| Genetic Information‐Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes |
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| Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome |
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| Erratum to: How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing? |
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| Reviewing Manuscripts for the Journal of Genetic Counseling: Practical Suggestions |
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| Genetic Counselors and Health Literacy: The Role of Genetic Counselors in Developing a Web‐Based Resource About the Affordable Care Act |
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| The Long and Short of Genetic Counseling Summary Letters: A Case–control Study |
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| Creation of a National, At‐home Model for Ashkenazi Jewish Carrier Screening |
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✓ |
✓ |
Ashkenazi Jewish; Jewish |
| Personalized Medicine Through SNP Testing for Breast Cancer Risk: Clinical Implementation |
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| How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing? |
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| Public Health Genetic Counselors: Activities, Skills, and Sources of Learning |
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| Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice |
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| Perceptions of Latinas on the Traditional Prenatal Genetic Counseling Model |
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| 2015 NSGC Presidential Address: Gifts of Genetic Counselors: Life's Leadership Lessons |
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| Storage and use of Newborn Screening Blood Specimens for Research: Assessing Public Opinion in Illinois |
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✓ |
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| Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling |
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| Congruence‐Incongruence Patterns in Alpha‐1 Antitrypsin Deficiency Couples’ Genetic Determinist Beliefs and Perceived Control over Genes: Implications for Clinical and Public Health Genomic Communicat |
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| A Genetic Lung Cancer Susceptibility Test may have a Positive Effect on Smoking Cessation |
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| Adults with Chromosome 18 Abnormalities |
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| Congenital Hypothyroidism Long‐Term Follow‐up Project: Navigating the Rough Waters of a Multi‐Center, Multi‐State Public Health Project |
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| Education and Parental Involvement in Decision‐Making About Newborn Screening: Understanding Goals to Clarify Content |
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| Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice? |
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| Ethical and Professional Challenges Encountered by Laboratory Genetic Counselors |
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| Health‐Related Quality of Life in Patients with MPS II |
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| Case Report: Concurrent Wilson Disease and Huntington Disease: Lightning Can Strike Twice |
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| Presented Abstracts from the Thirty Third Annual Education Conference of the National Society of Genetic Counselors (New Orleans, LA, September 2014) |
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| Genetics Health Professionals’ Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late‐Onset Neurological Diseases in Portugal: Core Components, Specific Challenges |
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| Ethical Considerations in Biobanks: How a Public Health Ethics Perspective Sheds New Light on Old Controversies |
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| Genetic Counseling for Indigenous Australians: an Exploratory Study from the Perspective of Genetic Health Professionals |
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| Genetics Professionals’ Opinions of Whole‐Genome Sequencing in the Newborn Period |
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| Genetic Counselors’ and Genetic Counseling Students’ Attitudes Around the Clinical Doctorate and Other Advanced Educational Options for Genetic Counselors: A Report from the Genetic Counseling Advance |
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| Applying Public Health Screening Criteria: How Does Universal Newborn Screening Compare to Universal Tumor Screening for Lynch Syndrome in Adults with Colorectal Cancer? |
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| Non‐Invasive Prenatal Testing: UK Genetic Counselors’ Experiences and Perspectives |
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| Family Communication in a Population at Risk for Hypertrophic Cardiomyopathy |
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| Perceptions and Attitudes About Genetic Counseling Among Residents of a Midwestern Rural Area |
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| Reduced Uptake of Family Screening in Genotype‐Negative Versus Genotype‐Positive Long QT Syndrome |
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| A Qualitative Evaluation of the Psychosocial Impact of Family History Screening in Australian Primary Care |
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| Patient Expectations and Attitudes Towards Specialist Genetic Eye Services |
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| “Is it Going to Hurt?”: The Impact of the Diagnostic Odyssey on Children and Their Families |
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| Public Awareness of Genetic Nondiscrimination Laws in Four States and Perceived Importance of Life Insurance Protections |
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| Genetic Counseling for Fanconi Anemia: Crosslinking Disciplines |
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| Assessment of Parental Understanding of Positive Newborn Screening Results and Carrier Status for Cystic Fibrosis with the use of a Short Educational Video |
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| The Psychological Impact of Predictive Genetic Testing for Huntington′s Disease: A Systematic Review of the Literature |
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| Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman |
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| Creation of a Network to Promote Universal Screening for Lynch Syndrome: The Lynch Syndrome Screening Network |
