| Editorial: The JOGC Journey Continues |
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| Psychiatric Disorders in Clinical Genetics II: Individualizing Recurrence Risks |
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| 2007 National Society of Genetic Counselors Presidential Address: Embracing Change to Race Forward |
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| Emotional Reaction to Fragile X Premutation Carrier Tests Among Infertile Women |
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| How Risk is Perceived, Constructed and Interpreted by Clients in Clinical Genetics, and the Effects on Decision Making: Systematic Review |
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| Psychiatric Disorders in Clinical Genetics I: Addressing Family Histories of Psychiatric Illness |
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| Culture and Acculturation Influences on Palestinian Perceptions of Prenatal Genetic Counseling |
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| Presented Abstracts from the Twenty‐Sixth Annual Education Conference of the National Society of Genetic Counselors (Kansas City, Missouri, October 2007) |
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| Genetics Education for Health Professionals: A Context |
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| Ethnic Differences in Parental Perceptions of Genetic Testing for Deaf Infants |
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Hispanic; Asian |
| Rejoinder to: Sahar et al.'s “Letter to the Editor” |
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| Engaging Nurses in Genetics: The Strategic Approach of the NHS National Genetics Education and Development Centre |
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| Family‐based Detection for Hereditary Hemochromatosis |
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| Letter to the Editor Journal of Genetic Counseling |
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| Employability of Genetic Counselors with a PhD in Genetic Counseling |
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| Living at Risk: Concealing Risk and Preserving Hope in Huntington Disease |
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| Coming Full Circle: A Reciprocal‐Engagement Model of Genetic Counseling Practice |
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| Why We Do What We Do: Commentary on A Reciprocal‐Engagement Model of Genetic Counseling Practice |
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| Women with <i>BRCA1</i> or <i>BRCA2</i> Mutations Renegotiating a Post‐Prophylactic Mastectomy Identity: Self‐Image and Self‐Disclosure. |
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| A National Survey of Genetic Counselors’ Personal Values |
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| Predictors of Cancer Worry in Unaffected Women from High Risk Breast Cancer Families: Risk Perception is not the Primary Issue |
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| Living with Hereditary Non‐polyposis Colorectal Cancer; Experiences from and Impact of Genetic Testing |
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| The Influence of Cancer‐related Distress and Sense of Coherence on Anxiety and Depression in Patients with Hereditary Cancer |
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| Assessment of Psychosocial Outcomes in Genetic Counseling Research: An Overview of Available Measurement Scales |
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| Psychosocial Issues in Families Affected by Maple Syrup Urine Disease |
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| What I Wish I Knew Then…Reflections from Personal Experiences in Counseling about Down Syndrome |
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| Distress and Family Functioning in Oncogenetic Counselling for Hereditary and Familial Breast and/or Ovarian Cancers |
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| Factors Influencing Perceptions of Breast Cancer Genetic Counseling among Women in an Urban Health Care System |
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African American |
| Infertility Counseling: A Comprehensive Handbook for Clinicians (2nd ed) |
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| Parental Narratives About Genetic Testing for Hearing Loss: A One Year Follow Up Study |
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| An Investigation of Genetic Counselor Experiences in Peer Group Supervision |
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| Career Research Interests and Training of Genetic Counseling Students |
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| Awareness and Attitudes Regarding Prenatal Testing among Texas Women of Childbearing Age |
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black; Hispanic; non‑Hispanic whites |
| Recommendation Recall and Satisfaction After Attending Breast/Ovarian Cancer Risk Counseling |
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| Neurofibromatosis Type 1 in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors |
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| Health Beliefs and Behaviors of Women Who Have Received Genetic Counseling For Breast Cancer |
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| Results of an Intervention for Individuals and Families with <i>BRCA</i> Mutations: A Model for Providing Medical Updates and Psychosocial Support Following Genetic Testing |
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| Successful Use of Peer Educators for Sharing Genetic Information |
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| The Impact of Breast Cancer Genetic Risk Assessment on Intentions to Perform Cancer Surveillance Behaviors |
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| Disclosure of Genetics Research Results after the Death of the Patient Participant: A Qualitative Study of the Impact on Relatives |
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| What do Patients Prefer: Informed Consent Models for Genetic Carrier Testing |
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| Providing a Transcultural Genetic Counseling Service in the UK |
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| Stigmatization, Culture and Counseling A Commentary on Growing Up and Living with NF1: a UK–Bangladeshi Case Study—by Santi Rozario |
