By Ms Mary-Anne Young

Journal articles

Purvis R; Forrest LE; Young MA; Limb S; James P; Taylor N, 2025, 'Defining next steps in the clinical implementation of polygenic scores: A landscape analysis of professional groups’ perspectives', Genetics in Medicine, 27, http://dx.doi.org/10.1016/j.gim.2025.101414

Yanes T; Courtney E; Young MA; Pearn A; McInerney-Leo A; Ingles J, 2025, 'Genetic counsellors: facilitating the integration of genomics into health care', Medical Journal of Australia, 222, pp. 114 - 117, http://dx.doi.org/10.5694/mja2.52568

Phillips KA; Kotsopoulos J; Domchek SM; Terry MB; Chamberlain JA; Bassett JK; Aeilts AM; Andrulis IL; Buys SS; Cui W; Daly MB; Eisen AF; Foulkes WD; Friedlander ML; Gronwald J; Hopper JL; John EM; Karlan BY; Kim RH; Kurian AW; Lubinski J; Metcalfe K; Nathanson KL; Singer CF; Southey MC; Symecko H; Tung N; Narod SA; Milne RL; Amor D; Andrews L; Antill Y; Balleine R; Beesley J; Bennett I; Bogwitz M; Bodek S; Botes L; Brennan M; Brown M; Buckley M; Burke J; Butow P; Caldon L; Campbell I; Cao M; Chakrabarti A; Chauhan D; Chauhan M; Chenevix-Trench G; Christian A; Cohen P; Colley A; Crook A; Cui J; Courtney E; Cummings M; Dawson SJ; Defazio A; Delatycki M; Dickson R; Dixon J; Edwards S; Farshid G; Fellows A; Fenton G; Field M; Flanagan J; Fong P; Forrest L; Fox S; French J; Gaff C; Gattas M; George P; Greening S; Harris M; Hart S; Harraka P; Hayward N; Hopper J; Hoskins C; Hunt C; James P; Jenkins M; Kidd A; Kirk J; Koehler J; Kollias J; Lakhani S; Lawrence M; Lee J; Li S; Lindeman G; Lippey J; Lipton L; Lobb L; Loi S; Mann G, 2025, 'Hormonal Contraception and Breast Cancer Risk for Carriers of Germline Mutations in BRCA1 and BRCA2', Journal of Clinical Oncology, 43, pp. 422 - 431, http://dx.doi.org/10.1200/JCO.24.00176

Fehlberg Z; Fisher L; Liu C; Kugenthiran N; Milne RL; Young MA; Willis A; Southey MC; Goranitis I; Best S, 2025, 'Using a behaviour-change approach to support uptake of population genomic screening and management options for breast or prostate cancer', European Journal of Human Genetics, 33, pp. 108 - 120, http://dx.doi.org/10.1038/s41431-024-01729-1

Mitchell LA; Jivani K; Young MA; Jacobs C; Willis AM, 2024, 'Systematic review of the uptake and outcomes from returning secondary findings to adult participants in research genomic testing', Journal of Genetic Counseling, 33, pp. 1145 - 1158, http://dx.doi.org/10.1002/jgc4.1865

McInerny S; Mascarenhas L; Yanes T; Petelin L; Chenevix-Trench G; Southey MC; Young MA; James PA, 2024, 'Using polygenic risk modification to improve breast cancer prevention: Study protocol for the PRiMo multicentre randomised controlled trial', BMJ Open, 14, http://dx.doi.org/10.1136/bmjopen-2024-087874

Pearce A; Mitchell LA; Best S; Young MA; Terrill B, 2024, 'Publics’ knowledge of, attitude to and motivation towards health-related genomics: a scoping review', European Journal of Human Genetics, 32, pp. 747 - 758, http://dx.doi.org/10.1038/s41431-024-01547-5

Terrill B; Pearce A; Chau A; Young M-A, 2024, 'Navigating genomic testing: Evaluation of an e-learning module with general practitioners', FOCUS ON HEALTH PROFESSIONAL EDUCATION-A MULTIDISCIPLINARY JOURNAL, 25, pp. 37 - 50

Yanes T; Wallingford CK; Young MA; McInerney-Leo AM; Willis AM; McKnight L; Terrill B; McInerny S; Forrest LE; Cicciarelli L; Williams R; Keane H; James PA, 2023, 'Development and evaluation of a novel educational program for providers on the use of polygenic risk scores', Genetics in Medicine, 25, http://dx.doi.org/10.1016/j.gim.2023.100876

