Yue-Qiu Tan (Juan Du, Yueqiu Tan, Y-Q Tan)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 52

Top Topics

Binding Protein

Polycystic Kidney Disease

Acute Lymphoblastic Leukemia

Top Venues

Clinical genetics

Journal of medical genetics

Signal transduction and targeted therapy

Molecular human reproduction

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

Publications

Dehua Cheng, Chang-Fu Lu, Fei Gong, Juan Du, Shimin Yuan, Ke-Li Luo, Yue-Qiu Tan, Guang-Xiu Lu, Ge Lin
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. Human reproduction (Oxford, England) 39 (4) (2024)
Sibing Yi, Weili Wang, Lilan Su, Lanlan Meng, Yong Li, Chen Tan, Qiang Liu, Huan Zhang, Liqing Fan, Guangxiu Lu, Liang Hu, Juan Du, Ge Lin, Yue-Qiu Tan, Chaofeng Tu, Qianjun Zhang
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Molecular human reproduction (2024)
Han Gong, Peihe Zhang, Qiang Liu, Yuxuan Tian, Fuxin Chen, Siyi Qian, Chaofeng Tu, Yue-Qiu Tan, Xingming Hu, Bin Zhang
XRCC2 driven homologous recombination subtypes and therapeutic targeting in lung adenocarcinoma metastasis. NPJ precision oncology 8 (1) (2024)
Dehua Cheng, Hebatallah Ibrahim, Keli Luo, Yifan Gu, Pingyuan Xie, Yanqin Xiao, Jingpeng Cai, Xianhong Wu, Ge Lin, Yue-Qiu Tan, Liang Hu
Characterization of cryptic complex chromosome rearrangements in balanced chromosomal rearrangement carriers and their PGT-SR clinical outcome assessments. Scientific reports 14 (1) (2024)
Chen Luo, Zixu Chen, Lanlan Meng, Chen Tan, Wenbin He, Chaofeng Tu, Juan Du, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan, Tong-Yao Hu
A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Clinical genetics 106 (1) (2024)
Gui-Quan Meng, Yaling Wang, Chen Luo, Yu-Mei Tan, Yong Li, Chen Tan, Chaofeng Tu, Qian-Jun Zhang, Liang Hu, Huan Zhang, Lan-Lan Meng, Chun-Yu Liu, Leiyu Deng, Guang-Xiu Lu, Ge Lin, Juan Du, Yue-Qiu Tan, Yanwei Sha, Lingbo Wang, Wen-Bin He
Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice. Human reproduction open 2024 (1) (2024)
Sibing Yi, Weili Wang, Lilan Su, Lanlan Meng, Yong Li, Chen Tan, Qiang Liu, Huan Zhang, Liqing Fan, Guangxiu Lu, Liang Hu, Juan Du, Ge Lin, Yue-Qiu Tan, Chaofeng Tu, Qianjun Zhang
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Molecular human reproduction 30 (2) (2024)
Sibing Yi, Weili Wang, Lilan Su, Lanlan Meng, Yong Li, Chen Tan, Qiang Liu, Huan Zhang, Liqing Fan, Guangxiu Lu, Liang Hu, Juan Du, Ge Lin, Yue-Qiu Tan, Chaofeng Tu, Qianjun Zhang
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Molecular human reproduction 30 (2) (2024)
Dehua Cheng, Chang-Fu Lu, Fei Gong, Juan Du, Shimin Yuan, Ke-Li Luo, Yue-Qiu Tan, Guang-Xiu Lu, Ge Lin
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. Human reproduction (Oxford, England) 39 (4) (2024)
Han Gong, Peihe Zhang, Qiang Liu, Yuxuan Tian, Fuxin Chen, Siyi Qian, Chaofeng Tu, Yue-Qiu Tan, Xingming Hu, Bin Zhang
XRCC2 driven homologous recombination subtypes and therapeutic targeting in lung adenocarcinoma metastasis. NPJ precision oncology 8 (1) (2024)
Gui-Quan Meng, Yaling Wang, Chen Luo, Yu-Mei Tan, Yong Li, Chen Tan, Chaofeng Tu, Qian-Jun Zhang, Liang Hu, Huan Zhang, Lan-Lan Meng, Chun-Yu Liu, Leiyu Deng, Guang-Xiu Lu, Ge Lin, Juan Du, Yue-Qiu Tan, Yanwei Sha, Lingbo Wang, Wen-Bin He
Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice. Human reproduction open 2024 (1) (2024)
Chen Luo, Zixu Chen, Lanlan Meng, Chen Tan, Wenbin He, Chaofeng Tu, Juan Du, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan, Tong-Yao Hu
A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Clinical genetics (2024)
Dehua Cheng, Chang-Fu Lu, Fei Gong, Juan Du, Shimin Yuan, Ke-Li Luo, Yue-Qiu Tan, Guang-Xiu Lu, Ge Lin
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. Human reproduction (Oxford, England) (2024)
Yang Li, Yuanyuan Wang, Yue-Qiu Tan, Qiuling Yue, Yueshuai Guo, Ruoyu Yan, Lanlan Meng, Huicong Zhai, Lingxiu Tong, Zihan Yuan, Wu Li, Cuicui Wang, Shenglin Han, Sen Ren, Yitong Yan, Weixu Wang, Lei Gao, Chen Tan, Tongyao Hu, Hao Zhang, Liya Liu, Pinglan Yang, Wanyin Jiang, Yiting Ye, Huanhuan Tan, Yanfeng Wang, Chenyu Lu, Xin Li, Jie Xie, Gege Yuan, Yiqiang Cui, Bin Shen, Cheng Wang, Yichun Guan, Wei Li, Qinghua Shi, Ge Lin, Ting Ni, Zheng Sun, Lan Ye, Anastasios Vourekas, Xue-Jiang Guo, Mingyan Lin, Zheng Sun
The landscape of RNA-binding proteins in mammalian spermatogenesis. Science (New York, N.Y.) (2024)
Han Gong, Peihe Zhang, Qiang Liu, Yuxuan Tian, Fuxin Chen, Siyi Qian, Chaofeng Tu, Yue-Qiu Tan, Xingming Hu, Bin Zhang
XRCC2 driven homologous recombination subtypes and therapeutic targeting in lung adenocarcinoma metastasis. NPJ precision oncology 8 (1) (2024)
Jingpeng Zhao, Zhiyong Ji, Guiquan Meng, Jiaqiang Luo, Yuxiang Zhang, Ningjing Ou, Haowei Bai, Ruhui Tian, Erlei Zhi, Yuhua Huang, Nachuan Liu, Wenbin He, Yue-Qiu Tan, Zheng Li, Chencheng Yao, Peng Li
Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia. Journal of human genetics (2023)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics 103 (4) (2023)
Shixiong Tian, Chaofeng Tu, Xiao-Jin He, Lanlan Meng, Jiaxiong Wang, Shuyan Tang, Yang Gao, Chunyu Liu, Huan Wu, Yiling Zhou, Mingrong Lv, Jing Guo, Li Jin, Yunxia Cao, Dongdong Tang, Feng Zhang, Yue-Qiu Tan
Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA. Journal of medical genetics (2023)
Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan
DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice. Signal transduction and targeted therapy 8 (1) (2023)
Chaofeng Tu, Junfei Wen, Weili Wang, Qifan Zhu, Ying Chen, Jianglu Cheng, Zeye Li, Lanlan Meng, Yong Li, Wenbin He, Chen Tan, Chunbo Xie, Shao-Mei Fu, Juan Du, Guangxiu Lu, Ge Lin, Lan-Tao Gou, Yue-Qiu Tan
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression. Cell discovery 9 (1) (2023)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics 103 (4) (2023)
Weili Wang, Lilan Su, Lanlan Meng, Jiaxin He, Chen Tan, Duo Yi, Dehua Cheng, Huan Zhang, Guangxiu Lu, Juan Du, Ge Lin, Qianjun Zhang, Chaofeng Tu, Yue-Qiu Tan
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Human reproduction (Oxford, England) (2023)
Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan
DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice. Signal transduction and targeted therapy 8 (1) (2023)
Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan
DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice. Signal transduction and targeted therapy 8 (1) (2023)
Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan
DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice. Signal transduction and targeted therapy 8 (1) (2023)
Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan
DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice. Signal transduction and targeted therapy 8 (1) (2023)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics 103 (4) (2023)
Yiyuan Liu, Yuqian Li, Lanlan Meng, Kuokuo Li, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Xiaojin He, Yunxia Cao, Huan Wu, Yue-Qiu Tan, Rong Hua
Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia due to acrosomal hypoplasia and reduced progressive motility. Human molecular genetics (2023)
Tongyao Hu, Lanlan Meng, Chen Tan, Chen Luo, Wen-Bin He, Chaofeng Tu, Huan Zhang, Juan Du, Hongchuan Nie, Guang-Xiu Lu, Jing Guo, Yue-Qiu Tan
Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia. Journal of medical genetics (2022)
Chunbo Xie, Weili Wang, Chaofeng Tu, Lanlan Meng, Guangxiu Lu, Ge Lin, Lin-Yu Lu, Yue-Qiu Tan
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia. Human reproduction update 28 (6) (2022)
Weili Wang, Lanlan Meng, Jiaxin He, Lilan Su, Yong Li, Chen Tan, Xilin Xu, Hongchuan Nie, Huan Zhang, Juan Du, Guangxiu Lu, Mengcheng Luo, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice. Molecular human reproduction 28 (6) (2022)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics (2022)
Wen-Bin He, Wen-Juan Xiao, Cong-Ling Dai, Yu-Rong Wang, Xiu-Rong Li, Fei Gong, Lan-Lan Meng, Chen Tan, Si-Cong Zeng, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan, Hao Hu, Juan Du
RNA splicing analysis contributes to reclassifying variants of uncertain significance and improves the diagnosis of monogenic disorders. Journal of medical genetics 59 (10) (2022)
Rui-Qi Bai, Wen-Bin He, Qian Peng, Su-Hui Shen, Qian-Qian Yu, Juan Du, Yue-Qiu Tan, Yue-Hong Wang, Bin-Jie Liu
