Frans J.M. Trijbels

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

Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease

Godfried H.J. Boers, Antony G.H. Smals, Frans J.M. Trijbels et al. · New England Journal of Medicine · 1985 · 740 citations

Vascular Disease, Genetics, Genetic Epidemiology +17

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Leo A. J. Kluijtmans, Lambertus P. van den Heuvel, G. H. J. Boers et al. · PubMed · 1996 · 660 citations · Full text

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

The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh Syndrome

Jan Loeffen, Ralf Triepels, Roel Smeets et al. · The American Journal of Human Genetics · 1998 · 282 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8