Journal of Genetic Counseling - 2018

109 articles | Last updated: 2025-12-03 14:12:57
Caucasian
1
White
1
European
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Other
9
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners
Genetic counselor workflow study: The times are they a‐changin’?
Whole exome sequencing for prenatal diagnosis in cases with fetal anomalies: Criteria to improve diagnostic yield
Patient decision‐making and the role of the prenatal genetic counselor: An exploratory study
Indigenous Peoples and genomics: Starting a conversation 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
Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making
Genetic counseling considerations with rapid genome‐wide sequencing in a neonatal intensive care unit
Patient goals, motivations, and attitudes in a patient‐driven variant reclassification study
Issue Highlights
Evolving Decisions: Perspectives of Active and Athletic Individuals with Inherited Heart Disease Who Exercise Against Recommendations
Interpretations of the Term “Actionable” when Discussing Genetic Test Results: What you Mean Is Not What I Heard
User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia diverse ethnic and backgrounds
The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation
Relation Between Religious Perspectives and Views on Sickle Cell Disease Research and Associated Public Health Interventions in Ghana
Issue Highlights
Alone in a Crowd? Parents of Children with Rare Diseases’ Experiences of Navigating the Healthcare System
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
Undergraduate Student Perceptions and Awareness of Genetic Counseling Asian and Hispanic ethnicity
All Along the Watchtower: a Case of Long QT Syndrome Misdiagnosis Secondary to Genetic Testing Misinterpretation
Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study
Assessing Shared Decision‐Making Clinical Behaviors Among Genetic Counsellors
Risk Communication in Families of Children with Familial Hypercholesterolemia: Identifying Motivators and Barriers to Cascade Screening to Improve Diagnosis at a Single Medical Center European countries
Precision Medicine: Familiarity, Perceived Health Drivers, and Genetic Testing Considerations Across Health Literacy Levels in a Diverse Sample
Effects of Genetic Counselor Self‐Disclosure: an Experimental Analog Study
Letter to the Editor: Response to Cox (2018)
Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions
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
Correction to: Talking with Children about Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents
Adrenal Insufficiency in Young Children: a Mixed Methods Study of Parents’ Experiences
Experiences of Women Who Have Had Carrier Testing for Duchenne Muscular Dystrophy and Becker Muscular Dystrophy During Adolescence
“I Am Uncertain About What My Uncertainty Even Is”: Men's Uncertainty and Information Management of Their BRCA‐Related Cancer Risks
Response to Costa, Lemos, and Paneque Letter to the Editor
Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease
Issue Highlights
Genetic Counselors’ Perspectives About Cell‐Free DNA: Experiences, Challenges, and Expectations for Obstetricians
Utilization of Genetic Testing for <i>RET</i> Mutations in Patients with Medullary Thyroid Carcinoma: a Single‐Center Experience
Training Methods for Delivering Difficult News in Genetic Counseling and Genetics Residency Training Programs
Cancer Susceptibility Genetic Testing in a High‐Risk Cohort of Urban Ashkenazi Jewish Individuals Ashkenazi Jewish (AJ)
The Contribution of the Reciprocal‐Engagement Model as a Theoretical Framework of a Portuguese Scale for Quality Assessment of Genetic Counseling
The Relationship Between the Supervisory Working Alliance and Student Self‐Efficacy in Genetic Counseling Training
Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization
Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study
The Influence of Adolescence on Parents’ Perspectives of Testing and Discussing Inherited Cancer Predisposition
Uptake of Preimplantation Genetic Diagnosis in Female BRCA1 and BRCA2 Mutation Carriers
Impact of Appointment Waiting Time on Attendance Rates at a Clinical Cancer Genetics Service
Creation and Implementation of an Environmental Scan to Assess Cancer Genetics Services at Three Oncology Care Settings
Patients’ Views of Treatment‐Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of <i>BRCA1</i> and <i>BRCA2</i> Testing
Message from the Editor‐in‐Chief
Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings
What to Do with a Second Chance in Life? Long‐Term Experiences of Non‐carriers of Huntington's Disease
Commentary on “Commercial Genetic Testing and the Future of the Genetic Counseling Profession”
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
Adopted Individuals’ Views on the Utility and Value of Expanded Carrier Screening
Identifying Factors Underlying the Decision for Sickle Cell Carrier Screening Among African Americans Within Middle Reproductive Age African Americans
Response to Commercial Genetic Testing and the Future of the Genetic Counseling Profession
Managing Couple Conflict During Prenatal Counseling Sessions: An Investigation of Genetic Counselor Experiences and Perceptions
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
Talking Points: Women's Information Needs for Informed Decision‐Making About Noninvasive Prenatal Testing for Down Syndrome
Development and Validation of the Genetic Counseling Self‐Efficacy Scale (GCSES)
The Process of Disclosure: Mothers’ Experiences of Communicating X‐Linked Carrier Risk Information to At‐Risk Daughters
Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting
Attitudes Toward and Uptake of Prenatal Genetic Screening and Testing in Twin Pregnancies
A Commentary on Opportunities for the Genetic Counseling Profession through Genomic Variant Interpretation: Reflections from an Ex‐Lab Rat
A Commentary on Commercial Genetic Testing and the Future of the Genetic Counseling Profession
Mindfulness Among Genetic Counselors Is Associated with Increased Empathy and Work Engagement and Decreased Burnout and Compassion Fatigue
Informed Decision‐Making in the Context of Prenatal Chromosomal Microarray
Pregnant Genetic Counselors in an Era of Advanced Genomic Tests: What Do the Experts Test Prenatally?
