Natasha T Strande
7PUBLICATIONS
29CO-AUTHORS
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Publications (7)
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|Jun 29, 2023
Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening.Samuel S Gidding, H Lester Kirchner, Andrew Brangan
|Jan 20, 2022
Massively parallel reporter assays discover de novo exonic splicing mutants in paralogs of Autism genes.Christy L Rhine, Christopher Neil, Jing Wang
|Feb 12, 2021
Leveraging population-based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project.Melissa A Kelly, Joseph B Leader, Karen E Wain
|Nov 12, 2020
Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients.Matthew T Oetjens, Jonathan Z Luo, Alexander Chang
|Dec 18, 2018
Increasing the diagnostic yield of exome sequencing by copy number variant analysis.Daniel S Marchuk, Kristy Crooks, Natasha Strande
|Aug 14, 2015
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel
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Frequent Collaborators
1 joint publications
Daniel S Marchuk
1 joint publications
Alicia Brandt
1 joint publications
Christian R Tilley
1 joint publications
Jonathan S Berg
1 joint publications
Julianne M O'Daniel
1 joint publications
Kristy R Crooks
1 joint publications
Kristy Lee
1 joint publications
Bradford C Powell
1 joint publications
Cynthia M Powell
1 joint publications
Myra I Roche
