1. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores. (28th July 2021) Authors: Barnes, Daniel R; Silvestri, Valentina; Leslie, Goska; McGuffog, Lesley; Dennis, Joe; Yang, Xin; Adlard, Julian; Agnarsson, Bjarni A; Ahmed, Munaza; Aittomäki, Kristiina; Andrulis, Irene L; Arason, Adalgeir; Arnold, Norbert; Auber, Bernd; Azzollini, Jacopo; Balmaña, Judith; Barkardottir, Rosa B; ... Journal: Journal of the National Cancer Institute Issue: Volume 114:Number 1(2022) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Ethical and practical implications of returning genetic research results: two Australian case studies. Issue 6 (8th November 2020) Authors: Tiller, Jane; Trainer, Alison H; Campbell, Ian; Lacaze, Paul A Journal: Medical journal of Australia Issue: Volume 214:Issue 6(2021) Page Start: 259 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. Issue 12 (9th November 2020) Authors: Tudini, Emma; Davidson, Aimee L; Dressel, Uwe; Andrews, Lesley; Antill, Yoland; Crook, Ashley; Field, Michael; Gattas, Michael; Harris, Rebecca; Kirk, Judy; Pachter, Nicholas; Salmon, Lucinda; Susman, Rachel; Townshend, Sharron; Trainer, Alison H; Tucker, Katherine M; Mitchell, Gillian; James, Pa... Journal: Journal of medical genetics Issue: Volume 58:Issue 12(2021) Page Start: 853 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mutational spectrum in a worldwide study of 29, 700 families with BRCA1 or BRCA2 mutations. Issue 5 (12th March 2018) Authors: Rebbeck, Timothy R.; Friebel, Tara M.; Friedman, Eitan; Hamann, Ute; Huo, Dezheng; Kwong, Ava; Olah, Edith; Olopade, Olufunmilayo I.; Solano, Angela R.; Teo, Soo‐Hwang; Thomassen, Mads; Weitzel, Jeffrey N.; Chan, TL; Couch, Fergus J.; Goldgar, David E.; Kruse, Torben A.; Palmero, Edenir Inêz; Par... Journal: Human mutation Issue: Volume 39:Issue 5(2018) Page Start: 593 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Rare variants in XRCC2 as breast cancer susceptibility alleles. Issue 10 (10th October 2012) Authors: Hilbers, Florentine S; Wijnen, Juul T; Hoogerbrugge, Nicoline; Oosterwijk, Jan C; Collee, Margriet J; Peterlongo, Paolo; Radice, Paolo; Manoukian, Siranoush; Feroce, Irene; Capra, Fabio; Couch, Fergus J; Wang, Xianshu; Guidugli, Lucia; Offit, Kenneth; Shah, Sohela; Campbell, Ian G; Thompson, Ella... Journal: Journal of medical genetics Issue: Volume 49:Issue 10(2012) Page Start: 618 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The genomic landscape of phaeochromocytoma. Issue 1 (2nd February 2015) Authors: Flynn, Aidan; Benn, Diana; Clifton‐Bligh, Roderick; Robinson, Bruce; Trainer, Alison H; James, Paul; Hogg, Annette; Waldeck, Kelly; George, Joshy; Li, Jason; Fox, Stephen B; Gill, Anthony J; McArthur, Grant; Hicks, Rodney J; Tothill, Richard W Journal: Journal of pathology Issue: Volume 236:Issue 1(2015) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The predicted impact and cost‐effectiveness of systematic testing of people with incident colorectal cancer for Lynch syndrome. Issue 2 (8th October 2019) Authors: Kang, Yoon‐Jung; Killen, James; Caruana, Michael; Simms, Kate; Taylor, Natalie; Frayling, Ian M; Snowsill, Tristan; Huxley, Nicola; Coupe, Veerle MH; Hughes, Suzanne; Freeman, Victoria; Boussioutas, Alex; Trainer, Alison H; Ward, Robyn L; Mitchell, Gillian; Macrae, Finlay A; Canfell, Karen Journal: Medical journal of Australia Issue: Volume 212:Issue 2(2020) Page Start: 72 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