Works matching AU Meng, Lanlan

Results: 38

Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermia.

Published in:

Journal of Assisted Reproduction & Genetics, 2025, v. 42, n. 5, p. 1601, doi. 10.1007/s10815-025-03480-y

By:

Wei, Chunjia;
Lu, Yingchi;
Yi, Sibing;
Liang, Yaoqiong;
Meng, Lanlan;
Tan, Chen;
Du, Juan;
Lin, Ge;
Tan, Yue-Qiu;
Gan, Xianyou;
Tu, Chaofeng;
Qin, Zailong

Publication type:

Article

Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 6, p. 1485, doi. 10.1007/s10815-024-03106-9

By:

Lu, Wenqing;
Li, Yong;
Meng, Lanlan;
Tan, Chen;
Nie, Hongchuan;
Zhang, Qianjun;
Song, Yuying;
Zhang, Huan;
Tan, Yue-Qiu;
Tu, Chaofeng;
Guo, Haichun;
Wu, Longxiang;
Du, Juan

Publication type:

Article

Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 5, p. 1297, doi. 10.1007/s10815-024-03087-9

By:

Zhao, Siyi;
Liu, Qiong;
Su, Lilan;
Meng, Lanlan;
Tan, Chen;
Wei, Chunjia;
Zhang, Huan;
Luo, Tao;
Zhang, Qianjun;
Tan, Yue-Qiu;
Tu, Chaofeng;
Chen, Houyang;
Gao, Xingcheng

Publication type:

Article

Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.

Published in:

2023

By:

Li, Yunhao;
Li, Yong;
Wang, Ying;
Meng, Lanlan;
Tan, Chen;
Du, Juan;
Tan, Yue-Qiu;
Nie, Hongchuan;
Zhang, Qianjun;
Lu, Guangxiu;
Lin, Ge;
Li, Huanzhu;
Zhang, Huan;
Tu, Chaofeng

Publication type:

Case Study

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 4, p. 811, doi. 10.1007/s10815-020-01735-4

By:

Wang, Ying;
Tu, Chaofeng;
Nie, Hongchuan;
Meng, Lanlan;
Li, Dongyan;
Wang, Weili;
Zhang, Huan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu;
Du, Juan

Publication type:

Article

Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature.

Published in:

2018

By:

Li, Haiyu;
Du, Juan;
Li, Wen;
Cheng, Dehua;
He, Wenbin;
Yi, Duo;
Xiong, Bo;
Yuan, Shimin;
Tu, Chaofeng;
Meng, Lanlan;
Luo, Aixiang;
Lin, Ge;
Lu, Guangxiu;
Tan, Yue-Qiu

Publication type:

Case Study

ZnCl<sub>2</sub>-Promoted One-Pot Three-Component Synthesis of Multisubstituted Thiazolo[4,5- b]pyridines and Thieno[2,3- b:4,5- b′]dipyridines.

Published in:

European Journal of Organic Chemistry, 2015, v. 2015, n. 3, p. 631, doi. 10.1002/ejoc.201403156

By:

Luo, Laichun;
Meng, Lanlan;
Peng, Yangqiu;
Xing, Yongning;
Sun, Qi;
Ge, Zemei;
Li, Runtao

Publication type:

Article

Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.

Published in:

2022

By:

Xie, Chunbo;
Wang, Weili;
Tu, Chaofeng;
Meng, Lanlan;
Lu, Guangxiu;
Lin, Ge;
Lu, Lin-Yu;
Tan, Yue-Qiu

Publication type:

journal article

Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect.

Published in:

SCIENCE CHINA Life Sciences, 2019, v. 62, n. 1, p. 144, doi. 10.1007/s11427-018-9329-3

By:

Meng, Lanlan;
Tu, Chaofeng;
Lu, Guangxiu;
Lin, Ge;
Tan, Yueqiu

Publication type:

Article

Diverse associations observed between pregnancy complications and RBC or plasma folates determined by an in-house developed LC-MS/MS method.

Published in:

Annals of Medicine, 2023, v. 55, n. 2, p. 1, doi. 10.1080/07853890.2023.2265381

By:

Xu, Zhengwen;
Li, Youran;
Liu, Ying;
Liu, Shengmin;
Zhang, Lin;
Wang, Jing;
Su, Shaofei;
Liu, Lin;
Meng, Lanlan;
Zhu, Hongyuan;
Sun, Jingru;
Shao, Lijun;
Li, Lin;
Zhai, Yanhong;
Li, Guanghui;
Cao, Zheng

Publication type:

Article

Delivery prediction by quantitative analysis of four steroid metabolites with liquid chromatography tandem mass spectrometry in asymptomatic pregnant women.

Published in:

Annals of Medicine, 2022, v. 54, n. 1, p. 1150, doi. 10.1080/07853890.2022.2067895

By:

Meng, Lanlan;
Su, Shaofei;
Li, Lin;
Liu, Shengmin;
Li, Youran;
Liu, Ying;
Lu, Yifan;
Xu, Zhengwen;
Liu, Lin;
He, Qixin;
Zheng, Yuanyuan;
Liu, Xiaowei;
Cong, Yuting;
Zhai, Yanhong;
Zhao, Zhen;
Cao, Zheng

Publication type:

Article

Establishment of trimester-specific reference intervals of serum lipids and the associations with pregnancy complications and adverse perinatal outcomes: a population-based prospective study.

Published in:

Annals of Medicine, 2021, v. 53, n. 1, p. 1632, doi. 10.1080/07853890.2021.1974082

By:

Lu, Yifan;
Jia, Zhaoxia;
Su, Shaofei;
Han, Lican;
Meng, Lanlan;
Tang, Guodong;
Wang, Jing;
Zhang, Chunhong;
Xie, Xin;
Zhang, Yi;
Zhang, Yue;
Zhai, Yanhong;
Cao, Zheng

Publication type:

Article

Establishment of trimester-specific reference intervals of serum lipids and the associations with pregnancy complications and adverse perinatal outcomes: a population-based prospective study.

Published in:

Annals of Medicine, 2021, v. 53, n. 1, p. 1632, doi. 10.1080/07853890.2021.1974082

By:

Yifan Lu;
Zhaoxia Jia;
Shaofei Su;
Lican Han;
Lanlan Meng;
Guodong Tang;
Jing Wang;
Chunhong Zhang;
Xin Xie;
Yi Zhang;
Yue Zhang;
Yanhong Zhai;
Zheng Cao

Publication type:

Article

An observational association study between maternal homocysteine and pregnancy complications or perinatal outcomes with established trimester-specific reference intervals in pregnant women.

Published in:

Laboratory Medicine, 2024, v. 55, n. 3, p. 355, doi. 10.1093/labmed/lmad092

By:

Tang, Guodong;
Su, Shaofei;
Lu, Yifan;
Meng, Lanlan;
Han, Lican;
Xu, Zhengwen;
Liu, Lin;
Zeng, Jiazi;
Chen, Lu;
Wang, Jing;
Zhang, Yue;
Zhai, Yanhong;
Cao, Zheng

Publication type:

Article

RNF216 regulates meiosis and PKA stability in the testes.

Published in:

FASEB Journal, 2021, v. 35, n. 4, p. 1, doi. 10.1096/fj.202002294RR

By:

Dengfeng Li;
Fangfang Li;
Lanlan Meng;
Huafang Wei;
Qianjun Zhang;
Fang Jiang;
Dan-Na Chen;
Wei Li;
Yue-Qiu Tan;
Jia-Da Li

Publication type:

Article

Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.

Published in:

Human Reproduction, 2023, v. 38, n. 7, p. 1399, doi. 10.1093/humrep/dead095

By:

Wang, Weili;
Su, Lilan;
Meng, Lanlan;
He, Jiaxin;
Tan, Chen;
Yi, Duo;
Cheng, Dehua;
Zhang, Huan;
Lu, Guangxiu;
Du, Juan;
Lin, Ge;
Zhang, Qianjun;
Tu, Chaofeng;
Tan, Yue-Qiu

Publication type:

Article

Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression.

Published in:

Cell Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41421-023-00580-w

By:

Tu, Chaofeng;
Wen, Junfei;
Wang, Weili;
Zhu, Qifan;
Chen, Ying;
Cheng, Jianglu;
Li, Zeye;
Meng, Lanlan;
Li, Yong;
He, Wenbin;
Tan, Chen;
Xie, Chunbo;
Fu, Shao-Mei;
Du, Juan;
Lu, Guangxiu;
Lin, Ge;
Gou, Lan-Tao;
Tan, Yue-Qiu

Publication type:

Article

Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly.

Published in:

Cell Discovery, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41421-021-00327-5

By:

Lu, Shuai;
Gu, Yayun;
Wu, Yifei;
Yang, Shenmin;
Li, Chenmeijie;
Meng, Lanlan;
Yuan, Wenwen;
Jiang, Tao;
Zhang, Xin;
Li, Yang;
Wang, Cheng;
Liu, Mingxi;
Ye, Lan;
Guo, Xuejiang;
Shen, Hongbing;
Yang, Xiaoyu;
Tan, Yueqiu;
Hu, Zhibin

Publication type:

Article

Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly.

