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Page 1
Update on Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Achatz MI, Villani A, Bertuch AA, Bougeard G, Chang VY, Doria AS, Gallinger B, Godley LA, Greer MC, Kamihara J, Khincha PP, Kohlmann WK, Kratz CP, MacFarland SP, Maese LD, Maxwell KN, Mitchell SG, Nakano Y, Pfister SM, Wasserman JD, Woodward ER, Garber JE, Malkin D. Achatz MI, et al. Among authors: gallinger b. Clin Cancer Res. 2025 May 15;31(10):1831-1840. doi: 10.1158/1078-0432.CCR-24-3301. Clin Cancer Res. 2025. PMID: 40072304
Update on Pediatric Surveillance Recommendations for PTEN Hamartoma Tumor Syndrome, DICER1-Related Tumor Predisposition, and Tuberous Sclerosis Complex.
Schultz KAP, MacFarland SP, Perrino MR, Mitchell SG, Kamihara J, Nelson AT, Mallinger PHR, Brzezinski JJ, Maxwell KN, Woodward ER, Gallinger B, Kim SY, Greer MC, Schneider KW, Scollon SR, Das A, Wasserman JD, Eng C, Malkin D, Foulkes WD, Michaeli O, Bauer AJ, Stewart DR. Schultz KAP, et al. Among authors: gallinger b. Clin Cancer Res. 2025 Jan 17;31(2):234-244. doi: 10.1158/1078-0432.CCR-24-1947. Clin Cancer Res. 2025. PMID: 39540884 Free PMC article. Review.
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.
Villani A, Shore A, Wasserman JD, Stephens D, Kim RH, Druker H, Gallinger B, Naumer A, Kohlmann W, Novokmet A, Tabori U, Tijerin M, Greer ML, Finlay JL, Schiffman JD, Malkin D. Villani A, et al. Among authors: gallinger b. Lancet Oncol. 2016 Sep;17(9):1295-305. doi: 10.1016/S1470-2045(16)30249-2. Epub 2016 Aug 5. Lancet Oncol. 2016. PMID: 27501770
Update on Surveillance in Von Hippel-Lindau Disease.
Rednam SP, Becktell KD, Villani A, Brodeur GM, States LJ, Doria AS, Kamihara J, Schneider KW, Voss SD, Widjaja E, Zelley K, Nakano Y, Pajtler KW, Achatz MI, Malkin D, Diller LR, Gallinger B, Tamura C, Wasserman JD. Rednam SP, et al. Among authors: gallinger b. Clin Cancer Res. 2025 Jun 13;31(12):2271-2277. doi: 10.1158/1078-0432.CCR-24-3525. Clin Cancer Res. 2025. PMID: 40232410 Review.
Update on Tumor Surveillance for Children with Hereditary Pheochromocytoma/Paraganglioma Syndromes.
Rednam SP, Kamihara J, Becktell KD, Brodeur GM, States LJ, Voss SD, Villani A, Zelley K, Malkin D, Nakano Y, Doria AS, Widjaja E, Pajtler KW, Schneider KW, Achatz MI, Diller LR, Gallinger B, Tamura C, Wasserman JD. Rednam SP, et al. Among authors: gallinger b. Clin Cancer Res. 2025 Aug 14;31(16):3368-3376. doi: 10.1158/1078-0432.CCR-24-4354. Clin Cancer Res. 2025. PMID: 40549645 Review.
Pediatric imaging in DICER1 syndrome.
Bueno MT, Martínez-Ríos C, la Puente Gregorio A, Ahyad RA, Villani A, Druker H, van Engelen K, Gallinger B, Aronoff L, Grant R, Malkin D, Greer MC. Bueno MT, et al. Among authors: gallinger b. Pediatr Radiol. 2017 Sep;47(10):1292-1301. doi: 10.1007/s00247-017-3875-0. Epub 2017 May 4. Pediatr Radiol. 2017. PMID: 28474256
Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes.
Michaeli O, Kim SY, Mitchell SG, Jongmans MCJ, Wasserman JD, Perrino MR, Das A, MacFarland SP, Scollon SR, Greer MC, Sobreira N, Gallinger B, Lupo PJ, Malkin D, Schneider KW, Schultz KAP, Foulkes WD, Woodward ER, Stewart DR. Michaeli O, et al. Among authors: gallinger b. Clin Cancer Res. 2025 Feb 3;31(3):457-465. doi: 10.1158/1078-0432.CCR-24-2171. Clin Cancer Res. 2025. PMID: 39601780 Free PMC article. Review.
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol.
Farncombe KM, Hughes LK, Tuzlali E, Akbari MR, Andrulis IL, Aronson M, Bell K, Brazas MD, Cable-Cibula M, Chan B, Courtot M, Feilotter H, Harland J, Lark K, Lerner-Ellis J, MacDougall E, Malkin D, Narod SA, Panabaker K, Radvanyi L, Rusnak A, Stein L, Kim RH; OHCRN community. Farncombe KM, et al. BMJ Open. 2024 Nov 24;14(11):e087023. doi: 10.1136/bmjopen-2024-087023. BMJ Open. 2024. PMID: 39581712 Free PMC article.
Updated Recommendations for Pediatric Surveillance in Hereditary Endocrine Neoplasia Syndromes: Multiple Endocrine Neoplasias, Hyperparathyroidism-Jaw Tumor Syndrome, and Carney Complex.
Wasserman JD, Schneider KW, Achatz MI, Nakano Y, Zelley K, Gallinger B, Bauer AJ, Becktell KD, Wassner AJ, Raiti L, Doria AS, States LJ, Stratakis CA, Brodeur GM, Diller LR, Kamihara J, Malkin D, Pajtler KW, Tamura C, Villani A, Widjaja E, Das A, Rednam SP. Wasserman JD, et al. Among authors: gallinger b. Clin Cancer Res. 2025 Sep 2;31(17):3628-3637. doi: 10.1158/1078-0432.CCR-24-3860. Clin Cancer Res. 2025. PMID: 40560659
24 results