Physician interpretation of variants of uncertain significance

Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast Cancer

(2017) Allison W. Kurian et al.   JOURNAL OF CLINICAL ONCOLOGY

Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance

(2017) Ilana Solomon et al.   Journal of Genetic Counseling

Germline BRCA testing is moving from cancer risk assessment to a predictive biomarker for targeting cancer therapeutics

(2016) L. Moreno et al.   Clinical & Translational Oncology

Genetics/genomics education for nongenetic health professionals: a systematic literature review

(2016) Divya Talwar et al.   GENETICS IN MEDICINE

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer

(2016) Nadine Tung et al.   JOURNAL OF CLINICAL ONCOLOGY

Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service

(2016) Irena Vrečar et al.   JOURNAL OF MEDICAL SYSTEMS

ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes

(2015) Sapna Syngal et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

BRCA1andBRCA2genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance

(2015) D. M. Eccles et al.   ANNALS OF ONCOLOGY

Understanding of BRCA VUS genetic results by breast cancer specialists

(2015) B. K. Eccles et al.   BMC CANCER

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

Sequence Variants of Uncertain Significance

(2015) Marc S. Greenblatt   Surgical Oncology Clinics of North America

Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes

(2014) Dmitry Pruss et al.   BREAST CANCER RESEARCH AND TREATMENT

A systematic review of factors that act as barriers to patient referral to genetic services

(2014) Türem Delikurt et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Comparison of risk management strategies between women testing positive for a BRCA variant of unknown significance and women with known BRCA deleterious mutations

(2014) Christine Garcia et al.   GENETICS IN MEDICINE

Systematic review of the psychological consequences of false-positive screening mammograms

(2014) M Bond et al.   HEALTH TECHNOLOGY ASSESSMENT

2015 NSGC Presidential Address: Gifts of Genetic Counselors: Life’s Leadership Lessons

(2014) Joy Larsen Haidle   Journal of Genetic Counseling

How well do doctors think they perform on the General Medical Council's Tests of Competence pilot examinations? A cross-sectional study

(2014) Leila Mehdizadeh et al.   BMJ Open

Variants of uncertain significance inBRCAtesting: evaluation of surgical decisions, risk perception, and cancer distress

(2013) JO Culver et al.   CLINICAL GENETICS

Barriers to integrating personalized medicine into clinical practice: a best–worst scaling choice experiment

(2012) Mehdi Najafzadeh et al.   GENETICS IN MEDICINE

Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors

(2011) Bronson D. Riley et al.   Journal of Genetic Counseling

BRCA1andBRCA2mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer

(2009) Michael J. Hall et al.   CANCER

Differential use of available genetic tests among primary care physicians in the United States: results of a national survey

(2008) Alexandra E Shields et al.   GENETICS IN MEDICINE

Physicians’ Experiences With BRCA1/2 Testing in Community Settings

(2008) Nancy L. Keating et al.   JOURNAL OF CLINICAL ONCOLOGY

The counsellees' view of an unclassified variant in BRCA1/2: recall, interpretation, and impact on life

(2007) Joël Vos et al.   PSYCHO-ONCOLOGY