Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories?

per Byrnes, Graham B, Southey, Melissa C, Hopper, John L
Publicat 2008

In silico analysis of missense substitutions using sequence-alignment based methods

per Tavtigian, Sean V, Greenblatt, Marc S, Lesueur, Fabienne, Byrnes, Graham B
Publicat 2008

Classification of Rare Missense Substitutions, Using Risk Surfaces, With Genetic- and Molecular-Epidemiology Applications

per Tavtigian, Sean V., Byrnes, Graham B., Goldgar, David E., Thomas, Alun
Publicat 2008

Dried venous blood samples for the detection and quantification of measles IgG using a commercial enzyme immunoassay.

per Riddell, Michaela A., Byrnes, Graham B., Leydon, Jennie A., Kelly, Heath A.
Publicat 2003

Genetic Evidence and Integration of Various Data Sources for Classifying Uncertain Variants Into a Single Model

per Goldgar, David E., Easton, Douglas F., Byrnes, Graham B., Spurdle, Amanda B., Iversen, Edwin S., Greenblatt, Marc S.
Publicat 2008

Predictors of mammographic density: insights gained from a novel regression analysis of a twin study

per Dite, Gillian S., Gurrin, Lyle C., Byrnes, Graham B., Stone, Jennifer, Gunasekara, Anoma, McCredie, Margaret R.E., English, Dallas R., Giles, Graham G., Cawson, Jennifer, Hegele, Robert A., Chiarelli, Anna M., Yaffe, Martin J., Boyd, Norman F., Hopper, John L.
Publicat 2008

A PALB2 mutation associated with high risk of breast cancer

per 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
Publicat 2010

Circulating tumour-derived KRAS mutations in pancreatic cancer cases are predominantly carried by very short fragments of cell-free DNA

per Zvereva, Maria, Roberti, Gabriel, Durand, Geoffroy, Voegele, Catherine, Nguyen, Minh Dao, Delhomme, Tiffany M., Chopard, Priscilia, Fabianova, Eleonora, Adamcakova, Zora, Holcatova, Ivana, Foretova, Lenka, Janout, Vladimir, Brennan, Paul, Foll, Matthieu, Byrnes, Graham B., McKay, James D., Scelo, Ghislaine, Le Calvez-Kelm, Florence
Publicat a EBioMedicine (2020)

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

per 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
Publicat 2013

KRAS mutations in blood circulating cell-free DNA: a pancreatic cancer case-control

per Le Calvez-Kelm, Florence, Foll, Matthieu, Wozniak, Magdalena B., Delhomme, Tiffany M., Durand, Geoffroy, Chopard, Priscilia, Pertesi, Maroulio, Fabianova, Eleonora, Adamcakova, Zora, Holcatova, Ivana, Foretova, Lenka, Janout, Vladimir, Vallee, Maxime P., Rinaldi, Sabina, Brennan, Paul, McKay, James D., Byrnes, Graham B., Scelo, Ghislaine
Publicat a Oncotarget (2016)

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screeni...

per Le Calvez-Kelm, Florence, Lesueur, Fabienne, Damiola, Francesca, Vallée, Maxime, Voegele, Catherine, Babikyan, Davit, Durand, Geoffroy, Forey, Nathalie, McKay-Chopin, Sandrine, Robinot, Nivonirina, Nguyen-Dumont, Tù, Thomas, Alun, Byrnes, Graham B, Hopper, John L, Southey, Melissa C, Andrulis, Irene L, John, Esther M, Tavtigian, Sean V
Publicat 2011

Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer

per Tavtigian, Sean V., Oefner, Peter J., Babikyan, Davit, Hartmann, Anne, Healey, Sue, Le Calvez-Kelm, Florence, Lesueur, Fabienne, Byrnes, Graham B., Chuang, Shu-Chun, Forey, Nathalie, Feuchtinger, Corinna, Gioia, Lydie, Hall, Janet, Hashibe, Mia, Herte, Barbara, McKay-Chopin, Sandrine, Thomas, Alun, Vallée, Maxime P., Voegele, Catherine, Webb, Penelope M., Whiteman, David C., Sangrajrang, Suleeporn, Hopper, John L., Southey, Melissa C., Andrulis, Irene L., John, Esther M., Chenevix-Trench, Georgia
Publicat 2009

Genetic polymorphisms in 15q25 and 19q13 loci, cotinine levels and risk of lung cancer in EPIC

per Timofeeva, Maria N., McKay, James D., Smith, George Davey, Johansson, Mattias, Byrnes, Graham B., Chabrier, Amélie, Relton, Caroline, Ueland, Per Magne, Vollset, Stein Emil, Midttun, Øivind, Nygård, Ottar, Slimani, Nadia, Romieu, Isabelle, Clavel-Chapelon, Françoise, Boutron-Ruault, Marie-Christine, Fagherazzi, Guy, Kaaks, Rudolf, Teucher, Birgit, Boeing, Heiner, Weikert, Cornelia, Bueno-de-Mesquita, H Bas, van Gils, Carla, Peeters, Petra HM, Agudo, Antonio, Barricarte, Aurelio, Huerta, Jose-Maria, Rodríguez, Laudina, Sánchez, Maria-José, Larrañaga, Nerea, Khaw, Kay-Tee, Wareham, Nick, Allen, Naomi E, Travis, Ruth C, Gallo, Valentina, Norat, Teresa, Krogh, Vittorio, Masala, Giovanna, Panico, Salvatore, Sacerdote, Carlotta, Tumino, Rosario, Trichopoulou, Antonia, Lagiou, Pagona, Trichopoulos, Dimitrios, Rasmuson, Torgny, Hallmans, Göran, Riboli, Elio, Vineis, Paolo, Brennan, Paul
Publicat a Cancer Epidemiol Biomarkers Prev (2011)