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 2005

Efficacy of Evolocumab in Monogenic vs Polygenic Hypercholesterolemia

por Lee, Timothy, Iacocca, Michael A., Ban, Matthew R., Hegele, Robert A.
Publicado 2019

Genetic determinants of statin intolerance

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

Clinical Utility and Practical Considerations of a Coronary Artery Disease Genetic Risk Score

por Liu, Robin, Cheng, Jiahui, Muzlera, Carlos, Robinson, John F., Ban, Matthew R., Hegele, Robert A.
Publicado 2019

Polygenic Contribution to Low-Density Lipoprotein Cholesterol Levels and Cardiovascular Risk in Monogenic Familial Hypercholesterolemia

por Trinder, Mark, Paquette, Martine, Cermakova, Lubomira, Ban, Matthew R., Hegele, Robert A., Baass, Alexis, Brunham, Liam R.
Publicado 2020

Genetic Determinants of Myocardial Infarction Risk in Familial Hypercholesterolemia

por Zhao, Pei Jun, Ban, Matthew R., Iacocca, Michael A., McIntyre, Adam D., Wang, Jian, Hegele, Robert A.
Publicado 2019

Six years’ experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias

por Dron, Jacqueline S., Wang, Jian, McIntyre, Adam D., Iacocca, Michael A., Robinson, John F., Ban, Matthew R., Cao, Henian, Hegele, Robert A.
Publicado 2020

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 2009

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 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 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 2008

Polygenic determinants in extremes of high-density lipoprotein cholesterol

por Dron, Jacqueline S., Wang, Jian, Low-Kam, Cécile, Khetarpal, Sumeet A., Robinson, John F., McIntyre, Adam D., Ban, Matthew R., Cao, Henian, Rhainds, David, Dubé, Marie-Pierre, Rader, Daniel J., Lettre, Guillaume, Tardif, Jean-Claude, Hegele, Robert A.
Publicado 2017