By Dr Amanda Willis

Journal articles

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

Morrow A; Speechly C; Young AL; Tucker K; Harris R; Poplawski N; Andrews L; Nguyen Dumont T; Kirk J; Southey MC; Willis A, 2024, '“Out of the blue”: A qualitative study exploring the experiences of women and next of kin receiving unexpected results from BRA-STRAP research gene panel testing', Journal of Genetic Counseling, 33, pp. 973 - 984, http://dx.doi.org/10.1002/jgc4.1803

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

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

Southey MC; Dowty JG; Riaz M; Steen JA; Renault AL; Tucker K; Kirk J; James P; Winship I; Pachter N; Poplawski N; Grist S; Park DJ; Pope BJ; Mahmood K; Hammet F; Mahmoodi M; Tsimiklis H; Theys D; Rewse A; Willis A; Morrow A; Speechly C; Harris R; Sebra R; Schadt E; Lacaze P; McNeil JJ; Giles GG; Milne RL; Hopper JL; Nguyen-Dumont T, 2021, 'Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing', npj Breast Cancer, 7, http://dx.doi.org/10.1038/s41523-021-00360-3

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

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

Savage SA; Viard M; O'hUigin C; Zhou W; Yeager M; Li SA; Wang T; Ramsuran V; Vince N; Vogt A; Hicks B; Burdett L; Chung C; Dean M; de Andrade KC; Freedman ND; Berndt SI; Rothman N; Lan Q; Cerhan JR; Slager SL; Zhang Y; Teras LR; Haagenson M; Chanock SJ; Spellman SR; Wang Y; Willis A; Askar M; Lee SJ; Carrington M; Gadalla SM, 2020, 'Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia', American Journal of Human Genetics, 106, pp. 264 - 271, http://dx.doi.org/10.1016/j.ajhg.2020.01.004

Creary LE; Guerra SG; Chong W; Brown CJ; Turner TR; Robinson J; Bultitude WP; Mayor NP; Marsh SGE; Saito K; Lam K; Duke JL; Mosbruger TL; Ferriola D; Monos D; Willis A; Askar M; Fischer G; Saw CL; Ragoussis J; Petrek M; Serra-Pagés C; Juan M; Stavropoulos-Giokas C; Dinou A; Ameen R; Al Shemmari S; Spierings E; Gendzekhadze K; Morris GP; Zhang Q; Kashi Z; Hsu S; Gangavarapu S; Mallempati KC; Yamamoto F; Osoegawa K; Vayntrub T; Chang CJ; Hansen JA; Fernández-Viňa MA, 2019, 'Next-generation HLA typing of 382 International Histocompatibility Working Group reference B-lymphoblastoid cell lines: Report from the 17th International HLA and Immunogenetics Workshop', Human Immunology, 80, pp. 449 - 460, http://dx.doi.org/10.1016/j.humimm.2019.03.001

Smith AG; Pereira S; Jaramillo A; Stoll ST; Khan FM; Berka N; Mostafa AA; Pando MJ; Usenko CY; Bettinotti MP; Pyo CW; Nelson WC; Willis A; Askar M; Geraghty DE, 2019, 'Comparison of sequence-specific oligonucleotide probe vs next generation sequencing for HLA-A, B, C, DRB1, DRB3/B4/B5, DQA1, DQB1, DPA1, and DPB1 typing: Toward single-pass high-resolution HLA typing in support of solid organ and hematopoietic cell transplant programs', HLA, 94, pp. 296 - 306, http://dx.doi.org/10.1111/tan.13619

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, 27, pp. 28 - 35, http://dx.doi.org/10.1038/s41431-018-0257-5

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, 27, pp. 1055 - 1066, http://dx.doi.org/10.1007/s10897-018-0223-y

Sousa M; Peate M; Lewis C; Jarvis S; Willis A; Hickey M; Friedlander M, 2018, 'Exploring knowledge, attitudes and experience of genitourinary symptoms in women with early breast cancer on adjuvant endocrine therapy', European Journal of Cancer Care, 27, http://dx.doi.org/10.1111/ecc.12820

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, 92, pp. 121 - 133, http://dx.doi.org/10.1111/cge.12868

Willis AM; Smith SK; Meiser B; Muller C; Lewis S; Halliday J, 2015, 'How do prospective parents prefer to receive information about prenatal screening and diagnostic testing?', Prenatal Diagnosis, 35, pp. 100 - 102, http://dx.doi.org/10.1002/pd.4493

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