Xenon Pharmaceuticals (Canada)

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee et al. · Nature Genetics · 1999 · 1.7K citations

Mendelian Disorder, Disease Mechanism, Genetic Disorder +13

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia

Cathryn M. Lewis, Douglas F. Levinson, Lesley H. Wise et al. · The American Journal of Human Genetics · 2003 · 1.1K citations · Full text

Psychiatry, Genetics, Schizophrenia +7

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

Mitoferrin is essential for erythroid iron assimilation

George Shaw, John J. Cope, Liangtao Li et al. · Nature · 2006 · 613 citations

Biochemistry, Iron Metabolism, Physiology +5

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