| Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners |
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| Genetic counselor workflow study: The times are they a‐changin’? |
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| Whole exome sequencing for prenatal diagnosis in cases with fetal anomalies: Criteria to improve diagnostic yield |
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| Patient decision‐making and the role of the prenatal genetic counselor: An exploratory study |
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| Indigenous Peoples and genomics: Starting a conversation |
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Compared to European ancestral groups |
| <i>“I didn’t take it too seriously because I’d just never heard of it”:</i> Experiential knowledge and genetic screening for thalassaemia in the UK |
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| Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making |
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| Genetic counseling considerations with rapid genome‐wide sequencing in a neonatal intensive care unit |
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| Patient goals, motivations, and attitudes in a patient‐driven variant reclassification study |
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| Issue Highlights |
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| Evolving Decisions: Perspectives of Active and Athletic Individuals with Inherited Heart Disease Who Exercise Against Recommendations |
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| Interpretations of the Term “Actionable” when Discussing Genetic Test Results: What you Mean Is Not What I Heard |
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| User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia |
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diverse ethnic and backgrounds |
| The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation |
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| Relation Between Religious Perspectives and Views on Sickle Cell Disease Research and Associated Public Health Interventions in Ghana |
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| Issue Highlights |
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| Alone in a Crowd? Parents of Children with Rare Diseases’ Experiences of Navigating the Healthcare System |
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| Practice Variation among an International Group of Genetic Counselors on when to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy |
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| Undergraduate Student Perceptions and Awareness of Genetic Counseling |
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Asian and Hispanic ethnicity |
| All Along the Watchtower: a Case of Long QT Syndrome Misdiagnosis Secondary to Genetic Testing Misinterpretation |
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| Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study |
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| Assessing Shared Decision‐Making Clinical Behaviors Among Genetic Counsellors |
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| Risk Communication in Families of Children with Familial Hypercholesterolemia: Identifying Motivators and Barriers to Cascade Screening to Improve Diagnosis at a Single Medical Center |
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European countries |
| Precision Medicine: Familiarity, Perceived Health Drivers, and Genetic Testing Considerations Across Health Literacy Levels in a Diverse Sample |
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| Effects of Genetic Counselor Self‐Disclosure: an Experimental Analog Study |
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| Letter to the Editor: Response to Cox (2018) |
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| Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions |
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| Response to “A Psychological Perspective on Factors Predicting Prophylactic Salpingo‐Oophorectomy in a Sample of Italian Women from the General Population. Results from a Hypothetical Study in the Con |
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| Correction to: Talking with Children about Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents |
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| Adrenal Insufficiency in Young Children: a Mixed Methods Study of Parents’ Experiences |
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| Experiences of Women Who Have Had Carrier Testing for Duchenne Muscular Dystrophy and Becker Muscular Dystrophy During Adolescence |
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| “I Am Uncertain About What My Uncertainty Even Is”: Men's Uncertainty and Information Management of Their BRCA‐Related Cancer Risks |
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| Response to Costa, Lemos, and Paneque Letter to the Editor |
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| Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease |
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| Issue Highlights |
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| Genetic Counselors’ Perspectives About Cell‐Free DNA: Experiences, Challenges, and Expectations for Obstetricians |
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| Utilization of Genetic Testing for <i>RET</i> Mutations in Patients with Medullary Thyroid Carcinoma: a Single‐Center Experience |
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| Training Methods for Delivering Difficult News in Genetic Counseling and Genetics Residency Training Programs |
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| Cancer Susceptibility Genetic Testing in a High‐Risk Cohort of Urban Ashkenazi Jewish Individuals |
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Ashkenazi Jewish (AJ) |
| The Contribution of the Reciprocal‐Engagement Model as a Theoretical Framework of a Portuguese Scale for Quality Assessment of Genetic Counseling |
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| The Relationship Between the Supervisory Working Alliance and Student Self‐Efficacy in Genetic Counseling Training |
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| Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization |
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| Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study |
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| The Influence of Adolescence on Parents’ Perspectives of Testing and Discussing Inherited Cancer Predisposition |
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| Uptake of Preimplantation Genetic Diagnosis in Female BRCA1 and BRCA2 Mutation Carriers |
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| Impact of Appointment Waiting Time on Attendance Rates at a Clinical Cancer Genetics Service |
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| Creation and Implementation of an Environmental Scan to Assess Cancer Genetics Services at Three Oncology Care Settings |
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| Patients’ Views of Treatment‐Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of <i>BRCA1</i> and <i>BRCA2</i> Testing |
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| Message from the Editor‐in‐Chief |
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| Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings |
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| What to Do with a Second Chance in Life? Long‐Term Experiences of Non‐carriers of Huntington's Disease |
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| Commentary on “Commercial Genetic Testing and the Future of the Genetic Counseling Profession” |
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| Involvement and Influence of Healthcare Providers, Family Members, and Other Mutation Carriers in the Cancer Risk Management Decision‐Making Process of <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers |
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| Adopted Individuals’ Views on the Utility and Value of Expanded Carrier Screening |
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| Identifying Factors Underlying the Decision for Sickle Cell Carrier Screening Among African Americans Within Middle Reproductive Age |
