27937091 28192596 26604852 34642594 27153269 30173949 29028368 26536838 33626791 27668172 26422737 30302274 28188191 27181684 30969158 27631194 29086656 29118898 26513348 26324366 32758032 33538426 29242914 26541391 27140283 27863196 27249770 2718168 - Search Results

Year	Number of Results
2015	14
2016	24
2017	11
2018	4
2019	4
2020	3
2021	4
2022	1
2023	0

1

Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics Study.

Gray SW, Gollust SE, Carere DA, Chen CA, Cronin A, Kalia SS, Rana HQ, Ruffin MT 4th, Wang C, Roberts JS, Green RC. Gray SW, et al. J Clin Oncol. 2017 Feb 20;35(6):636-644. doi: 10.1200/JCO.2016.67.1503. Epub 2016 Dec 12. J Clin Oncol. 2017. PMID: 27937091 Free PMC article.

2

Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.

Johnson LM, Valdez JM, Quinn EA, Sykes AD, McGee RB, Nuccio R, Hines-Dowell SJ, Baker JN, Kesserwan C, Nichols KE, Mandrell BN. Johnson LM, et al. Cancer. 2017 Jun 15;123(12):2352-2359. doi: 10.1002/cncr.30581. Epub 2017 Feb 13. Cancer. 2017. PMID: 28192596 Free PMC article.

3

Improving medical students' knowledge of genetic disease: a review of current and emerging pedagogical practices.

Wolyniak MJ, Bemis LT, Prunuske AJ. Wolyniak MJ, et al. Adv Med Educ Pract. 2015 Oct 29;6:597-607. doi: 10.2147/AMEP.S73644. eCollection 2015. Adv Med Educ Pract. 2015. PMID: 26604852 Free PMC article. Review.

4

Personalization of medical treatments in oncology: time for rethinking the disease concept to improve individual outcomes.

Bizzarri M, Fedeli V, Monti N, Cucina A, Jalouli M, Alwasel SH, Harrath AH. Bizzarri M, et al. EPMA J. 2021 Oct 7;12(4):545-558. doi: 10.1007/s13167-021-00254-1. eCollection 2021 Dec. EPMA J. 2021. PMID: 34642594 Free PMC article. Review.

5

Developing context-specific next-generation sequencing policy.

Curnutte MA, Frumovitz KL, Bollinger JM, Cook-Deegan RM, McGuire AL, Majumder MA. Curnutte MA, et al. Nat Biotechnol. 2016 May 6;34(5):466-70. doi: 10.1038/nbt.3545. Nat Biotechnol. 2016. PMID: 27153269 Free PMC article. No abstract available.

6

How should costs and cost-effectiveness be considered in prenatal genetic testing?

Sparks TN, Caughey AB. Sparks TN, et al. Semin Perinatol. 2018 Aug;42(5):275-282. doi: 10.1053/j.semperi.2018.07.003. Epub 2018 Jul 26. Semin Perinatol. 2018. PMID: 30173949 Free PMC article. Review.

7

A Window Into Clinical Next-Generation Sequencing-Based Oncology Testing Practices.

Nagarajan R, Bartley AN, Bridge JA, Jennings LJ, Kamel-Reid S, Kim A, Lazar AJ, Lindeman NI, Moncur J, Rai AJ, Routbort MJ, Vasalos P, Merker JD. Nagarajan R, et al. Arch Pathol Lab Med. 2017 Dec;141(12):1679-1685. doi: 10.5858/arpa.2016-0542-CP. Epub 2017 Oct 13. Arch Pathol Lab Med. 2017. PMID: 29028368 Free article.

8

Precision medicine in the age of big data: The present and future role of large-scale unbiased sequencing in drug discovery and development.

Vicini P, Fields O, Lai E, Litwack ED, Martin AM, Morgan TM, Pacanowski MA, Papaluca M, Perez OD, Ringel MS, Robson M, Sakul H, Vockley J, Zaks T, Dolsten M, Søgaard M. Vicini P, et al. Clin Pharmacol Ther. 2016 Feb;99(2):198-207. doi: 10.1002/cpt.293. Epub 2015 Dec 19. Clin Pharmacol Ther. 2016. PMID: 26536838 Review.

9

Response to the Proposed Food and Drug Administration Regulation of Laboratory-Developed Tests: It Is Past Time for Professional Consensus.

Konnick EQ. Konnick EQ. J Appl Lab Med. 2016 Sep 1;1(2):239-241. doi: 10.1373/jalm.2016.020909. J Appl Lab Med. 2016. PMID: 33626791 Free article. No abstract available.

10

Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel.

Messner DA, Al Naber J, Koay P, Cook-Deegan R, Majumder M, Javitt G, Deverka P, Dvoskin R, Bollinger J, Curnutte M, Chandrasekharan S, McGuire A. Messner DA, et al. Appl Transl Genom. 2016 May 25;10:19-24. doi: 10.1016/j.atg.2016.05.004. eCollection 2016 Sep. Appl Transl Genom. 2016. PMID: 27668172 Free PMC article.

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