Richard J. Rodenburg

Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations

Luís C. López, Markus Schuelke, Catarina M. Quinzii et al. · The American Journal of Human Genetics · 2006 · 389 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts

A.J.M. Janssen, Frans J.M. Trijbels, R. C. A. Sengers et al. · Clinical Chemistry · 2007 · 361 citations · Full text

A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

Kornelia Neveling, Ilse Feenstra, Christian Gilissen et al. · Human Mutation · 2013 · 336 citations · Full text

Exome Sequencing, Genetics, Genetic Epidemiology +23

Iron Deficiency Impairs Contractility of Human Cardiomyocytes Through Decreased Mitochondrial Function

Martijn F. Hoes, Niels Grote Beverborg, Jan David Kijlstra et al. · European Journal of Heart Failure · 2018 · 315 citations · Full text

Microbial stimulation of different Toll-like receptor signalling pathways induces diverse metabolic programmes in human monocytes

Ekta Lachmandas, Lily Boutens, Jacqueline M. Ratter et al. · Nature Microbiology · 2016 · 304 citations

Inflammation, Toll-like Receptors, Different Toll-like Receptor +13