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The development and evaluation of a nationwide training program for oncology health professionals in the provision of genetic testing for ovarian cancer patients.
Gleeson M, Kentwell M, Meiser B, Do J, Nevin S, Taylor N, Barlow-Stewart K, Kirk J, James P, Scott CL, Williams R, Gamet K, Burke J, Murphy M, Antill YC, Pearn A, Pachter N, Ebzery C, Poplawski N, Friedlander M, Tucker KM; Australian Genetic Testing Mainstreaming Collaborative Group. Gleeson M, et al. Among authors: kirk j. Gynecol Oncol. 2020 Aug;158(2):431-439. doi: 10.1016/j.ygyno.2020.05.001. Epub 2020 May 22. Gynecol Oncol. 2020. PMID: 32451123
When knowledge of a heritable gene mutation comes out of the blue: treatment-focused genetic testing in women newly diagnosed with breast cancer.
Meiser B, Quinn VF, Gleeson M, Kirk J, Tucker KM, Rahman B, Saunders C, Watts KJ, Peate M, Geelhoed E, Barlow-Stewart K, Field M, Harris M, Antill YC, Mitchell G. Meiser B, et al. Among authors: kirk j. Eur J Hum Genet. 2016 Nov;24(11):1517-1523. doi: 10.1038/ejhg.2016.69. Epub 2016 Jun 22. Eur J Hum Genet. 2016. PMID: 27329735 Free PMC article.
Cancer in the family. Part 2.
Kefford R, Tucker K, Friedlander M, Kirk J. Kefford R, et al. Among authors: kirk j. Aust Fam Physician. 1998 Jan-Feb;27(1-2):40-4. Aust Fam Physician. 1998. PMID: 9503704 Review.
Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics.
Meiser B, Kaur R, Kirk J, Morrow A, Peate M, Wong WKT, McPike E, Cops E, Dowson C, Austin R, Fine M, Thrupp L, Ward R, Macrae F, Hiller JE, Trainer AH, Mitchell G; ICCon Audit Study Collaborative Group. Meiser B, et al. Among authors: kirk j. Fam Cancer. 2020 Oct;19(4):337-346. doi: 10.1007/s10689-020-00183-4. Fam Cancer. 2020. PMID: 32385704
1,756 results