Area of research
Genetics · Neurology
Research interest
Research interests include Biology, Histone H3, Histone, Epigenetics, Cancer research, and ATRX.
FOXR2 Targets LHX6+/DLX+ Neural Lineages to Drive Central Nervous System Neuroblastoma
Single substitution in H3.3G34 alters DNMT3A recruitment to cause progressive neurodegeneration
K27M in canonical and noncanonical H3 variants occurs in distinct oligodendroglial cell lineages in brain midline gliomas
Histone H3.3G34-Mutant Interneuron Progenitors Co-opt PDGFRA for Gliomagenesis
H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
Pervasive H3K27 Acetylation Leads to ERV Expression and a Therapeutic Vulnerability in H3K27M Gliomas
Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors
Abstract LB-019: FGFR1 abnormalities in seizure-associated familial and sporadic dysembryoplastic neuroepithelial tumors
Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
Specific detection of methionine 27 mutation in histone 3 variants (H3K27M) in fixed tissue from high-grade astrocytomas
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas
Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma
K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas
Frequent ATRX mutations and loss of expression in adult diffuse astrocytic tumors carrying IDH1/IDH2 and TP53 mutations
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