Long Range Regulation of Human FXN Gene Expression

por Puspasari, Novita, Rowley, Simone M., Gordon, Lavinia, Lockhart, Paul J., Ioannou, Panos A., Delatycki, Martin B., Sarsero, Joseph P.
Publicado 2011

A simple consensus approach improves somatic mutation prediction accuracy

por Goode, David L, Hunter, Sally M, Doyle, Maria A, Ma, Tao, Rowley, Simone M, Choong, David, Ryland, Georgina L, Campbell, Ian G
Publicado 2013

Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer

por Thompson, Ella R., Rowley, Simone M., Sawyer, Sarah, kConFab, Eccles, Diana M., Trainer, Alison H., Mitchell, Gillian, James, Paul A., Campbell, Ian G.
Publicado 2013

Molecular comparison of pure ovarian fibroma with serous benign ovarian tumours

por Hunter, Sally M., Dall, Genevieve V., Doyle, Maria A., Lupat, Richard, Li, Jason, Allan, Prue, Rowley, Simone M., Bowtell, David, Campbell, Ian G., Gorringe, Kylie L.
Publicado 2020

MicroRNA Genes and Their Target 3′-Untranslated Regions Are Infrequently Somatically Mutated in Ovarian Cancers

por Ryland, Georgina L., Bearfoot, Jennifer L., Doyle, Maria A., Boyle, Samantha E., Choong, David Y. H., Rowley, Simone M., Tothill, Richard W., Gorringe, Kylie L., Campbell, Ian G.
Publicado 2012

Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes

por Subramanian, Deepak N., Zethoven, Magnus, McInerny, Simone, Morgan, James A., Rowley, Simone M., Lee, Jue Er Amanda, Li, Na, Gorringe, Kylie L., James, Paul A., Campbell, Ian G.
Publicado 2020

Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer

por 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.
Publicado 2022

Loss of heterozygosity: what is it good for?

por Ryland, Georgina L., Doyle, Maria A., Goode, David, Boyle, Samantha E., Choong, David Y.H., Rowley, Simone M., Li, Jason, Bowtell, David DL, Tothill, Richard W., Campbell, Ian G., Gorringe, Kylie L.
Publicado 2015

Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue

por Kader, Tanjina, Goode, David L., Wong, Stephen Q., Connaughton, Jacquie, Rowley, Simone M., Devereux, Lisa, Byrne, David, Fox, Stephen B., Mir Arnau, Gisela, Tothill, Richard W., Campbell, Ian G., Gorringe, Kylie L.
Publicado 2016

Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors

por Ryland, Georgina L., Hunter, Sally M., Doyle, Maria A., Caramia, Franco, Li, Jason, Rowley, Simone M., Christie, Michael, Allan, Prue E., Stephens, Andrew N., Bowtell, David D L, Campbell, Ian G., Gorringe, Kylie L.
Publicado 2015

Erratum to: Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors

por Ryland, Georgina L., Hunter, Sally M., Doyle, Maria A., Caramia, Franco, Li, Jason, Rowley, Simone M., Christie, Michael, Allan, Prue E., Stephens, Andrew N., Bowtell, David D. L., Campbell, Ian G., Gorringe, Kylie L.
Publicado 2017

Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context

por Thompson, Ella R., Gorringe, Kylie L., Rowley, Simone M., Li, Na, McInerny, Simone, Wong-Brown, Michelle W., Devereux, Lisa, Li, Jason, Trainer, Alison H., Mitchell, Gillian, Scott, Rodney J., James, Paul A., Campbell, Ian G.
Publicado 2015

Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs

por Li, Na, Rowley, Simone M., Thompson, Ella R., McInerny, Simone, Devereux, Lisa, Amarasinghe, Kaushalya C., Zethoven, Magnus, Lupat, Richard, Goode, David, Li, Jason, Trainer, Alison H., Gorringe, Kylie L., James, Paul A., Campbell, Ian G.
Publicado 2018

Evaluation of two population screening programmes for BRCA1/2 founder mutations in the Australian Jewish community: a protocol paper

por Cousens, Nicole E, Tiller, Jane, Meiser, Bettina, Barlow-Stewart, Kristine, Rowley, Simone, Ko, Yi-An, Mahale, Sakshi, Campbell, Ian G, Kaur, Rajneesh, Bankier, Agnes, Burnett, Leslie, Jacobs, Chris, James, Paul A, Trainer, Alison, Neil, Suzanne, Delatycki, Martin B, Andrews, Lesley
Publicado 2021

Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants

por Lim, Belle W X, Li, Na, Mahale, Sakshi, McInerny, Simone, Zethoven, Magnus, Rowley, Simone M, Huynh, Joanne, Wang, Theresa, Lee, Jue Er Amanda, Friedman, Mia, Devereux, Lisa, Scott, Rodney J, Sloan, Erica K, James, Paul A, Campbell, Ian G
Publicado 2022

Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study

por 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.
Publicado 2021

Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles

por Thompson, Ella R., Doyle, Maria A., Ryland, Georgina L., Rowley, Simone M., Choong, David Y. H., Tothill, Richard W., Thorne, Heather, Barnes, Daniel R., Li, Jason, Ellul, Jason, Philip, Gayle K., Antill, Yoland C., James, Paul A., Trainer, Alison H., Mitchell, Gillian, Campbell, Ian G.
Publicado 2012

Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls

por Thompson, Ella R., Gorringe, Kylie L., Rowley, Simone M., Wong-Brown, Michelle W., McInerny, Simone, Li, Na, Trainer, Alison H., Devereux, Lisa, Doyle, Maria A., Li, Jason, Lupat, Richard, Delatycki, Martin B., Mitchell, Gillian, James, Paul A., Scott, Rodney J., Campbell, Ian G.
Publicado 2015

The TP53 mutation rate differs in breast cancers that arise in women with high or low mammographic density

por Cheasley, Dane, Devereux, Lisa, Hughes, Siobhan, Nickson, Carolyn, Procopio, Pietro, Lee, Grant, Li, Na, Pridmore, Vicki, Elder, Kenneth, Bruce Mann, G., Kader, Tanjina, Rowley, Simone M., Fox, Stephen B., Byrne, David, Saunders, Hugo, Fujihara, Kenji M., Lim, Belle, Gorringe, Kylie L., Campbell, Ian G.
Publicado 2020

Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes

por Hunter, Sally M., Anglesio, Michael S., Ryland, Georgina L., Sharma, Raghwa, Chiew, Yoke-Eng, Rowley, Simone M., Doyle, Maria A., Li, Jason, Gilks, C. Blake, Moss, Phillip, Allan, Prue E., Stephens, Andrew N., Huntsman, David G., deFazio, Anna, Bowtell, David D., Gorringe, Kylie L., Campbell, Ian G.
Publicado 2015