| Genetic Counselors’ Current Use of Personal Health Records‐Based Family Histories in Genetic Clinics and Considerations for Their Future Adoption |
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| Family Communication Following <i>BRCA1/2</i> Genetic Testing: A Close Look at the Process |
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| Hoping to Live a “Normal” Life Whilst Living with Unpredictable Health and Fear of Death: Impact of Cystic Fibrosis on Young Adults |
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| Ethical Issues in Presymptomatic Genetic Testing for Minors: A dilemma in Li‐Fraumeni Syndrome |
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| Acceptance and Commitment Therapy in Genetic Counselling: A Case Study of Recurrent Worry |
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| Screening for Muir‐Torre Syndrome Using Mismatch Repair Protein Immunohistochemistry of Sebaceous Neoplasms |
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| When the Topic is You: Genetic Counselor Responses to Prenatal Patients’ Requests for Self‐Disclosure |
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| NSGC Practice Guideline: Risk Assessment and Genetic Counseling for Hereditary Breast and Ovarian Cancer |
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| Acceptance of Genetic Counseling and Testing in a Hospital‐Based Series of Patients with Gynecological Cancer |
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| NSGC Practice Guideline: Prenatal Screening and Diagnostic Testing Options for Chromosome Aneuploidy |
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| Response to Letter Written by Shelly Cummings, MS, CGC of Myriad Genetics Laboratories, Inc. Regarding the Paper, “Racial and Ethnic Differences in Direct‐to‐Consumer Genetic Tests Awareness in HINTS |
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| Response to Article: Langford et al. Racial and Ethnic Differences in Direct‐to‐Consumer Genetic Tests Awareness in HINTS 2007: Sociodemographic and Numeracy Correlates. <i>J Genet Counsel</i> (2012) |
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| Counseling Customers: Emerging Roles for Genetic Counselors in the Direct‐to‐Consumer Genetic Testing Market |
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| Talking to Children About Maternal <i>BRCA1/2</i> Genetic Test Results: A Qualitative Study of Parental Perceptions and Advice |
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| “I Didn't Know It Existed Before You Called”: Protestant Clergy Experience, Education and Perceptions Regarding Genetics |
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| Introduction to the Special Issue on Developmental Disabilities |
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| Uptake of Cardiac Screening and Genetic Testing Among Hypertrophic and Dilated Cardiomyopathy Families |
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| Knowledge, Attitudes, and Beliefs of Arab‐American Women Regarding Inherited Cancer Risk |
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✓ |
✓ |
Arab-American / Arab Americans / Arab‐American community |
| A Model for Peer Experiential and Reciprocal Supervision (PEERS) for Genetic Counselors: Development and Preliminary Evaluation Within Clinical Practice |
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| Variables Influencing Pregnancy Termination Following Prenatal Diagnosis of Fetal Chromosome Abnormalities |
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✓ |
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Filipina race; ethnicity |
| Erratum to: Genetic Counseling and Testing for <i>FMR1</i> Gene Mutations: Practice Guidelines of the National Society of Genetic Counselors |
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| On the Precarious Cusp of Genetic Medicine |
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| Amsterdam International |
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| Assessment of Parental Disclosure of a 22q11.2 Deletion Syndrome Diagnosis and Implications for Clinicians |
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| Genetic Disorders of Intellectual Disability: Expanding our Concepts of Phenotypes and of Family Outcomes |
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| Focusing on Patient Needs and Preferences May Improve Genetic Counseling for Colorectal Cancer |
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| Presented Abstracts from the Thirty First Annual Education Conference of the National Society of Genetic Counselors (Boston, MA, October 2012) |
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| <i>“Grasping the Grey”</i>: Patient Understanding and Interpretation of an Intermediate Allele Predictive Test Result for Huntington Disease |
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| Who Counsels Parents of Newborns Who Are Carriers of Sickle Cell Anemia or Cystic Fibrosis? |
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✓ |
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| “Is it Really Worth it to Get Tested?”: Primary Care Patients’ Impressions of Predictive SNP Testing for Colon Cancer |
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| Unintended Diagnosis of Von Hippel Lindau Syndrome Using Array Comparative Genomic Hybridization (CGH): Counseling Challenges Arising from Unexpected Information |
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| Full‐Spectrum Parenting |
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| The Road Less Traveled: One Genetic Counselor's Reflections on Disability and the Genetic Counseling Profession |
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| My Days of Counting Are Numbered |
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| Life Events may Contribute to Family Communication About Cancer Risk Following <i>BRCA1/2</i> Testing |
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| Children's Acceptance of Others with Disability: The Influence of a Disability‐Simulation Program |
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| Return of Genetic Results in the Familial Dilated Cardiomyopathy Research Project |
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| A Multi‐Case Report of the Pathways To and Through Genetic Testing and Cancer Risk Management for<i>BRCA</i>Mutation‐Positive Women Aged 18–25 |
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| Erratum to: Development and Evaluation of a Decision Aid for <i>BRCA</i> Carriers with Breast Cancer |
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| Enhancing Family Communication About Genetics: Ethical and Professional Dilemmas |
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| 22q11.2 Deletion Syndrome: Attitudes towards Disclosing the Risk of Psychiatric Illness |
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| Are Genetic Counselors and the Social Service System for People with Intellectual Disability Reaching Rapprochement? |
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| Parental Needs among Children with Birth Defects: Defining a Parent‐to‐Parent Support Network |
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| Genetic Counseling, Activism and ‘Genotype‐First’ Diagnosis of Developmental Disorders |
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| Young Adults’ Experience of Living with Neurofibromatosis Type 1 |
