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Vascular calcifications in homozygote familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 2008-04, Vol.28 (4), p.777-785

2008

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Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome

European journal of medical genetics, 2014-09, Vol.57 (9), p.524-526

2014

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The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia – A post-hoc analysis of a Phase 3, single-arm, open-label trial

Atherosclerosis, 2015-06, Vol.240 (2), p.408-414

2015

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Clinical and biochemical characteristics are varied in subjects with ABCA1 mutations

Atherosclerosis, 2015-07, Vol.241 (1), p.e37-e37

2015

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Familial chylomicronemia syndrome: an under‐recognized cause of severe hypertriglyceridaemia

Journal of internal medicine, 2020-04, Vol.287 (4), p.340-348

2020

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Activation of peroxisome proliferator-activated receptor gamma and retinoid X receptor results in net depletion of cellular cholesteryl esters in macrophages exposed to oxidized lipoproteins

Arteriosclerosis, thrombosis, and vascular biology, 2003-03, Vol.23 (3), p.475-482

2003

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Rationale and design of two trials assessing efficacy, safety and tolerability of Inclisiran in adolescents with homozygous and heterozygous familial hypercholesterolaemia

Atherosclerosis, 2022-08, Vol.355, p.150

2022

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PCV55 Cost-Effectiveness of Icosapent Ethyl (IPE) for the Reduction of the Risk of Ischemic Cardiovascular Events in Canada

Value in health, 2020-12, Vol.23, p.S496-S496

2020

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Evaluation of apolipoprotein A5 variants: A cohort of patients with severe hypertriglyceridemia from Turkiye

Journal of clinical lipidology, 2024-05, Vol.18 (3), p.e423-e429

2024

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Specification Of Acmg/Amp Guidelines For Variant Interpretation In Familial Hypercholesterolemia

Atherosclerosis, 2019-08, Vol.287, p.e68-e68

2019

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Characterization of the I4399M variant of apolipoprotein(a): implications for altered prothrombotic properties of lipoprotein(a)

Journal of thrombosis and haemostasis, 2017-09, Vol.15 (9), p.1834-1844

2017

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Adaptation of ACMG/AMP guidelines for variant interpretation in familial hypercholesterolemia - A clingen fh expert panel pilot study

Atherosclerosis, 2018-08, Vol.275, p.e98-e98

2018

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Specification of ACMG/AMP guidelines for standardized variant interpretation in familial hypercholesterolemia: On behalf of the clingen FH variant curation expert panel

Atherosclerosis, 2020-12, Vol.315, p.e5-e5

2020

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The HNF1A G319S variant is associated with C-reactive protein in an Aboriginal population

Canadian journal of diabetes, 2009, Vol.33 (3), p.194-194

2009

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Kinetics of lipolysis of very low density lipoproteins by lipoprotein lipase. Importance of particle number and noncompetitive inhibition by particles with low triglyceride content

The Journal of biological chemistry, 1994-08, Vol.269 (32), p.20554-20560

1994

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Copy number variation in metabolic phenotypes

Cytogenetic and genome research, 2008-01, Vol.123 (1-4), p.169-175

2008

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Postprandial lipemia in subjects with the threonine 54 variant of the fatty acid-binding protein 2 gene is dependent on the type of fat ingested

The American journal of clinical nutrition, 2004-06, Vol.79 (6), p.1110-1117

2004

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Relation of waist circumference and glycemic status to C-reactive protein in the Sandy Lake Oji-Cree

International Journal of Obesity, 2003-03, Vol.27 (3), p.347-354

2003

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Common chemokine receptor single nucleotide polymorphisms are associated with transplant vasculopathy in heart transplant recipients

The Journal of heart and lung transplantation, 2004-02, Vol.23 (2), p.S162-S163

2004

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Lipoprotein and Lipid Metabolism

Reference Module in Biomedical Research, 2014

Hegele, R.A.

2014

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Gene-environment interactions in atherosclerosis

Molecular and cellular biochemistry, 1992-08, Vol.113 (2), p.177-186

Hegele, R.A

1992

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4P-1154 Distinctive portfolios of determinants for different phenotypes of atherosclerosis

Atherosclerosis. Supplements, 2003, Vol.4 (2), p.328-328

2003

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Evidence for gene-diet interaction in the response of blood pressure to dietary fibre

Nutrition research (New York, N.Y.), 1997-08, Vol.17 (8), p.1229-1238

1997

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A hepatic lipase gene mutation associated with heritable lipolytic deficiency

The journal of clinical endocrinology and metabolism, 1991-03, Vol.72 (3), p.730-732

1991

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3.P.115 Modification of type III VLDL, their remnants and VLDL from apoE-knockout mice by p-hydroxyphenylacetaldehyde, causes marked macrophage cholesteryl ester accumulation

Atherosclerosis, 1997-10, Vol.134 (1-2), p.222-222

1997

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Vascular calcifications in homozygote familial hypercholesterolemia

Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome

The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia – A post-hoc analysis of a Phase 3, single-arm, open-label trial

Clinical and biochemical characteristics are varied in subjects with ABCA1 mutations

Familial chylomicronemia syndrome: an under‐recognized cause of severe hypertriglyceridaemia

Activation of peroxisome proliferator-activated receptor gamma and retinoid X receptor results in net depletion of cellular cholesteryl esters in macrophages exposed to oxidized lipoproteins

Rationale and design of two trials assessing efficacy, safety and tolerability of Inclisiran in adolescents with homozygous and heterozygous familial hypercholesterolaemia

PCV55 Cost-Effectiveness of Icosapent Ethyl (IPE) for the Reduction of the Risk of Ischemic Cardiovascular Events in Canada

Evaluation of apolipoprotein A5 variants: A cohort of patients with severe hypertriglyceridemia from Turkiye

Specification Of Acmg/Amp Guidelines For Variant Interpretation In Familial Hypercholesterolemia

Characterization of the I4399M variant of apolipoprotein(a): implications for altered prothrombotic properties of lipoprotein(a)

Adaptation of ACMG/AMP guidelines for variant interpretation in familial hypercholesterolemia - A clingen fh expert panel pilot study

Specification of ACMG/AMP guidelines for standardized variant interpretation in familial hypercholesterolemia: On behalf of the clingen FH variant curation expert panel

The HNF1A G319S variant is associated with C-reactive protein in an Aboriginal population

Kinetics of lipolysis of very low density lipoproteins by lipoprotein lipase. Importance of particle number and noncompetitive inhibition by particles with low triglyceride content

Copy number variation in metabolic phenotypes

Postprandial lipemia in subjects with the threonine 54 variant of the fatty acid-binding protein 2 gene is dependent on the type of fat ingested

Relation of waist circumference and glycemic status to C-reactive protein in the Sandy Lake Oji-Cree

Common chemokine receptor single nucleotide polymorphisms are associated with transplant vasculopathy in heart transplant recipients

Lipoprotein and Lipid Metabolism

Gene-environment interactions in atherosclerosis

4P-1154 Distinctive portfolios of determinants for different phenotypes of atherosclerosis

Evidence for gene-diet interaction in the response of blood pressure to dietary fibre

A hepatic lipase gene mutation associated with heritable lipolytic deficiency

3.P.115 Modification of type III VLDL, their remnants and VLDL from apoE-knockout mice by p-hydroxyphenylacetaldehyde, causes marked macrophage cholesteryl ester accumulation

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