Samuel J. Aronson

According to our database, Samuel J. Aronson authored at least 18 papers between 2009 and 2023.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of three.

2023

Using GPT-4 Prompts to Determine Whether Articles Contain Functional Evidence Supporting or Refuting Variant Pathogenicity.

Samuel J. Aronson, Kalotina Machini, Pranav Sriraman, Jiyeon Shin, Emma R. Henricks, Charlotte Mailly, Angie J. Nottage, Michael Oates, Matthew S. Lebo

CoRR, 2023

2022

I2b2-etl: Python application for importing electronic health data into the informatics for integrating biology and the bedside platform.

Kavishwar B. Wagholikar, Layne Ainsworth, David Zelle, Kira Chaney, Michael Mendis, Jeffrey G. Klann, Alexander J. Blood, Angela Miller, Rupendra Chulyadyo, Michael Oates, William J. Gordon, Samuel J. Aronson, Benjamin M. Scirica, Shawn N. Murphy

Bioinform., October, 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, George A. Mensah, Erin Ramos, Mary V. Relling, Dan M. Roden, Robb Rowley, Gil Alterovitz, Samuel J. Aronson, Lisa Bastarache, James J. Cimino, Erin L. Crowgey, Guilherme Del Fiol, Robert R. Freimuth, Mark A. Hoffman, Janina M. Jeff, Kevin B. Johnson, Kensaku Kawamoto, Subha Madhavan, Eneida A. Mendonça, Lucila Ohno-Machado, Siddharth Pratap, Casey Overby Taylor, Marylyn D. Ritchie, Nephi Walton, Chunhua Weng, Teresa Zayas-Cabán, Teri A. Manolio, Marc S. Williams

J. Am. Medical Informatics Assoc., 2022

2021

Genomic considerations for FHIR®; eMERGE implementation lessons.

Mullai Murugan, Lawrence J. Babb, Casey Overby Taylor, Luke V. Rasmussen, Robert R. Freimuth, Eric Venner, Fei Yan, Victoria Yi, Stephen J. Granite, Hana Zouk, Samuel J. Aronson, Kevin Power, Alexander Fedotov, David R. Crosslin, David Fasel, Gail P. Jarvik, Hakon Hakonarson, Hana Bangash, Iftikhar J. Kullo, John J. Connolly, Jordan G. Nestor, Pedro J. Caraballo, Wei-Qi Wei, Ken Wiley, Heidi L. Rehm, Richard A. Gibbs

J. Biomed. Informatics, 2021

Workflow Automation for a Virtual Hypertension Management Program.

Samuel J. Aronson, Benjamin M. Scirica, William J. Gordon, Alexander J. Blood, Kira Chaney, Eugene Clark, Corey Glynn, Remlee Green, John St. Laurent, Charlotte Mailly, Marian McPartlin, Shawn Murphy, Hunter Nichols, Michael Oates, Samantha Subramaniam, Matthew Varugheese, Kavishwar B. Wagholikar

Appl. Clin. Inform., 2021

2019

Dynamic Phenotyping to facilitate Accrual for Prospective Clinical studies: A Case Study in Heart Failure.

Kavishwar B. Wagholikar, Christina M. Fischer, Alyssa P. Goodson, Christopher Herrick, Taylor Maclean, Katelyn Smith, Liliana Fera, Thomas Gaziano, Jacqueline Dunning, Joshua Bosque-Hamilton, Lina Matta, Eloy Toscano, Brent Richter, Layne Ainsworth, Michael Oates, Samuel J. Aronson, Calum A. MacRae, Benjamin Morgan Scirica, Akshay S. Desai, Shawn N. Murphy

Proceedings of the AMIA 2019, 2019

Patient Stratification Process for enabling Clinical Interventions.

Kavishwar B. Wagholikar, Samuel J. Aronson, Benjamin Morgan Scirica, Akshay S. Desai, Shawn N. Murphy

Proceedings of the AMIA 2019, 2019

Initial Usage Patterns of a SMART-on-FHIR Point-Of-Care Platelet Transfusion Optimization Application.

William Gordon, Maria Aguad, Heather Appello, Samuel J. Aronson, Jane Baronas, Indira Guleria, Richard Kaufman, Edgar Milford, Michael Oates, Rory Dela Paz, Melissa Yeung, William Lane

Proceedings of the AMIA 2019, 2019

2018

Implications of Genomics for Clinical Informatics.

Mollie Ullman-Cullere, Eugene Clark, Samuel J. Aronson

Proceedings of the Encyclopedia of Database Systems, Second Edition, 2018

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, Emily Beth Devine, Shawn N. Murphy, Christopher G. Chute, Pedro J. Caraballo, Iftikhar J. Kullo, Robert R. Freimuth, Luke V. Rasmussen, Firas H. Wehbe, Josh F. Peterson, Jamie R. Robinson, Ken Wiley, Casey Overby Taylor, eMERGE Network EHRI Working Group

J. Am. Medical Informatics Assoc., 2018

A FHIR-based Application to Improve Platelet Utilization and Transfusion Workflow.

William Gordon, Samuel J. Aronson, William Lane

Proceedings of the AMIA 2018, 2018

2017

Design and Implementation of a Structured Sequencing Report Format: A Multi-Stakeholder Perspective from eMERGE.

Luke V. Rasmussen, Darren C. Ames, Samuel J. Aronson, Lawrence J. Babb, Casey L. Overby

Proceedings of the AMIA 2017, 2017

2016

Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates.

Stephanie Klinkenberg-Ramirez, Lynn A. Volk, Sara Samaha, Lisa P. Newmark, Stephanie E. Pollard, Matthew Varugheese, Samantha Baxter, Samuel J. Aronson, Heidi L. Rehm, David W. Bates, Pamela M. Neri

Appl. Clin. Inform., 2016

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, Christopher G. Chute, Robert R. Freimuth, Robert Grundmeier, Andrea L. Hartzler, Rongling Li, Peggy L. Peissig, Josh F. Peterson, Luke V. Rasmussen, Justin B. Starren, Marc S. Williams, Casey Lynnette Overby

J. Am. Medical Informatics Assoc., 2015

2013

A Novel Clinician Interface to Improve Access to Up-to-date Genetic Results.

Allison R. Wilcox, Pamela M. Neri, Lynn A. Volk, Lisa P. Newmark, Eugene Clark, Lawrence J. Babb, Matthew Varugheese, Samuel J. Aronson, Heidi L. Rehm, David W. Bates

Proceedings of the AMIA 2013, 2013

2012

Usability of a novel clinician interface for genetic results.

Pamela M. Neri, Stephanie E. Pollard, Lynn A. Volk, Lisa P. Newmark, Matthew Varugheese, Samantha Baxter, Samuel J. Aronson, Heidi L. Rehm, David W. Bates

J. Biomed. Informatics, 2012

Lessons Learned in the Implementation of Novel IT Infrastructure to Communicate Genetic Variant Updates.

Pamela M. Neri, Sara Samaha, Lynn A. Volk, Lisa P. Newmark, Stephanie E. Pollard, Matthew Varugheese, Samantha Baxter, Samuel J. Aronson, Heidi L. Rehm, David W. Bates

Proceedings of the AMIA 2012, 2012

2009

Implications of Genomics for Clinical Informatics.

Mollie Ullman-Cullere, Eugene Clark, Samuel J. Aronson

Proceedings of the Encyclopedia of Database Systems, 2009