Katarzyna A Ellsworth (Katarzyna Ellsworth, Kasia Ellsworth)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Topics

Mechanical Ventilation

Intensive Care Unit

Acute Respiratory Distress Syndrome

Top Venues

NPJ genomic medicine

Science translational medicine

Cold Spring Harbor molecular case studies

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

Publications

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)
Stephen F Kingsmore, Russell Nofsinger, Katarzyna A Ellsworth
Rapid genomic sequencing for genetic disease diagnosis and therapy in intensive care units: a review. NPJ genomic medicine 9 (1) (2024)
Stephen F Kingsmore, Russell Nofsinger, Katarzyna A Ellsworth
Rapid genomic sequencing for genetic disease diagnosis and therapy in intensive care units: a review. NPJ genomic medicine 9 (1) (2024)
Stephen F Kingsmore, Russell Nofsinger, Katarzyna A Ellsworth
Rapid genomic sequencing for genetic disease diagnosis and therapy in intensive care units: a review. 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)
Kiely N James, Megan Lau, Katayoon Shayan, Jerica Lenberg, Rebecca Mardach, Romeo C Ignacio, Jonathan Halbach, Lillian Choi, Soma Kumar, Katarzyna A Ellsworth
Expanding the genotypic spectrum of ACTG2-related visceral myopathy. Cold Spring Harbor molecular case studies 7 (3) (2021)
Michelle M Clark, Amber N Hildreth, Sergey Batalov, Yan Ding, Shimul Chowdhury, Kelly Watkins, Katarzyna A Ellsworth, Brandon Camp, Cyrielle I Kint, Calum Yacoubian, Lauge Farnaes, Matthew N Bainbridge, Curtis Beebe, Joshua J A Braun, Margaret Bray, Jeanne Carroll, Julie A Cakici, Sara A Caylor, Christina Clarke, Mitchell P Creed, Jennifer Friedman, Alison Frith, Richard Gain, Mary Gaughran, Shauna George, Sheldon Gilmer, Joseph G Gleeson, Jeremy Gore, Haiying Grunenwald, Raymond L Hovey, Marie L Janes, Kejia Lin, Paul D McDonagh, Kyle McBride, Patrick Mulrooney, Shareef A Nahas, Daeheon Oh, Albert Oriol, Laura Puckett, Zia Rady, Martin G Reese, Julie Ryu, Lisa Salz, Erica Sanford, Lawrence Stewart, Nathaly Sweeney, Mari Tokita, Luca Van Der Kraan, Sarah White, Kristen Wigby, Brett Williams, Terence Wong, Meredith S Wright, Catherine Yamada, Peter Schols, John Reynders, Kevin P Hall, David P Dimmock, Narayanan Veeraraghavan, Thomas Defay, Stephen F Kingsmore
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation. Science translational medicine 11 (489) (2020)