Integrating Genetic Information Resources with an EHR. - Guilherme Del Fiol; Marc S. Williams; Naveen Maram; Roberto A. Rocha; Grant M. Wood; Joyce A. Mitchell (AMIA, 2006)

Evaluation of LOINC for Representing Constitutional Cytogenetic Test Result Reports. - Yan Z. Heras; Joyce A. Mitchell; Marc S. Williams; Arthur R. Brothman; Stanley M. Huff (AMIA, 2009)

Deriving consumer-facing disease concepts for family health histories using multi-source sampling. - Nathan C. Hulse; Grant M. Wood; Peter J. Haug; Marc S. Williams (J. Biomed. Informatics, 2010)

Utility of gene-specific algorithms for predicting pathogenicity of uncertain gene variants. - David K. Crockett; Elaine Lyon; Marc S. Williams; Scott P. Narus; Julio C. Facelli; Joyce A. Mitchell (J. Am. Medical Informatics Assoc., 2012)

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project. - Casey L. Overby; Luke V. Rasmussen; Andrea L. Hartzler; John J. Connolly; Josh F. Peterson; RoseMary Hedberg; Robert R. Freimuth; Brian H. Shirts; Joshua C. Denny; Eric B. Larson; Christopher G. Chute; Gail P. Jarvik; et al. (AMIA, 2014)

Public Implementation Resources for Genomic Medicine. - Josh F. Peterson; Marc S. Williams; Casey L. Overby; Robert R. Freimuth; Iftikhar J. Kullo (AMIA, 2015)

Building the Computational Workforce for Precision Medicine. - Jessica D. Tenenbaum; Joshua C. Denny; David Flannery; Douglas B. Fridsma; Marc S. Williams (AMIA, 2015)

Desiderata for computable representations of electronic health records-driven phenotype algorithms. - Huan Mo; William K. Thompson; Luke V. Rasmussen; Jennifer A. Pacheco; Guoqian Jiang; Richard C. Kiefer; Qian Zhu 003; Jie Xu 011; Enid N. H. Montague; David S. Carrell; Todd Lingren; Frank D. Mentch; et al. (J. Am. Medical Informatics Assoc., 2015)

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record. - Brian H. Shirts; Joseph S. Salama; Samuel J. Aronson; Wendy K. Chung; Stacy W. Gray; Lucia A. Hindorff; Gail P. Jarvik; Sharon E. Plon; Elena M. Stoffel; Peter Tarczy-Hornoch; Eliezer M. Van Allen; Karen E. Weck; et al. (J. Am. Medical Informatics Assoc., 2015)

The Clinical Pharmacogenetics Implementation Consortium (CPIC) Term Standardization for Clinical Pharmacogenetic Test Results: Alleles and Phenotypes. - James M. Hoffman; Henry M. Dunnenberger; Jonathan D. Burlison; Michelle Whirl Carrillo; Robert R. Freimuth; Marc S. Williams; Stuart A. Scott; Josh F. Peterson; Heidi L. Rehm; Teri E. Klein; Mary V. Relling; Kelly E. Caudle (CRI, 2016)

Developing an Algorithm to Detect Early Childhood Obesity in Two Tertiary Pediatric Medical Centers. - Cassandra Brady; Bahram Namjou; Stephanie Kennebeck; Jonathan Bickel; Nandan Patibandla; Yizhao Ni; Sara Van Driest; Lixin Chen; Ashton Roach; Beth Cobb; Jacqueline Kirby; Joshua C. Denny; et al. (Appl. Clin. Inform., 2016)

Practical considerations for implementing genomic information resources. - Casey L. Overby; John J. Connolly; Christopher G. Chute; Joshua C. Denny; Robert R. Freimuth; Andrea L. Hartzler; Ingrid A. Holm; Shannon F. Manzi; Jyotishman Pathak; Peggy L. Peissig; Maureen E. Smith; Marc S. Williams; et al. (Appl. Clin. Inform., 2016)

Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard. - Casey L. Overby; Guilherme Del Fiol; Wendy S. Rubinstein; Donna R. Maglott; Tristan Nelson; Aleksandar Milosavljevic; Christa Martin; Scott Goehringer; Robert R. Freimuth; Marc S. Williams; Bret S. E. Heale (Appl. Clin. Inform., 2016)

Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC). - James M. Hoffman; Henry M. Dunnenberger; J. Kevin Hicks; Kelly E. Caudle; Michelle Whirl Carrillo; Robert R. Freimuth; Marc S. Williams; Teri E. Klein; Josh F. Peterson (J. Am. Medical Informatics Assoc., 2016)

The genomic CDS sandbox: An assessment among domain experts. - Ayesha Aziz; Kensaku Kawamoto; Karen Eilbeck; Marc S. Williams; Robert R. Freimuth; Mark A. Hoffman; Luke V. Rasmussen; Casey Lynnette Overby; Brian H. Shirts; James M. Hoffman; Brandon M. Welch (J. Biomed. Informatics, 2016)

