Works by Tan, Yue-Qiu

Results: 59

X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations.

Published in:

2019

By:

He, Wen‐Bin;
Du, Juan;
Xie, Ping‐Yuan;
Zhou, Shuang;
Zhang, Ya‐Xin;
Lu, Guang‐Xiu;
Lin, Ge;
Li, Wen;
Tan, Yue‐Qiu;
He, Wen-Bin;
Xie, Ping-Yuan;
Zhang, Ya-Xin;
Lu, Guang-Xiu;
Tan, Yue-Qiu

Publication type:

journal article

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

Extended application of PGT-M strategies for small pathogenic CNVs.

Published in:

Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 3, p. 739, doi. 10.1007/s10815-024-03028-6

By:

Hu, Xiao;
Wang, Weili;
Luo, Keli;
Dai, Jing;
Zhang, Yi;
Wan, Zhenxing;
He, Wenbin;
Zhang, Shuoping;
Yang, Lanlin;
Tan, Qin;
Li, Wen;
Zhang, Qianjun;
Gong, Fei;
Lu, Guangxiu;
Tan, Yue-Qiu;
Lin, Ge;
Du, Juan

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

The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 7, p. 1683, doi. 10.1007/s10815-022-02500-5

By:

Yuan, Shimin;
Guo, Liuliang;
Cheng, Dehua;
Li, Xiurong;
Hu, Hao;
Hu, Liang;
Lu, Guangxiu;
Lin, Ge;
Gong, Fei;
Tan, Yue-Qiu

Publication type:

Article

Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 3, p. 735, doi. 10.1007/s10815-020-02052-6

By:

Cheng, Dehua;
Hu, Liang;
Gong, Fei;
Yuan, Shimin;
Luo, Keli;
Wu, Xianhong;
Xie, Pingyuan;
Lu, Changfu;
Lu, Guangxiu;
Tan, Yue-Qiu;
Lin, Ge

Publication type:

Article

The genetic cause of intellectual deficiency and/or congenital malformations in two parental reciprocal translocation carriers and implications for assisted reproduction.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 1, p. 243, doi. 10.1007/s10815-020-01986-1

By:

Cheng, Dehua;
Yuan, Shimin;
Hu, Liang;
Yi, Duo;
Luo, Keli;
Gong, Fei;
Lu, Changfu;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu

Publication type:

Article

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

Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 12, p. 2533, doi. 10.1007/s10815-019-01611-w

By:

Cheng, Dehua;
Yuan, Shimin;
Yi, Duo;
Luo, Keli;
Xu, Fang;
Gong, Fei;
Lu, Changfu;
Lu, Guangxiu;
Lin, Ge;
Tan, Yue-Qiu

Publication type:

Article

Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby.

Published in:

2012

By:

Cheng, De-Hua;
Gong, Fei;
Lu, Chang-Fu;
Li, Lu-Yun;
Lu, Guang-Xiu;
Tan, Yue-Qiu

Publication type:

Report

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.

Published in:

Human Mutation, 2021, v. 42, n. 1, p. 31, doi. 10.1002/humu.24138

By:

Hu, Tong‐Yao;
Zhang, Huan;
Meng, Lan‐Lan;
Yuan, Shi‐Min;
Tu, Chao‐Feng;
Du, Juan;
Lu, Guang‐Xiu;
Lin, Ge;
Nie, Hong‐Chuan;
Tan, Yue‐Qiu

Publication type:

Article

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

Published in:

Human Reproduction Open, 2024, v. 2024, n. 1, p. 1, doi. 10.1093/hropen/hoae003

By:

Meng, Gui-Quan;
Wang, Yaling;
Luo, Chen;
Tan, Yu-Mei;
Li, Yong;
Tan, Chen;
Tu, Chaofeng;
Zhang, Qian-Jun;
Hu, Liang;
Zhang, Huan;
Meng, Lan-Lan;
Liu, Chun-Yu;
Deng, Leiyu;
Lu, Guang-Xiu;
Lin, Ge;
Du, Juan;
Tan, Yue-Qiu;
Sha, Yanwei;
Wang, Lingbo;
He, Wen-Bin

Publication type:

Article

Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies.

Published in:

Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00487-1

By:

Tan, Ya-Qi;
Tan, Yue-Qiu;
Cheng, De-Hua

Publication type:

Article

Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings.

