Strong, Alanna
Children's Hospital of Philadelphia
5 papers on CoChatORCID 0000-0001-9261-244X
Most cited papers
- Verified
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
Musunuru, K., Strong, A., Frank-Kamenetsky, M., Lee, N. E., Ahfeldt, T., Sachs, K. V., Li, X., Li, H., Kuperwasser, N., Ruda, V. M., et al. (2010) · Nature
Genetic Associations and EpidemiologyCholesterol and Lipid Metabolism
Cited by 1,140
- Verified
Permanent Alteration of PCSK9 With In Vivo CRISPR-Cas9 Genome Editing
Ding, Q., Strong, A., Patel, K. M., Ng, S.-L., Gosis, B. S., Regan, S. N., Cowan, C. A., Rader, D. J., & Musunuru, K. (2014) · Circulation Research
CRISPR and Genetic EngineeringLipoproteins and Cardiovascular Health
Cited by 522
- Verified
Hepatic sortilin regulates both apolipoprotein B secretion and LDL catabolism
Strong, A., Ding, Q., Edmondson, A. C., Millar, J. S., Sachs, K. V., Li, X., Kumaravel, A., Wang, M. Y., Ai, D., Guo, L., et al. (2012) · Journal of Clinical Investigation
Cholesterol and Lipid MetabolismLipoproteins and Cardiovascular Health
Cited by 222
- Verified
Macrophage Sortilin Promotes LDL Uptake, Foam Cell Formation, and Atherosclerosis
Patel, K. M., Strong, A., Tohyama, J., Jin, X., Morales, C. R., Billheimer, J., Millar, J., Kruth, H., & Rader, D. J. (2015) · Circulation Research
Atherosclerosis and Cardiovascular DiseasesCholesterol and Lipid Metabolism
Cited by 194
- Verified
Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype
Isidor, B., Ebstein, F., Hurst, A., Vincent, M., Bader, I., Rudy, N. L., Cogne, B., Mayr, J., Brehm, A., Bupp, C., et al. (2022) · Genetics in Medicine
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 24
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