About: Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes

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About: Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes Goto Sponge Distinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1997 (uk) article scientifique publié en 1997 (fr) im Dezember 1997 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57274836-09F0FD3C-12C6-4A04-9887-70EC2E465270
publication date	1997-12-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q57274836-03FADFC8-ADC6-45B6-8BF9-4E1D37DF3BDD wds:Q57274836-270DAFFC-35F3-452E-B8BA-4892F93DE57C wds:Q57274836-2FEE3E5D-72D8-4101-B04D-C400E7F86458 wds:Q57274836-352809F7-2037-4CB7-AC43-E0DBCB420B6A wds:Q57274836-3EDB983D-6539-4F5A-B313-0956FE8A3AE4 wds:Q57274836-5E5A55DC-FC2E-4F82-9059-3829F0017E6E wds:Q57274836-6E640D30-3986-4FE0-858F-7BBB8BCFE4FF wds:Q57274836-9FCAF0DC-AFC3-4A7F-B701-C2884D41AD5E wds:Q57274836-AC9E44A1-25EB-431D-A93B-3212E500C42D wds:Q57274836-BCEA548F-8010-4E03-85EC-43E73D459F74 wds:Q57274836-CF96D103-DCF5-479D-82B0-DC5F47713483 wds:Q57274836-E4DAAD29-B1D9-4AE7-A0AC-DB675C705AB4
author name string	L S Friedman T S Frank K Syrjäkoski M McClure S Pyrhönen B Ward M Luce T Muhonen H Eerola L Sarantaus P Vehmanen T Kainu
rdfs:label	Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (en) Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (nl)
skos:prefLabel	Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (en) Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (nl)
name	Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (en) Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (nl)
author	wds:Q57274836-638BEF1B-8B00-4AE0-A123-C002AA52C029 wds:Q57274836-728E1C18-ECEF-4F36-AC8F-2C7639643EEB
author	Heli Nevanlinna Olli-Pekka Kallioniemi
title	wds:Q57274836-D96DF386-8DB7-4781-8AE1-44C5E6AC08FE
title	Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes (en)
page(s)	wds:Q57274836-FEF3FECA-CB4E-440D-B07D-BBA08D64E8B0
page(s)	2309-2315
instance of	wds:Q57274836-35AFE84F-879F-4B74-9785-8532432E4B85
instance of	scholarly article
main subject	wds:Q57274836-4CEB07A3-F4C9-4BF6-AB22-CAF81B41FCE2
main subject	breast cancer
PubMed ID	wds:Q57274836-33F85480-C34D-445F-BCD9-70BCC4D7682C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9361038
PubMed ID	9361038
published in	wds:Q57274836-02E11C87-55FF-4615-952E-D81E5677A7B8
published in	Human Molecular Genetics
issue	wds:Q57274836-98AE2076-850C-41A8-8349-5DFC464E134A
volume	wds:Q57274836-B027FDF4-CAA5-4E36-8393-3A40CA550B26
issue	13
volume	6
DOI	wds:Q57274836-E411011D-5261-4388-82CE-32F7F3537CF0
DOI	http://dx.doi.org/10.1093/HMG/6.13.2309
DOI	10.1093/HMG/6.13.2309
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57274836
is cites work of	Testing for hereditary breast and ovarian cancer in the southeastern United States Relationship of patients' age to histopathological features of breast tumours in BRCA1 and BRCA2 and mutation-negative breast cancer families Familial breast cancer in southern Finland Mutational screening of breast cancer susceptibility gene 1 from early onset, bi-lateral, and familial breast cancer patients in Taiwan. No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22 Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families. Genetic predisposition, environment and cancer incidence: a nationwide twin study in Finland, 1976-1995. Evidence of founder mutations in Finnish BRCA1 and BRCA2 families Mutation analysis of the CHK2 gene in families with hereditary breast cancer Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families. A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families BRCA2 mutations in 154 finnish male breast cancer patients A probability model for predicting BRCA1 and BRCA2 mutations in breast and breast-ovarian cancer families ATM variants and cancer risk in breast cancer patients from Southern Finland Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families The DNA damage signalling kinase ATM is aberrantly reduced or lost in BRCA1/BRCA2-deficient and ER/PR/ERBB2-triple-negative breast cancer. Histopathological features of breast tumours in BRCA1, BRCA2 and mutation-negative breast cancer families Multi-variant pathway association analysis reveals the importance of genetic determinants of estrogen metabolism in breast and endometrial cancer susceptibility Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families. A role of BRCA1 and BRCA2 germline mutations in breast cancer susceptibility within Sardinian population Molecular epidemiology of sporadic breast cancer. The role of polymorphic genes involved in oestrogen biosynthesis and metabolism Germ line mutations associated with breast cancer susceptibility Spectrum and prevalence ofBRCA1 andBRCA2 germline mutations in Sardinian patients with breast carcinoma through hospital-based screening Prevalence of BRCA1 and BRCA2 gene mutations in families with medium and high risk of breast and ovarian cancer in Brazil. BRCA1/2 germline mutations and their clinical importance in Turkish breast cancer patients. NQO1 expression correlates inversely with NFκB activation in human breast cancer Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients No germline FH mutations in familial breast cancer patients Basal cytokeratins in breast tumours among BRCA1, BRCA2 and mutation-negative breast cancer families Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility Survival of breast cancer patients in BRCA1, BRCA2, and non-BRCA1/2 breast cancer families: a relative survival analysis from Finland A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer

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