标题
Update on multi‐gene panel testing and communication of genetic test results
作者
关键词
-
出版物
Breast Journal
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2020-07-08
DOI
10.1111/tbj.13971
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。- Therapeutic implications of germline genetic findings in cancer
- (2019) Subotheni Thavaneswaran et al. Nature Reviews Clinical Oncology
- An update on genetic risk assessment and prevention: the role of genetic testing panels in breast cancer
- (2019) Carolyn Piccinin et al. Expert Review of Anticancer Therapy
- Tumor Genomic Sequencing as an Impetus to Screen for Germline Mutations: Primum Non Nocere
- (2019) Saroj Niraula Journal of Oncology Practice
- When Should Tumor Genomic Profiling Prompt Consideration of Germline Testing?
- (2019) Kim DeLeonardis et al. Journal of Oncology Practice
- Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium
- (2019) Pooja Middha Kapoor et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Maternal perceptions of BRCA genetic counseling communication processes about disclosing cancer risk information to children and adult relatives
- (2018) Jada G. Hamilton et al. PSYCHO-ONCOLOGY
- Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries
- (2018) Freddie Bray et al. CA-A CANCER JOURNAL FOR CLINICIANS
- Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing
- (2018) Jacqueline Mersch et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
- (2018) Amit V. Khera et al. NATURE GENETICS
- Talazoparib in Patients with Advanced Breast Cancer and a Germline BRCA Mutation
- (2018) Jennifer K. Litton et al. NEW ENGLAND JOURNAL OF MEDICINE
- Breast Cancer Surgical Risk Reduction for Patients With Inherited Mutations in Moderate Penetrance Genes
- (2018) Anna Weiss et al. JAMA Surgery
- Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels
- (2018) Kristy Lee et al. GENETICS IN MEDICINE
- Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
- (2018) Peter D. Beitsch et al. JOURNAL OF CLINICAL ONCOLOGY
- Mutations in context: implications of BRCA testing in diverse populations
- (2017) Gabriela E. S. Felix et al. Familial Cancer
- Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk
- (2017) Jennifer L Caswell-Jin et al. GENETICS IN MEDICINE
- Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing
- (2017) Diana Mandelker et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
- (2017) Karoline B. Kuchenbaecker et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
- (2017) Julie Lecarpentier et al. JOURNAL OF CLINICAL ONCOLOGY
- National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer
- (2017) Christopher P. Childers et al. JOURNAL OF CLINICAL ONCOLOGY
- Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer
- (2017) Fergus J. Couch et al. JAMA Oncology
- Comparison of Breast Cancer Molecular Features and Survival by African and European Ancestry in The Cancer Genome Atlas
- (2017) Dezheng Huo et al. JAMA Oncology
- Gene Panel Testing for Inherited Cancer Risk
- (2017) Michael J. Hall et al. Journal of the National Comprehensive Cancer Network
- Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol
- (2016) F. Meric-Bernstam et al. ANNALS OF ONCOLOGY
- Risks of first and subsequent cancers amongTP53mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort
- (2016) Phuong L. Mai et al. CANCER
- Care delivery considerations for widespread and equitable implementation of inherited cancer predisposition testing
- (2016) Deborah Cragun et al. EXPERT REVIEW OF MOLECULAR DIAGNOSTICS
- Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
- (2016) Sarah S. Kalia et al. GENETICS IN MEDICINE
- Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age
- (2016) Ashley Elrick et al. Journal of Genetic Counseling
- Counselling framework for moderate-penetrance cancer-susceptibility mutations
- (2016) Nadine Tung et al. Nature Reviews Clinical Oncology
- Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA
- (2016) Kasmintan A. Schrader et al. JAMA Oncology
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility
- (2015) Mark E. Robson et al. JOURNAL OF CLINICAL ONCOLOGY
- Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
- (2015) Douglas F. Easton et al. NEW ENGLAND JOURNAL OF MEDICINE
- Personalized genomic analyses for cancer mutation discovery and interpretation
- (2015) Siân Jones et al. Science Translational Medicine
- Next-Generation Sequencing for Inherited Breast Cancer Risk: Counseling through the Complexity
- (2014) Irene R. Rainville et al. Current Oncology Reports
- Breast cancer genes: beyond BRCA1 and BRCA2
- (2013) Ana Vega Frontiers in Bioscience-Landmark
- Risk of Breast Cancer in Women With a CHEK2 Mutation With and Without a Family History of Breast Cancer
- (2011) Cezary Cybulski et al. JOURNAL OF CLINICAL ONCOLOGY
- Communication of BRCA Results and Family Testing in 1,103 High-Risk Women
- (2010) E. L. Cheung et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- Breast Cancer in the Personal Genomics Era
- (2010) Rachel E. Ellsworth et al. CURRENT GENOMICS
- 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
- The emerging landscape of breast cancer susceptibility
- (2007) Michael R Stratton et al. NATURE GENETICS
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started