Kim Jenny

Autophagy genes in biology and disease

Targeting the RAS/RAF/MAPK pathway for cancer therapy: from mechanism to clinical studies

Expanding the SHOC2 mutation associated phenotype of noonan syndrome with loose anagen hair: Structural brain anomalies and myelofibrosis

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome