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Year Number of Results
2004 1
2010 1
2011 3
2013 3
2014 3
2015 1
2016 2
2018 1
2021 2
2022 4
2024 1

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20 results

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Page 1
Optimizing the delivery of genetic and advanced diagnostic testing in the province of Ontario: challenges and implications for laboratory technology assessment and management in decentralized healthcare systems.
Husereau D, Sullivan T, Feilotter HE, Gomes MM, Juergens R, Sheffield BS, Kassam S, Stockley TL, Jacobs P. Husereau D, et al. Among authors: feilotter he. J Med Econ. 2022 Jan-Dec;25(1):993-1004. doi: 10.1080/13696998.2022.2101807. J Med Econ. 2022. PMID: 35850613 Free article.
BRCA1 Variant Assessment Using a Simple Analytic Assay.
Kim DM, Feilotter HE, Davey SK. Kim DM, et al. Among authors: feilotter he. J Appl Lab Med. 2022 May 4;7(3):674-688. doi: 10.1093/jalm/jfab163. J Appl Lab Med. 2022. PMID: 35021209 Free article.
Validation, Implementation, and Clinical Impact of the Oncomine Myeloid Targeted-Amplicon DNA and RNA Ion Semiconductor Sequencing Assay.
Ferrone CK, Wong H, Semenuk L, Werunga B, Snetsinger B, Zhang X, Zhang G, Lui J, Richard-Carpentier G, Crocker S, Good D, Hay AE, Quest G, Carson N, Feilotter HE, Rauh MJ. Ferrone CK, et al. Among authors: feilotter he. J Mol Diagn. 2021 Oct;23(10):1292-1305. doi: 10.1016/j.jmoldx.2021.07.010. Epub 2021 Aug 5. J Mol Diagn. 2021. PMID: 34365012 Free article.
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository.
Mighton C, Smith AC, Mayers J, Tomaszewski R, Taylor S, Hume S, Agatep R, Spriggs E, Feilotter HE, Semenuk L, Wong H, Lazo de la Vega L, Marshall CR, Axford MM, Silver T, Charames GS, Di Gioacchino V, Watkins N, Foulkes WD, Clavier M, Hamel N, Chong G, Lamont RE, Parboosingh J, Karsan A, Bosdet I, Young SS, Tucker T, Akbari MR, Speevak MD, Vaags AK, Lebo MS, Lerner-Ellis J; Canadian Open Genetics Repository Working Group. Mighton C, et al. Among authors: feilotter he. J Med Genet. 2022 Jun;59(6):571-578. doi: 10.1136/jmedgenet-2021-107738. Epub 2021 Apr 19. J Med Genet. 2022. PMID: 33875564 Free PMC article.
Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study.
Vaughn CP, Costa JL, Feilotter HE, Petraroli R, Bagai V, Rachiglio AM, Marino FZ, Tops B, Kurth HM, Sakai K, Mafficini A, Bastien RRL, Reiman A, Le Corre D, Boag A, Crocker S, Bihl M, Hirschmann A, Scarpa A, Machado JC, Blons H, Sheils O, Bramlett K, Ligtenberg MJL, Cree IA, Normanno N, Nishio K, Laurent-Puig P. Vaughn CP, et al. Among authors: feilotter he. BMC Cancer. 2018 Aug 16;18(1):828. doi: 10.1186/s12885-018-4736-4. BMC Cancer. 2018. PMID: 30115026 Free PMC article.
Discovering biomarkers for antidepressant response: protocol from the Canadian biomarker integration network in depression (CAN-BIND) and clinical characteristics of the first patient cohort.
Lam RW, Milev R, Rotzinger S, Andreazza AC, Blier P, Brenner C, Daskalakis ZJ, Dharsee M, Downar J, Evans KR, Farzan F, Foster JA, Frey BN, Geraci J, Giacobbe P, Feilotter HE, Hall GB, Harkness KL, Hassel S, Ismail Z, Leri F, Liotti M, MacQueen GM, McAndrews MP, Minuzzi L, Müller DJ, Parikh SV, Placenza FM, Quilty LC, Ravindran AV, Salomons TV, Soares CN, Strother SC, Turecki G, Vaccarino AL, Vila-Rodriguez F, Kennedy SH; CAN-BIND Investigator Team. Lam RW, et al. Among authors: feilotter he. BMC Psychiatry. 2016 Apr 16;16:105. doi: 10.1186/s12888-016-0785-x. BMC Psychiatry. 2016. PMID: 27084692 Free PMC article.
ATM gene mutations in sporadic breast cancer patients from Brazil.
Mangone FR, Miracca EC, Feilotter HE, Mulligan LM, Nagai MA. Mangone FR, et al. Among authors: feilotter he. Springerplus. 2015 Jan 15;4:23. doi: 10.1186/s40064-015-0787-z. eCollection 2015. Springerplus. 2015. PMID: 25625042 Free PMC article.
20 results