Published in:

Cell Discovery, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41421-021-00327-5

By:

Lu, Shuai;
Gu, Yayun;
Wu, Yifei;
Yang, Shenmin;
Li, Chenmeijie;
Meng, Lanlan;
Yuan, Wenwen;
Jiang, Tao;
Zhang, Xin;
Li, Yang;
Wang, Cheng;
Liu, Mingxi;
Ye, Lan;
Guo, Xuejiang;
Shen, Hongbing;
Yang, Xiaoyu;
Tan, Yueqiu;
Hu, Zhibin

Publication type:

Article

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 10, p. 1730, doi. 10.1093/hmg/ddad013

By:

Liu, Yiyuan;
Li, Yuqian;
Meng, Lanlan;
Li, Kuokuo;
Gao, Yang;
Lv, Mingrong;
Guo, Rui;
Xu, Yuping;
Zhou, Ping;
Wei, Zhaolian;
He, Xiaojin;
Cao, Yunxia;
Wu, Huan;
Tan, Yueqiu;
Hua, Rong

Publication type:

Article

Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development.

Published in:

Human Molecular Genetics, 2022, v. 31, n. 2, p. 219, doi. 10.1093/hmg/ddab234

By:

Zhang, Guohui;
Li, Dongyan;
Tu, Chaofeng;
Meng, Lanlan;
Tan, Yueqiu;
Ji, Zhiliang;
Cheng, Jiao;
Lu, Guangxiu;
Lin, Ge;
Zhang, Huan;
Sun, Jinpeng;
Wang, Mingwei;
Du, Juan;
Xu, Wenming

Publication type:

Article

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 24, p. 2240, doi. 10.1093/hmg/ddab185

By:

Wang, Weili;
Tian, Shixong;
Nie, Hongchuan;
Tu, Chaofeng;
Liu, Chunyu;
Li, Yong;
Li, Dongyan;
Yang, Xiaoxuan;
Meng, Lanlan;
Hu, Tongyao;
Zhang, Qianjun;
Du, Juan;
Fan, Liqing;
Lu, Guangxiu;
Lin, Ge;
Zhang, Feng;
Tan, Yue-Qiu

Publication type:

Article

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 23, p. 2240, doi. 10.1093/hmg/ddab185

By:

Wang, Weili;
Tian, Shixong;
Nie, Hongchuan;
Tu, Chaofeng;
Liu, Chunyu;
Li, Yong;
Li, Dongyan;
Yang, Xiaoxuan;
Meng, Lanlan;
Hu, Tongyao;
Zhang, Qianjun;
Du, Juan;
Fan, Liqing;
Lu, Guangxiu;
Lin, Ge;
Zhang, Feng;
Tan, Yue-Qiu

Publication type:

Article

A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia.

Published in:

Clinical Genetics, 2024, v. 106, n. 1, p. 27, doi. 10.1111/cge.14500

By:

Luo, Chen;
Chen, Zixu;
Meng, Lanlan;
Tan, Chen;
He, Wenbin;
Tu, Chaofeng;
Du, Juan;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu;
Hu, Tong‐Yao

Publication type:

Article

Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype.

Published in:

Clinical Genetics, 2023, v. 103, n. 4, p. 495, doi. 10.1111/cge.14281

By:

He, Jiaxin;
Liu, Qiang;
Wang, Weili;
Su, Lilan;
Meng, Lanlan;
Tan, Chen;
Zhang, Huan;
Zhang, Qianjun;
Lu, Guangxiu;
Du, Juan;
Lin, Ge;
Tu, Chaofeng;
Tan, Yue‐Qiu

Publication type:

Article

Front Cover.

Published in:

Clinical Genetics, 2020, v. 97, n. 5, p. i, doi. 10.1111/cge.13758

By:

Tu, Chaofeng;
Wang, Ying;
Nie, Hongchuan;
Meng, Lanlan;
Wang, Weili;
Li, Yong;
Li, Dongyan;
Zhang, Huan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue‐Qiu;
Du, Juan

Publication type:

Article

An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family.

Published in:

Clinical Genetics, 2020, v. 97, n. 5, p. 741, doi. 10.1111/cge.13712

By:

Tu, Chaofeng;
Wang, Ying;
Nie, Hongchuan;
Meng, Lanlan;
Wang, Weili;
Li, Yong;
Li, Dongyan;
Zhang, Huan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue‐Qiu;
Du, Juan

Publication type:

Article

TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.

Published in:

Autophagy, 2021, v. 17, n. 11, p. 3848, doi. 10.1080/15548627.2021.1894058

By:

Tu, Chaofeng;
Li, Haiyu;
Liu, Xuyang;
Wang, Ying;
Li, Wei;
Meng, Lanlan;
Wang, Weili;
Li, Yong;
Li, Dongyan;
Du, Juan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu

Publication type:

Article

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.936264

By:

Yurong Wang;
Ling Liu;
Chen Tan;
Guiquan Meng;
Lanlan Meng;
Hongchuan Nie;
Juan Du;
Guang-Xiu Lu;
Ge Lin;
Wen-Bin He;
Yue-Qiu Tan

Publication type:

Article

DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice.