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| Influence of Anchoring on Miscarriage Risk Perception Associated with Amniocentesis |
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| Increasing Participation in Genomic Research and Biobanking Through Community‐Based Capacity Building |
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| Informed Consent Form Challenges for Genetic Research in a Developing Arab Country with High Risk for Genetic Disease |
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| Evaluation of Patient Education Materials: The Example of Circulating cell free DNA Testing for Aneuploidy |
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| American BRCA Outcomes and Utilization of Testing (ABOUT) Study: A Pragmatic Research Model that Incorporates Personalized Medicine/Patient‐Centered Outcomes in a Real World Setting |
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| Using Formative Research to Develop a Counselor Training Program for Newborn Screening in Ghana |
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| To Reflex or Not: Additional BRCA1/2 Testing in Ashkenazi Jewish Individuals Without Founder Mutations |
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✓ |
✓ |
Ashkenazi Jewish |
| “She Came out of mum's Tummy the Wrong way” (Mis) Conceptions Among Siblings of Children with Rare Disorders |
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| “How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies |
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| Erratum to: The Impact of Supervision Training on Genetic Counselor Supervisory Identity Development |
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| Exploring Barriers to Payer Utilization of Genetic Counselors |
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| The Utilization of Counseling Skills by the Laboratory Genetic Counselor |
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| Interest in Genetic Testing in Ashkenazi Jewish Parkinson's Disease Patients and Their Unaffected Relatives |
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✓ |
✓ |
Ashkenazi Jewish (AJ) |
| BRCA Genetic Counseling Among At‐Risk Latinas in New York City: New Beliefs Shape New Generation |
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| Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients |
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| A Pilot Study of <i>BRCA</i> Mutation Carriers’ Knowledge About the Clinical Impact of Prophylactic‐oophorectomy and Views on Fertility Consultation: A Single‐Center Pilot Study |
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✓ |
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| Use of a Patient‐Entered Family Health History Tool with Decision Support in Primary Care: Impact of Identification of Increased Risk Patients on Genetic Counseling Attendance |
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| Mothers’ Experiences of Genetic Counselling in Johannesburg, South Africa |
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| Understanding the Experience of Myotonic Dystrophy. Mixed Method Study |
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| Parental Decisions Following Prenatal Diagnosis of Chromosomal Abnormalities: Implications for Genetic Counseling Practice in Japan |
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| Genetic Information, Non‐Discrimination, and Privacy Protections in Genetic Counseling Practice |
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| Assessing Deaf Awareness Training: Knowledge and Attitudes of Recent Genetic Counseling Graduates |
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| Commentary on “Conceptualizing Genetic Counseling as Psychotherapy in the era of Genomic Medicine” |
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| “We Don't Know Her History, Her Background”: Adoptive Parents’ Perspectives on Whole Genome Sequencing Results |
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✓ |
✓ |
ancestry / "biological family health history and ancestry" |
| A Survey of Genetic Counselors About the Needs of 18–25 Year Olds from Families with Hereditary Breast and Ovarian Cancer Syndrome |
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| Disparities in Current and Future Childhood and Newborn Carrier Identification |
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| An Assessment of Genetic Counseling Services for Individuals with Multiple Sclerosis |
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| Making the Decision to Participate in Predictive Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy |
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| Promoting Meaning‐Making to Help our Patients Grieve: An Exemplar for Genetic Counselors and Other Health Care Professionals |
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| Genetic Counseling in Direct‐to‐Consumer Exome Sequencing: A Case Report |
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| Information‐Seeking and Sharing Behavior Following Genomic Testing for Diabetes Risk |
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| An Internal Performance Assessment of CancerGene Connect: An Electronic Tool to Streamline, Measure and Improve the Genetic Counseling Process |
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✓ |
✓ |
racial and ethnic groups |
| Conceptualizing Genetic Counseling as Psychotherapy in the Era of Genomic Medicine |
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| The Impact of Supervision Training on Genetic Counselor Supervisory Identity Development |
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| Next Generation Genetic Counseling: Introduction to the Special Issue |
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| Cost Sharing and Hereditary Cancer Risk: Predictors of Willingness‐to‐Pay for Genetic Testing |
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| Attitudes Towards Potentially Carrying the FMR1 Premutation: Before vs After Testing of Non‐Carrier Females with Diminished Ovarian Reserve |
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| Barriers Impacting the Utilization of Supervision Techniques in Genetic Counseling |
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| Client Views and Attitudes to Non‐Invasive Prenatal Diagnosis for Sickle Cell Disease, Thalassaemia and Cystic Fibrosis |
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| It is Time: A Commentary on “An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing” |
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| Who is at Risk for Compassion Fatigue? An Investigation of Genetic Counselor Demographics, Anxiety, Compassion Satisfaction, and Burnout |
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✓ |
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| Provision of Cardiovascular Genetic Counseling Services: Current Practice and Future Directions |
