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility G Martinez, J Beurois, D Dacheux, C Cazin, M Bidart, ZE Kherraf, ... Journal of Medical Genetics 57 (10), 708-716, 2020 | 42 | 2020 |
