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Adam D McIntyre

Showing results (41-50 of 67) with videos related to

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Circulation. Genomic and Precision Medicine|February 1, 2021
Role of Common Genetic Variation in Lone Atrial FibrillationJulieta Lazarte, Jacqueline S Dron, Adam D McIntyre, et al.
Journal of Clinical Lipidology|November 24, 2018
Severe hypertriglyceridemia is primarily polygenicJacqueline S Dron, Jian Wang, Henian Cao, et al.
Journal of Clinical Lipidology|December 11, 2020
Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemiaPraneet K Gill, Jacqueline S Dron, Allison A Dilliott, et al.
Journal of Lipid Research|September 10, 2017
The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutationMeenakshi Sundaram, Kaitlin R Curtis, Mohsen Amir Alipour, et al.
Canadian Journal of Diabetes|October 4, 2020
Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the YoungAmanda J Berberich, Jian Wang, Henian Cao, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 26, 2020
Loss-of-Function <i>CREB3L3</i> Variants in Patients With Severe HypertriglyceridemiaJacqueline S Dron, Allison A Dilliott, Arden Lawson, et al.
The Canadian Journal of Cardiology|October 2, 2018
Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial HypercholesterolemiaMichael A Iacocca, Jian Wang, Samantha Sarkar, et al.
Journal of Lipid Research|September 15, 2019
Partial <i>LPL</i> deletions: rare copy-number variants contributing towards severe hypertriglyceridemiaJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
Kidney International|May 31, 2022
Defective KIM-1 phagocytosis does not predispose to acute graft dysfunction after kidney transplantation in humansRita S Suri, Ji Yun Lee, Matthew R Ban, et al.
Journal of Lipid Research|September 6, 2017
Polygenic determinants in extremes of high-density lipoprotein cholesterolJacqueline S Dron, Jian Wang, Cécile Low-Kam, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Circulation. Genomic and Precision Medicine|February 1, 2021
Role of Common Genetic Variation in Lone Atrial FibrillationJulieta Lazarte, Jacqueline S Dron, Adam D McIntyre, et al.
Journal of Clinical Lipidology|November 24, 2018
Severe hypertriglyceridemia is primarily polygenicJacqueline S Dron, Jian Wang, Henian Cao, et al.
Journal of Clinical Lipidology|December 11, 2020
Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemiaPraneet K Gill, Jacqueline S Dron, Allison A Dilliott, et al.
Journal of Lipid Research|September 10, 2017
The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutationMeenakshi Sundaram, Kaitlin R Curtis, Mohsen Amir Alipour, et al.
Canadian Journal of Diabetes|October 4, 2020
Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the YoungAmanda J Berberich, Jian Wang, Henian Cao, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 26, 2020
Loss-of-Function <i>CREB3L3</i> Variants in Patients With Severe HypertriglyceridemiaJacqueline S Dron, Allison A Dilliott, Arden Lawson, et al.
The Canadian Journal of Cardiology|October 2, 2018
Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial HypercholesterolemiaMichael A Iacocca, Jian Wang, Samantha Sarkar, et al.
Journal of Lipid Research|September 15, 2019
Partial <i>LPL</i> deletions: rare copy-number variants contributing towards severe hypertriglyceridemiaJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
Kidney International|May 31, 2022
Defective KIM-1 phagocytosis does not predispose to acute graft dysfunction after kidney transplantation in humansRita S Suri, Ji Yun Lee, Matthew R Ban, et al.
Journal of Lipid Research|September 6, 2017
Polygenic determinants in extremes of high-density lipoprotein cholesterolJacqueline S Dron, Jian Wang, Cécile Low-Kam, et al.
Pageof 7