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1. Cognitive function with evolocumab in pediatric heterozygous familial hypercholesterolemia

3. Lipid-modifying agents, from statins to PCSK9 inhibitors: JACC focus seminar

4. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

7. Reducing the Clinical and Public Health Burden of Familial Hypercholesterolemia: A Global Call to Action

8. Reducing the clinical and public health Burden of Familial hypercholesterolemia

10. Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

11. Defining the role of common variation in the genomic and biological architecture of adult human height

12. Defining severe familial hypercholesterolaemia and the implications for clinical management: a consensus statement from the International Atherosclerosis Society Severe Familial Hypercholesterolemia Panel

13. Triglyceride-rich lipoprotein cholesterol and risk of cardiovascular events among patients receiving statin therapy in the Treating to New Targets (TNT) trial

14. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 26, 2018)

15. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017)

17. Biological interpretation of genome-wide association studies using predicted gene functions

18. Cardiovascular Efficacy and Safety of Bococizumab in High-Risk Patients

19. Association of high-density lipoprotein-cholesterol versus apolipoprotein A-I with risk of coronary heart disease: The European prospective investigation into cancer-norfolk prospective population study, the atherosclerosis risk in communities study, and the Women'S Health Study

20. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

21. Genetically Determined Height and Coronary Artery Disease

22. Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

32. Loci influencing blood pressure identified using a cardiovascular gene-centric array (vol 22, pg 1663, 2013)

33. Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

34. The impact of LDLR function on fibroblast growth factor 21 levels

35. New genetic loci link adipose and insulin biology to body fat distribution.

36. Biological interpretation of genome-wide association studies using predicted gene functions

37. Impact of statin therapy on coronary plaque composition: a systematic review and meta-analysis of virtual histology intravascular ultrasound studies

38. New genetic loci link adipose and insulin biology to body fat distribution

39. Genetically determined height and coronary artery disease

40. Homozygous familial hypercholesterolaemia: New insights and guidance for clinicians to improve detection and clinical management. A position paper fromthe Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

44. Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population

45. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

46. Large-scale association analysis identifies new risk loci for coronary artery disease

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