Stacie L Taylor (Stacie Taylor)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Topics

Urinary Tract Infection

Top Venues

NPJ genomic medicine

Genome medicine

Journal of medical genetics

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

Publications

Kristen M Wigby, Deanna Brockman, Gregory Costain, Caitlin Hale, Stacie L Taylor, John W Belmont, David Bick, David P Dimmock, Susan Fernbach, John Greally, Vaidehi Jobanputra, Shashikant Kulkarni, Elizabeth Spiteri, Ryan J Taft
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. NPJ genomic medicine 9 (1) (2024)
Kristen M Wigby, Deanna Brockman, Gregory Costain, Caitlin Hale, Stacie L Taylor, John W Belmont, David Bick, David P Dimmock, Susan Fernbach, John Greally, Vaidehi Jobanputra, Shashikant Kulkarni, Elizabeth Spiteri, Ryan J Taft
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. NPJ genomic medicine 9 (1) (2024)
Vaidehi Jobanputra, Brock E Schroeder, Michael J Bamshad, Wei Shen, Elizabeth Spiteri, Ghunwa Nakouzi, Stacie L Taylor, Christian R Marshall, Linyan Meng, Stephen F Kingsmore, Katarzyna A Ellsworth, Euan Ashley, Ryan J Taft, null null
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action. NPJ genomic medicine 9 (1) (2024)
Olaf H Rieß, Marc Sturm, Benita Menden, Alexandra Liebmann, German Demidov, Dennis Witt, Nicolas Casadei, Jakob Admard, Leon Schütz, Stephan Ossowski, Stacie L Taylor, Sven Schaffer, Christopher Schroeder, Andreas Dufke, Tobias Haack
Genomes in clinical care. NPJ genomic medicine 9 (1) (2024)
Kristen M Wigby, Deanna Brockman, Gregory Costain, Caitlin Hale, Stacie L Taylor, John W Belmont, David Bick, David P Dimmock, Susan Fernbach, John Greally, Vaidehi Jobanputra, Shashikant Kulkarni, Elizabeth Spiteri, Ryan J Taft
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. NPJ genomic medicine 9 (1) (2024)
Olaf H Rieß, Marc Sturm, Benita Menden, Alexandra Liebmann, German Demidov, Dennis Witt, Nicolas Casadei, Jakob Admard, Leon Schütz, Stephan Ossowski, Stacie L Taylor, Sven Schaffer, Christopher Schroeder, Andreas Dufke, Tobias Haack
Genomes in clinical care. NPJ genomic medicine 9 (1) (2024)
Vaidehi Jobanputra, Brock E Schroeder, Michael J Bamshad, Wei Shen, Elizabeth Spiteri, Ghunwa Nakouzi, Stacie L Taylor, Christian R Marshall, Linyan Meng, Stephen F Kingsmore, Katarzyna A Ellsworth, Euan Ashley, Ryan J Taft, null null
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action. NPJ genomic medicine 9 (1) (2024)
Christian R Marshall, Shimul Chowdhury, Ryan J Taft, Matthew S Lebo, Jillian G Buchan, Steven M Harrison, Ross Rowsey, Eric W Klee, Pengfei Liu, Elizabeth A Worthey, Vaidehi Jobanputra, David P Dimmock, Hutton M Kearney, David Bick, Shashikant Kulkarni, Stacie L Taylor, John W Belmont, Dimitri J Stavropoulos, Niall J Lennon, null null
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. NPJ genomic medicine 5 (2020)
Robin Z Hayeems, David P Dimmock, David Bick, John W Belmont, Robert C Green, Brendan Lanpher, Vaidehi Jobanputra, Roberto Mendoza-Londono, Shashi Kulkarni, Megan E Grove, Stacie L Taylor, Euan Ashley, null null
Clinical utility of genomic sequencing: a measurement toolkit. NPJ genomic medicine 5 (1) (2020)
Christian R Marshall, David Bick, John W Belmont, Stacie L Taylor, Euan Ashley, David Dimmock, Vaidehi Jobanputra, Hutton M Kearney, Shashikant Kulkarni, Heidi Rehm, null null
The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic. Genome medicine 12 (1) (2020)
David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Journal of medical genetics 56 (12) (2019)