Orion J Buske

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 2

Top Topics

Staphylococcus Aureus

Cross Sectional

Genome Wide Analysis

Top Venues

Nature protocols

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Hannah G Driver, Taila Hartley, E Magda Price, Andrei L Turinsky, Orion J Buske, Matthew Osmond, Arun K Ramani, Emily Kirby, Kristin D Kernohan, Madeline Couse, Hillary Elrick, Kevin Lu, Pouria Mashouri, Aarthi Mohan, Delvin So, Conor Klamann, Hannah G B H Le, Andrea Herscovich, Christian R Marshall, Andrew Statia, Care Rare Canada Consortium, Bartha Maria Knoppers, Michael Brudno, Kym M Boycott
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery. Human mutation 43 (6) (2022)
Steven Laurie, Davide Piscia, Leslie Matalonga, Alberto Corvó, Marcos Fernandez-Callejo, Carles Garcia-Linares, Carles Hernandez-Ferrer, Cristina Luengo, Inés Martínez, Anastasios Papakonstantinou, Daniel Picó-Amador, Joan Protasio, Rachel Thompson, Raul Tonda, Mònica Bayés, Gemma Bullich, Jordi Camps-Puchadas, Ida Paramonov, Jean-Rémi Trotta, Angel Alonso, Marcella Attimonelli, Christophe Béroud, Virginie Bros-Facer, Orion J Buske, Andrés Cañada-Pallarés, José María Fernandez, Mats G Hansson, Rita Horvath, Julius O B Jacobsen, Rajaram Kaliyaperumal, Séverine Lair-Préterre, Luana Licata, Pedro Lopes, Estrella López-Martín, Deborah Mascalzoni, Lucia Monaco, Luis A Pérez-Jurado, Manuel Posada-de-la-Paz, Jordi Rambla De Argila, Ana Rath, Olaf H Rieß, Peter Nick Robinson, David Salgado, Damian Smedley, J Dylan Spalding, Peter A C 't Hoen, Ana Topf, Irina T Zaharieva, Holm Graessner, Ivo Glynne Gut, Hanns Lochmüller, Sergi Beltran
The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases. Human mutation 43 (6) (2022)
Damian Smedley, Julius O B Jacobsen, Marten Jäger, Sebastian Koehler, Manuel Holtgrewe, Max Schubach, Enrico Siragusa, Tomasz Zemojtel, Orion J Buske, Nicole L Washington, William P Bone, Melissa A Haendel, Peter Nick Robinson
Next-generation diagnostics and disease-gene discovery with the Exomiser. Nature protocols 10 (12) (2015)
William P Bone, Nicole L Washington, Orion J Buske, David R Adams, Joie Davis, David Draper, Elise D Flynn, Marta Girdea, Rena Godfrey, Gretchen Golas, Catherine Groden, Julius Jacobsen, Sebastian Köhler, Elizabeth M J Lee, Amanda E Links, Thomas C Markello, Christopher J Mungall, Michele Nehrebecky, Peter N Robinson, Murat Sincan, Ariane G Soldatos, Cynthia J Tifft, Camilo Toro, Heather Trang, Camillo Toro, Nicole A Vasilevsky, Colleen Wahl, Lynne A Wolfe, Elizabeth M J Lee, Michael Brudno, Melissa A Haendel, William A Gahl, Damian Smedley
Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency. Genetics in medicine : official journal of the American College of Medical Genetics 18 (6) (2015)