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Adam D McIntyre

Showing results (51-60 of 67) with videos related to

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Circulation. Cardiovascular Genetics|November 22, 2014
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populationsJoseph B Dubé, Jian Wang, Henian Cao, et al.
NPJ Genomic Medicine|December 22, 2017
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegenerationSali M K Farhan, Allison A Dilliott, Mahdi Ghani, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 8, 2021
Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillationJulieta Lazarte, Zachary W Laksman, Jian Wang, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 22, 2016
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained ClinicallyJian Wang, Jacqueline S Dron, Matthew R Ban, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2017
A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and PancreatitisMasako Ueda, Richard L Dunbar, Anna Wolska, et al.
American Journal of Human Genetics|January 10, 2012
Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1Lina Basel-Vanagaite, Noam Zevit, Adi Har Zahav, et al.
Gene|June 29, 2024
Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6Clara Schott, Allison A Dilliott, Jian Wang, et al.
Journal of Visualized Experiments : Jove|April 24, 2018
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional DiseaseAllison A Dilliott, Sali M K Farhan, Mahdi Ghani, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Circulation. Cardiovascular Genetics|November 22, 2014
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populationsJoseph B Dubé, Jian Wang, Henian Cao, et al.
NPJ Genomic Medicine|December 22, 2017
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegenerationSali M K Farhan, Allison A Dilliott, Mahdi Ghani, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 8, 2021
Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillationJulieta Lazarte, Zachary W Laksman, Jian Wang, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 22, 2016
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained ClinicallyJian Wang, Jacqueline S Dron, Matthew R Ban, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2017
A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and PancreatitisMasako Ueda, Richard L Dunbar, Anna Wolska, et al.
American Journal of Human Genetics|January 10, 2012
Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1Lina Basel-Vanagaite, Noam Zevit, Adi Har Zahav, et al.
Gene|June 29, 2024
Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6Clara Schott, Allison A Dilliott, Jian Wang, et al.
Journal of Visualized Experiments : Jove|April 24, 2018
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional DiseaseAllison A Dilliott, Sali M K Farhan, Mahdi Ghani, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Pageof 7