Area of research
Molecular Biology · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Biology, Embryonic stem cell, Induced pluripotent stem cell, Genetics, Aneuploidy, and Ploidy.
Predicting tumour resistance to paclitaxel and carboplatin utilising genome‐wide screening in haploid human embryonic stem cells
Genome-wide screening reveals essential roles for HOX genes and imprinted genes during caudal neurogenesis of human embryonic stem cells
Genome‐wide screen for anticancer drug resistance in haploid human embryonic stem cells
Generation, genomic characterization, and differentiation of triploid human embryonic stem cells
Genome-wide analysis of haploinsufficiency in human embryonic stem cells
The Chromatin Regulator ZMYM2 Restricts Human Pluripotent Stem Cell Growth and Is Essential for Teratoma Formation
Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells
FMR1 Reactivating Treatments in Fragile X iPSC-Derived Neural Progenitors In Vitro and In Vivo
Genome-wide Screen for Culture Adaptation and Tumorigenicity-Related Genes in Human Pluripotent Stem Cells
Derivation and differentiation of haploid human embryonic stem cells
Molecular Characterization of Down Syndrome Embryonic Stem Cells Reveals a Role for RUNX1 in Neural Differentiation
Genomic Instability in Human Pluripotent Stem Cells Arises from Replicative Stress and Chromosome Condensation Defects
Oncogenes create a unique landscape of fragile sites
Aneuploidy induces profound changes in gene expression, proliferation and tumorigenicity of human pluripotent stem cells
Comparable Frequencies of Coding Mutations and Loss of Imprinting in Human Pluripotent Cells Derived by Nuclear Transfer and Defined Factors
Selective Elimination of Human Pluripotent Stem Cells by an Oleate Synthesis Inhibitor Discovered in a High-Throughput Screen
The in vitro survival of human monosomies and trisomies as embryonic stem cells