Area of research
Public Health, Environmental and Occupational Health · Reproductive Medicine
Research interest
Research focused on Oocyte and Genetics, with related work in Embryonic stem cell, Phenotype, Infertility. Notable publications include 'Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest', 'Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility', and 'Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest'.
Single-cell multi-omics analysis reveals cellular subpopulations associated with relapse in high-risk B-ALL following intensified chemotherapy
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects
The impact of a previous tubal ectopic pregnancy on live birth and perinatal outcomes in vitrified-warmed cycles
Novel biallelic mutations in <i>MEI1:</i> expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development
Research Progress of Metal Fuel Motor Technology
Mutations in <i>NLRP2</i> and <i>NLRP5</i> cause female infertility characterised by early embryonic arrest
A pannexin 1 channelopathy causes human oocyte death
Homozygous mutations in <i>REC114</i> cause female infertility characterised by multiple pronuclei formation and early embryonic arrest
Assessment of a Novel Standardized Training System for Mandibular Contour Surgeries
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility
Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility
Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest
Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest
Novel mutations and structural deletions in<i>TUBB8</i>: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development
Dysmenorrhea and its severity are associated with increased uterine contractility and overexpression of oxytocin receptor (OTR) in women with symptomatic adenomyosis