Projects per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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Collaborations and top research areas from the last five years
Projects
- 1 Active
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Outcomes and late effects in pediatric and adolescent germ cell tumor survivors
Poynter, J. (PI), Pankratz, N. D. (CoI), Alch, S. (Other Role), Lane, J. A. (Other Role), Langer, E. K. (Other Role), Li, Y. (Other Role) & Roesler, M. A. (Other Role)
4/1/25 → 3/31/29
Project: Research project
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Exome sequencing findings in children with annular pancreas
Pitsava, G., Pankratz, N., Lane, J., Yang, W., Rigler, S., Shaw, G. M. & Mills, J. L., Oct 2023, In: Molecular Genetics and Genomic Medicine. 11, 10, e2233.Research output: Contribution to journal › Article › peer-review
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Exploratory Study of the Association of Genetic Factors With Recovery of Adrenal Function in Cushing Disease
Nguyen, M. H., Zhang, W., Pankratz, N., Lane, J., Chitiboina, P., Faucz, F. R., Mills, J. L., Stratakis, C. A. & Tatsi, C., Jun 1 2023, In: Journal of the Endocrine Society. 7, 6, bvad046.Research output: Contribution to journal › Article › peer-review
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Predicted leukocyte telomere length and risk of myeloid neoplasms
Sullivan, S. M., Cole, B., Lane, J., Meredith, J. J., Langer, E., Hooten, A. J., Roesler, M., McGraw, K. L., Pankratz, N. & Poynter, J. N., Oct 15 2023, In: Human molecular genetics. 32, 20, p. 2996-3005 10 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores
Folsom, A. R., Tang, W., Hong, C. P., Rosamond, W. D., Lane, J. A., Cushman, M. & Pankratz, N., Jan 2023, In: PloS one. 18, 1 January, e0280657.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number
Pillalamarri, V., Shi, W., Say, C., Yang, S., Lane, J., Guallar, E., Pankratz, N. & Arking, D. E., Jan 12 2023, In: Human Genetics and Genomics Advances. 4, 1, 100147.Research output: Contribution to journal › Article › peer-review
Open Access7 Scopus citations