1. A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females. Issue 1 (1st June 2022) Authors: Loeuillet, Corinne; Dhellemmes, Magali; Cazin, Caroline; Kherraf, Zine‐Eddine; Fourati Ben Mustapha, Selima; Zouari, Raoudha; Thierry‐Mieg, Nicolas; Arnoult, Christophe; Ray, Pierre F. Journal: Clinical genetics Issue: Volume 102:Issue 1(2022) Page Start: 22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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) ↗
3. Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility. Issue 10 (11th March 2020) Authors: Martinez, Guillaume; Beurois, Julie; Dacheux, Denis; Cazin, Caroline; Bidart, Marie; Kherraf, Zine-Eddine; Robinson, Derrick R; Satre, Véronique; Le Gac, Gerald; Ka, Chandran; Gourlaouen, Isabelle; Fichou, Yann; Petre, Graciane; Dulioust, Emmanuel; Zouari, Raoudha; Thierry-Mieg, Nicolas; Touré, A... Journal: Journal of medical genetics Issue: Volume 57:Issue 10(2020) Page Start: 708 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Expanding the sperm phenotype caused by mutations in SPATA20: A novel splicing mutation in an infertile patient with partial globozoospermia. Issue 5 (10th January 2023) Authors: Martinez, Guillaume; Metzler‐Guillemain, Catherine; Cazin, Caroline; Kherraf, Zine‐Eddine; Paulmyer‐Lacroix, Odile; Arnoult, Christophe; Ray, Pierre F.; Coutton, Charles Journal: Clinical genetics Issue: Volume 103:Issue 5(2023) Page Start: 612 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetics of teratozoospermia: Back to the head. Issue 6 (December 2020) Authors: Beurois, Julie; Cazin, Caroline; Kherraf, Zine-Eddine; Martinez, Guillaume; Celse, Tristan; Touré, Aminata; Arnoult, Christophe; Ray, Pierre F.; Coutton, Charles Journal: Best practice & research Issue: Volume 34:Issue 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. 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) ↗
8. KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole. (April 2021) Authors: Fatemi, Nayeralsadat; Ray, Pierre F.; Ramezanali, Fariba; Shahani, Tina; Amiri-Yekta, Amir; Kherraf, Zine-Eddine; Cazin, Caroline; Almadani, Navid; Varkiani, Maryam; Sarmadi, Soheila; Sodeifi, Niloofar; Gourabi, Hamid; Biglari, Alireza; Totonchi, Mehdi Journal: European journal of obstetrics, gynecology, and reproductive biology Issue: Volume 259(2021) Page Start: 100 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Issue 5 (17th July 2019) Authors: Kherraf, Zine‐Eddine; Cazin, Caroline; Coutton, Charles; Amiri‐Yekta, Amir; Martinez, Guillaume; Boguenet, Magalie; Fourati Ben Mustapha, Selima; Kharouf, Mahmoud; Gourabi, Hamid; Hosseini, Seyedeh Hanieh; Daneshipour, Abbas; Touré, Aminata; Thierry‐Mieg, Nicolas; Zouari, Raoudha; Arnoult, Christ... Journal: Clinical genetics Issue: Volume 96:Issue 5(2019) Page Start: 394 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