Lambert P. van den Heuvel

A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects?

N.M.J. van der Put, F. Gabreëls, E M Stevens et al. · The American Journal of Human Genetics · 1998 · 1.6K citations · Full text

Developmental Biology, Second Common Mutation, Neural-tube Defects +12

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

Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency

Marieke J. H. Coenen, Hana Antonická, Cristina Ugalde et al. · New England Journal of Medicine · 2004 · 192 citations · Full text

Mitophagy, Mitochondrial Biogenesis, Mitochondrial Function +15

Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins

Marina A. Schwab, Sven W. Sauer, Jürgen G. Okun et al. · Biochemical Journal · 2006 · 189 citations · Full text

Reconstructing the evolution of the mitochondrial ribosomal proteome

P. Smits, Jan A. M. Smeitink, Lambert P. van den Heuvel et al. · Nucleic Acids Research · 2007 · 183 citations · Full text

Genetics, Molecular Biology, Genomics +16