Journal of Genetic Counseling - 2017

138 articles | Last updated: 2025-12-03 14:12:57
Caucasian
0
White
3
European
0
Other
9
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
The Journal of Genetic Counseling: Continuing to Add Value to the Profession
Physicians’ Awareness and Utilization of Genetic Services in Texas
Genetic Counsellors and Private Practice: Professional Turbulence and Common Values
Managing Variant Interpretation Discrepancies in Hereditary Cancer: Clinical Practice, Concerns, and Desired Resources
An Evidence‐Based, Community‐Engaged Approach to Develop an Interactive Deliberation Tool for Pediatric Neuromuscular Trials
Bilingual Cancer Genetic Education Modules for the Deaf Community: Development and Evaluation of the Online Video Material
Investigation of the Use of a Family Health History Application in Genetic Counseling
Using Telemedicine in Mississippi to Improve Patient Access to Genetic Services
The Effect of Predictive Testing in Adult‐Onset Neurodegenerative Diseases on Social and Personal Life
Breast Cancer Genetics Knowledge and Testing Intentions among Nigerian Professional Women African populations; Nigerian
Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options
Evaluation of Breast Cancer Patients with Genetic Risk in a University Hospital: Before and After the Implementation of a Heredofamilial Cancer Unit
Comparison of Telephone and Televideo Modes for Delivery of Genetic Counseling: a Randomized Trial
Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies
Challenges, Dilemmas and Factors Involved in PGD Decision‐Making: Providers’ and Patients’ Views, Experiences and Decisions
Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team‐based Variant Classification
Development and Evaluation of a Telephone Communication Protocol for the Delivery of Personalized Melanoma Genomic Risk to the General Population
Implementing a Virtual Health Telemedicine Program in a Community Setting
Genesurance Counseling: Genetic Counselors’ Roles and Responsibilities in Regards to Genetic Insurance and Financial Topics
Tumor Screening in Beckwith‐Wiedemann Syndrome: Parental Perspectives
Impact of a Patient‐Facing Enhanced Genomic Results Report to Improve Understanding, Engagement, and Communication
High‐Risk Palliative Care Patients’ Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking
“Where Does it Come from?” Experiences Among Survivors and Parents of Children with Retinoblastoma in Kenya
Impact of Receiving Secondary Results from Genomic Research: A 12‐Month Longitudinal Study
Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks
“Yeah that Made a Big Difference!”: The Importance of the Relationship between Health Professionals and Fathers Who Have a Child with Down Syndrome
Clinician‐Stakeholders’ Perspectives on Using Patient Portals to Return Lynch Syndrome Screening Results
Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics‐Based Communities
Caregiver Quality of Life with Tyrosinemia Type 1
Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals
National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions
Parent Perspectives of Support Received from Physicians and/or Genetic Counselors Following a Decision to Continue a Pregnancy with a Prenatal Diagnosis of Trisomy 13/18
National Society of Genetic Counselors Code of Ethics
The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services
Women's Understanding and Attitudes towards Down Syndrome and Other Genetic Conditions in the Context of Prenatal Screening
Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study
Development of FOCUS‐GC: Framework for Outcomes of Clinical Communication Services in Genetic Counseling
Assessment of Current Genetic Counselor Practices in Post‐Visit Written Communications to Patients
Experiences of a High‐Risk Population with Prenatal Hemoglobinopathy Carrier Screening in a Primary Care Setting: a Qualitative Study
“My Plate is Full”: Reasons for Declining a Genetic Evaluation of Hearing Loss
Presented Abstracts from the Thirty Sixth Annual Conference of the National Society of Genetic Counselors (Columbus, OH, September 2017)
The Experience of Genetic Counselors Working with Patients Facing the Decision of Pregnancy Termination after 24 Weeks Gestation
Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At‐Risk Couples
Patients’ Opinions on Genetic Counseling on the Increased Risk of Parkinson Disease among Gaucher Disease Carriers
Psychosocial Distress and Knowledge Deficiencies in Parents of Children in Ireland Who Carry an Altered Cystic Fibrosis Gene
Evaluation of the Informational Content, Readability and Comprehensibility of Online Health Information on Monogenic Diabetes
