Lin Li (L Li)

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 17

Top Venues

Andrologia

Journal of clinical laboratory analysis

Clinical genetics

Archives of gynecology and obstetrics

Capital Medical University Beijing Obstetrics and Gynecology Hospital

Tsinghua University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Capital Medical University Beijing Obstetrics and Gynecology Hospital Aug 08 2016

China

Assistant Professor :: Central Laboratory

Education History

Tsinghua University Aug 23 2011 - Jul 15 2016

China

PHD :: School of Life Sciences

China Agricultural University - Jul 01 2009

China

BSC :: College of Biological Sciences

Publications

Yiqiu Wei, Jingxuan Wang, Rui Qu, Weiqian Zhang, Yiling Tan, Yanwei Sha, Lin Li, Tailang Yin
Genetic mechanisms of fertilization failure and early embryonic arrest: a comprehensive review. Human reproduction update (2023)
Yuxi Ding, Zequn He, Yanwei Sha, Kehkooi Kee, Lin Li
Eif4enif1 haploinsufficiency disrupts oocyte mitochondrial dynamics and leads to subfertility. Development (Cambridge, England) 150 (23) (2023)
Shao-Wen Wu, Lin Li, Fan Feng, Li Wang, Yuan-Yuan Kong, Xiao-Wei Liu, Chenghong Yin
Whole-exome sequencing reveals POLR3B variants associated with progeria-related Wiedemann-Rautenstrauch syndrome. Italian journal of pediatrics 47 (1) (2021)
Bo Chen, Gengzhen Zhu, An Yan, Jing He, Yang Liu, Lin Li, Xuerui Yang, Chen Dong, Kehkooi Kee
IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene. PLoS genetics 17 (9) (2021)
Lin Li, Fan Feng, Yipeng Wang, Jianying Guo, Wentao Yue
Mutational effect of human CFAP43 splice-site variant causing multiple morphological abnormalities of the sperm flagella. Andrologia 52 (6) (2020)
Li-Jing Luo, Fan Feng, Sheng-Hui Li, Dan Lu, Lin Li, Qi Zhou
Sequence variant in the CDC42BPB gene is potentially associated with Mullerian duct anomalies. The journal of obstetrics and gynaecology research 46 (5) (2020)
Lin Zhang, Zheng Cao, Fan Feng, Ya-Nan Xu, Lin Li, Hong Gao
A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing. BMC medical genetics 21 (1) (2020)
Ming-Bao Ren, Xiao-Rui Chai, Lin Li, Xin Wang, Chenghong Yin
Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole-exome sequencing. Molecular genetics & genomic medicine 8 (3) (2020)
Zheng Cao, Jingrui Liu, Xin Xie, Sien Zhan, Wei Song, Shaowen Wu, Zheng Sun, Ying Dong, Guodong Tang, Yilin Liu, Lin Li, Min Shen, Yanhong Zhai, Jihua Zou, Xiaowei Liu
Lipidomic profiling of amniotic fluid and its application in fetal lung maturity prediction. Journal of clinical laboratory analysis 34 (4) (2019)
Minying Zhao, Fan Feng, Chunfang Chu, Wentao Yue, Lin Li
A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing. Journal of ovarian research 12 (1) (2019)
Lin Li, Jin-Qi Zhao, Chengrong Wang, Nan Yang, Li-Fei Gong, Hai-He Yang, Chenghong Yin, Yuan-Yuan Kong
Whole-exome sequencing as a powerful tool for identifying genetic causes in a patient with POLG-related disorders and phenylketonuria. The Journal of international medical research 47 (3) (2019)
Ying Ma, Yan Pei, Chenghong Yin, Yuxin Jiang, Jingjing Wang, Xiaofei Li, Lin Li, Karl Oliver Kagan, Qingqing Wu
Subchromosomal anomalies in small for gestational-age fetuses and newborns. Archives of gynecology and obstetrics 300 (3) (2019)
Hongyuan Zhu, Meng Wang, Ying Dong, Honghai Hu, Qiaoli Zhang, Chen Qiao, Xin Xie, Fei Fan, Jiazi Zeng, Yan Jia, Lu Chen, Jingrui Liu, Lin Li, Yanhong Zhai, Zhen Zhao, Min Shen, Zheng Cao
Detection of non-criteria autoantibodies in women without apparent causes for pregnancy loss. Journal of clinical laboratory analysis 33 (9) (2019)
Y-W Sha, Y-K Sha, Z-Y Ji, L-B Mei, L Ding, Q Zhang, P-P Qiu, S-B Lin, X Wang, P Li, X Xu, Lin Li
TSGA10 is a novel candidate gene associated with acephalic spermatozoa. Clinical genetics 93 (4) (2018)
Lin Li, Y-W Sha, X Xu, L-B Mei, P-P Qiu, Z-Y Ji, S-B Lin, Z-Y Su, C Wang, C Yin, P Li
DNAH6 is a novel candidate gene associated with sperm head anomaly. Andrologia (2018)
Dajung Jung, Jie Xiong, Min Ye, Xunsi Qin, Lin Li, Shunfeng Cheng, Mengyuan Luo, Jia Peng, Ji Dong, Fuchou Tang, Wei Shen, Martin M Matzuk, Kehkooi Kee
In vitro differentiation of human embryonic stem cells into ovarian follicle-like cells. Nature communications 8 (2017)
X Xu, Y-W Sha, L-B Mei, Z-Y Ji, P-P Qiu, H Ji, P Li, T Wang, Lin Li
A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole-exome sequencing. Clinical genetics 93 (2) (2017)

Lin Li.css-eqlu8i{font-size:small;padding-left:4px;} (L Li)

Publication Activity (10 Years)

Top Topics

Top Venues

Lin Li (L Li)