Select Publications

Journal articles

Yanes T; Kaur R; Meiser B; Scheepers-Joynt M; McInerny S; Barlow-Stewart K; Antill Y; Salmon L; Smyth C; James PA; Young MA, 2020, 'Women’s responses and understanding of polygenic breast cancer risk information', Familial Cancer, vol. 19, pp. 297 - 306, http://dx.doi.org/10.1007/s10689-020-00185-2

Davies G; Butow P; Napier CE; Bartley N; Juraskova I; Meiser B; Ballinger ML; Thomas DM; Schlub TE; Best MC, 2020, 'Advanced Cancer Patient Knowledge of and Attitudes towards Tumor Molecular Profiling', Translational Oncology, vol. 13, pp. 100799, http://dx.doi.org/10.1016/j.tranon.2020.100799

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, 2020, 'The development and evaluation of a nationwide training program for oncology health professionals in the provision of genetic testing for ovarian cancer patients', Gynecologic Oncology, vol. 158, pp. 431 - 439, http://dx.doi.org/10.1016/j.ygyno.2020.05.001

Meiser B; Guo XY; Putt S; Fullerton JM; Schofield PR; Mitchell PB; Yanes T, 2020, 'Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature', American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 183, pp. 277 - 288, http://dx.doi.org/10.1002/ajmg.b.32786

McInerney-Leo AM; West J; Meiser B; West M; Brown MA; Duncan E, 2020, 'Causal Attributions in an Australian Aboriginal Family With Marfan Syndrome: A Qualitative Study', Frontiers in Genetics, vol. 11, pp. 461, http://dx.doi.org/10.3389/fgene.2020.00461

Butow P; Davies G; Napier CE; Schlub T; Best MC; Bartley N; Juraskova I; Meiser B; Ballinger ML; Biesecker B; Goldstein D; Thomas DM, 2020, 'Assessment of the Value of Tumor Variation Profiling Perceived by Patients With Cancer', JAMA network open, vol. 3, pp. e204721, http://dx.doi.org/10.1001/jamanetworkopen.2020.4721

Putt S; Yanes T; Meiser B; Kaur R; Fullerton JM; Barlow-Stewart K; Schofield PR; Toma C; Peay H; Mitchell PB, 2020, 'Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder', Journal of Affective Disorders, vol. 265, pp. 342 - 350, http://dx.doi.org/10.1016/j.jad.2020.01.037

Yanes T; Meiser B; Kaur R; Scheepers-Joynt M; McInerny S; Taylor S; Barlow-Stewart K; Antill Y; Salmon L; Smyth C; Young MA; James PA, 2020, 'Uptake of polygenic risk information among women at increased risk of breast cancer', Clinical Genetics, vol. 97, pp. 492 - 501, http://dx.doi.org/10.1111/cge.13687

Yanes T; Young MA; Meiser B; James PA, 2020, 'Clinical applications of polygenic breast cancer risk: A critical review and perspectives of an emerging field', Breast Cancer Research, vol. 22, pp. 21, http://dx.doi.org/10.1186/s13058-020-01260-3

Best MC; Butow P; Jacobs C; Savard J; Biesecker B; Ballinger ML; Bartley N; Davies G; Napier CE; Smit AK; Thomas DM; Newson AJ, 2020, 'Who should access germline genome sequencing? A mixed methods study of patient views', Clinical Genetics, vol. 97, pp. 329 - 337, http://dx.doi.org/10.1111/cge.13664

Bartley N; Best M; Jacobs C; Juraskova I; Newson AJ; Savard J; Meiser B; Ballinger ML; Thomas DM; Biesecker B; Butow P, 2020, 'Cancer patients' views and understanding of genome sequencing: A qualitative study', Journal of Medical Genetics, http://dx.doi.org/10.1136/jmedgenet-2019-106410

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; Susman R; Pachter N; Goodwin A; James P; Mascarenhas L; Morton C; Shanley S; Young MA; Andrews L; Morrow EA; Tucker K; Lindeman G; Field M; Monnik M; Poplawski N; Delatycki M; John T; Harris M; Kerr R; Vora B, 2020, 'Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics', Familial Cancer, http://dx.doi.org/10.1007/s10689-020-00183-4

O’Neill RS; Meiser B; Emmanuel S; Williams DB; Stoita A, 2020, 'Long-term positive psychological outcomes in an Australian pancreatic cancer screening program', Familial Cancer, vol. 19, pp. 23 - 35, http://dx.doi.org/10.1007/s10689-019-00147-3

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, 2019, 'Homologous recombination DNA repair defects in PALB2-associated breast cancers', npj Breast Cancer, vol. 5, http://dx.doi.org/10.1038/s41523-019-0115-9

Lázaro-Muñoz G; Sabatello M; Huckins L; Peay H; Degenhardt F; Meiser B; Lencz T; Soda T; Docherty A; Crepaz-Keay D; Austin J; Peterson RE; Davis LK, 2019, 'International Society of Psychiatric Genetics Ethics Committee: Issues facing us', American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 180, pp. 543 - 554, http://dx.doi.org/10.1002/ajmg.b.32736

Moldovan R; McGhee KA; Coviello D; Hamang A; Inglis A; Ingvoldstad Malmgren C; Johansson-Soller M; Laurino M; Meiser B; Murphy L; Paneque M; Papsuev O; Pawlak J; Rovira Moreno E; Serra-Juhe C; Shkedi-Rafid S; Laing N; Voelckel MA; Watson M; Austin JC, 2019, 'Psychiatric genetic counseling: A mapping exercise', American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 180, pp. 523 - 532, http://dx.doi.org/10.1002/ajmg.b.32735

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, 2019, '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)', npj Breast Cancer, vol. 5, http://dx.doi.org/10.1038/s41523-019-0140-8

Figlioli G; Bogliolo M; Catucci I; Caleca L; Lasheras SV; Pujol R; Kiiski JI; Muranen TA; Barnes DR; Dennis J; Michailidou K; Bolla MK; Leslie G; Aalfs CM; Balleine R; Baxter R; Braye S; Carpenter J; Dahlstrom J; Forbes J; Lee CS; Marsh D; Morey A; Pathmanathan N; Scott R; Simpson P; Spigelman A; Wilcken N; Yip D; Zeps N; Adank MA; Adlard J; Agata S; Cadoo K; Agnarsson BA; Ahearn T; Aittomäki K; Ambrosone CB; Andrews L; Anton-Culver H; Antonenkova NN; Arndt V; Arnold N; Aronson KJ; Arun BK; Asseryanis E; Auber B; Auvinen P; Azzollini J; Balmaña J; Barkardottir RB; Barrowdale D; Barwell J; Beane Freeman LE; Beauparlant CJ; Beckmann MW; Behrens S; Benitez J; Berger R; Bermisheva M; Blanco AM; Blomqvist C; Bogdanova NV; Bojesen A; Bojesen SE; Bonanni B; Borg A; Brady AF; Brauch H; Brenner H; Brüning T; Burwinkel B; Buys SS; Caldés T; Caliebe A; Caligo MA; Campa D; Campbell IG; Canzian F; Castelao JE; Chang-Claude J; Chanock SJ; Claes KBM; Clarke CL; Collavoli A; Conner TA; Cox DG; Cybulski C; Czene K; Daly MB; de la Hoya M; Devilee P; Diez O; Ding YC; Dite GS; Ditsch N; Domchek SM; Dorfling CM; dos-Santos-Silva I; Durda K, 2019, 'The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer', npj Breast Cancer, vol. 5, http://dx.doi.org/10.1038/s41523-019-0127-5

Tutty E; Petelin L; McKinley J; Young MA; Meiser B; Rasmussen VM; Forbes Shepherd R; James PA; Forrest LE, 2019, 'Evaluation of telephone genetic counselling to facilitate germline BRCA1/2 testing in women with high-grade serous ovarian cancer', European Journal of Human Genetics, vol. 27, pp. 1186 - 1196, http://dx.doi.org/10.1038/s41431-019-0390-9

Cheng L; Meiser B, 2019, 'The relationship between psychosocial factors and biomarkers in cancer patients: A systematic review of the literature', European Journal of Oncology Nursing, vol. 41, pp. 88 - 96, http://dx.doi.org/10.1016/j.ejon.2019.06.002

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, 'Patient perspectives on molecular tumor profiling: "why wouldn't you?"', BMC Cancer, vol. 19, pp. 753, http://dx.doi.org/10.1186/s12885-019-5920-x

Smith SK; Cabrera-Aguas M; Shaw J; Shepherd H; Naehrig D; Meiser B; Jackson M; Saade G; Bucci J; Halkett GKB; Turner RM; Milross C; Dhillon HM, 2019, 'A low literacy targeted talking book about radiation therapy for cancer: development and acceptability', Supportive Care in Cancer, vol. 27, pp. 2057 - 2067, http://dx.doi.org/10.1007/s00520-018-4446-0

Kaur R; Meiser B; Zilliacus E; Tim Wong WK; Woodland L; Watts K; Tomkins S; Kissane D; Girgis A; Butow P; Hale S; Perry A; Aranda SK; Shaw T; Tebble H; Norris C; Goldstein D, 2019, 'Evaluation of an online communication skills training programme for oncology nurses working with patients from minority backgrounds', Supportive Care in Cancer, vol. 27, pp. 1951 - 1960, http://dx.doi.org/10.1007/s00520-018-4507-4

Josephi-Taylor S; Barlow-Stewart K; Selvanathan A; Roscioli T; Bittles A; Meiser B; Worgan L; Rajagopalan S; Colley A; Kirk EP, 2019, 'User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia', Journal of Genetic Counseling, vol. 28, pp. 240 - 250, http://dx.doi.org/10.1007/s10897-018-0298-5

Mills L; Meiser B; Ahmad R; Schofield PR; Peate M; Levitan C; Trevena L; Barlow-Stewart K; Dobbins T; Christensen H; Sherman KA; Dunlop K; Mitchell PB, 2019, 'A cluster randomized controlled trial of an online psychoeducational intervention for people with a family history of depression 11 Medical and Health Sciences 1117 Public Health and Health Services 11 Medical and Health Sciences 1103 Clinical Sciences', BMC Psychiatry, vol. 19, pp. 29, http://dx.doi.org/10.1186/s12888-018-1994-2

Sutherland S; Meiser B; Kaur R; Mitchell G; Kirk J; Peate M; Tim Wong WK; Goodwin A, 2019, 'Assessing the medical workforces perceived barriers to the prescription of risk-reducing medication for women at high-risk of breast cancer', Breast Journal, vol. 25, pp. 34 - 40, http://dx.doi.org/10.1111/tbj.13157

Grimmett C; Brooks C; Recio-Saucedo A; Armstrong A; Cutress RI; Gareth Evans D; Copson E; Turner L; Meiser B; Wakefield CE; Eccles D; Foster C, 2019, 'Development of Breast Cancer Choices: a decision support tool for young women with breast cancer deciding whether to have genetic testing for BRCA1/2 mutations', Supportive Care in Cancer, vol. 27, pp. 297 - 309, http://dx.doi.org/10.1007/s00520-018-4307-x

Yanes T; Willis AM; Meiser B; Tucker KM; Best M, 2019, 'Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review', European Journal of Human Genetics, vol. 27, pp. 28 - 35, http://dx.doi.org/10.1038/s41431-018-0257-5

Josephi-Taylor S; Barlow-Stewart K; Selvanathan A; Roscioli T; Bittles A; Meiser B; Worgan L; Rajagopalan S; Colley A; Kirk EP, 2019, 'User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia.', J Genet Couns, vol. 28, pp. 240 - 250, http://dx.doi.org/10.1007/s10897-018-0298-5

Smith SK; Cai A; Wong M; Sousa MS; Peate M; Welsh A; Bettina M; Kaur R; Halliday J; Lewis S; Trevena L; Yanes T; Barlow-Stewart K; Barclay M, 2018, 'Improving women’s knowledge about prenatal screening in the era of non-invasive prenatal testing for Down syndrome – development and acceptability of a low literacy decision aid', BMC Pregnancy and Childbirth, vol. 18, pp. 499, http://dx.doi.org/10.1186/s12884-018-2135-0

Sutherland S; Meiser B; Kaur R; Mitchell G; Kirk J; Peate M; Wong WKT; Goodwin A, 2018, 'Assessing the medical workforce's perceived barriers to the prescription of risk- reducing medication for women at high-risk of breast cancer', The Breast Journal, http://dx.doi.org/10.1111/tbj.13157

Kaur R; Meiser B; Ziliacus E; Wong WKT; Woodland L; Watts K; Tomkins S; Kissane D; Girgis A; Butow P; Hale S; Perry A; Aranda SK; Shaw T; Tebble H; Norris C; Goldstein D, 2018, 'Evaluation of an online communication skills training programme for oncology nurses working with patients from minority backgrounds', Supportive Care in Cancer, http://dx.doi.org/10.1007/s00520-018-4507-4

Hedelund Lausen L; Smith SK; Cai A; Meiser B; Yanes T; Ahmad R; Rowlands G, 2018, 'How is health literacy addressed in primary care? Strategies that general practitioners use to support patients', Journal of Communication in Healthcare, vol. 11, pp. 278 - 287, http://dx.doi.org/10.1080/17538068.2018.1531477

Kaur R; Meiser B; Yanes T; Young M-A; Barlow-Stewart K; Roscioli T; Smith S; James PA, 2018, 'Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk', Familial Cancer, http://dx.doi.org/10.1007/s10689-018-0104-4

Willis AM; Smith SK; Meiser B; Ballinger ML; Thomas DM; Tattersall M; Young MA, 2018, 'Development and Pilot Testing of a Decision Aid for Genomic Research Participants Notified of Clinically Actionable Research Findings for Cancer Risk', Journal of Genetic Counseling, vol. 27, pp. 1055 - 1066, http://dx.doi.org/10.1007/s10897-018-0223-y

Butow P; Price M; Coll J; Tucker K; Meiser B; Milne R; Wilson J; Heiniger L; Baylock B; Bullen T; Weideman P; Phillips KA, 2018, 'Does stress increase risk of breast cancer? A 15-year prospective study', Psycho-Oncology, vol. 27, pp. 1908 - 1914, http://dx.doi.org/10.1002/pon.4740

Meiser B; Quinn VF; Mitchell G; Tucker K; Watts KJ; Rahman B; Peate M; Saunders C; Geelhoed E; Gleeson M; Barlow-Stewart K; Field M; Harris M; Antill YC; Susman R; Bowen MT; Mills L; Kirk J, 2018, 'Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history', European Journal of Human Genetics, vol. 26, pp. 972 - 983, http://dx.doi.org/10.1038/s41431-017-0057-3

Best M; Newson AJ; Meiser B; Juraskova I; Goldstein D; Tucker K; Ballinger ML; Hess D; Schlub TE; Biesecker B; Vines R; Vines K; Thomas D; Young MA; Savard J; Jacobs C; Butow P, 2018, 'The PiGeOn project: Protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer', BMC Cancer, vol. 18, http://dx.doi.org/10.1186/s12885-018-4366-x

Halliday JL; Muller C; Charles T; Norris F; Kennedy J; Lewis S; Meiser B; Donath S; Stark Z; McGillivray G; Menezes M; Smith SK; Forster D; Walker S; Pertile M; Amor DJ, 2018, 'Offering pregnant women different levels of genetic information from prenatal chromosome microarray: A prospective study', European Journal of Human Genetics, vol. 26, pp. 485 - 494, http://dx.doi.org/10.1038/s41431-017-0084-0

Peay HL; Meiser B; Kinnett K; Tibben A, 2018, 'Psychosocial Needs and Facilitators of Mothers Caring for Children with Duchenne/Becker Muscular Dystrophy', Journal of Genetic Counseling, vol. 27, pp. 197 - 203, http://dx.doi.org/10.1007/s10897-017-0141-4

Grimmett C; Pickett K; Shepherd J; Welch K; Recio-Saucedo A; Streit E; Seers H; Armstrong A; Cutress RI; Evans DG; Copson E; Meiser B; Eccles D; Foster C, 2018, 'Systematic review of the empirical investigation of resources to support decision-making regarding BRCA1 and BRCA2 genetic testing in women with breast cancer', Patient Education and Counseling, http://dx.doi.org/10.1016/j.pec.2017.11.016

Liang R; Meiser B; Smith S; Kasparian NA; Lewis CR; Chin M; Long GV; Ward R; Menzies AM; Harris-Wai JN; Kaur R, 2017, 'Advanced cancer patients’ attitudes towards, and experiences with, screening for somatic mutations in tumours: a qualitative study', European Journal of Cancer Care, vol. 26, http://dx.doi.org/10.1111/ecc.12600

Meiser B; Wong WKT; Peate M; Julian-Reynier C; Kirk J; Mitchell G, 2017, 'Motivators and barriers of tamoxifen use as risk-reducing medication amongst women at increased breast cancer risk: A systematic literature review', Hereditary Cancer in Clinical Practice, vol. 15, http://dx.doi.org/10.1186/s13053-017-0075-8

Watts KJ; Meiser B; Zilliacus E; Kaur R; Taouk M; Girgis A; Butow P; Kissane D; Hale S; Perry A; Aranda SK; Goldstein D, 2017, 'Perspectives of oncology nurses and oncologists regarding barriers to working with patients from a minority background: systemic issues and working with interpreters.', European Journal of Cancer Care, vol. 27, pp. e12758, http://dx.doi.org/10.1111/ecc.12758

Willis AM; Smith SK; Meiser B; Ballinger ML; Thomas DM; Young MA, 2017, 'Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review', Clinical Genetics, vol. 92, pp. 121 - 133, http://dx.doi.org/10.1111/cge.12868

Yanes T; meiser B; Young MA; Kaur R; Mitchell G; Barlow-Stewart K; Roscioli T; Halliday J; James P, 2017, 'Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study', BMC Cancer, vol. 17, http://dx.doi.org/10.1186/s12885-017-3485-0

Taouk M; Meiser B; Hadzi-Pavlovic D; Dudley M; Mitchell PB, 2017, 'Development of a potential screening measure for adolescent depression', Australian and New Zealand Journal of Psychiatry, vol. 51, pp. 624 - 633, http://dx.doi.org/10.1177/0004867416672726

Meiser B; Peate M; Levitan C; Mitchell PB; Trevena L; Barlow-Stewart K; Dobbins T; Christensen H; Sherman KA; Dunlop K; Schofield PR, 2017, 'A Psycho-Educational Intervention for People with a Family History of Depression: Pilot Results', Journal of Genetic Counseling, vol. 26, pp. 312 - 321, http://dx.doi.org/10.1007/s10897-016-0011-5

Quinn VF; Meiser B; Kirk J; Tucker KM; Watts KJ; Rahman B; Peate M; Saunders C; Geelhoed E; Gleeson M; Barlow-Stewart K; Field M; Harris M; Antill YC; Cicciarelli L; Crowe K; Bowen MT; Mitchell G; Gregory P; Lipton L; McKay L; Senior J; Lobb L; Crowe P; Matthews A; Neil G; Parasyn A; Thomson D; Duffy J; Andrews L; Gale J; Fox J; Hart S; Smythe C; White M; Creighton L; D'arcy J; Grieve S; Secomb E; Henderson M; O'Brien J; Poliness C; Hattam A; Susman R; Ung O; DIckson R; Moore K; Bastick P; Inder S; Lynch J; Schwartz P; Zia R; Mak C; Snook K; Spillane A; Hopper J; Bowman M; Cheung D; Edirimanne S; Edwards E; Elder E; French J; Moon D, 2017, 'Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: A randomized controlled noninferiority trial', Genetics in Medicine, vol. 19, pp. 448 - 456, http://dx.doi.org/10.1038/gim.2016.130

Quinn VF; Meiser B; Kirk J; Tucker KM; Watts KJ; Rahman B; Peate M; Saunders C; Geelhoed E; Gleeson M; Barlow-Stewart K; Field M; Harris M; Antill YC; Cicciarelli L; Crowe K; Bowen MT; Mitchell G, 2017, 'Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial', GENETICS IN MEDICINE, vol. 19, pp. 448 - 456, http://dx.doi.org/10.1038/gim.2016.130


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