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| Genetic Counseling and Testing for <i>FMR1</i> Gene Mutations: Practice Guidelines of the National Society of Genetic Counselors |
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| Low Rates of African American Participation in Genetic Counseling and Testing for BRCA1/2 Mutations: Racial Disparities or Just a Difference? |
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| Factors Associated with Psychological Distress among Women of African Descent at High Risk for BRCA Mutations |
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| Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study |
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✓ |
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| Genetic Counseling Supervisor Competencies: Results of a Delphi Study |
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| Effects of Second Language Usage on Genetic Counseling Training and Supervision |
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| Prenatal Treatment of Congenital Adrenal Hyperplasia—Not Standard of Care |
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| In Memoriam: Rose Grobstein (1917–2011) |
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| Personal Genomic Testing as Part of the Complete Breast Cancer Risk Assessment: A Case Report |
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| The Laboratory‐Clinician Team: A Professional Call to Action to Improve Communication and Collaboration for Optimal Patient Care in Chromosomal Microarray Testing |
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| Attitudes and Practices Among Internists Concerning Genetic Testing |
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✓ |
✓ |
African‐American |
| Report from the National Society of Genetic Counselors Service Delivery Model Task Force: A Proposal to Define Models, Components, and Modes of Referral |
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| Genetic Counseling for Personal Genomic Testing: Optimizing Client Uptake of Post‐Test Telephonic Counseling Services |
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| Genetic Counseling for the Orthodox Jewish Couple Undergoing Preimplantation Genetic Diagnosis |
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| Development of an Evidence‐Based Information Booklet to Support Parents of Children Without a Diagnosis |
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| You Want to Do What? My Mother's Choice to Have Direct‐to‐Consumer Genetic Testing |
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| Prenatal Genetic Testing: An Investigation of Determining Factors Affecting the Decision‐Making Process |
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| Direct‐to‐Consumer Genetic Testing: Introduction to the Special Issue |
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| Gay, Lesbian, and Bisexual Patients’ Recommendations for Genetic Counselors: A Qualitative Investigation |
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| Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C): A Review of Molecular and Clinical Literature |
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| Underutilization of Genetics Services for Autism: The Importance of Parental Awareness and Provider Recommendation |
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| Understanding of Genetic Inheritance among Xhosa‐Speaking Caretakers of Children with Hemophilia |
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| Direct‐to‐Consumer Genetic Testing: What Are We Talking About? |
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| Biotech 101: An Educational Outreach Program in Genetics and Biotechnology |
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| Quality of Life and Autonomy in Emerging Adults with Early‐Onset Neuromuscular Disorders |
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| Young Adults with MSUD and Their Transition to Adulthood: Psychosocial Issues |
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| Hispanic Infants with Cystic Fibrosis Show Low <i>CFTR</i> Mutation Detection Rates in the Illinois Newborn Screening Program |
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✓ |
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| Remembering and Listening |
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| Genetic Counseling as a Tool for Type 2 Diabetes Prevention: A Genetic Counseling Framework for Common Polygenetic Disorders |
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| Genetic Counseling for Prenatal Testing: Where is the Discussion About Disability? |
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| Genetic Counseling and the Ethical Issues Around Direct to Consumer Genetic Testing |
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| Explanatory Models of Illness May Facilitate Cultural Competence in Genetic Counseling |
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| Perception of Direct‐To‐Consumer Genetic Testing and Direct‐To‐Consumer Advertising of Genetic Tests among Members of a Large Managed Care Organization |
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✓ |
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| Couples’ Coping in Prodromal Huntington Disease: A Mixed Methods Study |
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| Risky Business: Risk Perception and the Use of Medical Services among Customers of DTC Personal Genetic Testing |
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| Direct‐to‐Consumer Personal Genomic Testing: A Case Study and Practical Recommendations for “Genomic Counseling” |
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| We Are ‘Woman’, after All |
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| It's a Small World: Fusion of Cultures in Genetic Counseling |
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| Ten Years Later: No Longer A Student, But Still Learning |
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| How I Learned that One Mistake Does not Define Me |
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| National Society of Genetic Counselors Natalie Weissburger Paul Lifetime Achievement Award Address: <b><i>The Power of Connecting</i></b> |
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| Racial and Ethnic Differences in Direct‐to‐Consumer Genetic Tests Awareness in HINTS 2007: Sociodemographic and Numeracy Correlates |
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✓ |
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| The Use of a Family History Risk Assessment Tool within a Community Health Care System: Views of Primary Care Providers |
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| Psychological Distress with Direct‐to‐Consumer Genetic Testing: A Case Report of an Unexpected<i>BRCA</i>Positive Test Result |
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| Genetic Testing Integration Panels (GTIPs): A Novel Approach for Considering Integration of Direct‐To‐Consumer and Other New Genetic Tests into Patient Care |
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| Bias in the Reporting of Family History: Implications for Clinical Care |
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| A Family Experience of Personal Genomics |
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| Communication about DTC Testing: Commentary on a ‘Family Experience of Personal Genomics’ |
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