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The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliability.
Hayeems RZ, Luca S, Ungar WJ, Venkataramanan V, Tsiplova K, Bashir NS, Costain G, Inglese C, McNiven V, Quercia N, Shugar A, Yoon G, Cytrynbaum C, Dupuis L, Shao Z, Hewson S, Shuman C, Aul R, Liston E, Babul-Hirji R, Bushby A, Pullenayegum E, Chad L, Meyn MS. Hayeems RZ, et al. Among authors: venkataramanan v. Genet Med. 2022 Feb;24(2):430-438. doi: 10.1016/j.gim.2021.10.005. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906486 Free article.
The complexity of diagnosing rare disease: An organizing framework for outcomes research and health economics based on real-world evidence.
Hayeems RZ, Michaels-Igbokwe C, Venkataramanan V, Hartley T, Acker M, Gillespie M, Ungar WJ, Mendoza-Londona R, Bernier FP, Boycott KM, Marshall DA. Hayeems RZ, et al. Among authors: venkataramanan v. Genet Med. 2022 Mar;24(3):694-702. doi: 10.1016/j.gim.2021.11.005. Epub 2021 Dec 3. Genet Med. 2022. PMID: 34906497 Free article.
Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario.
Hayeems RZ, Marshall CR, Gillespie MK, Szuto A, Chisholm C, Stavropoulos DJ, Venkataramanan V, Tsiplova K, Sawyer S, Price EM, Lau L, Khan R, Lee W, Huang L, Jarinova O, Ungar WJ, Mendoza-Londono R, Somerville MJ, Boycott KM. Hayeems RZ, et al. Among authors: venkataramanan v. CMAJ Open. 2022 May 24;10(2):E460-E465. doi: 10.9778/cmajo.20210272. Print 2022 Apr-Jun. CMAJ Open. 2022. PMID: 35609929 Free PMC article.
Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.
Ungar WJ, Hayeems RZ, Marshall CR, Gillespie MK, Szuto A, Chisholm C, James Stavropoulos D, Huang L, Jarinova O, Wu V, Tsiplova K, Lau L, Lee W, Venkataramanan V, Sawyer S, Mendoza-Londono R, Somerville MJ, Boycott KM; Genome Sequencing Ontario Secondary Findings Study Team. Ungar WJ, et al. Among authors: venkataramanan v. Clin Ther. 2023 Aug;45(8):702-709. doi: 10.1016/j.clinthera.2023.06.004. Epub 2023 Jul 14. Clin Ther. 2023. PMID: 37453830
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: venkataramanan v. 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
Cross-cultural validation of the ICOAP and physical function short forms of the HOOS and KOOS in a multi-country study of patients with hip and knee osteoarthritis.
Mehta SP, Sankar A, Venkataramanan V, Lohmander LS, Katz JN, Hawker GA, Gossec L, Roos EM, Maillefert JF, Kloppenburg M, Dougados M, Davis AM. Mehta SP, et al. Among authors: venkataramanan v. Osteoarthritis Cartilage. 2016 Dec;24(12):2077-2081. doi: 10.1016/j.joca.2016.07.014. Epub 2016 Aug 4. Osteoarthritis Cartilage. 2016. PMID: 27497697 Free article.
Expectations of recovery from revision knee replacement.
Venkataramanan V, Gignac MA, Mahomed NN, Davis AM. Venkataramanan V, et al. Arthritis Rheum. 2006 Apr 15;55(2):314-21. doi: 10.1002/art.21856. Arthritis Rheum. 2006. PMID: 16583381 Free article.
31 results