Published in:

2018

By:

Luo, Aixiang;
Li, Haiyu;
Cheng, Dehua;
Du, Juan;
Lin, Ge;
Tan, Yue-Qiu;
Yuan, Shimin;
Zhang, Yang;
Yang, Chuanchun;
Zhang, Wenyong

Publication type:

Case Study

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

Tumor progression of culture-adapted human embryonic stem cells during long-term culture.

Published in:

Genes, Chromosomes & Cancer, 2008, v. 47, n. 8, p. 665, doi. 10.1002/gcc.20574

By:

Yang, Sheng;
Lin, Ge;
Tan, Yue-Qiu;
Zhou, Di;
Deng, Lei-Yu;
Cheng, De-Hua;
Luo, Shu-Wei;
Liu, Tian-Cheng;
Zhou, Xiao-Ying;
Sun, Zheng;
Xiang, Yang;
Chen, Tian-Ji;
Wen, Ji-Fang;
Lu, Guang-Xiu

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

A case of megalencephalic leukoencephalopathy with subcortical cysts type 1 was identified with a novel compound heterozygous alteration (c.135delC; c.423+2dupT) in China.

Published in:

Clinical Case Reports, 2017, v. 5, n. 6, p. 961, doi. 10.1002/ccr3.986

By:

Dai, Cong‐Ling;
He, Wen‐Bin;
Du, Juan;
Tan, Yue‐Qiu;
Lu, Guang‐Xiu;
Li, Wen

Publication type:

Article

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Published in:

SCIENCE CHINA Life Sciences, 2025, v. 68, n. 3, p. 777, doi. 10.1007/s11427-024-2757-7

By:

Zhou, Yiling;
Tu, Chaofeng;
Coutton, Charles;
Tang, Jianan;
Tian, Shixiong;
Tang, Shuyan;
Martinez, Guillaume;
Zhou, Dapeng;
Tebbakh, Célia;
Wang, Jiaxiong;
Zouari, Raoudha;
Zhou, Xuehai;
Ben Mustapha, Selima Fourati;
Wang, Xuemei;
Wu, Bangguo;
Geng, Xinyan;
Liu, Shuang;
Jin, Li;
Shi, Huijuan;
Tan, Yue-Qiu

Publication type:

Article

The PIWI-specific insertion module helps load longer piRNAs for translational activation essential for male fertility.

Published in:

SCIENCE CHINA Life Sciences, 2023, v. 66, n. 7, p. 1459, doi. 10.1007/s11427-023-2390-5

By:

Wang, Xin;
Lin, Di-Hang;
Yan, Yue;
Wang, An-Hui;
Liao, Jiaoyang;
Meng, Qian;
Yang, Wen-Qing;
Zuo, Heng;
Hua, Min-Min;
Zhang, Fengjuan;
Zhu, Hongwen;
Zhou, Hu;
Huang, Tian-Yu;
He, Rui;
Li, Guangyong;
Tan, Yue-Qiu;
Shi, Hui-Juan;
Gou, Lan-Tao;
Li, Dangsheng;
Wu, Ligang

Publication type:

Article

Non-invasive preimplantation genetic testing for conventional IVF blastocysts.

Published in:

2022

By:

Xie, Pingyuan;
Zhang, Shuoping;
Gu, Yifang;
Jiang, Bo;
Hu, Liang;
Tan, Yue-qiu;
Yao, Yaxin;
Tang, Yi;
Wan, Anqi;
Cai, Sufen;
Zou, Yangyun;
Lu, Guangxiu;
Wan, Cheng;
Gong, Fei;
Lu, Sijia;
Lin, Ge

Publication type:

journal article

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination.

Published in:

Human Reproduction, 2024, v. 39, n. 4, p. 849, doi. 10.1093/humrep/deae026

By:

Cheng, Dehua;
Lu, Chang-Fu;
Gong, Fei;
Du, Juan;
Yuan, Shimin;
Luo, Ke-Li;
Tan, Yue-Qiu;
Lu, Guang-Xiu;
Lin, Ge

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

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

XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans.

Published in:

Clinical Genetics, 2019, v. 95, n. 3, p. 442, doi. 10.1111/cge.13475

By:

Zhang, Ya‐Xin;
Li, Hai‐Yu;
Tu, Chaofeng;
He, Wen‐Bin;
Du, Juan;
Li, Wen;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu;
Yang, Yongjia

Publication type:

Article

Front Cover.

