Celestial determinants of success in research

Por Pollex, Rebecca, Hegele, Bob, Ban, Matthew R.
Publicado em 2001

NPC1L1 haplotype is associated with inter-individual variation in plasma low-density lipoprotein response to ezetimibe

Por Hegele, Robert A, Guy, Justin, Ban, Matthew R, Wang, Jian
Publicado em 2005

Genetic determinants of statin intolerance

Por Oh, Jisun, Ban, Matthew R, Miskie, Brooke A, Pollex, Rebecca L, Hegele, Robert A
Publicado em 2007

Carnitine palmitoyltransferase IA polymorphism P479L is common in Greenland Inuit and is associated with elevated plasma apolipoprotein A-I

Por Rajakumar, Chandheeb, Ban, Matthew R., Cao, Henian, Young, T. Kue, Bjerregaard, Peter, Hegele, Robert A.
Publicado em 2009

A common hypofunctional genetic variant of GPER is associated with increased blood pressure in women

Por Feldman, Ross D, Gros, Robert, Ding, Qingming, Hussain, Yasin, Ban, Matthew R, McIntyre, Adam D, Hegele, Robert A
Publicado no Br J Clin Pharmacol (2014)

A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia

Por Hegele, Robert A., Ban, Matthew R., Hsueh, Neil, Kennedy, Brooke A., Cao, Henian, Zou, Guang Yong, Anand, Sonia, Yusuf, Salim, Huff, Murray W., Wang, Jian
Publicado em 2009

APOC1 T45S polymorphism is associated with reduced obesity indices and lower plasma concentrations of leptin and apolipoprotein C-I in aboriginal Canadians

Por 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.
Publicado em 2010

Association between the -455T>C promoter polymorphism of the APOC3 gene and the metabolic syndrome in a multi-ethnic sample

Por 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
Publicado em 2007

Inheritance of rare functional GCKR variants and their contribution to triglyceride levels in families

Por Rees, Matthew G., Raimondo, Anne, Wang, Jian, Ban, Matthew R., Davis, Mindy I., Barrett, Amy, Ranft, Jessica, Jagdhuhn, David, Waterstradt, Rica, Baltrusch, Simone, Simeonov, Anton, Collins, Francis S., Hegele, Robert A., Gloyn, Anna L.
Publicado em 2014

Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample

Por 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
Publicado em 2008

The common LDLR p.G116S variant has a large effect on plasma LDL cholesterol in circumpolar Inuit populations

Por Dubé, Joseph B., Wang, Jian, Cao, Henian, McIntyre, Adam, Johansen, Christopher T., Hopkins, Scarlett E., Stringer, Randa, Hosseinzadeh, Siyavash, Kennedy, Brooke A., Ban, Matthew R., Young, T. Kue, Connelly, Philip W., Dewailly, Eric, Bjerregaard, Peter, Boyer, Bert B., Hegele, Robert A.
Publicado no Circ Cardiovasc Genet (2014)

Excess of Rare Variants in Non-GWAS Candidate Genes in Patients with Hypertriglyceridemia

Por Johansen, Christopher T., Wang, Jian, McIntyre, Adam D., Martins, Rebecca A., Ban, Matthew R., Lanktree, Matthew B., Huff, Murray W., Péterfy, Miklós, Mehrabian, Margarete, Lusis, Aldons J., Kathiresan, Sekar, Anand, Sonia S., Yusuf, Salim, Lee, Ann-Hwee, Glimcher, Laurie H., Cao, Henian, Hegele, Robert A.
Publicado em 2011

Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution

Por Patel, Aniruddh P., Peloso, Gina M., Pirruccello, James P., Johansen, Christopher T., Dubé, Joseph B., Larach, Daniel B., Ban, Matthew R., Dallinge-Thie, Geesje M., Gupta, Namrata, Boehnke, Michael, Abecasis, Gonçalo R., Kastelein, John J.P., Kees Hovingh, G., Hegele, Robert A., Rader, Daniel J., Kathiresan, Sekar
Publicado no Atherosclerosis (2016)

Mutation skew in genes identified by genome-wide association study of hypertriglyceridemia

Por Johansen, Christopher T., Wang, Jian, Lanktree, Matthew B., Cao, Henian, McIntyre, Adam D., Ban, Matthew R., Martins, Rebecca A., Kennedy, Brooke A., Hassell, Reina G., Visser, Maartje E., Schwartz, Stephen M., Voight, Benjamin F., Elosua, Roberto, Salomaa, Veikko, O'Donnell, Christopher J., Dallinga-Thie, Geesje M., Anand, Sonia S., Yusuf, Salim, Huff, Murray W., Kathiresan, Sekar, Hegele, Robert A.
Publicado em 2010

An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia

Por Johansen, Christopher T., Wang, Jian, Lanktree, Matthew B., McIntyre, Adam D., Ban, Matthew R., Martins, Rebecca A., Kennedy, Brooke A., Hassell, Reina G., Visser, Maartje E., Schwartz, Stephen M., Voight, Benjamin F., Elosua, Roberto, Salomaa, Veikko, O’Donnell, Christopher J., Dallinga-Thie, Geesje M., Anand, Sonia S., Yusuf, Salim, Huff, Murray W., Kathiresan, Sekar, Cao, Henian, Hegele, Robert A.
Publicado em 2011

TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone

Por Huang, Lijia, Szymanska, Katarzyna, Jensen, Victor L., Janecke, Andreas R., Innes, A. Micheil, Davis, Erica E., Frosk, Patrick, Li, Chunmei, Willer, Jason R., Chodirker, Bernard N., Greenberg, Cheryl R., McLeod, D. Ross, Bernier, Francois P., Chudley, Albert E., Müller, Thomas, Shboul, Mohammad, Logan, Clare V., Loucks, Catrina M., Beaulieu, Chandree L., Bowie, Rachel V., Bell, Sandra M., Adkins, Jonathan, Zuniga, Freddi I., Ross, Kevin D., Wang, Jian, Ban, Matthew R., Becker, Christian, Nürnberg, Peter, Douglas, Stuart, Craft, Cheryl M., Akimenko, Marie-Andree, Hegele, Robert A., Ober, Carole, Utermann, Gerd, Bolz, Hanno J., Bulman, Dennis E., Katsanis, Nicholas, Blacque, Oliver E., Doherty, Dan, Parboosingh, Jillian S., Leroux, Michel R., Johnson, Colin A., Boycott, Kym M.
Publicado em 2011