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| Genetics Support to Primary Care Practitioners—A Demonstration Project |
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| Recommendations from Multi‐disciplinary Focus Groups on Cascade Testing and Genetic Counseling for Fragile X‐associated Disorders |
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| Growing Up and Living with Neurofibromatosis1 (NF1): A British Bangladeshi Case‐study |
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general European and American population; Bangladeshi; non‐Bangladeshi; UK |
| Risk Assessment and Genetic Counseling for Hereditary Breast and Ovarian Cancer: Recommendations of the National Society of Genetic Counselors |
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| Accuracy of Self‐Reported Personal History of Cancer in an Outpatient Breast Center |
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Asian/Pacific Islanders; Jewish ancestry |
| Picking a Frame for Communicating About Genetics: Stigmas or Challenges |
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| Decision‐Making About Reproductive Choices Among Individuals At‐Risk for Huntington's Disease |
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| Information Processing in the Context of Genetic Risk: Implications for Genetic‐Risk Communication |
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| Inherited Thrombophilia: Key Points for Genetic Counseling |
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| Using Adult Learning Theory Concepts to Address Barriers to Cancer Genetic Risk Assessment in the African American Community |
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| Risky Communication: Pitfalls in Counseling About Risk, and How to Avoid Them |
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| Genetic Counselling: A Psychological Approach |
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| Are You Really Listening? Keys to Successful Communication |
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| Development and Pilot Testing of Two Decision Aids for Individuals Considering Genetic Testing for Cancer Risk |
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| Cancer Family History Reporting: Impact of Method and Psychosocial Factors |
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| Parents’ Perceptions of Functioning in Families Having a Child with a Genetic Condition |
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| Knowledge and Attitudes Towards Genetic Testing: A Two Year Follow‐Up Study in Patients with Asthma, Diabetes Mellitus and Cardiovascular Disease |
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| Sharing <i>GJB2</i>/<i>GJB6</i> Genetic Test Information with Family Members |
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| Psychological Follow‐up of Presymptomatic Genetic Testing for Spinocerebellar Ataxia Type 2 (SCA2) in Cuba |
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| When You Care Enough to Do Your Very Best: Genetic Counselor Experiences of Compassion Fatigue |
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| Clinical Characterization and Risk Profile of Individuals Seeking Genetic Counseling for Hereditary Breast Cancer in Brazil |
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| Knowledge and Expectations of Women Undergoing Cancer Genetic Risk Assessment: A Qualitative Analysis of Free‐Text Questionnaire Comments |
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| Probability Biases in Genetic Problem Solving: A Comparison of Undergraduates, Genetic Counseling Graduate Students, and Genetic Counselors |
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| 2006 National Society of Genetic Counselors Presidential Address: Join Me on the NSGC Journey |
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| Report from the UK and Eire Association of Genetic Nurses and Counsellors (AGNC) Supervision Working Group on Genetic Counselling Supervision |
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| Editorial on Supervision |
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| Reflections on the Experience of Counseling Supervision by a Team of Genetic Counselors from the UK |
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| Bayesian Risk Assessment in Genetic Testing for Autosomal Dominant Disorders with Age‐Dependent Penetrance |
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| What Is It Like To Be in the Minority? Ethnic and Gender Diversity in the Genetic Counseling Profession |
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ethnic minority |
| Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families |
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| Cancer Genetic Counseling: Communication and Counselees’ Post‐Visit Satisfaction, Cognitions, Anxiety, and Needs Fulfillment |
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| Attitudes Toward Fragile X Mutation Carrier Testing from Women Identified in a General Population Survey |
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| Presented Abstracts from the Twenty‐Fifth Annual Education Conference of the National Society of Genetic Counselors (Nashville, Tennessee, November 2006) |
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| Knowledge About Genetics Among African Americans |
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African Americans |
| Risk Perception, Worry and Satisfaction Related to Genetic Counseling for Hereditary Cancer |
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| Living with Multiple Endocrine Neoplasia Type 1: Decent Care‐Insufficient Medical and Genetic Information A Qualitative Study of MEN 1 Patients in a Swedish Hospital |
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| The Effect of Disruptions During Counseling on Recall of Genetic Risk Information: The Case of Cystic Fibrosis |
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| Assessing the Informational Needs of Adolescents with a Genetic Condition: What Do They Want to Know? |
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| Characterization of the Practice and Attitudes of Genetic Counselors with Doctoral Degrees |
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| Increasing Utilization of Cancer Genetic Counseling Services Using a Patient Navigator Model |
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| Spiritual Assessment in Genetic Counseling |
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