E Andres Rivera-Munoz (Edgar A Rivera-Muñoz)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 10

Top Venues

bioRxiv : the preprint server for biology

Human mutation

University of North Carolina at Chapel Hill School of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of North Carolina at Chapel Hill School of Medicine Mar 01 2015

United States

Research Assistant :: Genetics

Publications

Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
Jessica Xiao-Ling Chong, Seth I Berger, Samantha Baxter, Erica D Smith, Changrui Xiao, Daniel G Calame, Megan H Hawley, E Andres Rivera-Munoz, Stephanie DiTroia, null null, Michael J Bamshad, Michael J Bamshad
Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. bioRxiv : the preprint server for biology (2024)
E Andres Rivera-Munoz, Laura V Milko, Steven M Harrison, Danielle R Azzariti, C Lisa Kurtz, Kristy Lee, Jessica L Mester, Meredith A Weaver, Erin Currey, William Craigen, Charis Eng, Birgit Funke, Madhuri Hegde, Ray E Hershberger, Rong Mao, Robert D Steiner, Lisa M Vincent, Christa L Martin, Sharon E Plon, Erin Ramos, Michael J Bamshad, Michael Watson, Jonathan S Berg
ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation. Human mutation 39 (11) (2019)
Sarah E Brnich, E Andres Rivera-Munoz, Jonathan S Berg
Quantifying the potential of functional evidence to reclassify variants of uncertain significance in the categorical and Bayesian interpretation frameworks. Human mutation 39 (11) (2018)

E Andres Rivera-Munoz.css-eqlu8i{font-size:small;padding-left:4px;} (Edgar A Rivera-Muñoz)

Publication Activity (10 Years)

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E Andres Rivera-Munoz (Edgar A Rivera-Muñoz)