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- Lin, L. et al. Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin. Blood, Volume 106, 2884-2889, October, 2005
- Papanikolaou, G. et al. Hepcidin in iron overload disorders. Blood, Volume 105, 4103-4105, May, 2005
- MacDonald, ML. et al. Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity, Clinical Genetics, Volume 67, 363-366, April, 2005
- Delatycki, MB. et al. A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosis, Clinical Genetics, Volume 65, 378-383, May, 2004
- Lafreniere, RG. et al. Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates, American Journal of Human Genetics, Volume 74, 1064-1073, May, 2004
- Hovingh, GK. et al. A novel apoA-I mutation (L178P) leads to endothelial dysfunction, increased arterial wall thickness, and premature coronary artery disease, Journal of the American College of Cardiology, Volume 44, 1429-1435, October, 2004
- Papanikolaou, G. et al. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis, Nature Genetics, Volume 36, 77-82, January, 2004
- Hovingh, GK. et Al. The role of the ABCA1 transporter and cholesterol efflux in familial hypoalphalipoproteinemia, Journal of Lipid Research, Volume 44, 1251-1255, June, 2003
- Wellington, CL. et al. Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol, Journal of Lipid Research, Volume 43, 1939-1949, November, 2002
- Robitaille, J. et al. Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy, Nature Genetics, Volume 32, 326-330, October 1, 2002
- Attie, A. et al. Relationship between Stearoyl-CoA Desaturase Activity and Plasma Triglyceride in Human and Mouse Hypertriglyceridemia, Journal of Lipid Research, Volume 43, 1899-1907, August 16, 2002
- Ntambi, J. et al. Loss of stearoyl-CoA desaturase-1 function protects mice against adiposity, Proc. Natl. Acad. Sci., Volume 99, 11482-11486, August, 2002
- Singaraja, R. et al. Increased ABCA1 activity protects against atherosclerosis, Journal of Clinical Investigation, Volume 110, 35-42, July, 2002
- Cohen, P. et al. Role of Stearoyl-CoA Desaturase-1 in Leptin-Mediated Weight Loss, Science, Volume 297, 240-243, July 12, 2002
- Bu, L. et al. Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner contact, Nature Genetics, Volume 31, 276-278, July 2002
- Cossette, P. et al, Mutation of GABRA1 in autosomal dominant form of juvenile myoclonic epilepsy, Nature Genetics, Volume 31, 184-189, June 2002
- Clee, S.M. et al, Common Genetics Variation in ABCA1 Is Associated With Altered Lipoprotein Levels and a Modified Risk for Coronary Artery Disease, Circulation, Volume 103, 1198-1205, February 12, 2001
- Miyazaki, M. et al. A lipogenic diet in mice with a disruption of the stearoyl-CoA desaturase 1 gene reveals a stringent requirement of endogenous monosaturated fatty acids for triglyceride synthesis, Journal of Lipid Research, Volume 42, 1018-1024, 2001
- Nadler, S.T. et al. The expression of adipogenic genes is decreased in obesity and diabetes mellitus, PNAS, Volume 97, 11371-11376, October 10, 2000
- Miyazaki, M. et al. The Biosynthesis of Hepatic Cholesterol Esters and Triglycerides Is Impaired in Mice with a Disruption of the Gene for Stearoyl-CoA Desaturase 1*, The Journal of Biological Chemistry, Volume 275, 30132-30138, September 29, 2000
- Brooks-Wilson, A. et al. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency, Nature Genetics, Volume 22, 336-345, August 1999
- Scott, J. Good cholesterol news, Nature, Volume 400, 816-819, August 26, 1999
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