| Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study |
41 |
| Alone in a Crowd? Parents of Children with Rare Diseases' Experiences of Navigating the Healthcare System |
17 |
| Genetic Counselors' Experiences and Interest in Telegenetics and Remote Counseling |
13 |
| Patient assessment of chatbots for the scalable delivery of genetic counseling |
12 |
| Review and Comparison of Electronic Patient-Facing Family Health History Tools |
12 |
| Secondary findings: How did we get here, and where are we going? |
9 |
| Development of FOCUS-GC: Framework for Outcomes of Clinical Communication Services in Genetic Counseling |
9 |
| Clinical models of telehealth in genetics: A regional telegenetics landscape |
9 |
| Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit |
8 |
| Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification |
8 |
| Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? |
8 |
| Blue Genes? Understanding and Mitigating Negative Consequences of Personalized Information about Genetic Risk for Depression |
8 |
| Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review |
8 |
| Patient perspectives on the process and outcomes of psychiatric genetic counseling: An Empowering Encounter |
7 |
| Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium |
7 |
| Impact of Appointment Waiting Time on Attendance Rates at a Clinical Cancer Genetics Service |
7 |
| Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies |
7 |
| Genetic counselor workflow study: The times are they a-changin'? |
7 |
| Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates |
6 |
| Patients' perspectives of variants of uncertain significance and strategies for uncertainty management |
6 |
| Bridge to the Literature? Third-Party Genetic Interpretation Tools and the Views of Tool Developers |
6 |
| Identifying Symptoms of Distress in Youth Living with Neurofibromatosis Type 1 (NF1) |
6 |
| Comparison of Telephone and Televideo Modes for Delivery of Genetic Counseling: a Randomized Trial |
6 |
| Mindfulness Among Genetic Counselors Is Associated with Increased Empathy and Work Engagement and Decreased Burnout and Compassion Fatigue |
6 |
| A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer-Related Germline Mutations |
6 |
| Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
6 |
| Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals |
6 |
| Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study |
6 |
| Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks |
6 |
| The Psychosocial Impact of Carrying a Debated Variant in the GLA Gene |
5 |
| The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease |
5 |
| Talking with Children About Adult-Onset Hereditary Cancer Risk: A Developmental Approach for Parents |
5 |
| Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era |
5 |
| Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census |
5 |
| Indigenous Peoples and genomics: Starting a conversation |
5 |
| Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics-Based Communities |
5 |
| Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing |
5 |
| Precision Medicine: Familiarity, Perceived Health Drivers, and Genetic Testing Considerations Across Health Literacy Levels in a Diverse Sample |
5 |
| Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges |
4 |
| Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions |
4 |
| Genetic counseling, 2030: An on-demand service tailored to the needs of a price conscious, genetically literate, and busy world |
4 |
| Relieving the Bottleneck: An Investigation of Barriers to Expansion of Supervision Networks at Genetic Counseling Training Programs |
4 |
| Cancer genetic counselors' experiences with transgender patients: A qualitative study |
4 |
| Trans-counseling: A case series of transgender individuals at high risk for BRCA1 pathogenic variants |
4 |
| Genesurance Counseling: Patient Perspectives |
4 |
| Uptake of Preimplantation Genetic Diagnosis in Female BRCA1 and BRCA2 Mutation Carriers |
4 |
| Patients' Views of Treatment-Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of BRCA1 and BRCA2 Testing |
4 |
| The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life |
4 |
| Patient decision-making and the role of the prenatal genetic counselor: An exploratory study |
4 |
| Parenting a Child with Phenylketonuria (PKU): an Interpretative Phenomenological Analysis (IPA) of the Experience of Parents |
4 |
