Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance

Cancer statistics, 2016

(2016) Rebecca L. Siegel et al.   CA-A CANCER JOURNAL FOR CLINICIANS

Understanding of BRCA VUS genetic results by breast cancer specialists

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

Cancer statistics, 2015

(2015) Rebecca L. Siegel et al.   CA-A CANCER JOURNAL FOR CLINICIANS

Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification fromBRCAtesting

(2015) C.L. Scherr et al.   CLINICAL GENETICS

A preliminary investigation of genetic counselors’ information needs when receiving a variant of uncertain significance result: a mixed methods study

(2015) Courtney L. Scherr et al.   GENETICS IN MEDICINE

More genes, more problems? Benefits and risks of multiplex genetic testing

(2015) Barbara M. Norquist et al.   GYNECOLOGIC ONCOLOGY

Rescreening for genetic mutations using multi-gene panel testing in patients who previously underwent non-informative genetic screening

(2015) Melissa K. Frey et al.   GYNECOLOGIC ONCOLOGY

Guidelines on Genetic Evaluation and Management of Lynch Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer

(2014) Francis M Giardiello et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

Use of panel tests in place of single gene tests in the cancer genetics clinic

(2014) A. Yorczyk et al.   CLINICAL 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

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility

(2014) Angela R. Bradbury et al.   GENETICS IN MEDICINE

The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?

(2013) FSM Hilbers et al.   CLINICAL GENETICS

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

(2013) JO Culver et al.   CLINICAL GENETICS

Commentary: Ambiguity and Uncertainty: Neglected Elements of Medical Education Curricula?

(2011) Vera P. Luther et al.   ACADEMIC MEDICINE

Family communication matters: The impact of telling relatives about unclassified variants and uninformative DNA-test results

(2011) Joël Vos et al.   GENETICS IN MEDICINE

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: Variant reclassification and surgical decisions

(2011) Mitzi L. Murray et al.   GENETICS IN MEDICINE

Varieties of Uncertainty in Health Care: A Conceptual Taxonomy

(2011) P. K. J. Han et al.   MEDICAL DECISION MAKING

Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review

(2010) Scott M. Weissman et al.   Journal of Genetic Counseling

Women’s Perceptions of the Personal and Family Impact of Genetic Cancer Risk Assessment: Focus Group Findings

(2009) Deborah J. MacDonald et al.   Journal of Genetic Counseling

Subjective interpretation of inconclusive BRCA1/2 cancer genetic test results and transmission of information to the relatives

(2008) C. Cypowyj et al.   PSYCHO-ONCOLOGY

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

(2007) Joël Vos et al.   PSYCHO-ONCOLOGY