Projects per year
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Dive into the research topics where Iftikhar Jan Kullo is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Polygenic Risk of Disease in Populations of Diverse Ancestry
Kullo, I. J., Schaid, D. J., Kullo, I. J. & Schaid, D. J.
National Human Genome Research Institute
9/8/21 → 6/30/23
Project: Research project
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EHR-based Genomic Discovery and Implementation
Kullo, I. I. J., Chute, C. G., Kullo, I. J., Sharp, R. R. R., Sharp, R. R. & Thibodeau, S. N.
National Human Genome Research Institute
8/15/11 → 4/30/23
Project: Research project
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Patient-Oriented Research in Genomic Discovery and Implementation
National Heart, Lung, and Blood Institute
7/15/17 → 6/30/22
Project: Research project
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EHR-Based Strategies to Improve Outcomes in Familial Hypercholesterolemia
National Heart, Lung, and Blood Institute
7/1/17 → 5/31/21
Project: Research project
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Plasma Osteoprotegerin and Adverse Outcomes in CHD Patients
National Heart, Lung, and Blood Institute
5/15/12 → 4/30/13
Project: Research project
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Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index
Hui, D., Xiao, B., Dikilitas, O., Freimuth, R. R., Irvin, M. R., Jarvik, G. P., Kottyan, L., Kullo, I., Limdi, N. A., Liu, C., Luo, Y., Namjou, B., Puckelwartz, M. J., Schaid, D., Tiwari, H., Wei, W. Q., Verma, S., Kim, D. & Ritchie, M. D., 2023, In: Pacific Symposium on Biocomputing. 2023, p. 437-448 12 p.Research output: Contribution to journal › Conference article › peer-review
Open Access -
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
Million Veterans Program & Global Lipids Genetics Consortium, Aug 4 2022, In: American journal of human genetics. 109, 8, p. 1366-1387 22 p.Research output: Contribution to journal › Article › peer-review
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A pragmatic clinical trial of cascade testing for familial hypercholesterolemia
Miller, A. A., Bangash, H., Smith, C. Y., Wood-Wentz, C. M., Bailey, K. R. & Kullo, I. J., Dec 2022, In: Genetics in Medicine. 24, 12, p. 2535-2543 9 p.Research output: Contribution to journal › Article › peer-review
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Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study
Glazer, A. M., Davogustto, G., Shaffer, C. M., Vanoye, C. G., Desai, R. R., Farber-Eger, E. H., Dikilitas, O., Shang, N., Pacheco, J. A., Yang, T., Muhammad, A., Mosley, J. D., Van Driest, S. L., Wells, Q. S., Shaffer, L. L., Kalash, O. R., Wada, Y., Bland, S., Yoneda, Z. T., Mitchell, D. W., & 30 others, Mar 22 2022, In: Circulation. 145, 12, p. 877-891 15 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases (Nature Communications, (2021), 12, 1, (6031), 10.1038/s41467-021-26174-2)
FEIRI investigators, International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group, MEGASTROKE & ARCADIA Investigators, Dec 2022, In: Nature communications. 13, 1, 2251.Research output: Contribution to journal › Comment/debate › peer-review
Open Access