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