Mark Samuels

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

George Papanikolaou, Mark Samuels, E H Ludwig et al. · Nature Genetics · 2003 · 976 citations · Full text

Juvenile Hemochromatosis, Heme Homeostasis, Iron Metabolism +8

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

Johane M. Robitaille, Marcia L.E. MacDonald, Ajamete Kaykas et al. · Nature Genetics · 2002 · 473 citations

Ocular Disease, Vitreous Body, Familial Exudative Vitreoretinopathy +6

De novo mutations in the gene encoding the synaptic scaffolding protein <i>SHANK3</i> in patients ascertained for schizophrenia

Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière et al. · Proceedings of the National Academy of Sciences · 2010 · 379 citations · Full text

A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

Kirsten M. Timms, Susanne Wagner, Mark Samuels et al. · Human Genetics · 2004 · 313 citations

Lipid Disorder, Genetic Disorder, Genetics +7

[35] In Vitro transcription: Whole-cell extract

James L. Manley, Andrew Fire, Mark Samuels et al. · Methods in enzymology on CD-ROM/Methods in enzymology · 1983 · 307 citations

Transcription Regulation, Cell Biology, Whole-cell Extract +1