Young MA; Yanes T; Cust AE; Dunlop K; Limb S; Newson AJ; Purvis R; Thiyagarajan L; Scott RJ; Verma K; James PA; Steinberg J, 2023, 'Human Genetics Society of Australasia Position Statement: Use of Polygenic Scores in Clinical Practice and Population Health', Twin Research and Human Genetics, 26, pp. 40 - 48, http://dx.doi.org/10.1017/thg.2023.10

Wallingford CK; Kovilpillai H; Jacobs C; Turbitt E; Primiero CA; Young MA; Brockman DG; Soyer HP; McInerney-Leo AM; Yanes T, 2023, 'Models of communication for polygenic scores and associated psychosocial and behavioral effects on recipients: A systematic review', Genetics in Medicine, 25, pp. 1 - 11, http://dx.doi.org/10.1016/j.gim.2022.09.008

Primiero CA; Baker AM; Wallingford CK; Maas EJ; Yanes T; Fowles L; Janda M; Young MA; Nisselle A; Terrill B; Lodge JM; Tiller JM; Lacaze P; Andersen H; McErlean G; Turbitt E; Soyer HP; McInerney-Leo AM, 2022, 'Attitudes of Australian dermatologists on the use of genetic testing: A cross-sectional survey with a focus on melanoma', Frontiers in Genetics, 13, http://dx.doi.org/10.3389/fgene.2022.919134

Pearce A; Terrill B; Alffenaar JW; Patanwala AE; Kummerfeld S; Day R; Young MA; Stocker SL, 2022, 'Pharmacogenomic testing: perception of clinical utility, enablers and barriers to adoption in Australian hospitals', Internal Medicine Journal, 52, pp. 1135 - 1143, http://dx.doi.org/10.1111/imj.15719

Forrest LE; Shepherd RF; Tutty E; Pearce A; Campbell I; Devereux L; Trainer AH; James PA; Young MA, 2022, 'The Clinical and Psychosocial Outcomes for Women Who Received Unexpected Clinically Actionable Germline Information Identified through Research: An Exploratory Sequential Mixed-Methods Comparative Study', Journal of Personalized Medicine, 12, http://dx.doi.org/10.3390/jpm12071112

Delahunty R; Nguyen L; Craig S; Creighton B; Ariyaratne D; Garsed DW; Christie E; Fereday S; Andrews L; Lewis A; Limb S; Pandey A; Hendley J; Traficante N; Carvajal N; Spurdle AB; Thompson B; Parsons MT; Beshay V; Volcheck M; Semple T; Lupat R; Doig K; Yu J; Chen XQ; Marsh A; Love C; Bilic S; Beilin M; Nichols CB; Greer C; Lee YC; Gerty S; Gill L; Newton E; Howard J; Williams R; Norris C; Stephens AN; Tutty E; Smyth C; O'connell S; Jobling T; Stewart CJR; Tan A; Fox SB; Pachter N; Li J; Ellul J; Mir Arnau G; Young MA; Gordon L; Forrest L; Harris M; Livingstone K; Hill J; Chenevix-Trench G; Cohen PA; Webb PM; Friedlander M; James P; Bowtell D; Alsop K, 2022, 'TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members', Journal of Clinical Oncology, 40, pp. 2036 - 2047, http://dx.doi.org/10.1200/JCO.21.02108

Lacaze PA; Tiller J; Winship I; Brotchie A; McNeil J; Zalcberg J; Thomas D; Milne R; James P; Delatycki M; Young MA; Nowak K; Nguyen-Dumont T; Southey M; Ademi Z; Bruinsma F; Riaz M; Terrill B; Kirk J; Tucker K; Andrews L; Pachter N; Susman R; Poplawski N; Wallis M; Watts G; Nicholls S; Macrae F; Sturm A; Green R; Ahern S; Revote J; Von Saldern S; Powell S; Rice T, 2022, 'Population DNA screening for medically actionable disease risk in adults', Medical Journal of Australia, 216, pp. 278 - 280, http://dx.doi.org/10.5694/mja2.51454

Willis AM; Terrill B; Pearce A; McEwen A; Ballinger ML; Young MA, 2022, 'My Research Results: a program to facilitate return of clinically actionable genomic research findings', European Journal of Human Genetics, 30, pp. 363 - 366, http://dx.doi.org/10.1038/s41431-021-00973-z

