1. Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice. Issue 2 (9th September 2019) Authors: Li, Weiyu; Wu, Huan; Li, Fuping; Tian, Shixiong; Kherraf, Zine-Eddine; Zhang, Jintao; Ni, Xiaoqing; Lv, Mingrong; Liu, Chunyu; Tan, Qing; Shen, Ying; Amiri-Yekta, Amir; Cazin, Caroline; Zhang, Jingjing; Liu, Wangjie; Zheng, Yan; Cheng, Huiru; Wu, Yingbi; Wang, Jiajia; Gao, Yang Journal: Journal of medical genetics Issue: Volume 57:Issue 2(2020) Page Start: 89 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report. Issue 3 (18th December 2020) Authors: Arafah, Karim; Lopez, Fabrice; Cazin, Caroline; Kherraf, Zine-Eddine; Tassistro, Virginie; Loundou, Anderson; Arnoult, Christophe; Thierry-Mieg, Nicolas; Bulet, Philippe; Guichaoua, Marie-Roberte; Ray, Pierre F Journal: Human reproduction Issue: Volume 36:Issue 3(2021) Page Start: 693 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. (22nd January 2018) Authors: Lorès, Patrick; Coutton, Charles; El Khouri, Elma; Stouvenel, Laurence; Givelet, Maëlle; Thomas, Lucie; Rode, Baptiste; Schmitt, Alain; Louis, Bruno; Sakheli, Zeinab; Chaudhry, Marhaba; Fernandez-Gonzales, Angeles; Mitsialis, Alex; Dacheux, Denis; Wolf, Jean-Philippe; Papon, Jean-François; Gacon,... Journal: Human molecular genetics Issue: Volume 27:Number 7(2018:Apr. 01) Page Start: 1196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice. Issue 7 (4th August 2021) Authors: Cong, Jiangshan; Wang, Xiong; Amiri-Yekta, Amir; Wang, Lingbo; Kherraf, Zine-Eddine; Liu, Chunyu; Cazin, Caroline; Tang, Shuyan; Hosseini, Seyedeh Hanieh; Tian, Shixiong; Daneshipour, Abbas; Wang, Jiaxiong; Zhou, Yiling; Zeng, Yuyan; Yang, Shenmin; He, Xiaojin; Li, Jinsong; Cao, Yunxia; Jin, Li; ... Journal: Journal of medical genetics Issue: Volume 59:Issue 7(2022) Page Start: 710 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome and recurrent intrauterine fetal death. Issue 9982 (23rd May 2015) Authors: Vasiljevic, Alexandre; Poreau, Brice; Bouvier, Raymonde; Lachaux, Alain; Arnoult, Christophe; Fauré, Julien; Cordier, Marie Pierre; Ray, Pierre F Journal: Lancet Issue: Volume 385:Issue 9982(2015) Page Start: 2120 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice. Issue 5 (16th April 2018) Authors: Christou‐Kent, Marie; Kherraf, Zine‐Eddine; Amiri‐Yekta, Amir; Le Blévec, Emilie; Karaouzène, Thomas; Conne, Béatrice; Escoffier, Jessica; Assou, Said; Guttin, Audrey; Lambert, Emeline; Martinez, Guillaume; Boguenet, Magalie; Fourati Ben Mustapha, Selima; Cedrin Durnerin, Isabelle; Halouani, Lazh... Journal: EMBO molecular medicine Issue: Volume 10:Issue 5(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans. Issue 7 (7th March 2017) Authors: Le Tanno, Pauline; Breton, Julie; Bidart, Marie; Satre, Véronique; Harbuz, Radu; Ray, Pierre F; Bosson, Caroline; Dieterich, Klaus; Jaillard, Sylvie; Odent, Sylvie; Poke, Gemma; Beddow, Rachel; Digilio, Maria Christina; Novelli, Antonio; Bernardini, Laura; Pisanti, Maria Antonietta; Mackenroth, L... Journal: Journal of medical genetics Issue: Volume 54:Issue 7(2017) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Slo3 K+ channel blocker clofilium extends bull and mouse sperm-fertilizing competence. Issue 6 (December 2018) Authors: Abi Nahed, Roland; Martinez, Guillaume; Hograindleur, Jean Pascal; Le Blévec, Emilie; Camugli, Sabine; Le Boucher, Richard; Ray, Pierre F; Escoffier, Jessica; Schmitt, Eric; Arnoult, Christophe Journal: Reproduction Issue: Volume 156:Issue 6(2018) Page Start: 463 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes. Issue 8 (29th May 2017) Authors: Kherraf, Zine‐Eddine; Christou‐Kent, Marie; Karaouzene, Thomas; Amiri‐Yekta, Amir; Martinez, Guillaume; Vargas, Alexandra S; Lambert, Emeline; Borel, Christelle; Dorphin, Béatrice; Aknin‐Seifer, Isabelle; Mitchell, Michael J; Metzler‐Guillemain, Catherine; Escoffier, Jessica; Nef, Serge; Grepilla... Journal: EMBO molecular medicine Issue: Volume 9:Issue 8(2017) Page Start: 1132 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The sperm-associated antigen 6 interactome and its role in spermatogenesis. Issue 2 (August 2019) Authors: Liu, Yunhao; Zhang, Ling; Li, Wei; Huang, Qian; Yuan, Shuo; Li, Yuhong; Liu, Junpin; Zhang, Shiyang; Pin, Guanglun; Song, Shizhen; Ray, Pierre F; Arnoult, Christophe; Cho, Chunghee; Garcia-Reyes, Balbina; Knippschild, Uwe; Strauss, Jerome F; Zhang, Zhibing Journal: Reproduction Issue: Volume 158:Issue 2(2019) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