Bailey Gallinger
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 26 publications
Timely and accurate RB1 genetic testing guides familial risk stratification in heritable retinoblastoma.
Journal: Ophthalmic genetics
Published: February 10, 2026
Two cases of mosaic germline SVA insertions in SMARCB1: implications for rhabdoid tumour predisposition diagnosis.
Journal: NPJ genomic medicine
Published: December 24, 2025
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel-Lindau (VHL) Disease.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 20, 2025
Multiplatform curation in the development of ACMG/AMP specifications for Von Hippel-Lindau (VHL) disease.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 20, 2025
Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel Lindau (VHL) Disease.
Journal: medRxiv : the preprint server for health sciences
Published: September 05, 2025
Update on Tumor Surveillance for Children with Hereditary Pheochromocytoma/Paraganglioma Syndromes.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: December 27, 2024
Updated Recommendations for Pediatric Surveillance in Hereditary Endocrine Neoplasia Syndromes: Multiple Endocrine Neoplasias, Hyperparathyroidism-Jaw Tumor Syndrome, and Carney Complex.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: November 27, 2024
Implementing a consultation service for translating genomic research findings into the clinic: Lessons from the SickKids Genome Board.
Journal: Paediatrics & child health
Published: November 13, 2024
Update on Surveillance in Von Hippel-Lindau Disease.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: October 22, 2024
Update on Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: October 04, 2024
Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: August 17, 2024
Update on Pediatric Surveillance Recommendations for PTEN Hamartoma Tumor Syndrome, DICER1-Related Tumor Predisposition, and Tuberous Sclerosis Complex.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: July 02, 2024
Last Updated: 09/26/2026