Young-In Chi

A Multi-Layered Computational Structural Genomics Approach Enhances Domain-Specific Interpretation of Kleefstra Syndrome Variants in EHMT1

B. Volkman, G. Lomberk, A. Mathison, 2023, bioRxiv.

Deep computational phenotyping of genomic variants impacting the SET domain of KMT2C reveal molecular mechanisms for their dysfunction

Jose Lizarraga Mazaba, B. Volkman, G. Lomberk, 2023, Frontiers in genetics.

A multi-layered computational structural genomics approach enhances domain-specific interpretation of Kleefstra syndrome variants in EHMT1

B. Volkman, G. Lomberk, A. Mathison, 2023, Computational and structural biotechnology journal.

Computational structural genomics and clinical evidence suggest BCKDK gain‐of‐function may cause a potentially asymptomatic maple syrup urine disease phenotype

J. S. Schwoerer, Young-In Chi, Raul Urrutia, 2024, JIMD reports.

Emergent properties of the lysine methylome reveal regulatory roles via protein interactions and histone mimicry.

G. Lomberk, A. Mathison, Young-In Chi, 2024, Epigenomics.