Meiser B; Butow P; Davies G; Napier CE; Schlub TE; Bartley N; Juraskova I; Ballinger ML; Thomas DM; Tucker K; Goldstein D; Biesecker BB; Best MC; Young M-A, 2022, 'Psychological predictors of advanced cancer patients’ preferences for return of results from comprehensive tumor genomic profiling', American Journal of Medical Genetics Part A, 188, pp. 725 - 734, http://dx.doi.org/10.1002/ajmg.a.62563

Gregory G; Das Gupta K; Meiser B; Barlow-Stewart K; Geelan-Small P; Kaur R; Scheepers-Joynt M; McInerny S; Taylor S; Antill Y; Salmon L; Smyth C; Young MA; James PA; Yanes T, 2022, 'Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk', Journal of Genetic Counseling, 31, pp. 120 - 129, http://dx.doi.org/10.1002/jgc4.1458

Yanes T; Meiser B; Kaur R; Young MA; Mitchell PB; Scheepers-Joynt M; McInerny S; Taylor S; Barlow-Stewart K; Antill Y; Salmon L; Smyth C; Betz-Stablein B; James PA, 2021, 'Breast cancer polygenic risk scores: a 12-month prospective study of patient reported outcomes and risk management behavior', Genetics in Medicine, 23, pp. 2316 - 2323, http://dx.doi.org/10.1038/s41436-021-01288-6

Meiser B; Kaur R; Morrow A; Peate M; Wong WKT; McPike E; Cops E; Nichols C; Austin R; Fine M; Thrupp L; Ward R; Macrae F; Hiller JE; Trainer AH; Mitchell G; Susman R; Pachter N; Goodwin A; James PA; Mascarenhas L; Morton C; Shanley S; Young MA; Andrews L; Morrow EA; Tucker K; Lindeman G; Mascarenhas L; Morton C; Field M; Goodwin A; Monnik M; Poplawski N; Delatycki M; John T; Harris M; Kerr R; Vora B, 2021, 'Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice', Hereditary Cancer in Clinical Practice, 19, http://dx.doi.org/10.1186/s13053-021-00180-3

Forbes Shepherd R; Forrest LE; Tutty E; Pearce A; Devereux L; James PA; Campbell IG; Trainer A; Young MA, 2021, 'Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study', Genetic Testing and Molecular Biomarkers, 25, pp. 741 - 748, http://dx.doi.org/10.1089/gtmb.2021.0115

Butow P; Müller F; Napier CE; Bartley N; Ballinger ML; Biesecker B; Juraskova I; Meiser B; Schlub TE; Thomas DM; Goldstein D; Best MC; Newson A; Tucker K; Vines R; Vines K; Kirk J; Young MA; Savard J; Jacobs C, 2021, 'Longitudinal patterns in fear of cancer progression in patients with rare, advanced cancers undergoing comprehensive tumour genomic profiling', Psycho Oncology, 30, pp. 1920 - 1929, http://dx.doi.org/10.1002/pon.5764

Das Gupta K; Gregory G; Meiser B; Kaur R; Scheepers-Joynt M; McInerny S; Taylor S; Barlow-Stewart K; Antill Y; Salmon L; Smyth C; McInerney-Leo A; Young MA; James PA; Yanes T, 2021, 'Communicating polygenic risk scores in the familial breast cancer clinic', Patient Education and Counseling, 104, pp. 2512 - 2521, http://dx.doi.org/10.1016/j.pec.2021.02.046

Smit AK; Sharman AR; Espinoza D; Wallingford C; Young MA; Dunlop K; Tiller J; Newson AJ; Meiser B; Cust AE; Yanes T, 2021, 'Knowledge, views and expectations for cancer polygenic risk testing in clinical practice: A cross-sectional survey of health professionals', Clinical Genetics, 100, pp. 430 - 439, http://dx.doi.org/10.1111/cge.14025

McKnight L; Pearce A; Willis A; Young MA; Terrill B, 2021, 'Supporting teachers to use genomics as a context in the classroom: an evaluation of learning resources for high school biology', Journal of Community Genetics, 12, pp. 653 - 662, http://dx.doi.org/10.1007/s12687-021-00550-3

Holland L; Young MA; Lewin J; Pearce A; Thompson K, 2021, 'Education in youth-friendly genetic counseling', Journal of Genetic Counseling, 30, pp. 1133 - 1142, http://dx.doi.org/10.1002/jgc4.1397

Hemming P; Kaur R; Meiser B; McKinley J; Young MA; James PA; Forrest LE, 2021, 'Oncologists’ perspectives of telephone genetic counseling to facilitate germline BRCA1/2 testing for their patients with high-grade serous ovarian cancer', Journal of Community Genetics, 12, pp. 449 - 457, http://dx.doi.org/10.1007/s12687-021-00530-7

Willis AM; Smith SK; Meiser B; James PA; Ballinger ML; Thomas DM; Yanes T; Young MA, 2021, 'Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’', Journal of Genetic Counseling, 30, pp. 849 - 860, http://dx.doi.org/10.1002/jgc4.1384

Hoskins C; Gaff C; McEwen A; Macciocca I; Pearn A; Shalhoub C; Salvemini H; Berkman J; Riley KE; Williams R; Milward M; Young MA, 2021, 'Professional regulation for Australasian genetic counselors', Journal of Genetic Counseling, 30, pp. 361 - 369, http://dx.doi.org/10.1002/jgc4.1344

Forrest LE; Forbes Shepherd R; Young MA; Keogh LA; James PA, 2021, 'Finding the five-year window: A qualitative study examining young women's decision-making and experience of using tamoxifen to reduce BRCA1/2 breast cancer risk', Psycho-Oncology, 30, pp. 159 - 166, http://dx.doi.org/10.1002/pon.5556

Leighton S; Forrest LE; Young MA; Delatycki MB; Lynch E, 2021, 'Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’', Journal of Genetic Counseling, 30, pp. 180 - 190, http://dx.doi.org/10.1002/jgc4.1307

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, 19, pp. 337 - 346, http://dx.doi.org/10.1007/s10689-020-00183-4

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, 19, pp. 297 - 306, http://dx.doi.org/10.1007/s10689-020-00185-2

Butow P; Davies G; Napier C; Thomas DM; Bartley N; Goldstein D; Ballinger ML; Juraskova I; Schlub TE; Tucker K; Meiser B; Young M-A, 2020, 'Return of results after somatic tumor mutation profiling in advanced cancer: Psychological impacts.', Journal of Clinical Oncology, 38, pp. 1541 - 1541, http://dx.doi.org/10.1200/jco.2020.38.15_suppl.1541

Young MA; Thompson K; Lewin J; Holland L, 2020, 'A framework for youth-friendly genetic counseling', Journal of Community Genetics, 11, pp. 161 - 170, http://dx.doi.org/10.1007/s12687-019-00439-2

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, 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, 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, 97, pp. 329 - 337, http://dx.doi.org/10.1111/cge.13664

Fachal L; Aschard H; Beesley J; Barnes DR; Allen J; Kar S; Pooley KA; Dennis J; Michailidou K; Turman C; Soucy P; Lemaçon A; Lush M; Tyrer JP; Ghoussaini M; Marjaneh MM; Jiang X; Agata S; Aittomäki K; Alonso MR; Andrulis IL; Anton-Culver H; Antonenkova NN; Arason A; Arndt V; Aronson KJ; Arun BK; Auber B; Auer PL; Azzollini J; Balmaña J; Barkardottir RB; Barrowdale D; Beeghly-Fadiel A; Benitez J; Bermisheva M; Bialkowska K; Blanco AM; Blomqvist C; Blot W; Bogdanova NV; Bojesen SE; Bolla MK; Bonanni B; Borg A; Bosse K; Brauch H; Brenner H; Briceno I; Brock IW; Brooks-Wilson A; Brüning T; Burwinkel B; Buys SS; Cai Q; Caldés T; Caligo MA; Camp NJ; Campbell I; Canzian F; Carroll JS; Carter BD; Castelao JE; Chiquette J; Christiansen H; Chung WK; Claes KBM; Clarke CL; Mari V; Berthet P; Castera L; Vaur D; Lallaoui H; Bignon YJ; Uhrhammer N; Bonadona V; Lasset C; Révillion F; Vennin P; Muller D; Gomes DM; Ingster O; Coupier I; Pujol P; Collonge-Rame MA; Mortemousque I; Bera O; Rose M; Baurand A; Bertolone G; Faivre L; Dreyfus H; Leroux D; Venat-Bouvet L; Bézieau S; Delnatte C; Chiesa J; Gilbert-Dussardier B; Gesta P; Prieur FP, 2020, 'Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes', Nature Genetics, 52, pp. 56 - 73, http://dx.doi.org/10.1038/s41588-019-0537-1

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, 5, http://dx.doi.org/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, 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, 5, http://dx.doi.org/10.1038/s41523-019-0140-8

McCabe M; Gauthier M-E; Chan C-L; Thompson T; De Sousa S; Puttick C; Grady J; Gayevskiy V; Tao J; Ying K; Cipponi A; Deng N; Swarbrick A; Thomas M; kConFab ; Lord R; Johns A; Kohonen-Corish M; O'Toole S; Clark J; Mueller S; Gupta R; McCormack A; Dinger M; Cowley M; Bastick P; Friedlander M; Colley A; Andrews L; Young M-A; Tucker K; Williams R, 2019, 'Development and validation of a targeted gene sequencing panel for application to disparate cancers', Scientific Reports, 9, pp. 17052, http://dx.doi.org/10.1038/s41598-019-52000-3

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, 27, pp. 1186 - 1196, http://dx.doi.org/10.1038/s41431-019-0390-9

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, 19, pp. 753, http://dx.doi.org/10.1186/s12885-019-5920-x

Forrest LE; Sawyer SD; Hallowell N; James PA; Young MA, 2019, 'High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information', Journal of Community Genetics, 10, pp. 197 - 206, http://dx.doi.org/10.1007/s12687-018-0378-0

Rowley SM; Mascarenhas L; Devereux L; Li N; Amarasinghe KC; Zethoven M; Lee JEA; Lewis A; Morgan JA; Limb S; Young MA; James PA; Trainer AH; Campbell IG, 2019, 'Population-based genetic testing of asymptomatic women for breast and ovarian cancer susceptibility', Genetics in Medicine, 21, pp. 913 - 922, http://dx.doi.org/10.1038/s41436-018-0277-0

Mavaddat N; Michailidou K; Dennis J; Lush M; Fachal L; Lee A; Tyrer JP; Chen TH; Wang Q; Bolla MK; Yang X; Adank MA; Ahearn T; Aittomäki K; Allen J; Andrulis IL; Anton-Culver H; Antonenkova NN; Arndt V; Aronson KJ; Auer PL; Auvinen P; Barrdahl M; Beane Freeman LE; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Bernstein L; Blomqvist C; Bogdanova NV; Bojesen SE; Bonanni B; Børresen-Dale AL; Brauch H; Bremer M; Brenner H; Brentnall A; Brock IW; Brooks-Wilson A; Brucker SY; Brüning T; Burwinkel B; Campa D; Carter BD; Castelao JE; Chanock SJ; Chlebowski R; Christiansen H; Clarke CL; Collée JM; Cordina-Duverger E; Cornelissen S; Couch FJ; Cox A; Cross SS; Czene K; Daly MB; Devilee P; Dörk T; dos-Santos-Silva I; Dumont M; Durcan L; Dwek M; Eccles DM; Ekici AB; Eliassen AH; Ellberg C; Engel C; Eriksson M; Evans DG; Fasching PA; Figueroa J; Fletcher O; Flyger H; Försti A; Fritschi L; Gabrielson M; Gago-Dominguez M; Gapstur SM; García-Sáenz JA; Gaudet MM; Georgoulias V; Giles GG; Gilyazova IR; Glendon G; Goldberg MS; Goldgar DE; González-Neira A; Grenaker Alnæs GI; Grip M; Gronwald J; Grundy A; Guénel P; Haeberle L; Hahnen E; Haiman CA; Håkansson N; Hamann U; Hankinson SE, 2019, 'Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes', American Journal of Human Genetics, 104, pp. 21 - 34, http://dx.doi.org/10.1016/j.ajhg.2018.11.002

McGill BC; Wakefield CE; Vetsch J; Barlow-Stewart K; Kasparian NA; Patenaude AF; Young MA; Cohn RJ; Tucker KM, 2019, 'Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review', Clinical Genetics, 95, pp. 10 - 22, http://dx.doi.org/10.1111/cge.13253

Rasmussen V; Forbes Shepherd R; Forrest LE; James PA; Young MA, 2019, 'Men's experiences of recontact about a potential increased risk of prostate cancer due to Lynch Syndrome: “Just another straw on the stack”', Journal of Genetic Counseling, 28, pp. 750 - 759, http://dx.doi.org/10.1002/jgc4.1110

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