Translation and Cross‐Cultural Adaptation with Preliminary Validation of GCOS‐24 for Use in Spain
Working with the Hmong Population in a Genetics Setting: an Interpreter Perspective Hmong
Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood
Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results
Perspectives of Women Considering Bilateral Prophylactic Mastectomy and their Peers towards a Telephone‐Based Peer Support Intervention
Referrals to Mental Health Services: Exploring the Referral Process in Genetic Counseling
Training to Provide Psychiatric Genetic Counseling: How Does It Impact Recent Graduates’ and Current Students’ Readiness to Provide Genetic Counseling for Individuals with Psychiatric Illness and Atti
Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention
Relieving the Bottleneck: An Investigation of Barriers to Expansion of Supervision Networks at Genetic Counseling Training Programs
Experiences of Genetic Counselors Practicing in Rural Areas
Physician Experiences and Understanding of Genomic Sequencing in Oncology
Counseling Close to Home: Genetic Counselors’ Experiences with their own Family Members
Attitudes of Individuals with Gaucher Disease toward Substrate Reduction Therapies
Psychosocial Needs and Facilitators of Mothers Caring for Children with Duchenne/Becker Muscular Dystrophy
The Psychosocial Impact of Carrying a Debated Variant in the GLA Gene
Online Module for Carrier Screening in Ashkenazi Jewish Individuals Compared with In‐Person Genetics Education: A Randomized Controlled Trial Ashkenazi Jewish
Cancer Counseling of Low‐Income Limited English Proficient Latina Women Using Medical Interpreters: Implications for Shared Decision‐Making
FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices
When to Consider Risk‐Reducing Mastectomy in <i>BRCA1/BRCA2</i> Mutation Carriers with Advanced Stage Ovarian Cancer: a Case Study Illustrating the Genetic Counseling Challenges
Blue Genes? Understanding and Mitigating Negative Consequences of Personalized Information about Genetic Risk for Depression
Cancer Genetic Counseling and Testing: Perspectives of Epithelial Ovarian Cancer Patients and Gynecologic Oncology Healthcare Providers
Identifying Symptoms of Distress in Youth Living with Neurofibromatosis Type 1 (NF1)
Patients’ Knowledge of Prenatal Screening for Trisomy 21
Variation among Consent Forms for Clinical Whole Exome Sequencing
Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy
A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia
Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
Working with the Hmong Population in a Genetics Setting: Genetic Counselor Perspectives Hmong ancestry; Hmong patients; Hmong individuals
Is Low <i>FMR1</i> CGG Repeat Length in Males Correlated with Family History of <i>BRCA</i>‐Associated Cancers? An Exploratory Analysis of Medical Records
Family Communication, Risk Perception and Cancer Knowledge of Young Adults from <i>BRCA1/2</i> Families: a Systematic Review
Impairment Experiences, Identity and Attitudes Towards Genetic Screening: the Views of People with Spinal Muscular Atrophy
Women's Experience with Non‐Invasive Prenatal Testing and Emotional Well‐being and Satisfaction after Test‐Results
Connecting Gaucher and Parkinson Disease: Considerations for Clinical and Research Genetic Counseling Settings
Elaboration of the Reciprocal‐Engagement Model of Genetic Counseling Practice: a Qualitative Investigation of Goals and Strategies
The Efficacy of Genetic Counseling for Psychiatric Disorders: a Meta‐Analysis
Invasive Prenatal Diagnostic Testing Recommendations are Influenced by Maternal Age, Statistical Misconception and Perceived Liability
“If It Helps, It's Worth a Try”: an Investigation of Perceptions and Attitudes about Genetic Counseling among Southern Manitoba Hutterites
The Genetics Journey: A Case Report of a Genetic Diagnosis Made 30 Years Later
Perspectives and Practices of Athletic Trainers and Team Physicians Implementing the 2010 NCAA Sickle Cell Trait Screening Policy race and ancestry
Universal <i>BRCA1/BRCA2</i> Testing for Ovarian Cancer Patients is Welcomed, but with Care: How Women and Staff Contextualize Experiences of Expanded Access
Anxiety and Hereditary Testing Results
Pediatric Predispositional Genetic Risk Communication: Potential Utility for Prevention and Control of Melanoma Risk as an Exemplar
“It was a lot Tougher than I Thought It would be”. A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier
Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome
Response to Dr. Sorscher
Utilization of Genetic Counseling after Direct‐to‐Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study
