Area of research
Molecular Biology · Health, Toxicology and Mutagenesis
Research interest
Research interests include Effects and risks of endocrine disrupting chemicals, Epigenetics and DNA Methylation, Genetics, Aging, and Longevity in Model Organisms, and Pluripotent Stem Cells Research.
TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system
Metabolo-epigenetics: the interplay of metabolism and epigenetics during early germ cells development†
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation
Perinatal nicotine exposure‐induced transgenerational asthma: Effects of reexposure in F1 gestation
Diagnostic utility of transcriptome sequencing for rare Mendelian diseases
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
IRF2BPL Is Associated with Neurological Phenotypes
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder
The Memory of Environmental Chemical Exposure in C. elegans Is Dependent on the Jumonji Demethylases jmjd-2 and jmjd-3/utx-1
<i>Caenorhabditis elegans</i> as an emerging model system in environmental epigenetics
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3
Exposure to the BPA-Substitute Bisphenol S Causes Unique Alterations of Germline Function