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Shuyan Tang
Shuyan Tang
在 fudan.edu.cn 的电子邮件经过验证
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引用次数
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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
2622017
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
1202020
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
1152019
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
862021
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
792020
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
702019
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
702019
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
552023
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
552019
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
452019
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
202020
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
192022
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
152020
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
142022
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
132019
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
122023
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
82023
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
72021
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
62023
Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism
J Zhang, SY Tang, XB Zhu, P Li, JQ Lu, JS Cong, LB Wang, F Zhang, Z Li
Asian Journal of Andrology 23 (3), 288, 2021
62021
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