Marc S. Williams

Orcid: 0000-0001-6165-8701

According to our database1, Marc S. Williams authored at least 30 papers between 2006 and 2024.

Collaborative distances:

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

On csauthors.net:

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

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

Infobuttons for Genomic Medicine: Requirements and Barriers.
Appl. Clin. Inform., 2021

Creating a Home for Genomic Data in the Electronic Health Record.
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
Portable Precision Phenotype Algorithm for Chronic Rhinosinusitis.
Proceedings of the AMIA 2017, 2017

2016
User-centered design of multi-gene sequencing panel reports for clinicians.
J. Biomed. Informatics, 2016

The genomic CDS sandbox: An assessment among domain experts.
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

Practical considerations for implementing genomic information resources.
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

Building the Computational Workforce for Precision Medicine.
Proceedings of the AMIA 2015, 2015

Public Implementation Resources for Genomic Medicine.
Proceedings of the AMIA 2015, 2015

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
Evaluation of LOINC for Representing Constitutional Cytogenetic Test Result Reports.
Proceedings of the AMIA 2009, 2009

2006
Integrating Genetic Information Resources with an EHR.
Proceedings of the AMIA 2006, 2006


  Loading...