669 related articles for article (PubMed ID: 31980526)
1. Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging.
Hou YC; Yu HC; Martin R; Cirulli ET; Schenker-Ahmed NM; Hicks M; Cohen IV; Jönsson TJ; Heister R; Napier L; Swisher CL; Dominguez S; Tang H; Li W; Perkins BA; Barea J; Rybak C; Smith E; Duchicela K; Doney M; Brar P; Hernandez N; Kirkness EF; Kahn AM; Venter JC; Karow DS; Caskey CT
Proc Natl Acad Sci U S A; 2020 Feb; 117(6):3053-3062. PubMed ID: 31980526
[TBL] [Abstract][Full Text] [Related]
2. Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adults.
Perkins BA; Caskey CT; Brar P; Dec E; Karow DS; Kahn AM; Hou YC; Shah N; Boeldt D; Coughlin E; Hands G; Lavrenko V; Yu J; Procko A; Appis J; Dale AM; Guo L; Jönsson TJ; Wittmann BM; Bartha I; Ramakrishnan S; Bernal A; Brewer JB; Brewerton S; Biggs WH; Turpaz Y; Venter JC
Proc Natl Acad Sci U S A; 2018 Apr; 115(14):3686-3691. PubMed ID: 29555771
[TBL] [Abstract][Full Text] [Related]
3. Genomic Autopsy of Sudden Deaths in Young Individuals.
Webster G; Puckelwartz MJ; Pesce LL; Dellefave-Castillo LM; Vanoye CG; Potet F; Page P; Kearns SD; Pottinger T; White S; Arunkumar P; Olson R; Kofman A; Ibrahim N; Ing A; Brew C; Yap KL; Kadri S; George AL; McNally EM
JAMA Cardiol; 2021 Nov; 6(11):1247-1256. PubMed ID: 34379075
[TBL] [Abstract][Full Text] [Related]
4. Precision Medicine: Functional Advancements.
Caskey T
Annu Rev Med; 2018 Jan; 69():1-18. PubMed ID: 29261360
[TBL] [Abstract][Full Text] [Related]
5. Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.
Zoltick ES; Linderman MD; McGinniss MA; Ramos E; Ball MP; Church GM; Leonard DGB; Pereira S; McGuire AL; Caskey CT; Sanderson SC; Schadt EE; Nielsen DE; Crawford SD; Green RC;
Genome Med; 2019 Feb; 11(1):10. PubMed ID: 30808425
[TBL] [Abstract][Full Text] [Related]
6. Genomic medicine and risk prediction across the disease spectrum.
Kotze MJ; Lückhoff HK; Peeters AV; Baatjes K; Schoeman M; van der Merwe L; Grant KA; Fisher LR; van der Merwe N; Pretorius J; van Velden DP; Myburgh EJ; Pienaar FM; van Rensburg SJ; Yako YY; September AV; Moremi KE; Cronje FJ; Tiffin N; Bouwens CS; Bezuidenhout J; Apffelstaedt JP; Hough FS; Erasmus RT; Schneider JW
Crit Rev Clin Lab Sci; 2015; 52(3):120-37. PubMed ID: 25597499
[TBL] [Abstract][Full Text] [Related]
7. Plasma metabolomic profiles enhance precision medicine for volunteers of normal health.
Guo L; Milburn MV; Ryals JA; Lonergan SC; Mitchell MW; Wulff JE; Alexander DC; Evans AM; Bridgewater B; Miller L; Gonzalez-Garay ML; Caskey CT
Proc Natl Acad Sci U S A; 2015 Sep; 112(35):E4901-10. PubMed ID: 26283345
[TBL] [Abstract][Full Text] [Related]
8. Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Glazer AM; Davogustto G; Shaffer CM; Vanoye CG; Desai RR; Farber-Eger EH; Dikilitas O; Shang N; Pacheco JA; Yang T; Muhammad A; Mosley JD; Van Driest SL; Wells QS; Shaffer LL; Kalash OR; Wada Y; Bland HT; Yoneda ZT; Mitchell DW; Kroncke BM; Kullo IJ; Jarvik GP; Gordon AS; Larson EB; Manolio TA; Mirshahi T; Luo JZ; Schaid D; Namjou B; Alsaied T; Singh R; Singhal A; Liu C; Weng C; Hripcsak G; Ralston JD; McNally EM; Chung WK; Carrell DS; Leppig KA; Hakonarson H; Sleiman P; Sohn S; Glessner J; ; Denny J; Wei WQ; George AL; Shoemaker MB; Roden DM
Circulation; 2022 Mar; 145(12):877-891. PubMed ID: 34930020
[TBL] [Abstract][Full Text] [Related]