Review and Comparison of Electronic Patient‐Facing Family Health History Tools
Movement of Genetic Counselors from Clinical to Non‐clinical Positions: Identifying Driving Forces
A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer‐Related Germline Mutations
Parkinson's Disease: Patients’ Knowledge, Attitudes, and Interest in Genetic Counseling
Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium
Introduction to the “Technology in Practice” Special Issue
Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review
Pregnant Women's Perspectives on Expanded Carrier Screening 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
The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease
Psychosocial Impact of a Positive Gene Result for Asymptomatic Relatives at Risk of Hypertrophic Cardiomyopathy
Parenting a Child with Phenylketonuria (PKU): an Interpretative Phenomenological Analysis (IPA) of the Experience of Parents
Development and Pilot Testing of a Decision Aid for Genomic Research Participants Notified of Clinically Actionable Research Findings for Cancer Risk
Comparison of Practice Guidelines, BRCAPRO, and Genetic Counselor Estimates to Identify Germline <i>BRCA1</i> and <i>BRCA2</i> Mutations in Pancreatic Cancer
Pediatric and Adult Recommendations Vary for Sibling Testing in Cystic Fibrosis
An iPhone Application Intervention to Promote Surveillance Among Women with a <i>BRCA</i> Mutation: Pre‐intervention Data
Health Survey of Adults with Neurofibromatosis 1 Compared to Population Study Controls
Reduction of Health Care Costs and Improved Appropriateness of Incoming Test Orders: the Impact of Genetic Counselor Review in an Academic Genetic Testing Laboratory
“Bridge to the Literature”? Third‐Party Genetic Interpretation Tools and the Views of Tool Developers
Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing
Perceived Changes to Obstetric Care and the Integration of Personal and Professional Life as a Pregnant Prenatal Genetic Counselor
A Two‐Phase Approach to Developing SNAP: an iPhone Application to Support Appointment Scheduling and Management for Women with a <i>BRCA</i> Mutation
“Second‐Class Status?” Insight into Communication Patterns and Common Concerns Among Men with Hereditary Breast and Ovarian Cancer Syndrome 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 indigenous ancestry
The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor's Perspective
Children's at Home: Pilot Study Assessing Dedicated Social Media for Parents of Adolescents with Neurofibromatosis Type 1
Talking with Children About Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents
How Might the Genetics Profession Better Utilize Social Media
Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists
Utilization of the Tablet Application Proband in Pedigree Construction and Assessment
Investigating Pregnancy Outcomes After Abnormal Cell‐Free DNA Test Results
Genetic Counseling in the Era of Genomics: What's all the Fuss about?
Genetic Counselors’ Experiences and Interest in Telegenetics and Remote Counseling
Genetic Test Reporting and Counseling for Melanoma Risk in Minors May Improve Sun Protection Without Inducing Distress
Genesurance Counseling: Patient Perspectives African Americans; Hispanics
Identification as a Mutation Carrier and Effects on Life According to Experiences of Finnish Male BRCA1/2 Mutation Carriers Finnish
Have You Ever Googled a Patient or Been Friended by a Patient? Social Media Intersects the Practice of Genetic Counseling
Thank You to Reviewers
2018 National Society of Genetic Counselors Presidential Address
Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?