Objects
Thompson, Ella R., Gorringe, Kylie L., Lupat, Richard, Delatycki, Martin B., LifePool Investigators,, Mitchell , Gillian, James , Paul A., Scott, Rodney J., Campbell, Ian G., Rowley, Simone M., Wong-Brown, Michelle W., McInerny, Simone, Li, Na, Trainer, Alison H., Devereux, Lisa, Doyle, Maria A., Li, Jason. BioMed Central; 2015. Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.
Lim, Belle W. X., Li, Na, Devereux, Lisa, Scott, Rodney J., Sloan, Erica K., James, Paul A., Campbell, Ian G., Mahale, Sakshi, McInerny, Simone, Zethoven, Magnus, Rowley, Simone M., Huynh, Joanne, Wang, Theresa, Lee, Jue Er Amanda, Friedman, Mia. Oxford University Press; 2023. Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants.
Thompson, Ella R., Rowley, Simone M., Campbell, Ian G., Li, Na, McInerny, Simone, Devereux, Lisa, Wong-Brown, Michelle W., Trainer, Alison H., Mitchell, Gillian, Scott, Rodeny J., James, Paul A.. American Society of Clinical Oncology; 2016. Panel testing for familial breast cancer: calibrating the tension between research and clinical care.
Lim, Belle W. X., Li, Na, Rowley, Simone M., Thompson, Ella R., McInerny, Simone, Zethoven, Magnus, Scott, Rodney J., Devereux, Lisa, Sloan, Erica K., James, Paul A., Campbell, Ian G.. Nature Publishing Group; 2022. Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer.
Li, Na, Thompson, Ella R., Gorringe, Kylie L., James, Paul A., Campbell, Ian G., Rowley, Simone M., McInerny, Simone, Devereux, Lisa, Goode, David, LifePool Investigators,, Wong-Brown, Michelle W., Scott, Rodney J., Trainer, Alison H.. Springer; 2016. Reevaluation of RINT1 as a breast cancer predisposition gene.
Li, Na, Zethoven, Magnus, Nguyen-Dumont, Tu, Southey, Melissa C., Hopper, John L., Simard, Jacques, Dumont, Martine, Soucy, Penny, Meindl, Alfons, Schmutzler, Rita, Schmidt, Marjanka K., Adank, Muriel A., McInerny, Simone, Andrulis, Irene L., Hahnen, E, Engel, C, Lesueur, F, Girard, E, Neuhausen, SL, Ziv, E, Allen, J, Easton, DF, Scott, Rodney J., Devereux, Lisa, Gorringe, KL, James, PA, Campbell, IG, Huang, Yu-Kuan, Thio, Niko, Cheasley, Dane, Gutiérrez-Enríquez, Sara, Moles-Fernández, Alejandro, Diez, Orland. Nature Publishing Group; 2021. Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.
Li, Na, Lim, Belle W. X., Thompson, Ella R., McInerny, Simone, Zethoven, Magnus, Cheasley, Dane, Rowley, Simone M., Wong-Brown, Michelle W., Devereux, Lisa, Gorringe, Kylie L., Sloan, Erica K., Trainer, Alison, Scott, Rodney J., James, Paul A., Campbell, Ian G.. Nature Publishing Group; 2021. Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study.
Wang, Yanliang, Feng, Yu Chen, Zhang, Lina, Wang, Limeng, Thorne, Rick F., Zhang, Xu Dong, Cao, Huixia, Shao, Feng-Min, Gan, Yujin, Teng, Liu, Wang, Li, La, Ting, Wang, Peilin, Gu, Yue, Yan, Lei, Li, Na. BioMed Central (BMC); 2022. LncRNA MILIP links YBX1 to translational activation of Snai1 and promotes metastasis in clear cell renal cell carcinoma.
Thompson, Ella R., Gorringe, Kylie L., Mitchell, Gillian, Scott, Rodney J., James, Paul A., Campbell, Ian G., Rowley, Simone M., Li, Na, McInerny, Simone, Wong-Brown, Michelle W., Devereux, Lisa, Li, Jason, Lifepool Investigators,, Trainer, Alison H.. Nature Publishing Group; 2015. Reevaluation of the BRCA₂ truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context.