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African Americans |
| Response to Commercial Genetic Testing and the Future of the Genetic Counseling Profession |
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| Managing Couple Conflict During Prenatal Counseling Sessions: An Investigation of Genetic Counselor Experiences and Perceptions |
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| Factors Influencing Clinical Follow‐Up for Individuals with a Personal History of Breast and/or Ovarian Cancer and Previous Uninformative <i>BRCA1</i> and <i>BRCA2</i> Testing |
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| Talking Points: Women's Information Needs for Informed Decision‐Making About Noninvasive Prenatal Testing for Down Syndrome |
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| Development and Validation of the Genetic Counseling Self‐Efficacy Scale (GCSES) |
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| The Process of Disclosure: Mothers’ Experiences of Communicating X‐Linked Carrier Risk Information to At‐Risk Daughters |
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| Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting |
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| Attitudes Toward and Uptake of Prenatal Genetic Screening and Testing in Twin Pregnancies |
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| A Commentary on Opportunities for the Genetic Counseling Profession through Genomic Variant Interpretation: Reflections from an Ex‐Lab Rat |
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| A Commentary on Commercial Genetic Testing and the Future of the Genetic Counseling Profession |
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| Mindfulness Among Genetic Counselors Is Associated with Increased Empathy and Work Engagement and Decreased Burnout and Compassion Fatigue |
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| Informed Decision‐Making in the Context of Prenatal Chromosomal Microarray |
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| Pregnant Genetic Counselors in an Era of Advanced Genomic Tests: What Do the Experts Test Prenatally? |
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| Review and Comparison of Electronic Patient‐Facing Family Health History Tools |
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| Movement of Genetic Counselors from Clinical to Non‐clinical Positions: Identifying Driving Forces |
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| A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer‐Related Germline Mutations |
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| Parkinson's Disease: Patients’ Knowledge, Attitudes, and Interest in Genetic Counseling |
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| Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network |
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| Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium |
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| Introduction to the “Technology in Practice” Special Issue |
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| Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review |
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| Pregnant Women's Perspectives on Expanded Carrier Screening |
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ethnicity; ethnicity-based carrier screening |
| Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing |
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| The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease |
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| Psychosocial Impact of a Positive Gene Result for Asymptomatic Relatives at Risk of Hypertrophic Cardiomyopathy |
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| Parenting a Child with Phenylketonuria (PKU): an Interpretative Phenomenological Analysis (IPA) of the Experience of Parents |
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| Development and Pilot Testing of a Decision Aid for Genomic Research Participants Notified of Clinically Actionable Research Findings for Cancer Risk |
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| Comparison of Practice Guidelines, BRCAPRO, and Genetic Counselor Estimates to Identify Germline <i>BRCA1</i> and <i>BRCA2</i> Mutations in Pancreatic Cancer |
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| Pediatric and Adult Recommendations Vary for Sibling Testing in Cystic Fibrosis |
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| An iPhone Application Intervention to Promote Surveillance Among Women with a <i>BRCA</i> Mutation: Pre‐intervention Data |
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| Health Survey of Adults with Neurofibromatosis 1 Compared to Population Study Controls |
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| Reduction of Health Care Costs and Improved Appropriateness of Incoming Test Orders: the Impact of Genetic Counselor Review in an Academic Genetic Testing Laboratory |
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| “Bridge to the Literature”? Third‐Party Genetic Interpretation Tools and the Views of Tool Developers |
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| Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing |
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| Perceived Changes to Obstetric Care and the Integration of Personal and Professional Life as a Pregnant Prenatal Genetic Counselor |
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| A Two‐Phase Approach to Developing SNAP: an iPhone Application to Support Appointment Scheduling and Management for Women with a <i>BRCA</i> Mutation |
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| “Second‐Class Status?” Insight into Communication Patterns and Common Concerns Among Men with Hereditary Breast and Ovarian Cancer Syndrome |
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Ashkenazi Jewish |
| Identifying and Addressing Genetic Counseling Challenges among Indigenous People of Oaxaca—One Center's Experience with Two Immigrant Farmworker Families in the Central Valley of California |
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indigenous ancestry |
| The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor's Perspective |
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| Children's at Home: Pilot Study Assessing Dedicated Social Media for Parents of Adolescents with Neurofibromatosis Type 1 |
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| Talking with Children About Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents |
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| How Might the Genetics Profession Better Utilize Social Media |
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| Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists |
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| Utilization of the Tablet Application Proband in Pedigree Construction and Assessment |
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| Investigating Pregnancy Outcomes After Abnormal Cell‐Free DNA Test Results |
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| Genetic Counseling in the Era of Genomics: What's all the Fuss about? |
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| Genetic Counselors’ Experiences and Interest in Telegenetics and Remote Counseling |
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| Genetic Test Reporting and Counseling for Melanoma Risk in Minors May Improve Sun Protection Without Inducing Distress |
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| Genesurance Counseling: Patient Perspectives |
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African Americans; Hispanics |
| Identification as a Mutation Carrier and Effects on Life According to Experiences of Finnish Male BRCA1/2 Mutation Carriers |
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Finnish |
| Have You Ever Googled a Patient or Been Friended by a Patient? Social Media Intersects the Practice of Genetic Counseling |
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| Thank You to Reviewers |
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| 2018 National Society of Genetic Counselors Presidential Address |
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| Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? |
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