Li-bin Mei

发表

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

Zhong-xian Lu, Shaobin Lin, S. Kong, 2019, Molecular genetics & genomic medicine.

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population

Yanru Huang, Yuhua Shi, Xuemei He, 2021, Frontiers in Medicine.

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant

Ping Li, H. Ji, Zhiyong Ji, 2017, Oncotarget.

A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole‐exome sequencing

X. Xu, Ping Li, H. Ji, 2018, Clinical genetics.

Congenital Short-Bowel Syndrome Is Associated With a Novel Deletion Mutation in the CLMP Gene: Mutations in CLMP Caused CSBS

Li-bin Mei, Xin Lin, Yan-Aan Wu, 2022, Frontiers in Pediatrics.

A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF).

Ping Li, Li-bin Mei, Yan-Wei Sha, 2017, Gene.

Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF)

Zhong-xian Lu, Shaobin Lin, S. Kong, 2019, Journal of Medical Genetics.

Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype

Shaobin Lin, Y. Sha, Xianjing Huang, 2020, Journal of Human Genetics.

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

C. Yin, Shaobin Lin, Ping Li, 2018, Gene.

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella

Shaobin Lin, Y. Sha, Xianjing Huang, 2019, Annals of human genetics.

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Ping Li, Zhiyong Ji, Li-bin Mei, 2018, Gene.

A familial analysis of two brothers with azoospermia caused by maternal 46,Y, t(X; 1) (q28; q21) chromosomal abnormality

Y. Sha, Wensheng Liu, Li-bin Mei, 2020, Andrologia.

DNAH6 is a novel candidate gene associated with sperm head anomaly

X. Xu, C. Yin, C. Wang, 2018, Andrologia.

Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.

Yanru Huang, Xuemei He, Ping Li, 2021, Molecular medicine reports.

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.

Shenmin Yang, Xiaoyu Yang, Ping Li, 2017, Fertility and sterility.

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia

Xiong Wang, Shaobin Lin, Jing Chen, 2019, Systems biology in reproductive medicine.

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella

Weibing Qin, Yunge Tang, Zhong-xian Lu, 2019, Clinical genetics.

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

C. Yin, Xiong Wang, Chengrong Wang, 2018, Gene.

TSGA10 is a novel candidate gene associated with acephalic spermatozoa

X. Xu, X. Wang, Q. Zhang, 2018, Clinical genetics.

Novel IFT140 variants cause spermatogenic dysfunction in humans

Xiong Wang, Jiahui Wang, Li-bin Mei, 2019, Molecular genetics & genomic medicine.

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing

Shaobin Lin, Ping Li, Xianjing Huang, 2018, Systems Biology in Reproductive Medicine.

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint

Ping Li, Zhiyong Ji, Li-bin Mei, 2017, Asian journal of andrology.

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Shaobin Lin, Yulin Zhou, Ping Li, 2018, Gene.

Biallelic mutations in PMFBP1 cause acephalic spermatozoa

Xiong Wang, S. Kong, Jing Chen, 2018, Clinical genetics.

Turner syndrome with Xp deletions and rare endometrial abnormalities

Jing Chen, Yanru Huang, Xuemei He, 2021, Medicine.

Two novel biallelic mutations in PSMC3IP in a Chinese patient affected by primary ovarian insufficiency: case report and review of the literature

Yanru Huang, Xuemei He, Ping Li, 2020 .

Author response for "DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella (MMAF)"

Weibing Qin, Yunge Tang, Zhong-xian Lu, 2019 .

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection

Xiong Wang, H. Bao, Ping Li, 2018, Andrologia.

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

Xiaoyu Yang, Shaobin Lin, Ping Li, 2018, BMC Medical Genetics.

Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsy.

Yanru Huang, J. Chen, Shaobin Lin, 2019, Clinica chimica acta; international journal of clinical chemistry.