1. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study. Issue 9 (September 2016) Authors: Villani, Anita; Shore, Ari; Wasserman, Jonathan D; Stephens, Derek; Kim, Raymond H; Druker, Harriet; Gallinger, Bailey; Naumer, Anne; Kohlmann, Wendy; Novokmet, Ana; Tabori, Uri; Tijerin, Marta; Greer, Mary-Louise C; Finlay, Jonathan L; Schiffman, Joshua D; Malkin, David Journal: Lancet oncology Issue: Volume 17:Issue 9(2016:Sep.) Page Start: 1295 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comprehensive characterization of a Canadian cohort of von Hippel‐Lindau disease patients. Issue 5 (6th August 2019) Authors: Salama, Yasser; Albanyan, Saleh; Szybowska, Marta; Bullivant, Garrett; Gallinger, Bailey; Giles, Rachel H.; Asa, Sylvia; Badduke, Chansonette; Chiorean, Andreea; Druker, Harriet; Ezzat, Shereen; Hannah‐Shmouni, Fady; Hernandez, Karen G.; Inglese, Cara; Jani, Payal; Kaur, Yuvreet; Krema, Hatem; Kr... Journal: Clinical genetics Issue: Volume 96:Issue 5(2019) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center. Issue 1 (27th September 2017) Authors: van Engelen, Kalene; Villani, Anita; Wasserman, Jonathan D.; Aronoff, Laura; Greer, Mary‐Louise C.; Tijerin Bueno, Marta; Gallinger, Bailey; Kim, Raymond H.; Grant, Ronald; Meyn, M. Stephen; Malkin, David; Druker, Harriet Journal: Pediatric blood & cancer Issue: Volume 65:Issue 1(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evidence for genetic anticipation in vonHippel-Lindau syndrome. Issue 6 (7th February 2018) Authors: Aronoff, Laura; Malkin, David; van Engelen, Kalene; Gallinger, Bailey; Wasserman, Jonathan; Kim, Raymond H; Villani, Anita; Meyn, M Stephen; Druker, Harriet Journal: Journal of medical genetics Issue: Volume 55:Issue 6(2018) Page Start: 395 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exome sequencing identifies PD‐L2 as a potential predisposition gene for lymphoma. Issue 3 (29th May 2022) Authors: Shao, Jianming; Gao, Lei; Leung, Marco L.; Gallinger, Bailey; Inglese, Cara; Meyn, M. Stephen; Del Gaudio, Daniela; Das, Soma; Li, Zejuan Journal: Hematological oncology Issue: Volume 40:Issue 3(2022) Page Start: 475 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Non‐rhabdomyosarcoma soft tissue sarcomas diagnosed in patients at a young age. An overview of clinical, pathological, and molecular findings. Issue 8 (25th March 2021) Authors: Renzi, Samuele; Cullinan, Noelle; Cohen‐Gogo, Sarah; Langenberg‐Ververgaert, Karin; Michaeli, Orli; Alkendi, Jalila; Kanwar, Nisha; Lo, Winnie; Villani, Anita; Shlien, Adam; Malkin, David; Ryan, Anne L.; Gallinger, Bailey; Ingley, Katrina; Hopyan, Sevan; Gupta, Abha; Chami, Rose Journal: Pediatric blood & cancer Issue: Volume 68:Issue 8(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. 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". (31st March 2022) Authors: Waldman, Larissa; Hancock, Kelly; Gallinger, Bailey; Johnstone, Brittney; Brunga, Ledia; Malkin, David; Barrera, Maru; Villani, Anita Journal: JCO precision oncology Issue: Volume 6(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases. Issue 10 (31st August 2015) Authors: Buske, Orion J.; Girdea, Marta; Dumitriu, Sergiu; Gallinger, Bailey; Hartley, Taila; Trang, Heather; Misyura, Andriy; Friedman, Tal; Beaulieu, Chandree; Bone, William P.; Links, Amanda E.; Washington, Nicole L.; Haendel, Melissa A.; Robinson, Peter N.; Boerkoel, Cornelius F.; Adams, David; Gahl, ... Journal: Human mutation Issue: Volume 36:Issue 10(2015:Oct.) Page Start: 931 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance. Issue 25 (1st September 2021) Authors: Durno, Carol; Ercan, Ayse Bahar; Bianchi, Vanessa; Edwards, Melissa; Aronson, Melyssa; Galati, Melissa; Atenafu, Eshetu G.; Abebe-Campino, Gadi; Al-Battashi, Abeer; Alharbi, Musa; Azad, Vahid Fallah; Baris, Hagit N.; Basel, Donald; Bedgood, Raymond; Bendel, Anne; Ben-Shachar, Shay; Blumenthal, De... Journal: Journal of clinical oncology Issue: Volume 39:Issue 25(2021) Page Start: 2779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The adrenal gland: an evolution of the roles of genetic counsellors and medical geneticists in endocrine cancers. Issue 3 (March 2016) Authors: Gallinger, Bailey; Druker, Harriet; Gill, Anthony J.; Wasserman, Jonathan D.; Kim, Raymond H. Journal: Diagnostic histopathology Issue: Volume 22:Issue 3(2016) Page Start: 108 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