Y. Tan

发表

Whole‐exome sequencing identifies a homozygous donor splice‐site mutation in STAG3 that causes primary ovarian insufficiency

H. Huang, G. Lin, Yueqiu Tan, 2018, Clinical genetics.

Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers.

G. Lin, K. Luo, De-Hua Cheng, 2013, Human reproduction.

Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts1

Xiuqing Zhang, Y. Liang, Hui Jiang, 2013, Biology of reproduction.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Y. Li, Yong-Gang Yao, Zhixi Su, 2023, American journal of human genetics.

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

G. Lin, De-Hua Cheng, Yueqiu Tan, 2018, Molecular Cytogenetics.

Differences between karyotypically normal and abnormal human embryonic stem cells

G. Lin, S. Yang, Y. Tan, 2010, Cell proliferation.

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA

L. Jin, Yunxia Cao, Huan Wu, 2023, Journal of Medical Genetics.

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

Yunxia Cao, Xiaojin He, G. Lin, 2021, American journal of human genetics.

C9orf131 and C10orf120 are not essential for male fertility in humans or mice.

G. Lin, Weili Wang, Y. Tan, 2023, Developmental biology.

Using SNP array to identify aneuploidy and segmental imbalance in translocation carriers

G. Lin, K. Luo, F. Gong, 2014, Genomics data.

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

G. Lin, Duo Yi, Weili Wang, 2023, Human reproduction.

Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella

G. Lin, L. Fan, Y. Tan, 2023, Frontiers in Cell and Developmental Biology.

A novel loss-of-function variant in PNLDC1 inducing oligo-astheno-teratozoospermia and male infertility

Xiong Wang, Y. Tan, Zhaoli Du, 2023, Asian journal of andrology.

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

G. Lin, Y. Tan, G. Lu, 2022, Journal of Assisted Reproduction and Genetics.

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice

Y. Liu, Chenyang Lu, Zhiping Tan, 2023, Frontiers of medicine.

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

Kuokuo Li, P. Zhou, Yiyuan Liu, 2023, Human molecular genetics.

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

Xiang-Dong Fu, Lan-Tao Gou, Mo-Fang Liu, 2023, Science China Life Sciences.

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

Lei Dai, Yongjia Yang, Yu Zheng, 2023, medRxiv.

Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia

Zheng Li, E. Zhi, Peng Li, 2023, Journal of Human Genetics.

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

Y. Tan, J. Du, C. Tu, 2024, Clinical genetics.

The landscape of RNA-binding proteins in mammalian spermatogenesis.

Qiuling Yue, Jie Xie, Ke Zheng, 2024, Science.