William J. Monis

Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome

Patrick R. Blackburn, Xu Zhi, Kathleen E. Tumelty et al. · The American Journal of Human Genetics · 2018 · 167 citations · Full text

Ehlers-danlos Syndrome, Defective Collagen Assembly, Fibrosis +9

BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia

William J. Monis, Victor Faúndez, Gregory J. Pazour · The Journal of Cell Biology · 2017 · 74 citations · Full text

Molecular Biology, Cytoskeleton, Cellular Physiology +16

Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration

Jillian N. Pearring, Jovenal T. San Agustin, Christopher Gabriel et al. · PLoS Genetics · 2017 · 36 citations · Full text

Ocular Disease, Pathology, Cellular Physiology +17

Mechanisms of aortic carboxypeptidase-like protein secretion and identification of an intracellularly retained variant associated with Ehlers–Danlos syndrome

Neya Vishwanath, William J. Monis, Gwendolyn A. Hoffmann et al. · Journal of Biological Chemistry · 2020 · 21 citations · Full text