HuGE Literature Finder
Records
1
-
10
| Genomic testing for copy number and single nucleotide variants in spermatogenic failure. Journal of assisted reproduction and genetics 2022 Jul . Hardy J, Pollock N, Gingrich T, Sweet P, Ramesh A, Kuong J, Basar A, Jiang H, Hwang K, Vukina J, Jaffe T, Olszewska M, Kurpisz M, Yatsenko A |
| Association of CATSPER1, SPATA16 and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian population. BMC medical genomics 2022 3 15 (1): 47. Behvarz Mohammadreza, Rahmani Seyyed Ali, Siasi Torbati Elham, Danaei Mehrabad Shahla, Bikhof Torbati Mary |
| Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia. Reproductive biology and endocrinology : RB&E 2022 4 20 (1): 63. Tang Dongdong, Li Kuokuo, Geng Hao, Xu Chuan, Lv Mingrong, Gao Yang, Wang Guanxiong, Yu Hui, Shao Zhongmei, Shen Qunshan, Jiang Hui, Zhang Xiansheng, He Xiaojin, Cao Yunx |
| A new TEX11 mutation causes azoospermia and testicular meiotic arrest. Asian journal of andrology 2021 3 23 (5): 510-515. Yu Xiao-Chen, Li Meng-Jing, Cai Fei-Fei, Yang Si-Jie, Liu Hong-Bin, Zhang Hao- |
| Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han Population. Frontiers in genetics 2021 10 12 741355. Ji Zhiyong, Yao Chencheng, Yang Chao, Huang Chuan, Zhao Liangyu, Han Xia, Zhu Zijue, Zhi Erlei, Liu Nachuan, Zhou Zhi, Li Zhe |
| Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Aug . Krausz Csilla, Riera-Escamilla Antoni, Moreno-Mendoza Daniel, Holleman Kaylee, Cioppi Francesca, Algaba Ferran, Pybus Marc, Friedrich Corinna, Wyrwoll Margot J, Casamonti Elena, Pietroforte Sara, Nagirnaja Liina, Lopes Alexandra M, Kliesch Sabine, Pilatz Adrian, Carrell Douglas T, Conrad Donald F, Ars Elisabet, Ruiz-Castañé Eduard, Aston Kenneth I, Baarends Willy M, Tüttelmann Fra |
| Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure. Asian journal of andrology 2020 Jul . Cannarella Rossella, Condorelli Rosita A, Paolacci Stefano, Barbagallo Federica, Guerri Giulia, Bertelli Matteo, La Vignera Sandro, Calogero Aldo |
| Development of a novel next-generation sequencing panel for diagnosis of quantitative spermatogenic impairment. Journal of assisted reproduction and genetics 2020 4 37 (4): 753-762. Rocca Maria Santa, Msaki Aichi, Ghezzi Marco, Cosci Ilaria, Pilichou Kalliopi, Celeghin Rudy, Foresta Carlo, Ferlin Alber |
| Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations. Andrology 2017 Jul 5 (4): 824-831. Nakamura S, Miyado M, Saito K, Katsumi M, Nakamura A, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Okada H, Hata K, Nakabayashi K, Okamura K, Ogata H, Matsubara Y, Ogata T, Nakai H, Fukami |
| Six polymorphisms in genes involved in DNA double-strand break repair and chromosome synapsis: association with male infertility. Systems biology in reproductive medicine 2015 61 (4): 187-93. Zhang Xiaohui, Ding Min, Ding Xianping, Li Tianjun, Chen Hongh |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 22, 2023
- Content source: