B F Meyer

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia

G. Morahan, N. Dzimiri, B. Meyer, 2017, Clinical genetics.

Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3.

M Kambouris, B. Meyer, S. Bohlega, 2000, American journal of human genetics.