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Submissions from 2009

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Narrative Review: Statin-Related Myopathy, Tisha R. Joy and Robert A. Hegele

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The 2009 Canadian Hypertension Education Program Recommendations for the Management of Hypertension: Part 2--Therapy, Nadia A. Khan, Brenda Hemmelgarn, Robert J. Herman, Chaim M. Bell, Jeff L. Mahon, Lawrence A. Leiter, Simon W. Rabkin, Michael D. Hill, Raj Padwal, Rhian M. Touyz, Pierre Larochelle, Ross D. Feldman, Ernesto L. Schiffrin, Norman R. C. Campbell, Gordon Moe, Ramesh Prasad, Malcolm O. Arnold, Tavis S. Campbell, Alain Milot, James A. Stone, Charlotte Jones, Richard I. Ogilvie, Pavel Hamet, George Fodor, George Carruthers, Kevin D. Burns, Marcel Ruzicka, Jacques deChamplain, George Pylypchuk, Robert Petrella, Jean-Martin Boulanger, Luc Trudeau, Robert A. Hegele, Vincent Woo, Phil McFarlane, Michel Vallée, Jonathan Howlett, Simon L. Bacon, Patrice Lindsay, Richard E. Gilbert, Richard Z. Lewanczuk, Sheldon Tobe, and Canadian Hypertension Education Program

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Cystathionine γ-lyase: Clinical, Metabolic, Genetic, and Structural Studies, Jan P. Kraus, Jindrich Hasek, Viktor Kozich, Renata Collard, Sarah Venezia, Bohumila Janosíková, Jian Wang, Sally P. Stabler, Robert H. Allen, Cornelis Jakobs, Christine T. Finn, Yin-Hsiu Chien, Wuh-Liang Hwu, Robert A. Hegele, and S. Harvey Mudd

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A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems, Piya Lahiry, Jian Wang, John F. Robinson, Jacob P. Turowec, David W. Litchfield, Matthew B. Lanktree, Gregory B. Gloor, Erik G. Puffenberger, Kevin A. Strauss, Mildred B. Martens, David A. Ramsay, C. Anthony Rupar, Victoria Siu, and Robert A. Hegele

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Replication of Genetic Associations with Plasma Lipoprotein Traits in a Multiethnic Sample, Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele, and SHARE Investigators

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Triple X Syndrome in a Patient with Partial Lipodystrophy Discovered Using a High-density Oligonucleotide Microarray: A Case Report, Matthew B. Lanktree, I. George Fantus, and Robert A. Hegele

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Gene-gene and Gene-environment Interactions: New Insights into the Prevention, Detection and Management of Coronary Artery Disease, Matthew B. Lanktree and Robert A. Hegele

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Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray, Matthew B. Lanktree, Robert A. Hegele, Salim Yusuf, and Sonia S. Anand

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Determination of Lipoprotein(a) Kringle Repeat Number from Genomic DNA: Copy Number Variation Genotyping Using qPCR, Matthew B. Lanktree, Chandheeb Rajakumar, J. Howard Brunt, Marlys L. Koschinsky, Philip W. Connelly, and Robert A. Hegele

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Metabolic Syndrome and Its Components as Predictors of Incident Type 2 Diabetes Mellitus in an Aboriginal Community, Sylvia H. Ley, Stewart B. Harris, Mary Mamakeesick, Tina Noon, Edith Fiddler, Joel Gittelsohn, Thomas M. S. Wolever, Philip W. Connelly, Robert A. Hegele, Bernard Zinman, and Anthony J. G. Hanley

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Naringenin Prevents Dyslipidemia, Apolipoprotein B Overproduction, and Hyperinsulinemia in LDL Receptor-null Mice with Diet-induced Insulin Resistance, Erin E. Mulvihill, Emma M. Allister, Brian G. Sutherland, Dawn E. Telford, Cynthia G. Sawyez, Jane Y. Edwards, Janet M. Markle, Robert A. Hegele, and Murray W. Huff

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Novel LPL Mutations Associated with Lipoprotein Lipase Deficiency: Two Case Reports and a Literature Review, Amit R. Rahalkar, Fiona Giffen, Bryan Har, Josephine Ho, Katherine M. Morrison, John Hill, Jian Wang, Robert A. Hegele, and Tisha Joy

