Heidi L. Rehm

According to our database, Heidi L. Rehm authored at least 7 papers between 2012 and 2023.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2023

FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.

Hufeng Zhou, Theodore Arapoglou, Xihao Li, Zilin Li, Xiuwen Zheng, Jill Moore, Abhijith Asok, Sushant Kumar, Elizabeth E. Blue, Steven Buyske, Nancy J. Cox, Adam Felsenfeld, Mark Gerstein, Eimear Kenny, Bingshan Li, Tara Cox Matise, Anthony Philippakis, Heidi L. Rehm, Heidi J. Sofia, Grace Snyder, Zhiping Weng, Benjamin M. Neale, Shamil R. Sunyaev, Xihong Lin

Nucleic Acids Res., January, 2023

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

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

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

Proceedings of the Summit on Clinical Research Informatics, 2016

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