Maartje J. Geerlings

Monocarboxylate Transporter 1 Deficiency and Ketone Utilization

Peter M. van Hasselt, Sacha Ferdinandusse, Glen R. Monroe et al. · New England Journal of Medicine · 2014 · 118 citations · Full text

Genetics, Pathology, Molecular Genetics +18

Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation

Laura Lorés‐Motta, Constantin C. Paun, Jordi Corominas et al. · Ophthalmology · 2018 · 66 citations · Full text

Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration

Nicole T.M. Saksens, Maartje J. Geerlings, Bjorn Bakker et al. · JAMA Ophthalmology · 2016 · 61 citations · Full text

The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration

Maartje J. Geerlings, Mariann Kremlitzka, Bjorn Bakker et al. · JAMA Ophthalmology · 2016 · 53 citations · Full text

Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch’s Membrane

Jordi Corominas, Johanna M. Colijn, Maartje J. Geerlings et al. · Ophthalmology · 2018 · 43 citations · Full text