Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes

Por Lindor, Noralane M., Hopper, John, Dowty, James
Publicado no Fam Cancer (2016)

The CRISP colorectal cancer risk prediction tool: an exploratory study using simulated consultations in Australian primary care

Por Walker, Jennifer G, Bickerstaffe, Adrian, Hewabandu, Nadira, Maddumarachchi, Sanjay, Dowty, James G, Jenkins, Mark, Pirotta, Marie, Walter, Fiona M, Emery, Jon D
Publicado no BMC Med Inform Decis Mak (2017)

Population-Based Estimate of Prostate Cancer Risk for Carriers of the HOXB13 Missense Mutation G84E

Por MacInnis, Robert J., Severi, Gianluca, Baglietto, Laura, Dowty, James G., Jenkins, Mark A., Southey, Melissa C., Hopper, John L., Giles, Graham G.
Publicado em 2013

Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of LAMBDA, BRCAPRO, Myriad II, and modified Couch models

Por Lindor, Noralane M., Lindor, Rachel A., Apicella, Carmel, Dowty, James G., Ashley, Amanda, Hunt, Katherine, Mincey, Betty A., Wilson, Marcia, Smith, M. Cathie, Hopper, John L.
Publicado em 2007

CONSTITUTIONAL METHYLATION OF THE BRCA1 PROMOTER IS SPECIFICALLY ASSOCIATED WITH BRCA1 MUTATION-ASSOCIATED PATHOLOGY IN EARLY-ONSET BREAST CANCER

Por Wong, Ee Ming, Southey, Melissa C, Fox, Stephen B, Brown, Melissa A, Dowty, James G, Jenkins, Mark A, Giles, Graham G, Hopper, John L, Dobrovic, Alexander
Publicado em 2010

Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model

Por Dite, Gillian S, Mahmoodi, Maryam, Bickerstaffe, Adrian, Hammet, Fleur, Macinnis, Robert J, Tsimiklis, Helen, Dowty, James G, Apicella, Carmel, Phillips, Kelly-Anne, Giles, Graham G, Southey, Melissa C, Hopper, John L
Publicado em 2013

Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

Por Teo, Zhi L, Park, Daniel J, Provenzano, Elena, Chatfield, Catherine A, Odefrey, Fabrice A, Nguyen-Dumont, Tu, Dowty, James G, Hopper, John L, Winship, Ingrid, Goldgar, David E, Southey, Melissa C
Publicado em 2013

Breast cancer risk prediction using clinical models and 77 independent risk-associated SNPs for women aged under 50 years: Australian Breast Cancer Family Registry

Por Dite, Gillian S., MacInnis, Robert J., Bickerstaffe, Adrian, Dowty, James G., Allman, Richard, Apicella, Carmel, Milne, Roger L., Tsimiklis, Helen, Phillips, Kelly-Anne, Giles, Graham G., Terry, Mary Beth, Southey, Melissa C., Hopper, John L.
Publicado no Cancer Epidemiol Biomarkers Prev (2015)

Risks of cancers for carriers of monoallelic MUTYH mutation with a family history of colorectal cancer

Por Win, Aung K, Cleary, Sean P, Dowty, James G, Lindor, Noralane M, Newcomb, Polly A, Haile, Robert W, Young, Joanne P, Buchanan, Daniel D, Le Marchand, Loïc, Green, Roger, Hopper, John L, Gallinger, Steven, Jenkins, Mark A
Publicado em 2011

Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screening

Por Jenkins, Mark A, Makalic, Enes, Dowty, James G, Schmidt, Daniel F, Dite, Gillian S, MacInnis, Robert J, Ait Ouakrim, Driss, Clendenning, Mark, Flander, Louisa B, Stanesby, Oliver K, Hopper, John L, Win, Aung K, Buchanan, Daniel D
Publicado no Future Oncol (2016)

Dependence of Colorectal Cancer Risk on the Parent-of-Origin of Mutations in DNA Mismatch Repair Genes

Por van Vliet, Christine M., Dowty, James G., van Vliet, Jane L., Smith, Letitia, Mead, Leeanne J., Macrae, Finlay A., St. John, D. James B., Giles, Graham G., Southey, Melissa C., Jenkins, Mark A., Velan, Gary M., Hopper, John L.
Publicado em 2011

A PALB2 mutation associated with high risk of breast cancer

Por Southey, Melissa C, Teo, Zhi L, Dowty, James G, Odefrey, Fabrice A, Park, Daniel J, Tischkowitz, Marc, Sabbaghian, Nelly, Apicella, Carmel, Byrnes, Graham B, Winship, Ingrid, Baglietto, Laura, Giles, Graham G, Goldgar, David E, Foulkes, William D, Hopper, John L
Publicado em 2010

The clinical phenotype of Lynch syndrome due to germline PMS2 mutations

Por Senter, Leigha, Clendenning, Mark, Sotamaa, Kaisa, Hampel, Heather, Green, Jane, Potter, John D., Lindblom, Annika, Lagerstedt, Kristina, Thibodeau, Stephen N., Lindor, Noralane M., Young, Joanne, Winship, Ingrid, Dowty, James G., White, Darren M., Hopper, John L., Baglietto, Laura, Jenkins, Mark A., de la Chapelle, Albert
Publicado em 2008

Cancer risk in 680 000 people exposed to computed tomography scans in childhood or adolescence: data linkage study of 11 million Australians

Por Mathews, John D, Forsythe, Anna V, Brady, Zoe, Butler, Martin W, Goergen, Stacy K, Byrnes, Graham B, Giles, Graham G, Wallace, Anthony B, Anderson, Philip R, Guiver, Tenniel A, McGale, Paul, Cain, Timothy M, Dowty, James G, Bickerstaffe, Adrian C, Darby, Sarah C
Publicado em 2013

Rare variants in the ATM gene and risk of breast cancer

Por Goldgar, David E, Healey, Sue, Dowty, James G, Da Silva, Leonard, Chen, Xiaoqing, Spurdle, Amanda B, Terry, Mary Beth, Daly, Mary J, Buys, Saundra M, Southey, Melissa C, Andrulis, Irene, John, Esther M, Khanna, Kum Kum, Hopper, John L, Oefner, Peter J, Lakhani, Sunil, Chenevix-Trench, Georgia
Publicado em 2011

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

Por Win, Aung Ko, Cleary, Sean P., Dowty, James G., Baron, John A., Young, Joanne P., Buchanan, Daniel D., Southey, Melissa C., Burnett, Terrilea, Parfrey, Patrick S., Green, Roger C., Le Marchand, Loïc, Newcomb, Polly A., Haile, Robert W., Lindor, Noralane M., Hopper, John L., Gallinger, Steven, Jenkins, Mark A.
Publicado em 2011

Lynch Syndrome and Cervical Cancer

Por Antill, Yoland C, Dowty, James G, Win, Aung Ko, Thompson, Tina, Walsh, Michael D, Cummings, Margaret C, Gallinger, Steven, Lindor, Noralane M, Le Marchand, Loïc, Hopper, John L, Newcomb, Polly A, Haile, Robert W, Church, James, Tucker, Katherine M, Buchanan, Daniel D, Young, Joanne P, Winship, Ingrid M, Jenkins, Mark A
Publicado no Int J Cancer (2015)

Body Mass Index in Early Adulthood and Endometrial Cancer Risk for Mismatch Repair Gene Mutation Carriers

Por Win, Aung Ko, Dowty, James G., Antill, Yoland C., English, Dallas R., Baron, John A., Young, Joanne P., Giles, Graham G., Southey, Melissa C., Winship, Ingrid, Lipton, Lara, Parry, Susan, Thibodeau, Stephen N., Haile, Robert W., Gallinger, Steven, Le Marchand, Loïc, Lindor, Noralane M., Newcomb, Polly A., Hopper, John L., Jenkins, Mark A.
Publicado em 2011

Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

Por Win, Aung Ko, Hopper, John L., Buchanan, Daniel D., Young, Joanne P., Tenesa, Albert, Dowty, James G., Giles, Graham G., Goldblatt, Jack, Winship, Ingrid, Boussioutas, Alex, Young, Graeme P., Parry, Susan, Baron, John A., Duggan, David, Gallinger, Steven, Newcomb, Polly A., Haile, Robert W., Le Marchand, Loïc, Lindor, Noralane M., Jenkins, Mark A.
Publicado em 2013

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

Por Win, Aung Ko, Jenkins, Mark A., Dowty, James G., Antoniou, Antonis C., Lee, Andrew, Giles, Graham G., Buchanan, Daniel D., Clendenning, Mark, Rosty, Christophe, Ahnen, Dennis J., Thibodeau, Stephen N., Casey, Graham, Gallinger, Steven, Le Marchand, Loïc, Haile, Robert W., Potter, John D., Zheng, Yingye, Lindor, Noralane M., Newcomb, Polly A., Hopper, John L., MacInnis, Robert J.
Publicado no Cancer Epidemiol Biomarkers Prev (2016)