Published in:

Clinical Genetics, 2019, v. 95, n. 3, p. i, doi. 10.1111/cge.13520

By:

Zhang, Ya‐Xin;
Li, Hai‐Yu;
Tu, Chaofeng;
He, Wen‐Bin;
Du, Juan;
Li, Wen;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu;
Yang, Yongjia

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

Risk Factors Affecting Alternate Segregation in Blastocysts From Preimplantation Genetic Testing Cycles of Autosomal Reciprocal Translocations.

Published in:

Frontiers in Genetics, 2022, p. 1, doi. 10.3389/fgene.2022.880208

By:

Xie, Pingyuan;
Hu, Liang;
Peng, Yangqin;
Tan, Yue-qiu;
Luo, Keli;
Gong, Fei;
Lu, Guangxiu;
Lin, Ge

Publication type:

Article

Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients.

Published in:

PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0190776

By:

Gu, Yi-Fan;
Zhou, Qin-Wei;
Zhang, Shuo-Ping;
Lu, Chang-Fu;
Gong, Fei;
Tan, Yue-Qiu;
Lu, Guang-Xiu;
Lin, Ge

Publication type:

Article

Etiological analysis of neurodevelopmental disabilities: single-center eight-year clinical experience in south China.

Published in:

2011

By:

Guo, Li;
Li, Bing-Xiao;
Deng, Mei;
Wen, Fang;
Jiang, Jian-Hui;
Tan, Yue-Qiu;
Song, Yuan-Zong;
Liu, Zhen-Huan;
Zhang, Chun-Hua;
Kobayashi, Keiko;
Wang, Zi-Neng

Publication type:

Journal 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

A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 4, p. 1, doi. 10.1002/mgg3.1902

By:

Bai, Rui‐Qi;
He, Wen‐Bin;
Peng, Qian;
Shen, Su‐Hui;
Yu, Qian‐Qian;
Du, Juan;
Tan, Yue‐Qiu;
Wang, Yue‐Hong;
Liu, Bin‐Jie

Publication type:

Article

Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 5, p. 1, doi. 10.1002/mgg3.1662

By:

Hu, Xiao;
He, Wen‐Bin;
Zhang, Shuo‐Ping;
Luo, Ke‐Li;
Gong, Fei;
Dai, Jing;
Zhang, Yi;
Wan, Zhen‐Xing;
Li, Wen;
Yuan, Shi‐Min;
Tan, Yue‐Qiu;
Lu, Guang‐Xiu;
Lin, Ge;
Du, Juan

Publication type:

Article

Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 4, p. 1, doi. 10.1002/mgg3.1165

By:

Zhang, Ya‐Xin;
He, Wen‐Bin;
Xiao, Wen‐Juan;
Meng, Lan‐Lan;
Tan, Chen;
Du, Juan;
Lu, Guang‐Xiu;
Lin, Ge;
Tan, Yue‐Qiu

Publication type:

Article

Novel <italic>FOXL2</italic> mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 2, p. 261, doi. 10.1002/mgg3.366

By:

Yang, Xiao‐Wen;
He, Wen‐Bin;
Gong, Fei;
Li, Wen;
Li, Xiu‐Rong;
Zhong, Chang‐Gao;
Lu, Guang‐Xiu;
Lin, Ge;
Du, Juan;
Tan, Yue‐Qiu

Publication type:

Article

Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China.

Published in:

2019

By:

Meng, Lan-Lan;
Yuan, Shi-Min;
Tu, Chao-Feng;
Lin, Ge;
Lu, Guang-Xiu;
Tan, Yue-Qiu

Publication type:

Letter to the Editor

Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China.

Published in:

2018

By:

Meng, Lan-Lan;
Yuan, Shi-Min;
Tu, Chao-Feng;
Lin, Ge;
Lu, Guang-Xiu;
Tan, Yue-Qiu

Publication type:

Case Study

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

Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction.

Published in:

BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0693-7

By:

Xiao, Wen-Juan;
He, Wen-Bin;
Tan, Yue-Qiu;
Li, Wen;
Zhang, Qian-Jun;
Zhong, Chang-Gao;
Li, Xiu-Rong;
Hu, Liang;
Lu, Guang-Xiu;
Lin, Ge;
Du, Juan;
Zhao, Xiao-Meng

Publication type:

Article

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency.

Published in:

BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0525-9

By:

He, Wen-Bin;
Tan, Yue-Qiu;
Hu, Xiao;
Li, Wen;
Xiong, Bo;
Luo, Ke-Li;
Gong, Fei;
Lu, Guang-Xiu;
Lin, Ge;
Du, Juan

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