About: Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease

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About: Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease Goto Sponge NotDistinct Permalink

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scientific article published on 20 February 2014

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rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2014 (ast) наукова стаття, опублікована в лютому 2014 (uk) مقالة علمية نشرت في 20 فبراير 2014 (ar) scientific article published on 20 February 2014 (en)
publication date	wds:Q37650650-A9D3569D-4286-4A3C-84D9-D2241B1227C8
publication date	2014-02-20 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37650650-BFE9FE6D-1BCF-4C54-B360-33255BA43D13
language of work or name	English
exact match	wds:Q37650650-C814330A-3F79-4999-8E96-0084C4FCA615
exact match	https://scigraph.springernature.com/pub.10.1038/bjc.2014.30
cites work	wds:Q37650650-094A3805-F306-481A-87DE-EF5D090F79C0 wds:Q37650650-1B182D04-E028-4260-A5AC-7312D2F8B6EE wds:Q37650650-1F23FEE1-CF56-42D5-9768-83E080677167 wds:Q37650650-25CF913E-DFF8-49D1-861A-B49DC28CE567 wds:Q37650650-2CA0DCCB-E4DB-4E18-B490-C541B600E8B7 wds:Q37650650-341D16C0-ACD4-43CC-98E3-903A70D500D6 wds:Q37650650-38B26D38-5B5B-4BA1-A7E6-BCC095B32E2F wds:Q37650650-39107319-5ABE-4B2C-BFFE-B2AF5E56D4EC wds:Q37650650-3AB0DF79-4852-4795-A552-E65694F05545 wds:Q37650650-469752B7-35DC-451B-815F-664B02C5AEC2 wds:Q37650650-49C826D5-0D81-489C-B5BA-3B713D7F52E4 wds:Q37650650-4B7F4A5D-A89E-4521-A5E7-6A57537D9A15 wds:Q37650650-4D15E59D-F195-4E6D-9F54-FDAB8AB0C246 wds:Q37650650-608B2F7A-7008-40CC-B090-8BF13B9F10B5 wds:Q37650650-63F138E6-ED38-428B-8629-BC508EBF1A7A wds:Q37650650-64850CBA-518F-4C92-A67A-2626AA244506 wds:Q37650650-6D6C798C-4209-4D79-81B8-6DAAAAFAABCD wds:Q37650650-6DBBB1FB-8AFB-4F4C-965B-6C48D4017595 wds:Q37650650-755A31E9-955E-42A9-AF8D-E4A37A4D7EE9 wds:Q37650650-7A1C310F-9641-4C81-8DB2-204D9DD4E3A4 wds:Q37650650-7B8D7C6D-1C59-4C56-B82A-BBD1F6C36FB4 wds:Q37650650-8EB5B15F-6D20-46C5-BB51-7133FAC788EF wds:Q37650650-98144F25-10DE-4559-8F36-0B8CB6725D0A wds:Q37650650-9844B578-1BCD-4F5B-898C-830CFDD86852 wds:Q37650650-9D946EF6-EBF8-49ED-AEB8-E1F4810D12EF wds:Q37650650-9DAE5868-8681-4AB5-B388-B342EB63D603 wds:Q37650650-9E93C3F5-E752-4316-B74B-1C2E8CDA7B7A wds:Q37650650-A353D445-1891-4E1B-B639-49D1082BD71C wds:Q37650650-A71070B5-20E9-4537-BCD2-2D838AD63ED5 wds:Q37650650-AA6DEFE6-D1EF-4FEF-9FBB-810763D76D0A wds:Q37650650-B20DC19C-2373-41EF-92F5-E1102FF3F284 wds:Q37650650-B6F3C970-0E7F-4D81-ACDC-459593D364BB wds:Q37650650-B8C9B525-2840-42B1-915A-04EE078721C5 wds:Q37650650-BEE0AA17-6219-4DC3-A94A-FAB1FB9A8E40 wds:Q37650650-C54049D7-7E6D-40E0-A867-FE74DE3AAAE7 wds:Q37650650-C828AB2E-B7D0-4766-B0D9-3A86F39511A7 wds:Q37650650-C8B56B29-016F-4A55-9FE4-C98894F4D94C wds:Q37650650-DA923E06-7925-4340-9BB6-405806E94FAB wds:Q37650650-F1C3E835-D5BA-4124-A873-29605969BD95 wds:Q37650650-F5A4AE5D-702A-4EFF-A268-034975FCB852 wds:Q37650650-F6DC15DA-ABC3-4D41-926D-DA9BCC8B6685 wds:Q37650650-FD0F0B4B-9D21-4074-884D-F2CBC2DAC601
cites work	Large-scale genotyping identifies 41 new loci associated with breast cancer risk Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression Germline BRCA1 mutations increase prostate cancer risk The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia Genome-wide association studies identify four ER negative-specific breast cancer risk loci Cancer risks and mortality in heterozygous ATM mutation carriers Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes Global cancer statistics ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data Poly (ADP-ribose) polymerase (PARP) inhibitors for the treatment of advanced germline BRCA2 mutant prostate cancer Familial prostate cancer: the evidence and the Cancer Research Campaign/British Prostate Group (CRC/BPG) UK Familial Prostate Cancer Study dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array Fast and accurate short read alignment with Burrows-Wheeler transform A framework for variation discovery and genotyping using next-generation DNA sequencing data Fanconi anaemia and the repair of Watson and Crick DNA crosslinks Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies ATM polymorphisms as risk factors for prostate cancer development Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer Mutations in CHEK2 associated with prostate cancer risk Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study. Combining target enrichment with barcode multiplexing for high throughput SNP discovery Genetic variants associated with predisposition to prostate cancer and potential clinical implications BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients A risk prediction algorithm based on family history and common genetic variants: application to prostate cancer with potential clinical impact Mendel: the Swiss army knife of genetic analysis programs Commentary on "identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array." Eeles RA, Olama AA, Benlloch S, Saunders EJ, Leongamornlert DA, Tymrakiewicz M, Ghoussaini M, Luccarini C, Dennis J, Jugurnauth-Lit Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.

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