As genomic sequencing expands into more areas of patient care, an increasing number of patients learn of the variants of uncertain significance (VUSs) that they carry. Understanding the potential psychosocial consequences of the disclosure of a VUS can help inform pre- and post-test counseling discussions. Medical uncertainty in general elicits a variety of responses from patients, particularly in the growing field of medical genetics and genomics. It is important to consider patients’ responses to the ambiguous nature of VUSs across different indications and situational contexts. Genetic counselors and other providers ordering genetic testing should be prepared for the possibility of their patients’ misinterpretation of such results. Pre-t...
Background: The use of multigene panel testing for identifying individuals with hereditary cancer su...
Patients pursuing exome sequencing in their quest for diagnosis will most often receive a clinically...
Genetic testing is becoming increasingly used to detect individuals who are predisposed to developin...
Establishing a genetic diagnosis may lead to major health benefits for the patient and their wider f...
Background: ACMG guidelines suggest that clinical laboratories use a variant classification system t...
Thesis (Ph.D.)--University of Washington, 2018The overall aim of this dissertation was to study how ...
The number of individuals being tested for hereditary cancer syndromes has greatly increased in the ...
Background Little is known about the impact of reclassification on patients’ perception of medical ...
Chromosomal microarray analysis (CMA) for unexplained anomalies and developmental delay has improved...
Genomic databases are one of many important tools used to classify variants as pathogenic, benign, o...
In genomics, the clinical application of Next Generation Sequencing technologies (such as Whole Geno...
Background: Many clients who undergo genetic testing (GT) for cancer risk assessment receive variant...
Various commercial laboratories are used in cancer genetics practice, which can lead to clinicians r...
Objective: Cancer genetic counseling increasingly involves discussing uncertain test results, for ex...
Organizations such as the American College of Medical Genetics (ACMG) and the National Society of Ge...
Background: The use of multigene panel testing for identifying individuals with hereditary cancer su...
Patients pursuing exome sequencing in their quest for diagnosis will most often receive a clinically...
Genetic testing is becoming increasingly used to detect individuals who are predisposed to developin...
Establishing a genetic diagnosis may lead to major health benefits for the patient and their wider f...
Background: ACMG guidelines suggest that clinical laboratories use a variant classification system t...
Thesis (Ph.D.)--University of Washington, 2018The overall aim of this dissertation was to study how ...
The number of individuals being tested for hereditary cancer syndromes has greatly increased in the ...
Background Little is known about the impact of reclassification on patients’ perception of medical ...
Chromosomal microarray analysis (CMA) for unexplained anomalies and developmental delay has improved...
Genomic databases are one of many important tools used to classify variants as pathogenic, benign, o...
In genomics, the clinical application of Next Generation Sequencing technologies (such as Whole Geno...
Background: Many clients who undergo genetic testing (GT) for cancer risk assessment receive variant...
Various commercial laboratories are used in cancer genetics practice, which can lead to clinicians r...
Objective: Cancer genetic counseling increasingly involves discussing uncertain test results, for ex...
Organizations such as the American College of Medical Genetics (ACMG) and the National Society of Ge...
Background: The use of multigene panel testing for identifying individuals with hereditary cancer su...
Patients pursuing exome sequencing in their quest for diagnosis will most often receive a clinically...
Genetic testing is becoming increasingly used to detect individuals who are predisposed to developin...