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Page 1
Update on Surveillance Guidelines in Emerging Wilms Tumor Predisposition Syndromes.
Brzezinski JJ, Becktell KD, Bougeard G, Brodeur GM, Diller LR, Doria AS, Hansford JR, Kohlmann WK, Kratz CP, MacFarland SP, Pajtler KW, Rednam SP, Schienda J, States LJ, Villani A, Weksberg R, Zelley K, Tomlinson GE, Kalish JM. Brzezinski JJ, et al. Among authors: kohlmann wk. Clin Cancer Res. 2025 Jan 6;31(1):18-24. doi: 10.1158/1078-0432.CCR-24-2488. Clin Cancer Res. 2025. PMID: 39466169 Review.
Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith-Wiedemann Syndrome and Other Predisposition Syndromes.
Kalish JM, Becktell KD, Bougeard G, Brodeur GM, Diller LR, Doria AS, Hansford JR, Klein SD, Kohlmann WK, Kratz CP, MacFarland SP, Pajtler KW, Rednam SP, Schienda J, States LJ, Villani A, Weksberg R, Zelley K, Tomlinson GE, Brzezinski JJ. Kalish JM, et al. Among authors: kohlmann wk. Clin Cancer Res. 2024 Dec 2;30(23):5260-5269. doi: 10.1158/1078-0432.CCR-24-2100. Clin Cancer Res. 2024. PMID: 39320341 Review.
Uptake of Cancer Genetic Services for Chatbot vs Standard-of-Care Delivery Models: The BRIDGE Randomized Clinical Trial.
Kaphingst KA, Kohlmann WK, Lorenz Chambers R, Bather JR, Goodman MS, Bradshaw RL, Chavez-Yenter D, Colonna SV, Espinel WF, Everett JN, Flynn M, Gammon A, Harris A, Hess R, Kaiser-Jackson L, Lee S, Monahan R, Schiffman JD, Volkmar M, Wetter DW, Zhong L, Mann DM, Ginsburg O, Sigireddi M, Kawamoto K, Del Fiol G, Buys SS. Kaphingst KA, et al. Among authors: kohlmann wk. JAMA Netw Open. 2024 Sep 3;7(9):e2432143. doi: 10.1001/jamanetworkopen.2024.32143. JAMA Netw Open. 2024. PMID: 39250153 Free PMC article. Clinical Trial.
Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies.
Perrino MR, Das A, Scollon SR, Mitchell SG, Greer MC, Yohe ME, Hansford JR, Kalish JM, Schultz KAP, MacFarland SP, Kohlmann WK, Lupo PJ, Maxwell KN, Pfister SM, Weksberg R, Michaeli O, Jongmans MCJ, Tomlinson GE, Brzezinski J, Tabori U, Ney GM, Gripp KW, Gross AM, Widemann BC, Stewart DR, Woodward ER, Kratz CP. Perrino MR, et al. Among authors: kohlmann wk. Clin Cancer Res. 2024 Nov 1;30(21):4834-4843. doi: 10.1158/1078-0432.CCR-24-1611. Clin Cancer Res. 2024. PMID: 39196581 Review.
Germline Testing in Patients With Breast Cancer: ASCO-Society of Surgical Oncology Guideline.
Bedrosian I, Somerfield MR, Achatz MI, Boughey JC, Curigliano G, Friedman S, Kohlmann WK, Kurian AW, Laronga C, Lynce F, Norquist BS, Plichta JK, Rodriguez P, Shah PD, Tischkowitz M, Wood M, Yadav S, Yao K, Robson ME. Bedrosian I, et al. Among authors: kohlmann wk. J Clin Oncol. 2024 Feb 10;42(5):584-604. doi: 10.1200/JCO.23.02225. Epub 2024 Jan 4. J Clin Oncol. 2024. PMID: 38175972
Enhanced family history-based algorithms increase the identification of individuals meeting criteria for genetic testing of hereditary cancer syndromes but would not reduce disparities on their own.
Bradshaw RL, Kawamoto K, Bather JR, Goodman MS, Kohlmann WK, Chavez-Yenter D, Volkmar M, Monahan R, Kaphingst KA, Del Fiol G. Bradshaw RL, et al. Among authors: kohlmann wk. J Biomed Inform. 2024 Jan;149:104568. doi: 10.1016/j.jbi.2023.104568. Epub 2023 Dec 9. J Biomed Inform. 2024. PMID: 38081564 Free PMC article.
35 results