David H. Evans

Hamburg, HH 20246, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Resequencing the untranslated regions of the lipoprotein lipase (LPL) gene reveals that variants in microRNA target sequences are associated with triglyceride levels.

Resequencing the untranslated regions of the lipoprotein lipase (LPL) gene reveals that variants in microRNA target sequences are associated with triglyceride levels.

Journal: Journal of clinical lipidology

Published: July 18, 2013

Resequencing the APOE gene reveals that rare mutations are not significant contributory factors in the development of type III hyperlipidemia.

Resequencing the APOE gene reveals that rare mutations are not significant contributory factors in the development of type III hyperlipidemia.

Journal: Journal of clinical lipidology

Published: February 11, 2013

Grading carotid stenosis using ultrasonic methods.

Grading carotid stenosis using ultrasonic methods.

Journal: Stroke

Published: February 21, 2012

The relative importance of common and rare genetic variants in the development of hypertriglyceridemia.

The relative importance of common and rare genetic variants in the development of hypertriglyceridemia.

Journal: Expert review of cardiovascular therapy

Published: May 28, 2011

Resequencing the apolipoprotein A5 (APOA5) gene in patients with various forms of hypertriglyceridemia.

Resequencing the apolipoprotein A5 (APOA5) gene in patients with various forms of hypertriglyceridemia.

Journal: Atherosclerosis

Published: April 26, 2011

Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia.

Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia.

Journal: Atherosclerosis

Published: September 13, 2010

The D9N, N291S and S447X variants in the lipoprotein lipase (LPL) gene are not associated with Type III hyperlipidemia.

The D9N, N291S and S447X variants in the lipoprotein lipase (LPL) gene are not associated with Type III hyperlipidemia.

Journal: BMC medical genetics

Published: February 12, 2007

The E670G SNP in the PCSK9 gene is associated with polygenic hypercholesterolemia in men but not in women.

The E670G SNP in the PCSK9 gene is associated with polygenic hypercholesterolemia in men but not in women.

Journal: BMC medical genetics

Published: May 16, 2006

Polymorphisms in the apolipoprotein A5 (APOA5) gene and type III hyperlipidemia.

Polymorphisms in the apolipoprotein A5 (APOA5) gene and type III hyperlipidemia.

Journal: Clinical genetics

Published: September 07, 2005

The single nucleotide polymorphism -1131T>C in the apolipoprotein A5 (APOA5) gene is associated with elevated triglycerides in patients with hyperlipidemia.

The single nucleotide polymorphism -1131T>C in the apolipoprotein A5 (APOA5) gene is associated with elevated triglycerides in patients with hyperlipidemia.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: February 14, 2003

The association of the R219K polymorphism in the ATP-binding cassette transporter 1 ( ABCA1) gene with coronary heart disease and hyperlipidaemia.

The association of the R219K polymorphism in the ATP-binding cassette transporter 1 ( ABCA1) gene with coronary heart disease and hyperlipidaemia.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: October 31, 2002

Association between polymorphisms in candidate genes and morbid obesity.

Association between polymorphisms in candidate genes and morbid obesity.

Journal: International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity

Published: July 24, 2001

Showing 1-12 of 15

Last Updated: 09/26/2026