Hjörvar Pétursson

Common Sequence Variants in the <i>LOXL1</i> Gene Confer Susceptibility to Exfoliation Glaucoma

Kristinn P. Magnússon, Patrick Sulem, G. Bragi Walters et al. · Science · 2007 · 673 citations

A Genetic Risk Factor for Periodic Limb Movements in Sleep

Hreinn Stefánsson, David B. Rye, Andrew A. Hicks et al. · New England Journal of Medicine · 2007 · 613 citations · Full text

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Laurie Robak, Iris E. Jansen, Jeroen van Rooij et al. · Brain · 2017 · 440 citations · Full text

Genetics, Genetic Epidemiology, Variant Burden +16

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Suzanne Lesage, Valérie Drouet, Elisa Majounie et al. · The American Journal of Human Genetics · 2016 · 427 citations · Full text

Cell Autophagy, Mitophagy, Mitochondrial Function +7

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich et al. · Proceedings of the National Academy of Sciences · 2014 · 362 citations · Full text