Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophyAngela Lek, Louis M. Kunkel, Vincent Ho et al.|Science Translational Medicine|2020Cited by 79
Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesisAnna Pakuła, Louis M. Kunkel, Angela Lek et al.|Human Molecular Genetics|2018Cited by 22
Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse modelQifei Li, Pankaj B. Agrawal, Jasmine Lin et al.|JCI Insight|2022Cited by 12