Общедоступные статьи - Georgia Chenevix-TrenchПодробнее...
8 статей недоступны нигде
Проверить
Mutations in EGFR, BRAF and RAS are rare in triple-negative and basal-like breast cancers from Caucasian women
E Tilch, T Seidens, S Cocciardi, LE Reid, D Byrne, PT Simpson, ...
Breast cancer research and treatment 143, 385-392, 2014
Финансирование: National Health and Medical Research Council, Australia
Проверить
Common genetic variants and cancer risk in Mendelian cancer syndromes
AC Antoniou, G Chenevix-Trench
Current opinion in genetics & development 20 (3), 299-307, 2010
Финансирование: Cancer Research UK
Проверить
The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case–control and family analysis
SE Johnatty, J Beesley, X Chen, JL Hopper, MC Southey, GG Giles, ...
Breast cancer research and treatment 115, 145-150, 2009
Финансирование: US National Institutes of Health
Проверить
No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers
AB Spurdle, AJ Deans, D Duffy, DE Goldgar, X Chen, J Beesley, kConFaB, ...
Breast cancer research and treatment 115, 307-313, 2009
Финансирование: US National Institutes of Health, Cancer Research UK
Проверить
Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient
J Johnson, DC Bessette, JM Saunus, CE Smart, S Song, RL Johnston, ...
Breast Cancer Research and Treatment 170, 179-188, 2018
Финансирование: Australian Research Council, National Health and Medical Research Council …
Проверить
The CYP17A1 −34T > C polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers
B Kaufman, Y Laitman, E Ziv, U Hamann, D Torres, EL Lahad, R Beeri, ...
Breast cancer research and treatment 126, 521-527, 2011
Финансирование: Canadian Institutes of Health Research, Cancer Research UK
Проверить
Association between KRAS rs61764370 and triple-negative breast cancer—a false positive?
P Pharoah, A Antoniou, A Berchuck, G Chenevix-Trench, S Gayther, ...
The Lancet Oncology 12 (8), 723-724, 2011
Финансирование: Cancer Research UK
Проверить
Childhood, adolescent, and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers
S Li, L Madanat-Harjuoja, G Leslie, DR Barnes, MK Bolla, J Dennis, ...
JNCI: Journal of the National Cancer Institute, djae306, 2024
Финансирование: National Health and Medical Research Council, Australia, Cancer Research UK …
373 статьи доступны в некоторых источниках
Проверить
Genome-wide association study identifies novel breast cancer susceptibility loci
DF Easton, KA Pooley, AM Dunning, PDP Pharoah, D Thompson, ...
Nature 447 (7148), 1087-1093, 2007
Финансирование: Cancer Research UK
Проверить
Association analysis identifies 65 new breast cancer risk loci
K Michailidou, S Lindström, J Dennis, J Beesley, S Hui, S Kar, A Lemaçon, ...
Nature 551 (7678), 92-94, 2017
Финансирование: US National Institutes of Health, Canadian Institutes of Health Research …
Проверить
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
K Michailidou, P Hall, A Gonzalez-Neira, M Ghoussaini, J Dennis, ...
Nature genetics 45 (4), 353-361, 2013
Финансирование: US National Institutes of Health, Canadian Institutes of Health Research …
Проверить
Gene-panel sequencing and the prediction of breast-cancer risk
DF Easton, PDP Pharoah, AC Antoniou, M Tischkowitz, SV Tavtigian, ...
New England Journal of Medicine 372 (23), 2243-2257, 2015
Финансирование: US National Institutes of Health, National Health and Medical Research …
Проверить
Polygenic risk scores for prediction of breast cancer and breast cancer subtypes
N Mavaddat, K Michailidou, J Dennis, M Lush, L Fachal, A Lee, JP Tyrer, ...
The American Journal of Human Genetics 104 (1), 21-34, 2019
Финансирование: US National Institutes of Health, Canadian Institutes of Health Research …
Проверить
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies
XR Yang, J Chang-Claude, EL Goode, FJ Couch, H Nevanlinna, RL Milne, ...
Journal of the National Cancer Institute 103 (3), 250-263, 2011
Финансирование: US National Institutes of Health, Cancer Research UK
Проверить
Breast cancer risk genes—association analysis in more than 113,000 women
Breast Cancer Association Consortium
New England Journal of Medicine 384 (5), 428-439, 2021
Финансирование: Cancer Research UK, UK Medical Research Council, Wellcome Trust, European …
Проверить
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
N Mavaddat, D Barrowdale, IL Andrulis, SM Domchek, D Eccles, ...
Cancer Epidemiology, Biomarkers & Prevention 21 (1), 134-147, 2012
Финансирование: US National Institutes of Health, Canadian Institutes of Health Research …
Проверить
Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer
KL Bolton, G Chenevix-Trench, C Goh, S Sadetzki, SJ Ramus, BY Karlan, ...
Jama 307 (4), 382-389, 2012
Финансирование: US National Institutes of Health, Cancer Research UK, Government of Spain
Проверить
Prediction of breast cancer risk based on profiling with common genetic variants
N Mavaddat, PDP Pharoah, K Michailidou, J Tyrer, MN Brook, MK Bolla, ...
Journal of the National Cancer Institute 107 (5), djv036, 2015
Финансирование: US National Institutes of Health, National Health and Medical Research …
Проверить
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
K Michailidou, J Beesley, S Lindstrom, S Canisius, J Dennis, MJ Lush, ...
Nature genetics 47 (4), 373-380, 2015
Финансирование: US National Institutes of Health, Canadian Institutes of Health Research …
Проверить
A common coding variant in CASP8 is associated with breast cancer risk
A Cox, AM Dunning, M Garcia-Closas, S Balasubramanian, MWR Reed, ...
Nature genetics 39 (3), 352-358, 2007
Финансирование: German Research Foundation
Информация о публикациях и финансировании собрана автоматически.