Published in:

2023

By:

Zhou, Shushu;
Yuan, Shimin;
Zhang, Jintao;
Meng, Lanlan;
Zhang, Xin;
Liu, Siyu;
Lu, Guangxiu;
Lin, Ge;
Liu, Mingxi;
Tan, Yue-Qiu

Publication type:

Letter

YTHDC2 manipulates anti-tumoral macrophage polarization and predicts favorable outcomes in triple negative breast cancer.

Published in:

NPJ Precision Oncology, 2025, p. 1, doi. 10.1038/s41698-025-00880-2

By:

Jin, Hao;
Zhang, Dongbo;
Ma, Yufan;
Meng, Lanlan;
Huang, Songyin;
Su, Hongjun;
Xu, Jiannan;
Yao, Yandan

Publication type:

Article

Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia.

Published in:

Molecular Human Reproduction, 2024, v. 30, n. 2, p. 1, doi. 10.1093/molehr/gaae002

By:

Yi, Sibing;
Wang, Weili;
Su, Lilan;
Meng, Lanlan;
Li, Yong;
Tan, Chen;
Liu, Qiang;
Zhang, Huan;
Fan, Liqing;
Lu, Guangxiu;
Hu, Liang;
Du, Juan;
Lin, Ge;
Tan, Yue-Qiu;
Tu, Chaofeng;
Zhang, Qianjun

Publication type:

Article

Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.

Published in:

Molecular Human Reproduction, 2022, v. 28, n. 6, p. 1, doi. 10.1093/molehr/gaac015

By:

Wang, Weili;
Meng, Lanlan;
He, Jiaxin;
Su, Lilan;
Li, Yong;
Tan, Chen;
Xu, Xilin;
Nie, Hongchuan;
Zhang, Huan;
Du, Juan;
Lu, Guangxiu;
Luo, Mengcheng;
Lin, Ge;
Tu, Chaofeng;
Tan, Yue-Qiu

Publication type:

Article

CEP112 coordinates translational regulation of essential fertility genes during spermiogenesis through phase separation in humans and mice.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52705-8

By:

Zhang, Xueguang;
Huang, Gelin;
Jiang, Ting;
Meng, Lanlan;
Li, Tongtong;
Zhang, Guohui;
Wu, Nan;
Chen, Xinyi;
Zhao, Bingwang;
Li, Nana;
Wu, Sixian;
Guo, Junceng;
Zheng, Rui;
Ji, Zhiliang;
Xu, Zhigang;
Wang, Zhenbo;
Deng, Dong;
Tan, Yueqiu;
Xu, Wenming

Publication type:

Article

Large-scale prospective serum metabolomic profiling reveals candidate predictive biomarkers for suspected preeclampsia patients.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-87905-9

By:

Cao, Yan;
Meng, Lanlan;
Wang, Yifei;
Zhao, Shenglong;
Zheng, Yuanyuan;
Ran, Rui;
Du, Jie;
Wu, Hongqiang;
Han, Jiaqi;
Xu, Zhengwen;
Lu, Yifan;
Liu, Lin;
Chen, Lu;
Wang, Jing;
Li, Youran;
Zhai, Yanhong;
Sun, Zhi;
Cao, Zheng

Publication type:

Article

Elevated levels of renal function tests conferred increased risks of developing various pregnancy complications and adverse perinatal outcomes: insights from a population-based cohort study.

Published in:

Clinical Chemistry & Laboratory Medicine, 2023, v. 61, n. 10, p. 1760, doi. 10.1515/cclm-2023-0104

By:

Xu, Zhengwen;
Yang, He S.;
Liu, Lin;
Meng, Lanlan;
Lu, Yifan;
Han, Lican;
Tang, Guodong;
Wang, Jing;
Chen, Lu;
Zhang, Yue;
Zhai, Yanhong;
Su, Shaofei;
Cao, Zheng

Publication type:

Article

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-52436-7

By:

Tu, Chaofeng;
Nie, Hongchuan;
Meng, Lanlan;
Yuan, Shimin;
He, Wenbin;
Luo, Aixiang;
Li, Haiyu;
Li, Wen;
Du, Juan;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu

Publication type:

Article

Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.

Published in:

Human Genetics, 2020, v. 139, n. 2, p. 257, doi. 10.1007/s00439-020-02110-0

By:

Tu, Chaofeng;
Nie, Hongchuan;
Meng, Lanlan;
Wang, Weili;
Li, Haiyu;
Yuan, Shimin;
Cheng, Dehua;
He, Wenbin;
Liu, Gang;
Du, Juan;
Gong, Fei;
Lu, Guangxiu;
Lin, Ge;
Zhang, Qianjun;
Tan, Yue-Qiu

Publication type:

Article