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Carnitine Palmitoyltransferase IA Polymorphism P479L Is Common in Greenland Inuit and Is Associated with Elevated Plasma Apolipoprotein A-I, Chandheeb Rajakumar, Matthew R. Ban, Henian Cao, T Kue Young, Peter Bjerregaard, and Robert A. Hegele

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Enzyme-Sensitive Magnetic Resonance Imaging Targeting Myeloperoxidase Identifies Active Inflammation in Experimental Rabbit Atherosclerotic Plaques, John A. Ronald, John W. Chen, Yuanxin Chen, Amanda M. Hamilton, Elisenda Rodriguez, Fred Reynolds, Robert A. Hegele, Kem A. Rogers, Manel Querol, Alexei Bogdanov, Ralph Weissleder, and Brian K. Rutt

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Nuclear Degradation of Wilms Tumor 1-associating Protein and Survivin Splice Variant Switching Underlie IGF-1-mediated Survival, Theodore W. Small and J. Geoffrey Pickering

Submissions from 2008

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Association between the FTO rs9939609 Polymorphism and the Metabolic Syndrome in a Non-Caucasian Multi-ethnic Sample, Salam A. Al-Attar, Rebecca L. Pollex, Matthew R. Ban, T Kue Young, Peter Bjerregaard, Sonia S. Anand, Salim Yusuf, Bernard Zinman, Stewart B. Harris, Anthony J. G. Hanley, Philip W. Connelly, Murray W. Huff, and Robert A. Hegele

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Heterozygous CAV1 Frameshift Mutations (MIM 601047) in Patients with Atypical Partial Lipodystrophy and Hypertriglyceridemia, Henian Cao, Lindsay Alston, Jennifer Ruschman, and Robert A. Hegele

Submissions from 2007

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Quantitative and Qualitative Differences in Subcutaneous Adipose Tissue Stores across Lipodystrophy Types Shown by Magnetic Resonance Imaging, Salam A. Al-Attar, Rebecca L. Pollex, John F. Robinson, Brooke A. Miskie, Rhonda Walcarius, Cynthia Harper Little, Brian K. Rutt, and Robert A. Hegele

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Analysis of a Missense Variant of the Human N-formyl Peptide Receptor that Is Associated with Agonist-independent β-arrestin Association and Indices of Inflammation, M. Bhattacharya, J. Wang, F. M. Ribeiro, S. J. Dixon, R. D. Feldman, R. A. Hegele, and S. S. G. Ferguson

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Obstructive Sleep Apnea in 2 Women with Familial Partial Lipodystrophy due to a Heterozygous LMNA R482Q Mutation, Robert A. Hegele, Salam A. Al-Attar, and Brian K. Rutt

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Alstrom Syndrome (OMIM 203800): A Case Report and Literature Review, Tisha Joy, Henian Cao, Graeme Black, Rayaz Malik, Valentine Charlton-Menys, Robert A. Hegele, and Paul N. Durrington

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Genetic Determinants of Statin Intolerance, Jisun Oh, Matthew R. Ban, Brooke A. Miskie, Rebecca L. Pollex, and Robert A. Hegele

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Association Between the -455T>C Promoter Polymorphism of the APOC3 Gene and the Metabolic Syndrome in a Multi-ethnic Sample, Rebecca L. Pollex, Matthew R. Ban, T. Kue Young, Peter Bjerregaard, Sonia S. Anand, Salim Yusuf, Bernard Zinman, Stewart B. Harris, Anthony J. G. Hanley, Philip W. Connelly, Murray W. Huff, and Robert A. Hegele

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Homozygous Missense Mutation (G56R) in Glycosylphosphatidylinositol-anchored High-density Lipoprotein-binding Protein 1 (GPI-HBP1) in Two Siblings with Fasting Chylomicronemia (MIM 144650), Jian Wang and Robert A. Hegele

Submissions from 2006

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Semi-automated Segmentation and Quantification of Adipose Tissue in Calf and Thigh by MRI: A Preliminary Study in Patients with Monogenic Metabolic Syndrome, Salam A. Al-Attar, Rebecca L. Pollex, John F. Robinson, Brooke A. Miskie, Rhonda Walcarius, Brian K. Rutt, and Robert A. Hegele