The role of genetic testing in dyslipidaemia-Reference-Cited by-同舟云学术

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The role of genetic testing in dyslipidaemia

Published:2019-02 Issue:2 Volume:51 Page:184-192
ISSN:0031-3025
Container-title:Pathology
language:en
Short-container-title:Pathology

Author:

Berberich Amanda J.,Hegele Robert A.

Funder

Schulich School of Medicine & Dentistry

Western University

Canadian Society for Endocrinology

Jacob J. Wolfe Distinguished Medical Research Chair

Canadian Institutes of Health Research

Heart and Stroke Foundation of Ontario

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference59 articles.

1. Genotype-guided diagnosis in familial hypercholesterolemia: population burden and cascade screening;Hopkins;Curr Opin Lipidol,2017

2. Targeted next-generation sequencing in monogenic dyslipidemias;Hegele;Curr Opin Lipidol,2015

3. Polygenic influences on dyslipidemias;Dron;Curr Opin Lipidol,2018

4. Genetic diagnosis and testing in clinical practice;McPherson;Clin Med Res,2006

5. Clinical and biochemical features of different molecular etiologies of familial chylomicronemia;Hegele;J Clin Lipidol,2018

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1. Germline variant analysis from a cohort of patients with severe hypertriglyceridemia in Brazil;Molecular Genetics and Metabolism Reports;2024-09

2. Genetic testing for familial hypercholesterolemia: a review of the current state of its implementation in Canada;CJC Open;2024-08

3. Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene;BMC Endocrine Disorders;2024-04-15

4. Clinical impact of genetic testing for lipid disorders;Current Opinion in Cardiology;2024-02-29

5. Unveiling Familial Hypercholesterolemia—Review, Cardiovascular Complications, Lipid-Lowering Treatment and Its Efficacy;International Journal of Molecular Sciences;2024-01-29

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