| Genetic Counselors’ Experience with Cell‐Free Fetal DNA Testing as a Prenatal Screening Option for Aneuploidy |
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| Perceived Risk Following Melanoma Genetic Testing: A 2‐Year Prospective Study Distinguishing Subjective Estimates from Recall |
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| Prevalence of the <i>HOXB13</i> G84E Mutation Among Unaffected Men with a Family History of Prostate Cancer |
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✓ |
African descent; non‐African; Hispanic |
| Factors Which Impact the Delivery of Genetic Risk Assessment Services Focused on Inherited Cancer Genomics: Expanding the Role and Reach of Certified Genetics Professionals |
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| Informing Children of Their Newborn Screening Carrier Result for Sickle Cell or Cystic Fibrosis: Qualitative Study of Parents’ Intentions, Views and Support Needs |
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| Diagnostic Exome Sequencing Identifies Two Novel <i>IQSEC2</i> Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis |
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| Public Trust in Genomic Risk Assessment for Type 2 Diabetes Mellitus |
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| Seeking Balance: Decision Support Needs of Women Without Cancer and a Deleterious <i>BRCA1</i> or <i>BRCA2</i> Mutation |
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| Three Clinical Experiences with SNP Array Results Consistent with Parental Incest: A Narrative with Lessons Learned |
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| Looking Back and Moving Forward: An Historical Perspective from Laboratory Genetic Counselors |
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| An Exploration of the Experience of Huntington's Disease in Family Dyads: An Interpretative Phenomenological Analysis |
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| MPS II: Adaptive Behavior of Patients and Impact on the Family System |
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| African American Women's Limited Knowledge and Experiences with Genetic Counseling for Hereditary Breast Cancer |
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✓ |
✓ |
African American |
| Classifying Married Adults Diagnosed With Alpha‐1 Antitrypsin Deficiency Based on Spousal Communication Patterns Using Latent Class Analysis: Insights for Intervention |
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| The Value of a Genetic Counselor: Improving Identification of Cancer Genetic Counseling Patients with Chart Review |
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| Models of Service Delivery for Cancer Genetic Risk Assessment and Counseling |
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| A Genetic Counselor's Guide to Using Next‐Generation Sequencing in Clinical Practice |
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| Predictive Genetic Testing in Children: Constitutional Mismatch Repair Deficiency Cancer Predisposing Syndrome |
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| An Immense New Power to Heal: The Promise of Personalized Medicine |
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| Disclosure Pattern and Follow‐Up After the Molecular Diagnosis of BRCA/CHEK2 Mutations |
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| Jennifer Wiggins and Anna Middleton (eds): Getting the Message Across: Communication with Diverse Populations in Clinical Genetics |
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| Introduction to the Special Issue on Genetic Counseling: A Global Perspective |
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| Genetic Counseling/Consultation in South‐East Asia: A Report from the Workshop at the 10th Asia Pacific Conference on Human Genetics |
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| Genetic Screening Services Provided in Turkey |
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| The Development of Genetic Counseling Services and Training Program in Saudi Arabia |
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| International Genetic Counseling Students’ Perspective on Their Training Experience in the United States |
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| Presented Abstracts from the Thirty Second Annual Education Conference of the National Society of Genetic Counselors (Anaheim, CA, October 2013) |
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| A Qualitative Study of Healthcare Providers’ Perspectives on the Implications of Genome‐Wide Testing in Pediatric Clinical Practice |
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| Identifying Outcomes of Clinical Genetic Services: Qualitative Evidence and Methodological Considerations |
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| The Establishment of Core Competencies for Canadian Genetic Counsellors: Validation of Practice Based Competencies |
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| Genomic Counseling: Next Generation Counseling |
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| Practical Aspects of Recruitment and Retention in Clinical Trials of Rare Genetic Diseases: The Phenylketonuria (PKU) Experience |
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| Acceptability of Telemedicine and Other Cancer Genetic Counseling Models of Service Delivery in Geographically Remote Settings |
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| Molecular Testing for Cystic Fibrosis Carrier Status Practice Guidelines: Recommendations of the National Society of Genetic Counselors |
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| From Constraints to Opportunities? Provision of Psychosocial Support in Portuguese Oncogenetic Counseling Services |
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| Predictive Genetic Testing of a Bone Marrow Recipient–Ethical Issues Involving Unexpected Results, Gender Issues, Test Accuracy, and Implications for the Donor |
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| Genetic Counselor Perceptions of Genetic Counseling Session Goals: A Validation Study of the Reciprocal‐Engagement Model |
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| The Current State of Genetic Counseling Before and After Amniocentesis for Fetal Karyotyping in Japan: A Survey of Obstetric Hospital Clients of a Prenatal Testing Laboratory |
