G. H. J. Boers

The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

S. Harvey Mudd, Flemming Skovby, Harvey L. Levy et al. · PubMed · 1985 · 1.3K citations

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

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia.

A.M.T. Engbersen, D. G. Franken, G. H. J. Boers et al. · PubMed · 1995 · 424 citations

Hyperhomocysteinaemia and endothelial dysfunction in young patients with peripheral arterial occlusive disease

M. van den Berg, G. H. J. Boers, D. G. Franken et al. · European Journal of Clinical Investigation · 1995 · 226 citations

Evidence for McKusick's hypothesis of deficient collagen cross-linking in patients with homocystinuria

Barbara Lubec, Susanne Fang-Kircher, T. Lubec et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1996 · 211 citations

Deficient Collagen Cross-linking, Autoimmune Disease, Pathology +3