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Marc S. Williams
Marc S. Williams
Professor and Director Emeritus, Genomic Medicine Institute, Geisinger
Overená e-mailová adresa na: geisinger.edu - Domovská stránka
Názov
Citované v
Citované v
Rok
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
27332013
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
6052013
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
5972013
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
5861998
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
4812017
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
4412014
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
4272014
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
3322010
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
2772008
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
2562014
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
2342013
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
2062014
Family history and the natural history of colorectal cancer: systematic review
NB Henrikson, EM Webber, KA Goddard, A Scrol, M Piper, MS Williams, ...
Genetics in medicine 17 (9), 702-712, 2015
2052015
Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants
K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ...
JAMA Network Open 1 (5), e182140-e182140, 2018
1972018
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
1902016
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
1842016
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
1722015
A model for genome-first care: returning secondary genomic findings to participants and their healthcare providers in a large research cohort
MLB Schwartz, CZ McCormick, AL Lazzeri, ML D’Andra, MLG Hallquist, ...
The American Journal of Human Genetics 103 (3), 328-337, 2018
1532018
GA4GH: International policies and standards for data sharing across genomic research and healthcare
HL Rehm, AJH Page, L Smith, JB Adams, G Alterovitz, LJ Babb, ...
Cell genomics 1 (2), 2021
1412021
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
1412015
Systém momentálne nemôže vykonať operáciu. Skúste to neskôr.
Články 1–20