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Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants.
Haque B, Cheerie D, Pan A, Curtis M, Nalpathamkalam T, Nguyen J, Salhab C, Thiruvahindrapuram B, Zhang J, Couse M, Hartley T, Morrow MM, Price EM, Walker S, Malkin D, Roth FP, Costain G. Haque B, et al. Among authors: hartley t. PLoS Genet. 2025 Jan 6;21(1):e1011540. doi: 10.1371/journal.pgen.1011540. eCollection 2025 Jan. PLoS Genet. 2025. PMID: 39761285 Free PMC article.
Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?
Degeling K, Tagimacruz T, MacDonald KV, Seeger TA, Fooks K, Venkataramanan V, Boycott KM, Bernier FP, Mendoza-Londono R, Hartley T, Hayeems RZ, Marshall DA; Care4Rare Canada. Degeling K, et al. Among authors: hartley t. Appl Health Econ Health Policy. 2024 Dec 30. doi: 10.1007/s40258-024-00936-7. Online ahead of print. Appl Health Econ Health Policy. 2024. PMID: 39739296
A Modular Biosensor Design for Quantitative Measurement of Free Nedd8.
Davis ZW, Coyle K, Park MK, Oren T, Hartley T, Umphlett A, Monahan J, Light K, Hunter K, Choi YS. Davis ZW, et al. Among authors: hartley t. ACS Sens. 2024 Sep 27;9(9):4740-4747. doi: 10.1021/acssensors.4c01130. Epub 2024 Sep 10. ACS Sens. 2024. PMID: 39253816 Free PMC article.
Clinical decision aids and computed tomography coronary angiography in patients with suspected acute coronary syndrome.
Wang KL, Taggart C, McDermott M, O'Brien R, Oatey K, Keating L, Storey RF, Felmeden D, Curzen N, Kardos A, Roobottom C, Smith J, Goodacre S, Newby DE, Gray AJ; RAPID-CTCA Investigators. Wang KL, et al. Emerg Med J. 2024 Jul 22;41(8):488-494. doi: 10.1136/emermed-2024-213904. Emerg Med J. 2024. PMID: 38857986 Free article. Clinical Trial.
341 results