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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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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Community Based Genomic Medicine and Polygenic Scoring
Somers, V. (PI) & Kullo, I. J. (CoPI)
National Human Genome Research Institute
5/1/24 → 2/28/26
Project: Research project
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Polygenic Risk of Disease in Populations of Diverse Ancestry
Schaid, D. J. (PI) & Kullo, I. J. (CoPI)
National Human Genome Research Institute
9/8/21 → 6/30/26
Project: Research project
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EHR-based Genomic Discovery and Implementation [Funded Extension]
Sharp, R. R. (CoPI), Chute, C. G. (CoPI), Kullo, I. J. (CoPI) & Thibodeau, S. N. (CoPI)
National Human Genome Research Institute
8/15/11 → 4/30/26
Project: Research project
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Patient-Oriented Research in Genomic Discovery and Implementation
Kullo, I. J. (PI)
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
Kullo, I. J. (PI)
National Heart, Lung, and Blood Institute
7/1/17 → 5/31/21
Project: Research project
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Admixture Mapping of Lipid Traits in Hispanic Americans
Ding, K., Johar, A. S., Zaidi, A., Crane, P. K., Velez Edwards, D. R., Jarvik, G. P., Karlson, E. W., Rosenthal, E. A., Stanaway, I. B., Weng, C., Schaid, D. J. & Kullo, I. J., Nov 3 2025, In: Journal of the American Heart Association. 14, 21, p. 1-15 15 p., e036650.Research output: Contribution to journal › Article › peer-review
Open Access -
Clinical use of polygenic risk scores: current status, barriers and future directions
Kullo, I. J., 2025, (Accepted/In press) In: Nature Reviews Genetics.Research output: Contribution to journal › Review article › peer-review
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Clonal Hematopoiesis of Indeterminate Potential in Chronic Coronary Disease: A Report From the ISCHEMIA Trials Biorepository
Muller, M. A., Liu, R., Shah, F., Hu, J., Held, C., Kullo, I. J., Mcmanus, B. M., Wallentin, L., Newby, L. K., Sidhu, M. S., Bangalore, S., Reynolds, H. R., Hochman, J. S., Maron, D. J., Ruggles, K. V., Berger, J. S. & Newman, J. D., Jun 1 2025, In: Circulation: Genomic and Precision Medicine. 18, 3, e004921.Research output: Contribution to journal › Article › peer-review
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Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Penn Medicine BioBank, Apr 2025, In: Nature Genetics. 57, 4, p. 829-838 10 p., 163.Research output: Contribution to journal › Article › peer-review
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Constructing a multi-ancestry polygenic risk score for uterine fibroids using publicly available data highlights need for inclusive genetic research
Winters, J. L. G., Piekos, J. A., Hellwege, J. N., Dikilitas, O., Kullo, I. J., Schaid, D. J., Edwards, T. L. & Velez Edwards, D. R., 2025, In: Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing. 30, p. 268-280 13 p.Research output: Contribution to journal › Article › peer-review