Issue Date | Title | Author(s) |
2017-02 | A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public. | Smit, AK; Espinoza, D; Newson, AJ; Morton, RL; Fenton, G; Freeman, L; Dunlop, K; Butow, PN; Law, MH; Kimlin, MG; Keogh, LA; Dobbinson, SJ; Kirk, J; Kanetsky, PA; Mann, GJ; Cust, AE |
2022-09-26 | Communicating Personal Melanoma Polygenic Risk Information: Participants' Experiences of Genetic Counseling in a Community-Based Study. | Smit, AK; Espinoza, D; Fenton, GL; Kirk, J; Innes, JS; McGovern, M; Limb, S; On Behalf Of The Managing Your Risk Study Group,; Turbitt, E; Cust, AE |
2018-04 | Development and Evaluation of a Telephone Communication Protocol for the Delivery of Personalized Melanoma Genomic Risk to the General Population. | Fenton, GL; Smit, AK; Freeman, L; Badcock, C; Dunlop, K; Butow, PN; Kirk, J; Cust, AE |
2019-12-01 | Development and validation of a targeted gene sequencing panel for application to disparate cancers | McCabe, MJ; Gauthier, MEA; Chan, CL; Thompson, TJ; De Sousa, SMC; Puttick, C; Grady, JP; Gayevskiy, V; Tao, J; Ying, K; Cipponi, A; Deng, N; Swarbrick, A; Thomas, ML; Lord, RV; Johns, AL; Kohonen-Corish, M; O’Toole, SA; Clark, J; Mueller, SA; Gupta, R; McCormack, AI; Dinger, ME; Cowley, MJ; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Armitage, S; Arnold, L; Balleine, R; Bastick, P; Beesley, J; Beilby, J; Bennett, I; Blackburn, A; Bogwitz, M; Botes, L; Brennan, M; Brown, M; Buckley, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Callen, D; Campbell, I; Chauhan, D; Chauhan, M; Chenevix-Trench, G; Christian, A; Clarke, C; Cohen, P; Colley, A; Crook, A; Cui, J; Culling, B; Cummings, M; Dawson, SJ; deFazio, A; Delatycki, M; Dickson, R; Dixon, J; Dobrovic, A; Dudding, T; Edkins, T; Edwards, S; Eisenbruch, M; Farshid, G; Fellows, A; Fenton, G; Field, M; Flanagan, J; Fong, P; Forrest, L; Fox, S; French, J; Friedlander, M; Gaff, C; Ortega, DG; Gattas, M; George, P; Giles, G; Gill, G; Greening, S; Haan, E; Harris, M; Hart, S; Hayward, N; Heiniger, L; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kidd, A; Kirk, J; Koehler, J; Kollias, J; Lakhani, S |
2021-08 | Helping young children understand inherited cancer predisposition syndromes using bibliotherapy. | Schlub, GM; Crook, A; Barlow-Stewart, K; Fleming, J; Kirk, J; Tucker, K; Greening, S |
2019-12-01 | Homologous recombination DNA repair defects in PALB2-associated breast cancers | Li, A; Geyer, FC; Blecua, P; Lee, JY; Selenica, P; Brown, DN; Pareja, F; Lee, SSK; Kumar, R; Rivera, B; Bi, R; Piscuoglio, S; Wen, HY; Lozada, JR; Gularte-Mérida, R; Cavallone, L; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Balleine, R; Beesley, J; Blackburn, A; Bogwitz, M; Brown, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Campbell, I; Christian, A; Clarke, C; Cohen, P; Crook, A; Cui, J; Cummings, M; Dawson, SJ; De Fazio, A; Delatycki, M; Dobrovic, A; Dudding, T; Duijf, P; Edkins, E; Edwards, S; Farshid, G; Fellows, A; Field, M; Flanagan, J; Fong, P; Forbes, J; Forrest, L; Fox, S; French, J; Friedlander, M; Ortega, DG; Gattas, M; Giles, G; Gill, G; Gleeson, M; Greening, S; Haan, E; Harris, M; Hayward, N; Hickie, I; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kentwell, M; Kirk, J; Kollias, J; Lakhani, S; Lindeman, G; Lipton, L; Lobb, L; Lok, S; Macrea, F; Mann, G; Marsh, D; McLachlan, SA; Meiser, B; Milne, R; Nightingale, S; O’Connell, S; Pachter, N; Patterson, B; Phillips, K; Saleh, M; Salisbury, E; Saunders, C; Saunus, J; Scott, C; Scott, R; Sexton, A; Shelling, A; Simpson, P; Spigelman, A; Spurdle, M; Stone, J |
