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Title:	Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
Source:	Nature Genetics [1061-4036] Seal, Sheila yr:2006

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description	5.	Mathew, C G G. "Fanconi anaemia genes and susceptibility to cancer." Oncogene 25.43 (2006): 5875-84.
description	6.	Meyle, Kathrine D. "Genetic risk factors for melanoma." Human Genetics 126.4 (2009): 499-510.
description	7.	De Nicolo, A. "A Novel Breast Cancer-Associated BRIP1 (FANCJ/BACH1) Germ-line Mutation Impairs Protein Stability and Function." Clinical cancer research 14.14 (2008): 4672-80.
description	8.	Stacey, Thorarinn N. "The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland." PLoS medicine 3.7 (2006): 1103-1113.
description	9.	Hayes, N. "Genome-wide association study of prostate cancer identifies a second risk locus at 8q24." Nature genetics 39.5 (2007): 645-649.
description	10.	Bojesen, M. "Genome-wide association study identifies novel breast cancer susceptibility loci." Nature 447.7148 (2007): 1087-93.
description	11.	Easton, Douglas F. "Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk." The New England journal of medicine 372.ARRAY(0x2acea18) (2015): 2243-2257.
description	12.	Rahman, N. "PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene." Nature genetics 39.2 (2007): 165-7.
description	13.	Thompson, D. "The genetic epidemiology of breast cancer genes." Journal of Mammary Gland Biology and Neoplasia 9.3 (2004): 221-36.
description	14.	Barker, Anna D S. "Mapping the cancer genome. Pinpointing the genes involved in cancer will help chart a new course across the complex landscape of human malignancies." Scientific American 296.3 (2007): 50-7.
description	15.	Taniguchi, T. "Molecular pathogenesis of Fanconi anemia: recent progress." Blood 107.11 (2006): 4223-33.
description	16.	Erkko, Hannele, B. "A recurrent mutation in PALB2 in Finnish cancer families." Nature 446.7133 (2007): 316-319.
description	17.	Shuen, William Y. "Inherited Mutations in Breast Cancer Genes—Risk and Response." Journal of Mammary Gland Biology and Neoplasia 16.1 (2011): 3-15.
description	18.	Hall, Michael J. "BRCA2 mutation and the risk of hematologic malignancy." Leukemia & lymphoma 47.4 (2006): 765-7.
description	19.	Pujana, M. "Network modeling links breast cancer susceptibility and centrosome dysfunction." Nature genetics 39.11 (2007): 1338-1349.
description	20.	Hampe, J. "A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1." Nature genetics 39.2 (2007): 207-211.