| Biallelic mutations in CFAP43 and CFAP44 cause male infertility with multiple morphological abnormalities of the sperm flagella S Tang, X Wang, W Li, X Yang, Z Li, W Liu, C Li, Z Zhu, L Wang, J Wang, ... The American Journal of Human Genetics 100 (6), 854-864, 2017 | 284 | 2017 |
| 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 | 145 | 2020 |
| Bi-Allelic mutations in TTC21A induce Asthenoteratospermia in humans and mice W Liu, X He, S Yang, R Zouari, J Wang, H Wu, ZE Kherraf, C Liu, ... The American Journal of Human Genetics 104 (4), 738-748, 2019 | 123 | 2019 |
| Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility C Liu, C Tu, L Wang, H Wu, BJ Houston, FK Mastrorosa, W Zhang, Y Shen, ... The American Journal of Human Genetics 108 (2), 309-323, 2021 | 105 | 2021 |
| Landscape of pathogenic mutations in premature ovarian insufficiency H Ke, S Tang, T Guo, D Hou, X Jiao, S Li, W Luo, B Xu, S Zhao, G Li, ... Nature Medicine, 1-10, 2023 | 96 | 2023 |
| Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility C Liu, M Lv, X He, Y Zhu, A Amiri-Yekta, W Li, H Wu, ZE Kherraf, W Liu, ... Journal of Medical Genetics 57 (1), 31-37, 2020 | 84 | 2020 |
| Bi-allelic mutations in TTC29 cause male subfertility with asthenoteratospermia in humans and mice C Liu, X He, W Liu, S Yang, L Wang, W Li, H Wu, S Tang, X Ni, J Wang, ... The American Journal of Human Genetics 105 (6), 1168-1181, 2019 | 80 | 2019 |
| Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility W Li, X He, S Yang, C Liu, H Wu, W Liu, M Lv, D Tang, J Tan, S Tang, ... Journal of human genetics 64 (1), 49-54, 2019 | 76 | 2019 |
| Rare variants in FANCA induce premature ovarian insufficiency X Yang, X Zhang, J Jiao, F Zhang, Y Pan, Q Wang, Q Chen, B Cai, S Tang, ... Human genetics 138 (11), 1227-1236, 2019 | 61 | 2019 |
| Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia. W Liu, H Wu, L Wang, X Yang, C Liu, X He, W Li, J Wang, Y Chen, ... Journal of genetics and genomics= Yi chuan xue bao 46 (1), 53, 2019 | 49 | 2019 |
| Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice J Cong, X Wang, A Amiri-Yekta, L Wang, ZE Kherraf, C Liu, C Cazin, ... Journal of Medical Genetics 59 (7), 710-718, 2022 | 24 | 2022 |
| Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause Q Chen, H Ke, X Luo, L Wang, Y Wu, S Tang, J Li, L Jin, F Zhang, Y Qin, ... Human Molecular Genetics 29 (16), 2698-2707, 2020 | 22 | 2020 |
| Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis J Cong, Y Yang, X Wang, Y Shen, HT Qi, C Liu, S Tang, S Wu, S Tian, ... Cell Discovery 8 (1), 23, 2022 | 19 | 2022 |
| Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility C Liu, Y Shen, S Tang, J Wang, Y Zhou, S Tian, H Wu, J Cong, X He, L Jin, ... Journal of Medical Genetics 60 (2), 137-143, 2023 | 17 | 2023 |
| Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies L Wang, Y Zhang, X Fu, S Dong, S Tang, N Zhang, C Song, N Yang, ... Cell Research 30 (1), 91-94, 2020 | 17 | 2020 |
| A genome‐wide association study identifies new genes associated with developmental dysplasia of the hip W Yan, Z Hao, S Tang, J Dai, L Zheng, P Yu, W Yan, X Han, X Xu, D Shi, ... Clinical genetics 95 (3), 345-355, 2019 | 14 | 2019 |
| Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA S Tian, C Tu, X He, L Meng, J Wang, S Tang, Y Gao, C Liu, H Wu, Y Zhou, ... Journal of Medical Genetics, 2023 | 13 | 2023 |
| Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models C Liu, W Si, C Tu, S Tian, X He, S Wang, X Yang, C Yao, C Li, ZE Kherraf, ... The American Journal of Human Genetics 110 (3), 516-530, 2023 | 12 | 2023 |
| Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants W Luo, H Ke, S Tang, X Jiao, Z Li, S Zhao, F Zhang, T Guo, Y Qin Journal of Ovarian Research 16 (1), 1-13, 2023 | 11 | 2023 |
| Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility C Liu, Y Shen, Q Shen, W Zhang, J Wang, S Tang, H Wu, S Tian, J Cong, ... Cells 10 (7), 1594, 2021 | 9 | 2021 |
Feng ZhangProfessor of Genetics, Fudan UniversityΗ διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα fudan.edu.cn