2020-11-09 | Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. | Tudini, E; Davidson, AL; Dressel, U; Andrews, L; Antill, Y; Crook, A; Field, M; Gattas, M; Harris, R; Kirk, J; Pachter, N; Salmon, L; Susman, R; Townshend, S; Trainer, AH; Tucker, KM; Mitchell, G; James, PA; Ward, RL; Mar Fan, H; Poplawski, NK; Spurdle, AB |
2023-02-18 | Older age should not be a barrier to testing for somatic variants in homologous recombination DNA repair-related genes in patients with high-grade serous ovarian carcinoma. | Pitiyarachchi, O; Lee, YC; Sim, H-W; Srirangan, S; Mapagu, C; Kirk, J; Harnett, PR; Balleine, RL; Bowtell, DDL; Samimi, G; Brand, AH; Marsh, DJ; Beale, P; Anderson, L; Bouantoun, N; Provan, P; INOVATe Investigators,; Ramus, SJ; DeFazio, A; Friedlander, M |
2019-07-31 | Patient perspectives on molecular tumor profiling: "why wouldn't you?" | Best, MC; Bartley, N; Jacobs, C; Juraskova, I; Goldstein, D; Newson, AJ; Savard, J; Meiser, B; Ballinger, M; Napier, C; Thomas, D; Biesecker, B; Butow, P; Tucker, K; Schlub, T; Vines, R; Vines, K; Kirk, J; Young, MA |
2019-02-01 | Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations | Bancroft, EK; Saya, S; Page, EC; Myhill, K; Thomas, S; Pope, J; Chamberlain, A; Hart, R; Glover, W; Cook, J; Rosario, DJ; Helfand, BT; Selkirk, CH; Davidson, R; Longmuir, M; Eccles, DM; Gadea, N; Brewer, C; Barwell, J; Salinas, M; Greenhalgh, L; Tischkowitz, M; Henderson, A; Evans, DG; Buys, SS; Eeles, RA; Aaronson, NK; Eeles, R; Bancroft, E; Page, E; Kote-Jarai, Z; Ardern-Jones, A; Bangma, C; Castro, E; Dearnaley, D; Falconer, A; Foster, C; Gronberg, H; Hamdy, FC; Johannsson, OT; Khoo, V; Eccles, D; Lilja, H; Evans, G; Eyfjord, J; Lubinski, J; Maehle, L; Mikropoulos, C; Millner, A; Mitra, A; Offman, J; Moynihan, C; Rennert, G; Suri, M; Dias, A; Taylor, N; D'Mello, L; James, P; Mitchell, G; Shanley, S; Richardson, K; McKinley, J; Petelin, L; Murphy, M; Mascarenhas, L; Murphy, D; Lam, J; Taylor, L; Miller, C; Stapleton, A; Chong, M; Suthers, G; Poplawski, N; Tucker, K; Andrews, L; Duffy, J; Millard, R; Ward, R; Williams, R; Stricker, P; Kirk, J; Bowman, M; Patel, M; Harris, M; O'Connell, S; Hunt, C; Smyth, C; Frydenberg, M; Lindeman, G; Shackleton, K; Morton, C; Susman, R; McGaughran, J; Boon, M; Pachter, N; Townshend, S; Schofield, L; Nicholls, C; Spigelman, A; Gleeson, M; Amor, D; Burke, J; Patterson, B; Swindle, P; Scott, R; Foulkes, W; Boshari, T; Aprikian, A; Jensen, T; Bojeson, A; Osther, P; Skytte, A-B; Cruger, D; Tondering, MK; Gerdes, A-M; Schmutzler, R; Rhiem, K; Wihler, P; Kast, K; Griebsch, C; Johannsson, O; Stefansdottir, V; Murthy, V; Sarin, R; Awatagiri, K; Ghonge, S; Kowtal, P; Mulgund, G; Gallagher, D; Bambury, R; Farrell, M; Gallagher, F; Kiernan, I; Friedman, E; Chen-Shtoyerman, R; Basevitch, A; Leibovici, D; Melzer, E; Ben-Yehoshua, SJ; Nicolai, N; Radice, P; Valdagni, R; Magnani, T; Gay, S; Teo, SH; Tan, HM; Yoon, S-Y; Thong, MK; Vasen, H; Ringleberg, J; van Asperen, C; Kiemeney, B; van Zelst-Stams, W; Ausems, MGEM; van der Luijt, RB; van Os, T; Ruijs, MWG; Adank, MA; Oldenburg, RA; Helderman-van den Enden, APTJM; Caanen, BAH; Oosterwijk, JC; Moller, P; Brennhovd, B; Medvik, H; Hanslien, E; Grindedal, EM; Cybulski, C; Wokolorczyk, D; Teixeira, M; Maia, S; Peixoto, A; Henrique, R; Oliveira, J; Goncalves, N; Araujo, L; Seixas, M; Souto, JP; Nogueira, P; Copakova, L; Zgajnar, J; Krajc, M; Vrecar, A; Capella, G; Ramon y Cajal, T; Fisas, D; Mora, J; Esquena, S; Balmana, J; Morote, J; Liljegren, A; Hjalm-Eriksson, M; Ekdahl, K-J; Carlsson, S; George, A; Kemp, Z; Wiggins, J; Moss, C; Van As, N; Thompson, A; Ogden, C; Woodhouse, C; Kumar, P; Bulman, B; Rothwell, J; Tricker, K; Wise, G; Mercer, C; McBride, D; Costello, P; Pearce, A; Torokwa, A; Paterson, J; Clowes, V; Taylor, A; Newcombe, B; Walker, L; Halliday, D; Stayner, B; Fleming-Brown, D; Snape, K; Hanson, H; Hodgson, S; Brice, G; Homfray, T; Hammond, C; Kohut, K; Anjum, U; Dearing, A; Mencias, M; Potter, A; Renton, C; Searle, A; Hill, K; Goodman, S; Garcia, L; Devlin, G; Everest, S; Nadolski, M; Douglas, F; Jobson, I; Paez, E; Donaldson, A; Tomkins, S; Langman, C; Jacobs, C; Pichert, G; Shaw, A; Kulkarni, A; Tripathi, V; Rose, S; Compton, C; Watson, M; Reinholtz, C; Brady, A; Dorkins, H; Melville, A; Kosicka-Slawinska, M; Cummings, C; Kiesel, V; Bartlett, M; Randhawa, K; Ellery, N; Side, L; Male, A; Simon, K; Rees, K; Tidey, L; Gurasashvili, J; Nevitt, L; Ingram, S; Howell, A; Rosario, D; Catto, J; Howson, J; Ong, K-R; Chapman, C; Cole, T; Heaton, T; Hoffman, J; Burgess, L; Huber, C; Islam, F; Watt, C; Duncan, A; Kockelbergh, R; Mzazi, S; Dineen, A; Sattar, A; Kaemba, B; Sidat, Z; Patel, N; Siguake, K; Birt, A; Poultney, U; Umez-Eronini, N; Mom, J; Sutton, V; Cornford, P; Bermingham, N; Yesildag, P; Treherne, K; Griffiths, J; Cogley, L; Gott, H; Rubinstein, WS; Hulick, P; McGuire, M; Shevrin, D; Kaul, K; Weissman, S; Newlin, A; Vogel, K; Weiss, S; Hook, N; Buys, S; Goldgar, D; Conner, T; Venne, V; Stephenson, R; Dechet, C; Domchek, S; Powers, J; Rustgi, N; Strom, S; Arun, B; Davis, JW; Yamamura, Y; Obeid, E; Giri, V; Gross, L; Bealin, L; Cooney, K; Stoffel, E; Okoth, L |
2019-12-01 | Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9) | Li, A; Geyer, FC; Blecua, P; Lee, JY; Selenica, P; Brown, DN; Pareja, F; Lee, SSK; Kumar, R; Rivera, B; Bi, R; Piscuoglio, S; Wen, HY; Lozada, JR; Gularte-Mérida, R; Cavallone, L; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Balleine, R; Beesley, J; Blackburn, A; Bogwitz, M; Brown, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Campbell, I; Christian, A; Clarke, C; Cohen, P; Crook, A; Cui, J; Cummings, M; Dawson, SJ; De Fazio, A; Delatycki, M; Dobrovic, A; Dudding, T; Duijf, P; Edkins, E; Edwards, S; Farshid, G; Fellows, A; Field, M; Flanagan, J; Fong, P; Forbes, J; Forrest, L; Fox, S; French, J; Friedlander, M; Ortega, DG; Gattas, M; Giles, G; Gill, G; Gleeson, M; Greening, S; Haan, E; Harris, M; Hayward, N; Hickie, I; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kentwell, M; Kirk, J; Kollias, J; Lakhani, S; Lindeman, G; Lipton, L; Lobb, L; Lok, S; Macrea, F; Mann, G; Marsh, D; McLachlan, SA; Meiser, B; Milne, R; Nightingale, S; O’Connell, S; Pachter, N; Patterson, B; Phillips, K; Saleh, M; Salisbury, E; Saunders, C; Saunus, J; Scott, C; Scott, R; Sexton, A; Shelling, A; Simpson, P; Spigelman, A; Spurdle, M; Stone, J |
2022-02 | Rare germline variants in childhood cancer patients suspected of genetic predisposition to cancer. | Sylvester, DE; Chen, Y; Grima, N; Saletta, F; Padhye, B; Bennetts, B; Wright, D; Krivanek, M; Graf, N; Zhou, L; Catchpoole, D; Kirk, J; Latchoumanin, O; Qiao, L; Ballinger, M; Thomas, D; Jamieson, R; Dalla-Pozza, L; Byrne, JA |