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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2017 | 3 |
2019 | 2 |
2020 | 2 |
2024 | 0 |
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6 results
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Page 1
Settling the score: variant prioritization and Mendelian disease.
Nat Rev Genet. 2017 Oct;18(10):599-612. doi: 10.1038/nrg.2017.52. Epub 2017 Aug 14.
Nat Rev Genet. 2017.
PMID: 28804138
Free PMC article.
Review.
Combating subclonal evolution of resistant cancer phenotypes.
Brady SW, McQuerry JA, Qiao Y, Piccolo SR, Shrestha G, Jenkins DF, Layer RM, Pedersen BS, Miller RH, Esch A, Selitsky SR, Parker JS, Anderson LA, Dalley BK, Factor RE, Reddy CB, Boltax JP, Li DY, Moos PJ, Gray JW, Heiser LM, Buys SS, Cohen AL, Johnson WE, Quinlan AR, Marth G, Werner TL, Bild AH.
Brady SW, et al.
Nat Commun. 2017 Nov 1;8(1):1231. doi: 10.1038/s41467-017-01174-3.
Nat Commun. 2017.
PMID: 29093439
Free PMC article.
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Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.
Lubin IM, Aziz N, Babb LJ, Ballinger D, Bisht H, Church DM, Cordes S, Eilbeck K, Hyland F, Kalman L, Landrum M, Lockhart ER, Maglott D, Marth G, Pfeifer JD, Rehm HL, Roy S, Tezak Z, Truty R, Ullman-Cullere M, Voelkerding KV, Worthey EA, Zaranek AW, Zook JM.
Lubin IM, et al.
J Mol Diagn. 2017 May;19(3):417-426. doi: 10.1016/j.jmoldx.2016.12.001. Epub 2017 Mar 18.
J Mol Diagn. 2017.
PMID: 28315672
Free PMC article.
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Multi-platform discovery of haplotype-resolved structural variation in human genomes.
Chaisson MJP, Sanders AD, Zhao X, Malhotra A, Porubsky D, Rausch T, Gardner EJ, Rodriguez OL, Guo L, Collins RL, Fan X, Wen J, Handsaker RE, Fairley S, Kronenberg ZN, Kong X, Hormozdiari F, Lee D, Wenger AM, Hastie AR, Antaki D, Anantharaman T, Audano PA, Brand H, Cantsilieris S, Cao H, Cerveira E, Chen C, Chen X, Chin CS, Chong Z, Chuang NT, Lambert CC, Church DM, Clarke L, Farrell A, Flores J, Galeev T, Gorkin DU, Gujral M, Guryev V, Heaton WH, Korlach J, Kumar S, Kwon JY, Lam ET, Lee JE, Lee J, Lee WP, Lee SP, Li S, Marks P, Viaud-Martinez K, Meiers S, Munson KM, Navarro FCP, Nelson BJ, Nodzak C, Noor A, Kyriazopoulou-Panagiotopoulou S, Pang AWC, Qiu Y, Rosanio G, Ryan M, Stütz A, Spierings DCJ, Ward A, Welch AE, Xiao M, Xu W, Zhang C, Zhu Q, Zheng-Bradley X, Lowy E, Yakneen S, McCarroll S, Jun G, Ding L, Koh CL, Ren B, Flicek P, Chen K, Gerstein MB, Kwok PY, Lansdorp PM, Marth GT, Sebat J, Shi X, Bashir A, Ye K, Devine SE, Talkowski ME, Mills RE, Marschall T, Korbel JO, Eichler EE, Lee C.
Chaisson MJP, et al.
Nat Commun. 2019 Apr 16;10(1):1784. doi: 10.1038/s41467-018-08148-z.
Nat Commun. 2019.
PMID: 30992455
Free PMC article.
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Implementing the VMC Specification to Reduce Ambiguity in Genomic Variant Representation.
Watkins M, Rynearson S, Henrie A, Eilbeck K.
Watkins M, et al.
AMIA Annu Symp Proc. 2020 Mar 4;2019:1226-1235. eCollection 2019.
AMIA Annu Symp Proc. 2020.
PMID: 32308920
Free PMC article.
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FHIR Lab Reports: using SMART on FHIR and CDS Hooks to increase the clinical utility of pharmacogenomic laboratory test results.
Watkins M, Eilbeck K.
Watkins M, et al.
AMIA Jt Summits Transl Sci Proc. 2020 May 30;2020:683-692. eCollection 2020.
AMIA Jt Summits Transl Sci Proc. 2020.
PMID: 32477691
Free PMC article.
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