Journal of Genetic Counseling

Genetic counseling considerations with rapid genome‐wide sequencing in a neonatal intensive care unit

The current state of genetic counseling assistants in the United States

Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era

Genetic counseling in pediatric acute care: Reflections on ultra‐rapid genomic diagnoses in neonates

Talking across generations: Family communication about BRCA1 and BRCA2 genetic cancer risk

Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges

Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world

Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making

Demographic differences in the utilization of clinical and direct-to-consumer genetic testing.

Trans‐counseling: A case series of transgender individuals at high risk for BRCA1 pathogenic variants

Factors complicating the informed consent process for whole exome sequencing in neonatal and pediatic intensive care units

Practice variation of genetic counselor engagement in the cystic fibrosis newborn screen‐positive diagnostic resolution process

Genetic counselors’ comfort and knowledge of cancer risk assessment for transgender patients

Exploring genetic counselors’ perceptions of usefulness and intentions to use refined risk models in clinical care based on the Technology Acceptance Model (TAM)

Establishing the minimum clinically important difference for the Genetic Counseling Outcome Scale (GCOS‐24)

How to inform relatives at risk of hereditary diseases? A mixed‐methods systematic review on patient attitudes

A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system

Female family members lack understanding of indeterminate negative BRCA1/2 test results shared by probands

Patient goals, motivations, and attitudes in a patient‐driven variant reclassification study

Current genetic counseling practice in the United States following positive non‐invasive prenatal testing for sex chromosome abnormalities

The relationship between genetic counseling student self‐efficacy and clinical training

Genetic counselors with advanced skills: II. A new career trajectory framework

Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications

Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test results

Genetics professionals’ experiences of facilitating parent/child communication through the genetic clinic

How to inform at‐risk relatives? Attitudes of 1379 Dutch patients, relatives, and members of the general population

Evaluation of an automated process for disclosure of negative noninvasive prenatal test results

A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing

Genetic testing preferences and intentions in patients with clinically diagnosed familial hypercholesterolemia

Much ado about nothing: A qualitative study of the experiences of an average‐risk population receiving results of exome sequencing

Genetic counselor and proxy patient perceptions of genetic counselor responses to prenatal patient self‐disclosure requests: Skillfulness is in the eye of the beholder

Familial implications of autoimmune disease: Recurrence risks of alopecia areata and associated conditions in first‐degree relatives

Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results

Access barriers to genetic services for Spanish‐speaking families in states with rapidly growing migrant populations

A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27

The impact of health anxiety on perceptions of personal and children’s health in parents with Lynch syndrome

Examining genetic counselors’ implicit attitudes toward disability

Genetic counselors with advanced skills: I. Refining a model of advanced training

Issue Highlights

User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia.

Recontact practices of cancer genetic counselors and an exploration of professional, legal, and ethical duty

Health professional and at‐risk BRCA young adult perspectives about information needs: What does Gen Y need to know?

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.

Lessons learned from testing cardiac channelopathy and cardiomyopathy genes in individuals who died suddenly: A two‐year prospective study in a large medical examiner’s office with an in‐house molecular genetics laboratory and genetic counseling services

Alternative option labeling impacts decision‐making in noninvasive prenatal screening

Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients

Defining the role of a genetic counselor within pediatric hematology and oncology comprehensive care teams: Perspectives of the provider team and patients