9. Integration of Omics and Phenotypic Data for Precision Medicine.
Zhao J; Feng Q; Wei WQ
Methods Mol Biol; 2022; 2486():19-35. PubMed ID: 35437716
[TBL] [Abstract][Full Text] [Related]
10. Retrospective genotype-phenotype analysis in a 305 patient cohort referred for testing of a targeted epilepsy panel.
Hesse AN; Bevilacqua J; Shankar K; Reddi HV
Epilepsy Res; 2018 Aug; 144():53-61. PubMed ID: 29778030
[TBL] [Abstract][Full Text] [Related]
11. Precision phenotyping, panomics, and system-level bioinformatics to delineate complex biologies of atherosclerosis: rationale and design of the "Genetic Loci and the Burden of Atherosclerotic Lesions" study.
Voros S; Maurovich-Horvat P; Marvasty IB; Bansal AT; Barnes MR; Vazquez G; Murray SS; Voros V; Merkely B; Brown BO; Warnick GR
J Cardiovasc Comput Tomogr; 2014; 8(6):442-51. PubMed ID: 25439791
[TBL] [Abstract][Full Text] [Related]
12. Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations.
Johnston JJ; Lewis KL; Ng D; Singh LN; Wynter J; Brewer C; Brooks BP; Brownell I; Candotti F; Gonsalves SG; Hart SP; Kong HH; Rother KI; Sokolic R; Solomon BD; Zein WM; Cooper DN; Stenson PD; Mullikin JC; Biesecker LG
Am J Hum Genet; 2015 Jun; 96(6):913-25. PubMed ID: 26046366
[TBL] [Abstract][Full Text] [Related]
13. Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine.
Fang H; Wu Y; Yang H; Yoon M; Jiménez-Barrón LT; Mittelman D; Robison R; Wang K; Lyon GJ
BMC Med Genomics; 2017 Feb; 10(1):10. PubMed ID: 28228131
[TBL] [Abstract][Full Text] [Related]
14. Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review.
Fatkin D; Huttner IG; Kovacic JC; Seidman JG; Seidman CE
J Am Coll Cardiol; 2019 Dec; 74(23):2921-2938. PubMed ID: 31806137
[TBL] [Abstract][Full Text] [Related]
15. Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases.
Hitomi Y; Tokunaga K
Proc Jpn Acad Ser B Phys Biol Sci; 2017; 93(9):657-676. PubMed ID: 29129848
[TBL] [Abstract][Full Text] [Related]
16. Scientists on the Spot: Sequencing the human genome to influence patient healthcare.
Schmidt C; Hubbard T
Cardiovasc Res; 2018 Jul; 114(9):e66-e67. PubMed ID: 30052801
[No Abstract] [Full Text] [Related]
17. PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases.
Adler A; Kirchmeier P; Reinhard J; Brauner B; Dunger I; Fobo G; Frishman G; Montrone C; Mewes HW; Arnold M; Ruepp A
Orphanet J Rare Dis; 2018 Jan; 13(1):22. PubMed ID: 29370821
[TBL] [Abstract][Full Text] [Related]
18. Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.
Bagnall RD; Ingles J; Dinger ME; Cowley MJ; Ross SB; Minoche AE; Lal S; Turner C; Colley A; Rajagopalan S; Berman Y; Ronan A; Fatkin D; Semsarian C
J Am Coll Cardiol; 2018 Jul; 72(4):419-429. PubMed ID: 30025578
[TBL] [Abstract][Full Text] [Related]
19. Family history assessment significantly enhances delivery of precision medicine in the genomics era.
Bylstra Y; Lim WK; Kam S; Tham KW; Wu RR; Teo JX; Davila S; Kuan JL; Chan SH; Bertin N; Yang CX; Rozen S; Teh BT; Yeo KK; Cook SA; Jamuar SS; Ginsburg GS; Orlando LA; Tan P
Genome Med; 2021 Jan; 13(1):3. PubMed ID: 33413596
[TBL] [Abstract][Full Text] [Related]
20. Harnessing technology and molecular analysis to understand the development of cardiovascular diseases in Asia: a prospective cohort study (SingHEART).
Yap J; Lim WK; Sahlén A; Chin CW; Chew KMY; Davila S; Allen J; Goh V; Tan SY; Tan P; Lam CSP; Cook SA; Yeo KK
BMC Cardiovasc Disord; 2019 Nov; 19(1):259. PubMed ID: 31752689
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
