Marc S. Williams
Orcid: 0000-0001-6165-8701
According to our database1,
Marc S. Williams
authored at least 31 papers
between 2006 and 2024.
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Bibliography
2024
Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup.
J. Am. Medical Informatics Assoc., January, 2024
Genomics in nephrology: identifying informatics opportunities to improve diagnosis of genetic kidney disorders using a human-centered design approach.
J. Am. Medical Informatics Assoc., 2024
Genetically guided precision medicine clinical decision support tools: a systematic review.
J. Am. Medical Informatics Assoc., 2024
2022
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
J. Am. Medical Informatics Assoc., 2022
High-throughput assessment of genomic outcomes: development and validation of the HI-TAG knowledgebase.
Proceedings of the AMIA 2022, 2022
2021
Misdiagnosis: Burnout, moral injury, and implications for the electronic health record.
J. Am. Medical Informatics Assoc., 2021
A retrospective look at the predictions and recommendations from the 2009 AMIA policy meeting: did we see EHR-related clinician burnout coming?
J. Am. Medical Informatics Assoc., 2021
Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelines.
J. Am. Medical Informatics Assoc., 2021
Appl. Clin. Inform., 2021
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021
Evaluation of the Portability of Natural Language Processing-based Computable Phenotypes in the eMERGE Network.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021
2020
Translational Research of Machine Learning and Artificial Intelligence Advances in Clinical Settings - Experiences and Challenges.
Proceedings of the AMIA 2020, 2020
2018
Implementation of a patient-facing genomic test report in the electronic health record using a web-application interface.
BMC Medical Informatics Decis. Mak., 2018
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
J. Am. Medical Informatics Assoc., 2018
2017
Proceedings of the AMIA 2017, 2017
2016
J. Biomed. Informatics, 2016
J. Biomed. Informatics, 2016
Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).
J. Am. Medical Informatics Assoc., 2016
Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard.
Appl. Clin. Inform., 2016
Appl. Clin. Inform., 2016
Developing an Algorithm to Detect Early Childhood Obesity in Two Tertiary Pediatric Medical Centers.
Appl. Clin. Inform., 2016
The Clinical Pharmacogenetics Implementation Consortium (CPIC) Term Standardization for Clinical Pharmacogenetic Test Results: Alleles and Phenotypes.
Proceedings of the Summit on Clinical Research Informatics, 2016
2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
J. Am. Medical Informatics Assoc., 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithms.
J. Am. Medical Informatics Assoc., 2015
Proceedings of the AMIA 2015, 2015
Proceedings of the AMIA 2015, 2015
2014
A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.
Proceedings of the AMIA 2014, 2014
2012
Utility of gene-specific algorithms for predicting pathogenicity of uncertain gene variants.
J. Am. Medical Informatics Assoc., 2012
2010
Deriving consumer-facing disease concepts for family health histories using multi-source sampling.
J. Biomed. Informatics, 2010
2009
Proceedings of the AMIA 2009, 2009
2006
Proceedings of the AMIA 2006, 2006