Samuel Aronson
Samuel Aronson
Unknown affiliation
Verified email at partners.org
Title
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
11422014
Building the foundation for genomics in precision medicine
SJ Aronson, HL Rehm
Nature 526 (7573), 336-342, 2015
3302015
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
1382016
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
952012
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
732011
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
702015
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
642013
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
482018
Medical laboratory report message gateway
SJ Aronson, LJ Babb, M Ullman-Cullere, EH Clark
US Patent 7,908,293, 2011
392011
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
362018
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
332012
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
212019
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
182014
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
102016
Genomic information for clinicians in the electronic health record: lessons learned from ClinGen and eMERGE
MS Williams, CO Taylor, NA Walton, SR Goehringer, S Aronson, ...
Frontiers in genetics 10, 1059, 2019
82019
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
82018
Information technology support for clinical genetic testing within an Academic Medical Center
S Aronson, L Mahanta, LL Ros, E Clark, L Babb, M Oates, H Rehm, ...
Journal of personalized medicine 6 (1), 4, 2016
82016
Evaluation: a qualitative pilot study of novel information technology infrastructure to communicate genetic variant updates
S Klinkenberg-Ramirez, PM Neri, LA Volk, SJ Samaha, LP Newmark, ...
Applied clinical informatics 7 (2), 461, 2016
82016
Can semantic web technologies enable translational medicine?(or can translational medicine help enrich the semantic web?)
V Kashyap, T Hongsermeier, S Aronson
Tech Report No. CIRD-20041027-0, 2005
72005
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
52019
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