Soo‐Mi Park

Biomolecular condensates: organizers of cellular biochemistry

Molecular genetics of congenital nuclear cataract

The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity

Making Proteins in the Powerhouse

Mitochondrial dysfunction induces RNA interference in C. elegans through a pathway homologous to the mammalian RIG-I antiviral response

Functional mapping and annotation of genetic associations with FUMA

Phase Transition in Postsynaptic Densities Underlies Formation of Synaptic Complexes and Synaptic Plasticity

Cataracts

Liquid phase condensation in cell physiology and disease

X-linked cataract and Nance-Horan syndrome are allelic disorders

De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability

Pathogenic Mitochondrial t RNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease

De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability