Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella MB Khelifa, C Coutton, R Zouari, T Karaouzène, J Rendu, M Bidart, ... The American Journal of Human Genetics 94 (1), 95-104, 2014 | 426 | 2014 |
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 | 338 | 2015 |
Ca2+ Entry through Store-operated Channels in Mouse Sperm Is Initiated by Egg ZP3 and Drives the Acrosome Reaction CMB O'Toole, C Arnoult, A Darszon, RA Steinhardt, HM Florman Molecular biology of the cell 11 (5), 1571-1584, 2000 | 301 | 2000 |
Activation of mouse sperm T-type Ca2+ channels by adhesion to the egg zona pellucida C Arnoult, RA Cardullo, JR Lemos, HM Florman Proceedings of the National Academy of Sciences 93 (23), 13004-13009, 1996 | 299 | 1996 |
Control of the low voltage-activated calcium channel of mouse sperm by egg ZP3 and by membrane hyperpolarization during capacitation C Arnoult, IG Kazam, PE Visconti, GS Kopf, M Villaz, HM Florman Proceedings of the National Academy of Sciences 96 (12), 6757-6762, 1999 | 283 | 1999 |
A perspective on the control of mammalian fertilization by egg-activated ion channels in sperm: a tale of two channels HM Florman, C Arnoult, IG Kazam, C Li, CMB O'Toole Biology of Reproduction 59 (1), 12-16, 1998 | 239 | 1998 |
A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation R Harbuz, R Zouari, V Pierre, MB Khelifa, M Kharouf, C Coutton, ... The American Journal of Human Genetics 88 (3), 351-361, 2011 | 235 | 2011 |
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 | 209 | 2018 |
ZP3-dependent activation of sperm cation channels regulates acrosomal secretion during mammalian fertilization. C Arnoult, Y Zeng, HM Florman The Journal of cell biology 134 (3), 637-645, 1996 | 194 | 1996 |
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 | 190 | 2012 |
Genetic abnormalities leading to qualitative defects of sperm morphology or function PF Ray, A Toure, C Metzler‐Guillemain, MJ Mitchell, C Arnoult, C Coutton Clinical Genetics 91 (2), 217-232, 2017 | 169 | 2017 |
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 | 163 | 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 | 162 | 2016 |
Pharmacological properties of the T-type Ca2+ current of mouse spermatogenic cells C Arnoult, M Villaz, HM Florman Molecular pharmacology 53 (6), 1104-1111, 1998 | 156 | 1998 |
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion S Treves, C Franzini-Armstrong, L Moccagatta, C Arnoult, C Grasso, ... The Journal of cell biology 166 (4), 537-548, 2004 | 148 | 2004 |
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 | 143 | 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 | 138 | 2019 |
Bi-allelic DNAH8 variants lead to multiple morphological abnormalities of the sperm flagella and primary male infertility C Liu, H Miyata, Y Gao, Y Sha, S Tang, Z Xu, M Whitfield, C Patrat, H Wu, ... The American Journal of Human Genetics 107 (2), 330-341, 2020 | 129 | 2020 |
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations A Amiri-Yekta, C Coutton, ZE Kherraf, T Karaouzène, P Le Tanno, ... Human Reproduction, 1-9, 2016 | 128 | 2016 |
Voltage-dependent modulation of T-type calcium channels by protein tyrosine phosphorylation C Arnoult, JR Lemos, HM Florman The EMBO Journal 16 (7), 1593-1599, 1997 | 128 | 1997 |