Erratum to: At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease
An Exploration of Genetic Test Utilization, Genetic Counseling, and Consanguinity within the Inborn Errors of Metabolism Collaborative (IBEMC)
A Qualitative Look into Israeli Genetic Experts’ Insights Regarding Culturally Competent Genetic Counseling and Recommendations for Its Enhancement
Cancer Genetic Counseling and Testing in an Era of Rapid Change
Development of a Streamlined Work Flow for Handling Patients’ Genetic Testing Insurance Authorizations
Erratum to: Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients
Erratum to: A Qualitative Study to Explore the Views and Attitudes towards Prenatal Testing in Adults who Have Muenke Syndrome and their Partners
Influence of Genetic Counseling Graduate Program Websites on Student Application Decisions
Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI‐GENES) Randomized Clinical Trial
Insights into <i>BRCA1/2</i> Genetic Counseling from Ethnically Diverse Latina Breast Cancer Survivors
Prospective Evaluation of Predictive DNA Testing for Huntington's Disease in a Large German Center
A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes
Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice
Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients black or African American race, Hispanic origin
Genetic Counselors’ Perception of the Effect on Practice of Laws Restricting Abortion
Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports
A Qualitative Study to Explore the Views and Attitudes towards Prenatal Testing in Adults Who Have Muenke Syndrome and their Partners
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 Context of BRCA Italian women
Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing
Seekers, Finders, Settlers, and Stumblers: Identifying the Career Paths of Males in the Genetic Counseling Profession
Should Genetic Testing be Offered for Children? The Perspectives of Adolescents and Emerging Adults in Families with Li‐Fraumeni Syndrome
Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients
At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease
Risk Perception and Psychological Distress in Genetic Counselling for Hereditary Breast and/or Ovarian Cancer
Using Patient‐Reported Outcome Measures for Quality Improvement in Clinical Genetics: an Exploratory Study
Special Issue Introduction: Dealing with Psychological and Social Complexity in Genetic Counseling
Translation and Adaptation of the Genetic Counselling Outcome Scale (GCOS‐24) for Use in Denmark
Performing and Declining PGD: Accounts of Jewish Israeli Women Who Carry a <i>BRCA1/2</i> Mutation or Partners of Male Mutation Carriers Jewish Israeli; Ashkenazi founder mutations
Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States Asian; Southeast and East Asian; Asian population; Asian women; Asian patients
A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling
Genetic Counseling Dilemmas for a Patient with Sporadic Amyotrophic Lateral Sclerosis, Frontotemporal Degeneration &amp; Parkinson's Disease
Standards for the Reporting of Genetic Counseling Interventions in Research and Other Studies (GCIRS): an NSGC Task Force Report
Experiences of Pre‐Implantation Genetic Diagnosis (PGD) in Sweden: a Three‐Year Follow‐Up of Men and Women
Analysis of Reimbursement of Genetic Counseling Services at a Single Institution in a State Requiring Licensure
A Rapid Systematic Review of Outcomes Studies in Genetic Counseling
Genetic Counseling for Alcohol Addiction: Assessing Perceptions and Potential Utility in Individuals with Lived Experience and Their Family Members
“They Just Want to Know” ‐ Genetic Health Professionals' Beliefs About Why Parents Want to Know their Child's Carrier Status
“It was an Emotional Baby”: Previvors’ Family Planning Decision‐Making Styles about Hereditary Breast and Ovarian Cancer Risk
Commentary: “My Identical Twin Sequenced Our Genome”
Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance
Breast Cancer Risk Assessment at the Time of Screening Mammography: Perceptions and Clinical Management Outcomes for Women at High Risk
Prevalence and Characteristics of Patients with Suspected Inherited Renal Cell Cancer: Application of the ACMG/NSGC Genetic Referral Guidelines to Patient Cohorts
Thank You to Reviewers
Large, Prospective Analysis of the Reasons Patients Do Not Pursue <i>BRCA</i> Genetic Testing Following Genetic Counseling
Cancer Genetic Counselors’ Current Practices and Attitudes Related to the Use of Tumor Profiling
Characterizing Clinical Genetic Counselors’ Countertransference Experiences: an Exploratory Study