Stacie Taylor
7PUBLICATIONS
24CO-AUTHORS
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Publications (7)
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|Mar 28, 2024
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action.Vaidehi Jobanputra, Brock Schroeder, Heidi L Rehm
|Feb 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders.Kristen M Wigby, Deanna Brockman, Gregory Costain
|Dec 15, 2020
Clinical utility of genomic sequencing: a measurement toolkit.Robin Z Hayeems, David Dimmock, David Bick
|Oct 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease.Christian R Marshall, Shimul Chowdhury, Ryan J Taft
|May 29, 2020
The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic.Christian R Marshall, David Bick, John W Belmont
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Frequent Collaborators
4 joint publications
Vaidehi Jobanputra
3 joint publications
David Bick
3 joint publications
David Dimmock
2 joint publications
Christian R Marshall
1 joint publications
Mathew S Lebo
1 joint publications
Steven M Harrison
1 joint publications
Roberto Mendoza
1 joint publications
Megan E Grove
1 joint publications
Kristen M Wigby
1 joint publications
Gregory Costain
