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Samuel Aronson
Samuel Aronson
Unknown affiliation
Verified email at partners.org
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Cited by
Cited by
Year
Using multiplexed assays of oncogenic drivers in lung cancers to select targeted drugs
MG Kris, BE Johnson, LD Berry, DJ Kwiatkowski, AJ Iafrate, II Wistuba, ...
Jama 311 (19), 1998-2006, 2014
17812014
Building the foundation for genomics in precision medicine
SJ Aronson, HL Rehm
Nature 526 (7573), 336-342, 2015
5252015
Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine
RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ...
The American Journal of Human Genetics 98 (6), 1051-1066, 2016
1682016
Research directions in the clinical implementation of pharmacogenomics: an overview of US programs and projects
S Volpi, CJ Bult, RL Chisholm, PA Deverka, GS Ginsburg, HJ Jacob, ...
Clinical Pharmacology & Therapeutics 103 (5), 778-786, 2018
1142018
Communicating new knowledge on previously reported genetic variants
SJ Aronson, EH Clark, M Varugheese, S Baxter, LJ Babb, HL Rehm
Genetics in medicine 14 (8), 713-719, 2012
1122012
Harmonizing clinical sequencing and interpretation for the eMERGE III network
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
932019
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study
WJ Lane, CM Westhoff, NS Gleadall, M Aguad, R Smeland-Wagman, ...
The Lancet Haematology 5 (6), e241-e251, 2018
932018
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record
BH Shirts, JS Salama, SJ Aronson, WK Chung, SW Gray, LA Hindorff, ...
Journal of the American Medical Informatics Association 22 (6), 1231-1242, 2015
892015
The GeneInsight suite: a platform to support laboratory and provider use of DNA‐based genetic testing
SJ Aronson, EH Clark, LJ Babb, S Baxter, LM Farwell, BH Funke, ...
Human mutation 32 (5), 532-536, 2011
782011
A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record
P Tarczy-Hornoch, L Amendola, SJ Aronson, L Garraway, S Gray, ...
Genetics in Medicine 15 (10), 824-832, 2013
692013
Medical laboratory report message gateway
SJ Aronson, LJ Babb, M Ullman-Cullere, EH Clark
US Patent 7,908,293, 2011
602011
Genomic information for clinicians in the electronic health record: lessons learned from the clinical genome resource project and the electronic medical records and genomics …
MS Williams, CO Taylor, NA Walton, SR Goehringer, S Aronson, ...
Frontiers in genetics 10, 1059, 2019
492019
Usability of a novel clinician interface for genetic results
PM Neri, SE Pollard, LA Volk, LP Newmark, M Varugheese, S Baxter, ...
Journal of biomedical informatics 45 (5), 950-957, 2012
362012
Results of a remotely delivered hypertension and lipid program in more than 10 000 patients across a diverse health care network
AJ Blood, CP Cannon, WJ Gordon, C Mailly, T MacLean, S Subramaniam, ...
JAMA cardiology 8 (1), 12-21, 2023
282023
Genomic considerations for FHIR®; eMERGE implementation lessons
M Murugan, LJ Babb, CO Taylor, LV Rasmussen, RR Freimuth, E Venner, ...
Journal of biomedical informatics 118, 103795, 2021
192021
Rationale and design of a navigator‐driven remote optimization of guideline‐directed medical therapy in patients with heart failure with reduced ejection fraction
AJ Blood, CM Fischer, LE Fera, TE MacLean, KV Smith, JR Dunning, ...
Clinical Cardiology 43 (1), 4-13, 2020
192020
A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga
WJ Lane, M Aguad, R Smeland‐Wagman, S Vege, HH Mah, A Joseph, ...
Transfusion 59 (3), 908-915, 2019
192019
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example
S Aronson, L Babb, D Ames, RA Gibbs, E Venner, JJ Connelly, K Marsolo, ...
Journal of the American Medical Informatics Association 25 (10), 1375-1381, 2018
192018
A novel clinician interface to improve clinician access to up-to-date genetic results
AR Wilcox, PM Neri, LA Volk, LP Newmark, EH Clark, LJ Babb, ...
Journal of the American Medical Informatics Association 21 (e1), e117-e121, 2014
192014
Providing access to genomic variant knowledge in a healthcare setting: a vision for the ClinGen Electronic Health Records Workgroup
CL Overby, B Heale, S Aronson, JM Cherry, S Dwight, A Milosavljevic, ...
Clinical Pharmacology & Therapeutics 99 (2), 157-160, 2016
162016
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