|ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing|
RC Green, JS Berg, WW Grody, SS Kalia, BR Korf, CL Martin, AL McGuire, ...
Genetics in Medicine 15 (7), 565-574, 2013
|CHARGE association: an update and review for the primary pediatrician|
KD Blake, SLH Davenport, BD Hall, MA Hefner, RA Pagon, MS Williams, ...
Clinical pediatrics 37 (3), 159-173, 1998
|Implementing genomic medicine in the clinic: the future is here|
TA Manolio, RL Chisholm, B Ozenberger, DM Roden, MS Williams, ...
Genetics in Medicine 15 (4), 258-267, 2013
|The electronic medical records and genomics (eMERGE) network: past, present, and future|
O Gottesman, H Kuivaniemi, G Tromp, WA Faucett, R Li, TA Manolio, ...
Genetics in Medicine 15 (10), 761-771, 2013
|Return of genomic results to research participants: the floor, the ceiling, and the choices in between|
GP Jarvik, LM Amendola, JS Berg, K Brothers, EW Clayton, W Chung, ...
The American Journal of Human Genetics 94 (6), 818-826, 2014
|Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process|
K E Caudle, T E Klein, J M Hoffman, D J Muller, M Whirl-Carrillo, L Gong, ...
Current drug metabolism 15 (2), 209-217, 2014
|Pharmacogenetic testing of CYP2C9 and VKORC1 alleles for warfarin|
DA Flockhart, D O'Kane, MS Williams, MS Watson, B Gage, R Gandolfi, ...
Genetics in Medicine 10 (2), 139-150, 2008
|Population-based family history–specific risks for colorectal cancer: a constellation approach|
DP Taylor, RW Burt, MS Williams, PJ Haug, LA Cannon–Albright
Gastroenterology 138 (3), 877-885, 2010
|Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC)|
KE Caudle, HM Dunnenberger, RR Freimuth, JF Peterson, JD Burlison, ...
Genetics in Medicine 19 (2), 215-223, 2017
|Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from …|
AO Berg, K Armstrong, J Botkin, N Calonge, J Haddow, M Hayes, C Kaye, ...
Genetics in Medicine 11 (1), 35-41, 2009
|Design and anticipated outcomes of the eMERGE‐PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems|
LJ Rasmussen‐Torvik, SC Stallings, AS Gordon, B Almoguera, ...
Clinical Pharmacology & Therapeutics 96 (4), 482-489, 2014
|Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records|
SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ...
Jama 315 (1), 47-57, 2016
|Primary sclerosing cholangitis, autoimmune hepatitis, and overlap in Utah children: epidemiology and natural history|
M Deneau, MK Jensen, J Holmen, MS Williams, LS Book, SL Guthery
Hepatology 58 (4), 1392-1400, 2013
|Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5|
MJ McMillin, AE Beck, JX Chong, KM Shively, KJ Buckingham, ...
The American Journal of Human Genetics 94 (5), 734-744, 2014
|Global implementation of genomic medicine: we are not alone|
TA Manolio, M Abramowicz, F Al-Mulla, W Anderson, R Balling, ...
Science translational medicine 7 (290), 290ps13-290ps13, 2015
|A policy model to evaluate the benefits, risks and costs of warfarin pharmacogenomic testing|
LM Meckley, JM Gudgeon, JL Anderson, MS Williams, DL Veenstra
Pharmacoeconomics 28 (1), 61-74, 2010
|Further delineation of Kabuki syndrome in 48 well‐defined new individuals|
L Armstrong, AAE Moneim, K Aleck, DJ Aughton, C Baumann, ...
American Journal of Medical Genetics Part A 132 (3), 265-272, 2005
|Genetic variation among 82 pharmacogenes: the PGRNseq data from the eMERGE network|
WS Bush, DR Crosslin, A Owusu‐Obeng, J Wallace, B Almoguera, ...
Clinical Pharmacology & Therapeutics 100 (2), 160-169, 2016
|Pediatric advance care planning|
BJ Hammes, J Klevan, M Kempf, MS Williams
Journal of palliative medicine 8 (4), 766-773, 2005
|Desiderata for computable representations of electronic health records-driven phenotype algorithms|
H Mo, WK Thompson, LV Rasmussen, JA Pacheco, G Jiang, R Kiefer, ...
Journal of the American Medical Informatics Association 22 (6), 1220-1230, 2015