Defective Notch1 signaling in endothelial cells drives pathogenesis in a mouse model of Adams-Oliver syndrome. Journal of Clinical Investigation. 2025; 135(23).
The ALX4 dimer structure provides insight into how disease alleles impact function. Nature Communications. 2025; 16(1):4800.
Modelling a pathological GSX2 variant that selectively alters DNA binding reveals hypomorphic mouse brain defects. Disease Models & Mechanisms. 2025; 18(2).
Cooperative Gsx2-DNA binding requires DNA bending and a novel Gsx2 homeodomain interface. Nucleic Acids Research (NAR). 2024; 52(13):7987-8002.
Homeodomain complex formation and biomolecular condensates in Hox gene regulation. Seminars in Cell and Developmental Biology. 2024; 152-153:93-100.
Prediction of cooperative homeodomain DNA binding sites from high-throughput-SELEX data. Nucleic Acids Research (NAR). 2023; 51(12):6055-6072.
A Drosophila Su(H) model of Adams-Oliver Syndrome reveals cofactor titration as a mechanism underlying developmental defects. PLoS Genetics. 2022; 18(8):e1010335.
Olig2 defines a subset of neural stem cells that produce specific olfactory bulb interneuron subtypes in the subventricular zone of adult mice. Development. 2022; 149(5).
A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic Paraplegia. Movement Disorders. 2022; 37(2):375-383.