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| Specific Psychosocial Issues of Individuals Undergoing Genetic Counseling for Cancer – A Literature Review |
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| Awareness of Genetic Counseling and Perceptions of its Purpose: A Survey of the Canadian Public |
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| Attitude of Medical School Students in China Towards Genetic Testing and Counseling Issues in FXS |
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| A Qualitative Inquiry of the Financial Concerns of Couples Opting to Use Preimplantation Genetic Diagnosis to Prevent the Transmission of Known Genetic Disorders |
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| Iceland—Genetic Counseling Services |
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| An Overview of Genetic Counseling in Cuba |
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| Alpha‐1 Couples: Interpersonal and Intrapersonal Predictors of Spousal Communication and Stress |
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| Erratum to: Changes in Specialists’ Perspectives on Cancer Genetic Testing, Prophylactic Surgery and Insurance Discrimination: Then and Now |
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| Psychosocial Burden of Sickle Cell Disease on Parents with an Affected Child in Cameroon |
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| Newborn Screening: Education, Consent, and the Residual Blood Spot. The Position of the National Society of Genetic Counselors |
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| Aspirin Use is Associated with Lower Prostate Cancer Risk in Male Carriers of BRCA Mutations |
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| Fabry Disease Practice Guidelines: Recommendations of the National Society of Genetic Counselors |
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| Changes in Specialists’ Perspectives on Cancer Genetic Testing, Prophylactic Surgery and Insurance Discrimination: Then and Now |
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| Stakeholders’ Opinions on the Implementation of Pediatric Whole Exome Sequencing: Implications for Informed Consent |
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| Consumer Preferences for the Predictive Genetic Test for Alzheimer Disease |
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| ‘Battling my Biology’: Psychological Effects of Genetic Testing for Risk of Weight Gain |
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| Peering into a Chilean Black Box: Parental Storytelling in Pediatric Genetic Counseling |
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| Large Normal and Intermediate Alleles in the Context of SCA2 Prenatal Diagnosis |
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| Young Adults’ Pre‐Existing Knowledge of Cystic Fibrosis and Sickle Cell Diseases: Implications for Newborn Screening |
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| 3‐Dimensional Ultrasound Assisted Counseling for Conjoined Twins |
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| Effects of a Genetic Counseling Model on Mothers of Children with Down Syndrome: A Brazilian Pilot Study |
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| Evaluation of a Heredofamilial Cancer Unit in Increasing Family History Collection and Genetic Counseling Referrals Among Spanish Oncologists at a University Hospital |
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| The Transnational Alliance for Genetic Counseling: Promoting International Communication and Collaboration |
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| Use of Genetic Tests among Neurologists and Psychiatrists: Knowledge, Attitudes, Behaviors, and Needs for Training |
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| Longitudinal Interviews of Couples Diagnosed with Diminished Ovarian Reserve Undergoing Fragile X Premutation Testing |
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| Perceived Versus Predicted Risks of Colorectal Cancer and Self‐Reported Colonoscopies by Members of Mismatch Repair Gene Mutation‐Carrying Families Who Have Declined Genetic Testing |
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| Knowledge of and Interest in Genetic Results Among Parkinson Disease Patients and Caregivers |
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| What's the Harm? Genetic Counselor Perceptions of Adverse Effects of Genetics Service Provision by Non‐Genetics Professionals |
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| Medical Genetics and Genetic Counseling in Chile |
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| Views of Genetics Health Professionals on the Return of Genomic Results |
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| Ethical and Professional Challenges of Genetic Counseling – the Case of Austria |
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| Expansion of Genetic Services Utilizing a General Genetic Counseling Clinic |
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| Roles of Genetic Counselors in South Africa |
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| NIPT in a Clinical Setting: An analysis of Uptake in the First Months of Clinical Availability |
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| Incidental Findings from Clinical Genome‐Wide Sequencing: A Review |
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| Stress and Well‐Being Among Parents of Children with Potocki‐Lupski Syndrome |
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| Two Decades of Huntington Disease Testing: Patient's Demographics and Reproductive Choices |
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| French Professionals in Genetic Counselor Careers |
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| “There's a Whole Different Way of Working with Adolescents”: Interviews with Australian Genetic Counselors About their Experiences with Adolescent Clients |
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| Exploring Culture‐Specific Differences in Beliefs about Causes, Kinship and the Heritability of Major Depressive Disorder: The Views of Anglo‐Celtic and Chinese‐Australians |
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✓ |
✓ |
