| 1 |
The mutation c.346-1G?>?A in SOHLH1 impairs sperm production in the homozygous but not in the heterozygous condition |
|
|
| Mohan Liu, Yihong Yang, Yan Wang, Suren Chen, Ying Shen |
|
| Human Molecular Genetics. 2021; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 2 |
Functional role of piRNAs in animal models and its prospects in aquaculture |
|
|
| Christy Lite,Vasisht Varsh Sridhar,Swati Sriram,Melita Juliet,Aziz Arshad,Jesu Arockiaraj |
|
| Reviews in Aquaculture. 2021; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 3 |
Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertility |
|
|
| Hela Bellil,Farah Ghieh,Emeline Hermel,Béatrice Mandon-Pepin,François Vialard |
|
| Basic and Clinical Andrology. 2021; 31(1) |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 4 |
Preconception genome medicine: current state and future perspectives to improve infertility diagnosis and reproductive and health outcomes based on individual genomic data |
|
|
| Antonio Capalbo,Maurizio Poli,Antoni Riera-Escamilla,Vallari Shukla,Miya Kudo Høffding,Csilla Krausz,Eva R Hoffmann,Carlos Simon |
|
| Human Reproduction Update. 2020; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 5 |
Novel compound heterozygous DNAAF2 mutations cause primary ciliary dyskinesia in a Han Chinese family |
|
|
| Minghan Sun,Yi Zhang,Yi JiyunYang,Yi Wang,Hao Tan,Hailian Wang,Tiantian Lei,Xiaojie Li,Xiaojian Zhang,Wen Xiong,Ke Dou,Yongxin Ma |
|
| Journal of Assisted Reproduction and Genetics. 2020; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 6 |
Kartagener syndrome |
|
|
| Bi-cui Liu,Ting-xuan Huang,Chun-Tao Liu |
|
| The American Journal of the Medical Sciences. 2020; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 7 |
Dyskinésies ciliaires primitives de l’enfant |
|
|
| S. Blanchon,J.F. Papon,N. Beydon,A. Tamalet,E. Escudier,M. Legendre,G. Thouvenin |
|
| Journal de Pédiatrie et de Puériculture. 2020; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 8 |
TEX15 is an essential executor of MIWI2-directed transposon DNA methylation and silencing |
|
|
| Theresa Schöpp,Ansgar Zoch,Rebecca V. Berrens,Tania Auchynnikava,Yuka Kabayama,Lina Vasiliauskaite,Juri Rappsilber,Robin C. Allshire,Dónal O’Carroll |
|
| Nature Communications. 2020; 11(1) |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 9 |
Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes |
|
|
| T. F. Araujo,C. Friedrich,C. H. P. Grangeiro,L. R. Martelli,J. D. Grzesiuk,J. Emich,M. J. Wyrwoll,S. Kliesch,A. L. Simões,F. Tüttelmann |
|
| Andrology. 2019; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 10 |
Loss-of-function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype |
|
|
| Yanwei Sha,Xiong Wang,JinTing Yuan,Xingshen Zhu,Zhiying Su,Xuequan Zhang,Xiaohui Xu,Xiaoli Wei |
|
| Clinical Genetics. 2019; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 11 |
Genetic causes of nonsyndromic forms of azoospermia and severe oligozoospermia in infertility men |
|
|
| O. A. Solovova,V. B. Chernykh |
|
| Andrology and Genital Surgery. 2019; 20(2): 16 |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 12 |
Novel
IFT140
variants cause spermatogenic dysfunction in humans |
|
|
| Xiong Wang,Yan-wei Sha,Wen-ting Wang,Yuan-qing Cui,Jie Chen,Wei Yan,Xiao-tao Hou,Li-bin Mei,Cui-cui Yu,Jiahui Wang |
|
| Molecular Genetics & Genomic Medicine. 2019; |
|
| [Pubmed] [Google Scholar] [DOI] |
|
| 13 |
SCSA results correlated with rate of motility reduction after ejaculation in Asthenozoospermia |
|
|
| Zohreh Moradian Fard,Majid Naghdi,Peyman Salehi,Seyedeh Zahra Shahrokhi,Ali Ajami,Mohammad Reza Deemeh,Mohammad Hassan Meshkibaf |
|
| Andrologia. 2018; : e13146 |
|
| [Pubmed] [Google Scholar] [DOI] |
|
