Hutchinson-Gilford progeria syndrome von Pollex, RL, Hegele, RA

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Clinical and genetic associations with hypertriglyceridemic waist in a Canadian aboriginal population von Pollex, R L, Hanley, A J G, Zinman, B, Harris, S B, Hegele, R A

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Polygenic determinants of severe hypertriglyceridemia von Wang, Jian, Ban, Matthew R., Zou, Guang Yong, Cao, Henian, Lin, Tim, Kennedy, Brooke A., Anand, Sonia, Yusuf, Salim, Huff, Murray W., Pollex, Rebecca L., Hegele, Robert A.

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Synergism between mutant HNF1A and the metabolic syndrome in Oji-Cree Type 2 diabetes von Pollex, R. L., Hanley, A. J. G., Zinman, B., Harris, S. B., Khan, H. M. R., Hegele, R. A.

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Complex Trait Locus Linkage Mapping in Atherosclerosis: Time to Take a Step Back Before Moving Forward? von Pollex, Rebecca L, Hegele, Robert A

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Genetic and physiological insights into the metabolic syndrome von Hegele, Robert A, Pollex, Rebecca L

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Metabolic syndrome in aboriginal Canadians: Prevalence and genetic associations von Pollex, Rebecca L., Hanley, Anthony J.G., Zinman, Bernard, Harris, Stewart B., Khan, Hafiz M.R., Hegele, Robert A.

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Uncloaking the Genetic Determinants of Metabolic Syndrome von Lahiry, Piya, Pollex, Rebecca L., Hegele, Robert A.

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Longitudinal Differences in Familial Combined Hyperlipidemia Quantitative Trait Loci von Pollex, Rebecca L, Hegele, Robert A

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The metabolic syndrome in Inuit von Pollex, Rebecca L, Khan, Hafiz M R, Connelly, Philip W, Young, T Kue, Hegele, Robert A

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Genetic determinants of statin intolerance von Oh, Jisun, Ban, Matthew R, Miskie, Brooke A, Pollex, Rebecca L, Hegele, Robert A

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Quantitative examination of isometric tongue protrusion forces in children with oro‐facial dysfunctions or myofunctional disorders von Rohrbach, S., Buettner, F., Pollex, D., Mathmann, P., Weinhold, L., Schubert, R., Reilmann, R.

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Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample von Al-Attar, Salam A, Pollex, Rebecca L, Ban, Matthew R, Young, T Kue, Bjerregaard, Peter, Anand, Sonia S, Yusuf, Salim, Zinman, Bernard, Harris, Stewart B, Hanley, Anthony Jg, Connelly, Philip W, Huff, Murray W, Hegele, Robert A

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Resequencing Genomic DNA of Patients With Severe Hypertriglyceridemia (MIM 144650) von Wang, Jian, Cao, Henian, Ban, Matthew R, Kennedy, Brooke A, Zhu, Siqi, Anand, Sonia, Yusuf, Salim, Pollex, Rebecca L, Hegele, Robert A

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APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia von Wang, Jian, Ban, Matthew R, Kennedy, Brooke A, Anand, Sonia, Yusuf, Salim, Huff, Murray W, Pollex, Rebecca L, Hegele, Robert A

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Association between the -455T>C promoter polymorphism of the APOC3 gene and the metabolic syndrome in a multi-ethnic sample von Pollex, Rebecca L, Ban, Matthew R, Young, T Kue, Bjerregaard, Peter, Anand, Sonia S, Yusuf, Salim, Zinman, Bernard, Harris, Stewart B, Hanley, Anthony J G, Connelly, Philip W, Huff, Murray W, Hegele, Robert A

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APOC1 T45S polymorphism is associated with reduced obesity indices and lower plasma concentrations of leptin and apolipoprotein C-I in aboriginal Canadians von Lahiry, Piya, Cao, Henian, Ban, Matthew R., Pollex, Rebecca L., Mamakeesick, Mary, Zinman, Bernard, Harris, Stewart B., Hanley, Anthony J.G., Huff, Murray W., Connelly, Philip W., Hegele, Robert A.

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Emerging antidyslipidemic drugs von Pollex, Rebecca L, Joy, Tisha R, Hegele, Robert A

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Catalytic Inactivation of Protein Tyrosine Phosphatase CD45 and Protein Tyrosine Phosphatase 1B by Polyaromatic Quinones von Wang, Qingping, Dubé, Daniel, Friesen, Richard W, LeRiche, Tammy G, Bateman, Kevin P, Trimble, Laird, Sanghara, Joe, Pollex, Rebecca, Ramachandran, Chidambaram, Gresser, Michael J, Huang, Zheng

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Common variants APOC3, APOA5, APOE and PON1 are associated with variation in plasma lipoprotein traits in Greenlanders von Lahiry, Piya, Ban, Matthew R., Pollex, Rebecca L., Sawyez, Cynthia G., Huff, Murray W., Young, T. Kue, Bjerregaard, Peter, Hegele, Robert A.

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