Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 7 Similar Profiles
Mutation Medicine & Life Sciences
Hyperlipoproteinemia Type II Medicine & Life Sciences
Therapeutics Medicine & Life Sciences
Hydroxymethylglutaryl-CoA Reductase Inhibitors Medicine & Life Sciences
Lipids Medicine & Life Sciences
Triglycerides Medicine & Life Sciences
Hyperlipoproteinemia Type I Medicine & Life Sciences
Genotype Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2001 2017

1 Citations

ANGPTL3 inhibition in homozygous familial hypercholesterolemia

Gaudet, D., Gipe, D. A., Pordy, R., Ahmad, Z., Cuchel, M., Shah, P. K., Chyu, K. Y., Sasiela, W. J., Chan, K. C., Brisson, D., Khoury, E., Banerjee, P., Gusarova, V., Gromada, J., Stahl, N., Yancopoulos, G. D. & Hovingh, G. K. Jul 20 2017 In : New England Journal of Medicine. 377, 3, p. 296-298 3 p.

Research output: Research - peer-reviewLetter

1 Citations

Building a better understanding of the burden of disease in familial chylomicronemia syndrome

Ahmad, Z., Halter, R. & Stevenson, M. Jan 2 2017 In : Expert Review of Clinical Pharmacology. 10, 1, p. 1-3 3 p.

Research output: Research - peer-reviewEditorial

2 Citations

The burden of familial chylomicronemia syndrome: interim results from the IN-FOCUS study

Davidson, M., Stevenson, M., Hsieh, A., Ahmad, Z., Crowson, C. & Witztum, J. L. May 4 2017 In : Expert Review of Cardiovascular Therapy. 15, 5, p. 415-423 9 p.

Research output: Research - peer-reviewArticle

Hyperlipoproteinemia Type I
Quality of Life
Cost of Illness
Surveys and Questionnaires
Career Choice
4 Citations

Familial defective apolipoprotein B-100: A review

Andersen, L. H., Miserez, A. R., Ahmad, Z. & Andersen, R. L. Nov 1 2016 In : Journal of Clinical Lipidology. 10, 6, p. 1297-1302 6 p.

Research output: Research - peer-reviewReview article

Hyperlipoproteinemia Type II
Mutation
Apolipoprotein B-100
Inborn Genetic Diseases
LDL Receptors
4 Citations

Premature coronary heart disease and autosomal dominant hypercholesterolemia: Increased risk in women with LDLR mutations

Ahmad, Z., Li, X., Wosik, J., Mani, P., Petr, J., McLeod, G., Murad, S., Song, L., Adams-Huet, B. & Garg, A. Jan 1 2016 In : Journal of Clinical Lipidology. 10, 1, p. 101-108.e3

Research output: Research - peer-reviewArticle

Hyperlipoproteinemia Type II
LDL Receptors
Coronary Disease
Mutation
LDL Cholesterol