1. Basophil activation test shows high accuracy in the diagnosis of peanut and tree nut allergy: The Markers of Nut Allergy Study. Issue 6 (29th December 2020) Authors: Duan, Lucy; Celik, Alper; Hoang, Jennifer A.; Schmidthaler, Klara; So, Delvin; Yin, Xiaojun; Ditlof, Christina M.; Ponce, Marta; Upton, Julia E.M.; Lee, Jean‐Soo; Hung, Lisa; Breiteneder, Heimo; Palladino, Chiara; Atkinson, Adelle R.; Kim, Vy H.D.; Berenjy, Alireza; Asper, Maria; Hummel, David; W... Journal: Allergy Issue: Volume 76:Issue 6(2021) Page Start: 1800 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data. Issue 3 (29th November 2022) Authors: Hartley, Taila; Soubry, Élisabeth; Acker, Meryl; Osmond, Matthew; Couse, Madeline; Gillespie, Meredith K.; Ito, Yoko; Marshall, Aren E.; Lemire, Gabrielle; Huang, Lijia; Chisholm, Caitlin; Eaton, Alison J.; Price, E. Magda; Dowling, James J.; Ramani, Arun K.; Mendoza‐Londono, Roberto; Costain, Gr... Journal: Clinical genetics Issue: Volume 103:Issue 3(2023) Page Start: 288 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genomics4RD: An integrated platform to share Canadian deep‐phenotype and multiomic data for international rare disease gene discovery. Issue 6 (9th March 2022) Authors: Driver, Hannah G.; Hartley, Taila; Price, E. Magda; Turinsky, Andrei L.; Buske, Orion J.; Osmond, Matthew; Ramani, Arun K.; Kirby, Emily; Kernohan, Kristin D.; Couse, Madeline; Elrick, Hillary; Lu, Kevin; Mashouri, Pouria; Mohan, Aarthi; So, Delvin; Klamann, Conor; Le, Hannah G. B. H.; Herscovich... Other Names: Boycott Kym guestEditor.; Hamosh Ada guestEditor.; Rehm Heidi guestEditor. Journal: Human mutation Issue: Volume 43:Issue 6(2022) Page Start: 800 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Utilization of Whole Exome Sequencing Data to Identify Clinically Relevant Pharmacogenomic Variants in Pediatric Inflammatory Bowel Disease. Issue 12 (1st December 2020) Authors: Mulder, Daniel J.; Khalouei, Sam; Warner, Neil; Gonzaga-Jauregui, Claudia; Church, Peter C.; Walters, Thomas D.; Ramani, Arun K.; Griffiths, Anne M.; Cohn, Iris; Muise, Aleixo M. Journal: Clinical and translational gastroenterology Issue: Volume 11:Issue 12(2020) Page Start: e00263 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy. Issue 5 (11th February 2021) Authors: McMillan, Hugh J.; Marshall, Aren E.; Venkateswaran, Sunita; Hartley, Taila; Warman‐Chardon, Jodi; Ramani, Arun K.; Marshall, Christian R.; Michaud, Jean; Boycott, Kym M.; Dyment, David A.; Kernohan, Kristin D. Journal: Clinical genetics Issue: Volume 99:Issue 5(2021) Page Start: 746 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