Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control
出版年份 2010 全文链接
标题
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control
作者
关键词
-
出版物
EPMA Journal
Volume 1, Issue 3, Pages 397-412
出版商
Springer Nature
发表日期
2010-06-26
DOI
10.1007/s13167-010-0037-y
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- BRCA1gene mutations may explain more than 80% of excess number of ovarian cancer cases after breast cancer – a population based study from the Western Sweden Health Care region
- (2010) Zakaria Einbeigi et al. ACTA ONCOLOGICA
- Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene
- (2010) Ivana Ticha et al. BREAST CANCER RESEARCH AND TREATMENT
- Interlaboratory Diagnostic Validation of Conformation-Sensitive Capillary Electrophoresis for Mutation Scanning
- (2010) C. J. Mattocks et al. CLINICAL CHEMISTRY
- The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania
- (2010) P Elsakov et al. CLINICAL GENETICS
- High-resolution DNA melting analysis in clinical research and diagnostics
- (2010) Jesse L Montgomery et al. EXPERT REVIEW OF MOLECULAR DIAGNOSTICS
- Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2
- (2010) Nancie Petrucelli et al. GENETICS IN MEDICINE
- A role of BRCA1 and BRCA2germline mutations in breast cancer susceptibility within Sardinian population
- (2009) Grazia Palomba et al. BMC CANCER
- Two founder BRCA2 mutations predispose to breast cancer in young women
- (2009) Mar Infante et al. BREAST CANCER RESEARCH AND TREATMENT
- Is early onset breast cancer with no family history a good criterion for testingBRCA1andBRCA2genes? A small population-based study
- (2009) CLINICAL GENETICS
- The contribution of founder mutations to early-onset breast cancer in French-Canadian women
- (2009) P Ghadirian et al. CLINICAL GENETICS
- BRCA15272-1G>A andBRCA25374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin
- (2009) M Infante et al. CLINICAL GENETICS
- Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing
- (2009) Orland Diez et al. Familial Cancer
- A high frequent BRCA1 founder mutation identified in the Greenlandic population
- (2009) Theresa Larriba Harboe et al. Familial Cancer
- Pathologic Complete Response Rates in Young Women With BRCA1-Positive Breast Cancers After Neoadjuvant Chemotherapy
- (2009) Tomasz Byrski et al. JOURNAL OF CLINICAL ONCOLOGY
- Survival Analysis of Cancer Risk Reduction Strategies forBRCA1/2Mutation Carriers
- (2009) Allison W. Kurian et al. JOURNAL OF CLINICAL ONCOLOGY
- Meta-analysis of Risk Reduction Estimates Associated With Risk-Reducing Salpingo-oophorectomy in BRCA1 or BRCA2 Mutation Carriers
- (2009) T. R. Rebbeck et al. JNCI-Journal of the National Cancer Institute
- The Contribution of BRCA1 and BRCA2 to Ovarian Cancer
- (2009) Susan J. Ramus et al. Molecular Oncology
- Inhibition of Poly(ADP-Ribose) Polymerase in Tumors fromBRCAMutation Carriers
- (2009) Peter C. Fong et al. NEW ENGLAND JOURNAL OF MEDICINE
- MRI and Mammography Surveillance of Women at Increased Risk for Breast Cancer
- (2008) Elon J. Granader et al. ACADEMIC RADIOLOGY
- BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer
- (2008) Mads Thomassen et al. ACTA ONCOLOGICA
- Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic Analysis
- (2008) F. Marroni et al. ANNALS OF HUMAN GENETICS
- Spectrum and characterisation of BRCA1 and BRCA2deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer
- (2008) Eva Machackova et al. BMC CANCER
- Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families
- (2008) Katri Pylkäs et al. BMC CANCER
- Five recurrent BRCA1/2 mutations are responsible for cancer predisposition in the majority of Slovenian breast cancer families
- (2008) Mateja Krajc et al. BMC Medical Genetics
- Is BRCA1-5083del19, identified in breast cancer patients of Sicilian origin, a Calabrian founder mutation?
- (2008) Antonio Russo et al. BREAST CANCER RESEARCH AND TREATMENT
- A common Greenlandic Inuit BRCA1 RING domain founder mutation
- (2008) Thomas v. O. Hansen et al. BREAST CANCER RESEARCH AND TREATMENT
- Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania
- (2008) Ramūnas Janavičius et al. BREAST CANCER RESEARCH AND TREATMENT
- Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy
- (2008) Laura Papi et al. BREAST CANCER RESEARCH AND TREATMENT
- Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families
- (2008) Thomas v. O. Hansen et al. BREAST CANCER RESEARCH AND TREATMENT
- The c.156_157insAlu BRCA2 rearrangement accounts for more than one-fourth of deleterious BRCA mutations in northern/central Portugal
- (2008) Ana Peixoto et al. BREAST CANCER RESEARCH AND TREATMENT
- Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndrome
- (2008) E.C.B. da Costa et al. CANCER GENETICS AND CYTOGENETICS
- BRCA1 and BRCA2 Mutation Prevalence and Clinical Characteristics of a Population-Based Series of Ovarian Cancer Cases from Denmark
- (2008) M. Soegaard et al. CLINICAL CANCER RESEARCH
- Hereditary breast cancer: from bench to bedside
- (2008) Jacques De Grève et al. CURRENT OPINION IN ONCOLOGY
- Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate
- (2008) Brett T Chiquet et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The 4154delA mutation carriers in the BRCA1 gene share a common ancestry
- (2008) Silvija Ozolina et al. Familial Cancer
- MLPA screening in theBRCA1gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases
- (2008) Stefanie Engert et al. HUMAN MUTATION
- Risk-Reducing Salpingo-Oophorectomy for the Prevention of BRCA1- and BRCA2-Associated Breast and Gynecologic Cancer: A Multicenter, Prospective Study
- (2008) Noah D. Kauff et al. JOURNAL OF CLINICAL ONCOLOGY
- Risk reducing mastectomy: outcomes in 10 European centres
- (2008) D G R Evans et al. JOURNAL OF MEDICAL GENETICS
- Keeping Up With the Next Generation
- (2008) John R. ten Bosch et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- BRCA1p.Val1688del Is a Deleterious Mutation That Recurs in Breast and Ovarian Cancer Families From Northeast Italy
- (2007) Sandro Malacrida et al. JOURNAL OF CLINICAL ONCOLOGY
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started