Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)Soohyun Kim, Hudson H. Freeze, Vibeke Westphal et al.|Journal of Clinical Investigation|2000Cited by 178
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)Gert Matthijs, Bryan Winchester, Els Schollen et al.|Human Mutation|2000Cited by 163
Two Proteins Modulating Transendothelial Migration of Leukocytes Recognize Novel Carboxylated Glycans on Endothelial CellsGeetha Srikrishna, Hudson H. Freeze, Ajit Varki et al.|The Journal of Immunology|2001Cited by 143
Ablation of Mouse Phosphomannose Isomerase (Mpi) Causes Mannose 6-Phosphate Accumulation, Toxicity, and Embryonic LethalityCharles DeRossi, Hudson H. Freeze, Lars Bode et al.|Journal of Biological Chemistry|2005Cited by 112
Reduced Heparan Sulfate Accumulation in Enterocytes Contributes to Protein-Losing Enteropathy in a Congenital Disorder of GlycosylationVibeke Westphal, Hudson H. Freeze, Simon Murch et al.|American Journal Of Pathology|2000Cited by 99