User-centered design of multi-gene sequencing panel reports for clinicians. - Elizabeth M. Cutting; Meghan Banchero; Amber Beitelshees; James J. Cimino; Guilherme Del Fiol; Ayse P. Gurses; Mark A. Hoffman; Linda Jo Bone Jeng; Kensaku Kawamoto; Mark Kelemen; Harold Alan Pincus; Alan R. Shuldiner; et al. (J. Biomed. Informatics, 2016)

Portable Precision Phenotype Algorithm for Chronic Rhinosinusitis. - Jennifer A. Pacheco; Agnes S. Sundaresan; Kenneth M. Borthwick; Sergio E. Chiarella; David T. Coleman; Andy Yizhou Wu; Abel N. Kho; M. Geoffrey Hayes; Marc S. Williams (AMIA, 2017)

Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example. - Samuel J. Aronson; Lawrence J. Babb; Darren C. Ames; Richard A. Gibbs; Eric Venner; John J. Connelly; Keith Marsolo; Chunhua Weng; Marc S. Williams; Andrea L. Hartzler; Wayne H. Liang; James D. Ralston; et al. (J. Am. Medical Informatics Assoc., 2018)

Implementation of a patient-facing genomic test report in the electronic health record using a web-application interface. - Marc S. Williams; Melissa S. Kern; Virginia R. Lerch; Jonathan Billet; Janet L. Williams; Gregory J. Moore (BMC Medical Informatics Decis. Mak., 2018)

Translational Research of Machine Learning and Artificial Intelligence Advances in Clinical Settings - Experiences and Challenges. - William R. Hersh; Gretchen P. Jackson; Marc S. Williams; Colin G. Walsh; David A. Dorr (AMIA, 2020)

Evaluation of the Portability of Natural Language Processing-based Computable Phenotypes in the eMERGE Network. - Jennifer A. Pacheco; Luke V. Rasmussen; Ken Wiley; Thomas N. Person; David J. Cronkite; Sunghwan Sohn; Shawn N. Murphy; Justin H. Gundelach; Vivian S. Gainer; Victor M. Castro; Cong Liu 020; Todd Lingren; et al. (AMIA, 2021)

Creating a Home for Genomic Data in the Electronic Health Record. - Nephi Walton; Darren Johnson; Bret S. E. Heale; Thomas N. Person; Marc S. Williams (AMIA, 2021)

Infobuttons for Genomic Medicine: Requirements and Barriers. - Luke V. Rasmussen; John J. Connolly; Guilherme Del Fiol; Robert R. Freimuth; Douglas B. Pet; Josh F. Peterson; Brian H. Shirts; Justin B. Starren; Marc S. Williams; Nephi Walton; Casey Overby Taylor (Appl. Clin. Inform., 2021)

Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelines. - Aly Khalifa; Clinton C. Mason; Jennifer H. Garvin; Marc S. Williams; Guilherme Del Fiol; Brian R. Jackson; Steven B. Bleyl; Gil Alterovitz; Stanley M. Huff (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? - Justin B. Starren; William M. Tierney; Marc S. Williams; Paul C. Tang; Charlene R. Weir; Ross Koppel; Philip R. O. Payne; George Hripcsak; Don E. Detmer (J. Am. Medical Informatics Assoc., 2021)

Misdiagnosis: Burnout, moral injury, and implications for the electronic health record. - Marc S. Williams (J. Am. Medical Informatics Assoc., 2021)

High-throughput assessment of genomic outcomes: development and validation of the HI-TAG knowledgebase. - Jodell E. Linder; Ran Tao; Ni Ketut Wilmayani; Marc S. Williams; Josh F. Peterson (AMIA, 2022)

A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources. - Ken Wiley; Laura Findley; Madison Goldrich; Tejinder K. Rakhra-Burris; Ana Stevens; Pamela Williams; Carol J. Bult; Rex L. Chisholm; Patricia Deverka; Geoffrey S. Ginsburg; Eric D. Green; Gail P. Jarvik; et al. (J. Am. Medical Informatics Assoc., 2022)

Genetically guided precision medicine clinical decision support tools: a systematic review. - Darren Johnson; Guilherme Del Fiol; Kensaku Kawamoto; Katrina M. Romagnoli; Nathan Sanders; Grace Isaacson; Elden Jenkins; Marc S. Williams (J. Am. Medical Informatics Assoc., 2024)

Genomics in nephrology: identifying informatics opportunities to improve diagnosis of genetic kidney disorders using a human-centered design approach. - Katrina M. Romagnoli; Zachary M. Salvati; Darren Johnson; Heather M. Ramey; Alexander R. Chang; Marc S. Williams (J. Am. Medical Informatics Assoc., 2024)

Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup. - Nephi A. Walton; Radhakrishnan Nagarajan; Chen Wang 001; Murat Sincan; Robert R. Freimuth; David B. Everman; Derek C. Walton; Scott P. McGrath; Dominick J. Lemas; Panayiotis V. Benos; Alexander V. Alekseyenko; Qianqian Song; et al. (J. Am. Medical Informatics Assoc., 2024)