Research output per year
Research output 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):
Fingerprint
The Fingerprint is created by mining the titles and abstracts of the person's research outputs and projects/funding awards to create an index of weighted terms from discipline-specific thesauri.
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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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Exome sequencing findings in children with annular pancreas
Pitsava, G., Pankratz, N., Lane, J., Yang, W., Rigler, S., Shaw, G. M. & Mills, J. L., 2023, (Accepted/In press) In: Molecular Genetics and Genomic Medicine.Research output: Contribution to journal › Article › peer-review
Open Access -
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
Open Access -
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 Access -
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 Access1 Scopus citations -
Exome sequencing identifies variants in infants with sacral agenesis
UW Center for Mendelian Genomics, NISC Comparative Sequencing Program and the National Birth Defects Prevention Study, Apr 1 2022, In: Birth Defects Research. 114, 7, p. 215-227 13 p.Research output: Contribution to journal › Article › peer-review
2 Scopus citations