Sellers S, Cunningham B, Bonham V
J Racial Ethn Health Disparities. 2018; 6(1):110-116.
PMID: 29926440
PMC: 6309376.
DOI: 10.1007/s40615-018-0505-y.
Merdad L, Aldakhil L, Gadi R, Assidi M, Saddick S, Abuzenadah A
BMC Med Ethics. 2017; 18(1):32.
PMID: 28464877
PMC: 5414189.
DOI: 10.1186/s12910-017-0195-8.
Hall J, Ryan J, Bray B, Brown C, Lanfear D, Newby L
Circ Cardiovasc Genet. 2016; 9(2):193-202.
PMID: 26976545
PMC: 5646218.
DOI: 10.1161/HCG.0000000000000029.
Dunnenberger H, Crews K, Hoffman J, Caudle K, Broeckel U, Howard S
Annu Rev Pharmacol Toxicol. 2014; 55:89-106.
PMID: 25292429
PMC: 4607278.
DOI: 10.1146/annurev-pharmtox-010814-124835.
SanGiovanni J, Chew E
Cold Spring Harb Perspect Med. 2014; 4(10).
PMID: 25125423
PMC: 4200209.
DOI: 10.1101/cshperspect.a017228.
PG4KDS: a model for the clinical implementation of pre-emptive pharmacogenetics.
Hoffman J, Haidar C, Wilkinson M, Crews K, Baker D, Kornegay N
Am J Med Genet C Semin Med Genet. 2014; 166C(1):45-55.
PMID: 24619595
PMC: 4056586.
DOI: 10.1002/ajmg.c.31391.
Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.
Dotson W, Douglas M, Kolor K, Stewart A, Bowen M, Gwinn M
Clin Pharmacol Ther. 2014; 95(4):394-402.
PMID: 24398597
PMC: 4689130.
DOI: 10.1038/clpt.2013.226.
Genetics in population health science: strategies and opportunities.
Belsky D, Moffitt T, Caspi A
Am J Public Health. 2013; 103 Suppl 1:S73-83.
PMID: 23927511
PMC: 3786748.
DOI: 10.2105/AJPH.2012.301139.
Bringing genome-wide association findings into clinical use.
Manolio T
Nat Rev Genet. 2013; 14(8):549-58.
PMID: 23835440
DOI: 10.1038/nrg3523.
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Gottesman O, Kuivaniemi H, Tromp G, Andrew Faucett W, Li R, Manolio T
Genet Med. 2013; 15(10):761-71.
PMID: 23743551
PMC: 3795928.
DOI: 10.1038/gim.2013.72.
How can polygenic inheritance be used in population screening for common diseases?.
Khoury M, Janssens A, Ransohoff D
Genet Med. 2013; 15(6):437-43.
PMID: 23412608
PMC: 4692802.
DOI: 10.1038/gim.2012.182.
Pharmacogenomics discovery and implementation in genome-wide association studies era.
Ni X, Zhang W, Huang R
Wiley Interdiscip Rev Syst Biol Med. 2012; 5(1):1-9.
PMID: 23188748
PMC: 3527666.
DOI: 10.1002/wsbm.1199.
A population approach to precision medicine.
Khoury M, Gwinn M, Glasgow R, Kramer B
Am J Prev Med. 2012; 42(6):639-45.
PMID: 22608383
PMC: 3629731.
DOI: 10.1016/j.amepre.2012.02.012.
Atherosclerosis, inflammation, genetics, and stem cells: 2012 update.
Goldschmidt-Clermont P, Dong C, Seo D, Velazquez O
Curr Atheroscler Rep. 2012; 14(3):201-10.
PMID: 22476914
PMC: 3537163.
DOI: 10.1007/s11883-012-0244-1.
Resolving the variable genome and epigenome in human disease.
Knight J
J Intern Med. 2012; 271(4):379-91.
PMID: 22443201
PMC: 4442130.
DOI: 10.1111/j.1365-2796.2011.02508.x.
Looking back at genomic medicine in 2011.
Auffray C, Caulfield T, Khoury M, Lupski J, Schwab M, Veenstra T
Genome Med. 2012; 4(1):9.
PMID: 22293121
PMC: 3334557.
DOI: 10.1186/gm308.