Anglo‐Celtic‐Australians and Chinese‐Australians |
| Does a Duty of Disclosure Foster Special Treatment of Genetic Research Participants? |
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| Genetic Risk Assessment for Women with Epithelial Ovarian Cancer: Referral Patterns and Outcomes in a University Gynecologic Oncology Clinic |
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| Genetic Counseling: A Transnational Perspective |
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| Current Lynch Syndrome Tumor Screening Practices: A Survey of Genetic Counselors |
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| Family Communication of <i>BRCA1/2</i> Results and Family Uptake of <i>BRCA1/2</i> Testing in a Diverse Population of <i>BRCA1/2</i> Carriers |
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|
✓ |
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✓ |
✓ |
African American and Asian/Pacific Islander; racially and socioeconomically diverse |
| Genetic Counseling Services and Development of Training Programs in Malaysia |
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| More than 10 Years After the First ‘Savior Siblings’: Parental Experiences Surrounding Preimplantation Genetic Diagnosis |
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| Identification of Genetic Counseling Service Delivery Models in Practice: A Report from the NSGC Service Delivery Model Task Force |
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| The Decision to Continue a Pregnancy Affected by Down Syndrome: Timing of Decision and Satisfaction with Receiving a Prenatal Diagnosis |
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| A Review of Genetic Counseling for Charcot Marie Tooth Disease (CMT) |
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| “Nothing is Absolute in Life”: Understanding Uncertainty in the Context of Psychiatric Genetic Counseling from the Perspective of those with Serious Mental Illness |
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| Preimplantation Genetic Diagnosis: Understanding What Parents Plan to Tell Their Children About Their Conception |
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| Exploring the Perceptions and the Role of Genetic Counselors in the Emerging Field of Perinatal Palliative Care |
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| Development of Genetic Counseling Services in Taiwan |
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| A Closer Look at the Recommended Criteria for Disclosing Genetic Results: Perspectives of Medical Genetic Specialists, Genomic Researchers, and Institutional Review Board Chairs |
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| Effect of Direct‐to‐Consumer Genetic Tests on Health Behaviour and Anxiety: A Survey of Consumers and Potential Consumers |
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| Genetic Counseling Training in the Philippines |
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| The Views of Pakistani Doctors Regarding Genetic Counseling Services – Is there a Future? |
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| Receiving Enzyme Replacement Therapy for a Lysosomal Storage Disorder: A Preliminary Exploration of the Experiences of Young Patients and Their Families |
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| Erratum to: Effects of Second Language Usage on Genetic Counseling Training and Supervision |
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| Genetic Counseling Services and Training of Genetic Counselors in Israel: An Overview |
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| Educating Genetic Counselors in Australia—Developing a Masters Program |
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| Stem Cell Research and Therapy: The Position of the National Society of Genetic Counselors |
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| Deaf Genetic Testing and Psychological Well‐Being in Deaf Adults |
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| International Exchange Training in Genetic Counseling: An Exploration of the Value in Exchange Experiences |
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✓ |
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| Promoting Public Awareness and Engagement in Genome Sciences |
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| Non‐syndromic Sensorineural Prelingual Deafness: The Importance of Genetic Counseling in Demystifying Parents’ Beliefs About the Cause of Their Children's Deafness |
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| Provision of Genetics Services on Guam |
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| What Would You Say? Genetic Counseling Graduate Students’ and Counselors’ Hypothetical Responses to Patient Requested Self‐Disclosure |
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| Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors |
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| Delivering Genetic Education and Genetic Counseling for Rare Diseases in Rural Brazil |
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| Building the Genetic Counsellor Profession in the United Kingdom: Two Decades of Growth and Development |
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| Genetic Counseling Training and Certification in Australasia |
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| Comparison of the Screening Practices of Unaffected Noncarriers under 40 and between 40 and 49 in BRCA1/2 Families |
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| The Role of Religious and Existential Well‐being in Families with Lynch Syndrome: Prevention, Family Communication, and Psychosocial Adjustment |
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| Introduction |
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| What Counts as Effective Genetic Counselling for Presymptomatic Testing in Late‐Onset Disorders? A Study of the Consultand's Perspective |
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| A Mobile Colonoscopic Unit for Lynch Syndrome: Trends in Surveillance Uptake and Patient Experiences of Screening in a Developing Country |
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| How Do Partners Find out About the Risk of Huntington's Disease in Couple Relationships? |
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