Laura M Amendola

6PUBLICATIONS
39CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Communication technology and digital media studiesInformation systems development methodologies and practiceDiscourse and pragmaticsDisease surveillance
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Publications (6)

|Dec 05, 2025
Long-Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia.

Liora H Feshbach, Morgan Similuk, Laura M Amendola

|Apr 03, 2021
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium.

Sabrina A Suckiel, Julianne M O'Daniel, Katherine E Donohue

|Jan 13, 2017
Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing.

Patricia Himes, Tia L Kauffman, Kristin R Muessig

|Nov 05, 2016
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.

Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola

|Aug 05, 2016
Is "incidental finding" the best term?: a study of patients' preferences.

Nina Tan, Laura M Amendola, Julianne M O'Daniel

|Mar 06, 2015
Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing.

Adam A Nishimura, Brian H Shirts, Michael O Dorschner

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Frequent Collaborators

3 joint publications

Gail P Jarvik

3 joint publications

Julianne M O'Daniel

2 joint publications

C Sue Richards

2 joint publications

Katrina A Goddard