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| Interdisciplinary Education for Genetic Counselors: Developing the Concept and Assessing the Need in Australasia |
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| Collaboration of Colorado Cancer Genetic Counselors to Integrate Next Generation Sequencing Panels into Clinical Practice |
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| LQTS Parents’ Reflections About Genetic Risk Knowledge and their Need to Know or Not to Know their Children's Carrier Status |
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| The Utilization and Choices of Aneuploidy Screening in a Midwestern Population |
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| Maternal Uniparental Isodisomy Causing Autosomal Recessive GM1 Gangliosidosis: A Clinical Report |
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| Disclosure of Genetic Research Results to Members of a Founder Population |
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✓ |
✓ |
Hutterites |
| Amyotrophic Lateral Sclerosis in a Patient with a Family History of Huntington Disease: Genetic Counseling Challenges |
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| The Evolution of Cancer Risk Assessment in the Era of Next Generation Sequencing |
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| Predictors of Genetic Testing Decisions: A Systematic Review and Critique of the Literature |
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| Demographic and Experiential Correlates of Public Attitudes Towards Cell‐Free Fetal DNA Screening |
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✓ |
✓ |
Asian race |
| Genetic Counselors’ Views and Experiences with the Clinical Integration of Genome Sequencing |
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| Linking Genetic Counseling Content to Short‐Term Outcomes in Individuals at Elevated Breast Cancer Risk |
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| Birth Defects, Causal Attributions, and Ethnicity in the National Birth Defects Prevention Study |
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| Genomic Counseling in the Newborn Period: Experiences and Views of Genetic Counselors |
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| Genetic Counseling Practice in Next Generation Sequencing Research: Implications for the Ethical Oversight of the Informed Consent Process |
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| Motivation to Pursue Genetic Testing in Individuals with a Personal or Family History of Cardiac Events or Sudden Cardiac Death |
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| Genetic Testing of Children for Predisposition to Mood Disorders: Anticipating the Clinical Issues |
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| Evaluation of a Clinical Genetics Service – A Quality Initiative |
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| Cancer Risk Assessment Using Genetic Panel Testing: Considerations for Clinical Application |
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| The Incorporation of Predictive Genomic Testing into Genetic Counseling Programs |
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| Traditional Roles in a Non‐Traditional Setting: Genetic Counseling in Precision Oncology |
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| A Genetic Counseling Intervention to Facilitate Family Communication About Inherited Conditions |
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| Genetic Counseling Graduate Student Debt: Impact on Program, Career and Life Choices |
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| An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing |
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| An Investigation of Genetic Counselors’ Testing Recommendations: Pedigree Analysis and the Use of Multiplex Breast Cancer Panel Testing |
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| An Assessment of Time Involved in Pre‐test Case Review and Counseling for a Whole Genome Sequencing Clinical Research Program |
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| Psychosocial Stressors of Sickle Cell Disease on Adult Patients in Cameroon |
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| Personalized Genomic Results: Analysis of Informational Needs |
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| Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era |
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| NSGC 2014 Presidential Address: Just Own It |
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| Attitudes of Mothers of Children with Down Syndrome Towards Noninvasive Prenatal Testing |
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| Attitudes About Internet Support Groups Among Adolescents and Young Adults with Neurofibromatosis Type 1 and their Parents |
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| Adapting Genetic Counseling Training to the Genomic Era: More an Evolution than a Revolution |
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| Lynch Syndrome Patients’ Views of and Preferences for Return of Results Following Whole Exome Sequencing |
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| Next Generation Sequencing is the Impetus for the Next Generation of Laboratory‐Based Genetic Counselors |
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| The Ophthalmic Experience: Unanticipated Primary Findings in the Era of Next Generation Sequencing |
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| Assessing the Integration of Genomic Medicine in Genetic Counseling Training Programs |
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| Huntington Disease: Who Seeks Presymptomatic Genetic Testing, Why and What are the Outcomes? |
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| The Effect of Genetic Counseling for Adult Offspring of Patients with Type 2 Diabetes on Attitudes Toward Diabetes and its Heredity: A Randomized Controlled Trial |
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| Insufficient Referral for Genetic Counseling in the Management of Hereditary Haemochromatosis in Portugal: A Study of Perceptions of Health Professionals Requesting <i>HFE</i> Genotyping |
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| Balancing Life with an Increased Risk of Cancer: Lived Experiences in Healthy Individuals with Lynch Syndrome |
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| Points to Consider in the Clinical Use of NGS Panels for Mitochondrial Disease: An Analysis of Gene Inclusion and Consent Forms |
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| Preferences Regarding Targeted Education and Risk Assessment in People with a Family History of Major Depressive Disorder |
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