A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance. Molecular genetics & genomic medicine 10 (4) (2022)
Jiaxin He, Qiang Liu, Weili Wang, Lilan Su, Lanlan Meng, Chen Tan, Huan Zhang, Qianjun Zhang, Guangxiu Lu, Juan Du, Ge Lin, Chaofeng Tu, Yue-Qiu Tan
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clinical genetics (2022)
Chaofeng Tu, Haiyu Li, Xuyang Liu, Ying Wang, Wei Li, Lanlan Meng, Weili Wang, Yong Li, Dongyan Li, Juan Du, Guangxiu Lu, Ge Lin, Yue-Qiu Tan
TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation. Autophagy 17 (11) (2021)
Xiao Hu, Wen-Bin He, Shuo-Ping Zhang, Ke-Li Luo, Fei Gong, Jing Dai, Yi Zhang, Zhen-Xing Wan, Wen Li, Shi-Min Yuan, Yue-Qiu Tan, Guang-Xiu Lu, Ge Lin, Juan Du
Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism. Molecular genetics & genomic medicine 9 (5) (2021)
Chaofeng Tu, Ying Wang, Hongchuan Nie, Lanlan Meng, Weili Wang, Yong Li, Dongyan Li, Huan Zhang, Guangxiu Lu, Ge Lin, Yue-Qiu Tan, Juan Du
An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family. Clinical genetics 97 (5) (2020)
Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Weili Wang, Haiyu Li, Shimin Yuan, Dehua Cheng, Wenbin He, Gang Liu, Juan Du, Fei Gong, Guangxiu Lu, Ge Lin, Qianjun Zhang, Yue-Qiu Tan
Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD. Human genetics 139 (2) (2020)
Wen-Bin He, Chen Tan, Ya-Xin Zhang, Lan-Lan Meng, Fei Gong, Guang-Xiu Lu, Ge Lin, Juan Du, Yue-Qiu Tan
Homozygous variants in SYCP2L cause premature ovarian insufficiency. Journal of medical genetics 58 (3) (2020)
Tong-Yao Hu, Huan Zhang, Lan-Lan Meng, Shi-Min Yuan, Chao-Feng Tu, Juan Du, Guang-Xiu Lu, Ge Lin, Hong-Chuan Nie, Yue-Qiu Tan
Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility. Human mutation 42 (1) (2020)
Ya-Xin Zhang, Wen-Bin He, Wen-Juan Xiao, Lan-Lan Meng, Chen Tan, Juan Du, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan
Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency. Molecular genetics & genomic medicine 8 (4) (2020)
Wen-Bin He, Juan Du, Ping-Yuan Xie, Shuang Zhou, Ya-Xin Zhang, Guang-Xiu Lu, Ge Lin, Wen Li, Yue-Qiu Tan
X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations. Prenatal diagnosis 39 (8) (2019)
Weili Wang, Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Yong Li, Shimin Yuan, Qianjun Zhang, Juan Du, Junpu Wang, Fei Gong, Liqing Fan, Guang-Xiu Lu, Jing Guo, Yue-Qiu Tan
Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations. Journal of medical genetics 56 (11) (2019)
Wen-Bin He, Wen-Juan Xiao, Yue-Qiu Tan, Xiao-Meng Zhao, Wen Li, Qian-Jun Zhang, Chang-Gao Zhong, Xiu-Rong Li, Liang Hu, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan
Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction. BMC medical genetics 19 (1) (2018)
Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Juan Du, Yang Zhang, Chuanchun Yang, Ge Lin, Wenyong Zhang, Yue-Qiu Tan
Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings. Molecular cytogenetics 11 (2018)
Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, Yue-Qiu Tan
Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature. Molecular cytogenetics 11 (2018)
Lan-Lan Meng, Shi-Min Yuan, Chao-Feng Tu, Ge Lin, Guang-Xiu Lu, Yue-Qiu Tan
Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China. Annals of hematology 98 (1) (2018)
Wen-Bin He, Yue-Qiu Tan, Xiao Hu, Wen Li, Bo Xiong, Ke-Li Luo, Fei Gong, Guang-Xiu Lu, Ge Lin, Yue-Qiu Tan
Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency. BMC medical genetics 19 (1) (2018)
Xiao-Wen Yang, Wen-Bin He, Fei Gong, Wen Li, Xiu-Rong Li, Chang-Gao Zhong, Guang-Xiu Lu, Ge Lin, Juan Du, Yue-Qiu Tan
Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency. Molecular genetics & genomic medicine 6 (2) (2018)
Ya-Xin Zhang, Hai-Yu Li, Wen-Bin He, Chaofeng Tu, Juan Du, Wen Li, Guang-Xiu Lu, Ge Lin, Yongjia Yang, Yue-Qiu Tan
XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans. Clinical genetics 95 (3) (2018)
W-B He, S Banerjee, L-L Meng, J Du, F Gong, H Huang, X-X Zhang, Y-Y Wang, G-X Lu, G Lin, Yue-Qiu Tan
Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency. Clinical genetics 93 (2) (2017)