Marjolein A.W. van den Boogert

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation

Jos C. Jansen, Sharita Timal, Monique van Scherpenzeel et al. · The American Journal of Human Genetics · 2016 · 89 citations · Full text

Autoimmune Disease, Disease Mechanism, Abnormal Glycosylation +9

N-Glycosylation Defects in Humans Lower Low-Density Lipoprotein Cholesterol Through Increased Low-Density Lipoprotein Receptor Expression

Marjolein A.W. van den Boogert, Lars Emil Larsen, Lubna Ali et al. · Circulation · 2019 · 37 citations · Full text

Defective Lipid Droplet–Lysosome Interaction Causes Fatty Liver Disease as Evidenced by Human Mutations in TMEM199 and CCDC115

Lars Emil Larsen, Marjolein A.W. van den Boogert, W. Alfredo Ríos‐Ocampo et al. · Cellular and Molecular Gastroenterology and Hepatology · 2021 · 28 citations · Full text

Common gene variants in ASGR1 gene locus associate with reduced cardiovascular risk in absence of pleiotropic effects

Lubna Ali, Arjen J. Cupido, Maaike Rijkers et al. · Atherosclerosis · 2020 · 19 citations · Full text

Reduced CETP glycosylation and activity in patients with homozygous B4GALT1 mutations

Marjolein A.W. van den Boogert, Cleo L. Crunelle, Lubna Ali et al. · Journal of Inherited Metabolic Disease · 2019 · 11 citations · Full text