Multigene Panel Testing Detects Equal Rates of Pathogenic BRCA1/2 Mutations and has a Higher Diagnostic Yield Compared to Limited BRCA1/2 Analysis Alone in Patients at Risk for Hereditary Breast Cancer
出版年份 2015 全文链接
标题
Multigene Panel Testing Detects Equal Rates of Pathogenic BRCA1/2 Mutations and has a Higher Diagnostic Yield Compared to Limited BRCA1/2 Analysis Alone in Patients at Risk for Hereditary Breast Cancer
作者
关键词
National Comprehensive Cancer Network, Lynch Syndrome, National Comprehensive Cancer Network, Panel Testing, Breast Magnetic Resonance Imaging
出版物
ANNALS OF SURGICAL ONCOLOGY
Volume 22, Issue 10, Pages 3282-3288
出版商
Springer Nature
发表日期
2015-07-28
DOI
10.1245/s10434-015-4754-2
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。- Validation of a Next-Generation–Sequencing Cancer Panel for Use in the Clinical Laboratory
- (2015) Birgitte B. Simen et al. ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
- Frequency of mutations in individuals with breast cancer referred forBRCA1andBRCA2testing using next-generation sequencing with a 25-gene panel
- (2014) Nadine Tung et al. CANCER
- Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes
- (2014) Laurent Castéra et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients
- (2014) Holly LaDuca et al. GENETICS IN MEDICINE
- Population-Based Screening forBRCA1andBRCA2
- (2014) Mary-Claire King et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment
- (2014) Allison W. Kurian et al. JOURNAL OF CLINICAL ONCOLOGY
- Breast-Cancer Risk in Families with Mutations in PALB2
- (2014) Antonis C. Antoniou et al. NEW ENGLAND JOURNAL OF MEDICINE
- Multiplex Genetic Testing for Cancer Susceptibility: Out on the High Wire Without a Net?
- (2013) Susan M. Domchek et al. JOURNAL OF CLINICAL ONCOLOGY
- Supreme Court Ruling Broadens BRCA Testing Options
- (2013) A. Azvolinsky JNCI-Journal of the National Cancer Institute
- Integrating next-generation sequencing into the diagnostic testing of inherited cancer predisposition
- (2012) CS Ku et al. CLINICAL GENETICS
- Comprehensive molecular portraits of human breast tumours
- (2012) Daniel C. Koboldt et al. NATURE
- Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
- (2011) T. Walsh et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Pathology of hereditary breast cancer
- (2011) Petra van der Groep et al. CELLULAR ONCOLOGY
- Association of Risk-Reducing Surgery in BRCA1 or BRCA2 Mutation Carriers With Cancer Risk and Mortality
- (2010) Susan M. Domchek JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: a proof-of-concept trial
- (2010) Andrew Tutt et al. LANCET
- Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing
- (2010) Tom Walsh et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis
- (2009) Stefanie Vogt et al. GASTROENTEROLOGY
- Increased Colorectal Cancer Incidence in Obligate Carriers of Heterozygous Mutations in MUTYH
- (2009) Natalie Jones et al. GASTROENTEROLOGY
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