Publications by authors named "Bailey Gallinger"

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Updated Recommendations for Pediatric Surveillance in Hereditary Endocrine Neoplasia Syndromes: Multiple Endocrine Neoplasias, Hyperparathyroidism-Jaw Tumor Syndrome, and Carney Complex.
Jonathan D Wasserman, Kami Wolfe Schneider, Maria-Isabel Achatz, Yoshiko Nakano, Kristin Zelley, Bailey Gallinger

Clin Cancer Res· September 2025

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Implementing a consultation service for translating genomic research findings into the clinic: Lessons from the SickKids Genome Board.
Amy Y Pan, Kenzie Pulsifer, Michelle M Axford, Lena Dolman, Bailey Gallinger

Paediatr Child Health· September 2025

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Update on Tumor Surveillance for Children with Hereditary Pheochromocytoma/Paraganglioma Syndromes.
Surya P Rednam, Junne Kamihara, Kerri D Becktell, Garrett M Brodeur, Lisa J States, Bailey Gallinger

Clin Cancer Res· August 2025

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Update on Surveillance in Von Hippel-Lindau Disease.
Surya P Rednam, Kerri D Becktell, Anita Villani, Garrett M Brodeur, Lisa J States, Bailey Gallinger

Clin Cancer Res· June 2025

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Update on Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Maria Isabel Achatz, Anita Villani, Alison A Bertuch, Gaëlle Bougeard, Vivian Y Chang, Bailey Gallinger

Clin Cancer Res· May 2025

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Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes.
Orli Michaeli, Sun Young Kim, Sarah G Mitchell, Marjolijn C J Jongmans, Jonathan D Wasserman, Bailey Gallinger

Clin Cancer Res· February 2025

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Update on Pediatric Surveillance Recommendations for PTEN Hamartoma Tumor Syndrome, DICER1-Related Tumor Predisposition, and Tuberous Sclerosis Complex.
Kris Ann P Schultz, Suzanne P MacFarland, Melissa R Perrino, Sarah G Mitchell, Junne Kamihara, Bailey Gallinger

Clin Cancer Res· January 2025

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Late-onset tumors in rhabdoid tumor predisposition syndrome type-1 (RTPS1) and implications for surveillance.
Yoshiko Nakano, Meryl Acker, Harriet Druker, Kalene van Engelen, M Stephen Meyn, Bailey Gallinger

Eur J Hum Genet· November 2024

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Update on Genetic Counselor Practice and Recommendations for Pediatric Cancer Predisposition Evaluation and Surveillance.
Kristin Zelley, Jaclyn Schienda, Bailey Gallinger, Wendy K Kohlmann, Rose B McGee

Clin Cancer Res· September 2024

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The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations.
Anita Villani, Scott Davidson, Nisha Kanwar, Winnie W Lo, Yisu Li, Bailey Gallinger

Nat Cancer· February 2023

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Exome sequencing identifies PD-L2 as a potential predisposition gene for lymphoma.
Jianming Shao, Lei Gao, Marco L Leung, Bailey Gallinger, Cara Inglese

Hematol Oncol· August 2022

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Perspectives and Experiences of Parents and Adolescents Who Participate in a Pediatric Precision Oncology Program: "When You Feel Helpless, This Kind of Thing Is Very Helpful".
Larissa Waldman, Kelly Hancock, Bailey Gallinger, Brittney Johnstone, Ledia Brunga

JCO Precis Oncol· March 2022

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Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance.
Carol Durno, Ayse Bahar Ercan, Vanessa Bianchi, Melissa Edwards, Melyssa Aronson, Bailey Gallinger

J Clin Oncol· September 2021

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Non-rhabdomyosarcoma soft tissue sarcomas diagnosed in patients at a young age. An overview of clinical, pathological, and molecular findings.
Samuele Renzi, Noelle Cullinan, Sarah Cohen-Gogo, Karin Langenberg-Ververgaert, Orli Michaeli, Bailey Gallinger

Pediatr Blood Cancer· August 2021

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Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers.
Kalene van Engelen, Maru Barrera, Jonathan D Wasserman, Susan Randall Armel, David Chitayat, Bailey Gallinger

Pediatr Blood Cancer· August 2021

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Comprehensive characterization of a Canadian cohort of von Hippel-Lindau disease patients.
Yasser Salama, Saleh Albanyan, Marta Szybowska, Garrett Bullivant, Bailey Gallinger

Clin Genet· November 2019

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Evidence for genetic anticipation in vonHippel-Lindau syndrome.
Laura Aronoff, David Malkin, Kalene van Engelen, Bailey Gallinger, Jonathan Wasserman

J Med Genet· June 2018

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DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center.
Kalene van Engelen, Anita Villani, Jonathan D Wasserman, Laura Aronoff, Mary-Louise C Greer, Bailey Gallinger

Pediatr Blood Cancer· January 2018

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Pediatric imaging in DICER1 syndrome.
Marta Tijerin Bueno, Claudia Martínez-Ríos, Alejandro De la Puente Gregorio, Rayan A Ahyad, Anita Villani, Bailey Gallinger

Pediatr Radiol· September 2017

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Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.
Anita Villani, Ari Shore, Jonathan D Wasserman, Derek Stephens, Raymond H Kim, Bailey Gallinger

Lancet Oncol· September 2016

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PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases.
Orion J Buske, Marta Girdea, Sergiu Dumitriu, Bailey Gallinger, Taila Hartley

Hum Mutat· October 2015

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