Journal of Genetic Counseling - 2007

84 articles | Last updated: 2025-12-03 14:12:57
Caucasian
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White
2
European
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Other
7
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Editorial: The JOGC Journey Continues
Psychiatric Disorders in Clinical Genetics II: Individualizing Recurrence Risks
2007 National Society of Genetic Counselors Presidential Address: Embracing Change to Race Forward
Emotional Reaction to Fragile X Premutation Carrier Tests Among Infertile Women
How Risk is Perceived, Constructed and Interpreted by Clients in Clinical Genetics, and the Effects on Decision Making: Systematic Review
Psychiatric Disorders in Clinical Genetics I: Addressing Family Histories of Psychiatric Illness
Culture and Acculturation Influences on Palestinian Perceptions of Prenatal Genetic Counseling
Presented Abstracts from the Twenty‐Sixth Annual Education Conference of the National Society of Genetic Counselors (Kansas City, Missouri, October 2007)
Genetics Education for Health Professionals: A Context
Ethnic Differences in Parental Perceptions of Genetic Testing for Deaf Infants Hispanic; Asian
Rejoinder to: Sahar et al.'s “Letter to the Editor”
Engaging Nurses in Genetics: The Strategic Approach of the NHS National Genetics Education and Development Centre
Family‐based Detection for Hereditary Hemochromatosis
Letter to the Editor Journal of Genetic Counseling
Employability of Genetic Counselors with a PhD in Genetic Counseling
Living at Risk: Concealing Risk and Preserving Hope in Huntington Disease
Coming Full Circle: A Reciprocal‐Engagement Model of Genetic Counseling Practice
Why We Do What We Do: Commentary on A Reciprocal‐Engagement Model of Genetic Counseling Practice
Women with <i>BRCA1</i> or <i>BRCA2</i> Mutations Renegotiating a Post‐Prophylactic Mastectomy Identity: Self‐Image and Self‐Disclosure.
A National Survey of Genetic Counselors’ Personal Values
Predictors of Cancer Worry in Unaffected Women from High Risk Breast Cancer Families: Risk Perception is not the Primary Issue
Living with Hereditary Non‐polyposis Colorectal Cancer; Experiences from and Impact of Genetic Testing
The Influence of Cancer‐related Distress and Sense of Coherence on Anxiety and Depression in Patients with Hereditary Cancer
Assessment of Psychosocial Outcomes in Genetic Counseling Research: An Overview of Available Measurement Scales
Psychosocial Issues in Families Affected by Maple Syrup Urine Disease
What I Wish I Knew Then…Reflections from Personal Experiences in Counseling about Down Syndrome
Distress and Family Functioning in Oncogenetic Counselling for Hereditary and Familial Breast and/or Ovarian Cancers
Factors Influencing Perceptions of Breast Cancer Genetic Counseling among Women in an Urban Health Care System African American
Infertility Counseling: A Comprehensive Handbook for Clinicians (2nd ed)
Parental Narratives About Genetic Testing for Hearing Loss: A One Year Follow Up Study
An Investigation of Genetic Counselor Experiences in Peer Group Supervision
Career Research Interests and Training of Genetic Counseling Students
Awareness and Attitudes Regarding Prenatal Testing among Texas Women of Childbearing Age black; Hispanic; non‑Hispanic whites
Recommendation Recall and Satisfaction After Attending Breast/Ovarian Cancer Risk Counseling
Neurofibromatosis Type 1 in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors
Health Beliefs and Behaviors of Women Who Have Received Genetic Counseling For Breast Cancer
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
Successful Use of Peer Educators for Sharing Genetic Information
The Impact of Breast Cancer Genetic Risk Assessment on Intentions to Perform Cancer Surveillance Behaviors
Disclosure of Genetics Research Results after the Death of the Patient Participant: A Qualitative Study of the Impact on Relatives
What do Patients Prefer: Informed Consent Models for Genetic Carrier Testing
Providing a Transcultural Genetic Counseling Service in the UK
Stigmatization, Culture and Counseling A Commentary on Growing Up and Living with NF1: a UK–Bangladeshi Case Study—by Santi Rozario
Genetics Support to Primary Care Practitioners—A Demonstration Project
Recommendations from Multi‐disciplinary Focus Groups on Cascade Testing and Genetic Counseling for Fragile X‐associated Disorders
Growing Up and Living with Neurofibromatosis1 (NF1): A British Bangladeshi Case‐study 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
Accuracy of Self‐Reported Personal History of Cancer in an Outpatient Breast Center Asian/Pacific Islanders; Jewish ancestry
Picking a Frame for Communicating About Genetics: Stigmas or Challenges
Decision‐Making About Reproductive Choices Among Individuals At‐Risk for Huntington's Disease
Information Processing in the Context of Genetic Risk: Implications for Genetic‐Risk Communication
Inherited Thrombophilia: Key Points for Genetic Counseling
Using Adult Learning Theory Concepts to Address Barriers to Cancer Genetic Risk Assessment in the African American Community
Risky Communication: Pitfalls in Counseling About Risk, and How to Avoid Them
Genetic Counselling: A Psychological Approach
Are You Really Listening? Keys to Successful Communication
Development and Pilot Testing of Two Decision Aids for Individuals Considering Genetic Testing for Cancer Risk
Cancer Family History Reporting: Impact of Method and Psychosocial Factors
Parents’ Perceptions of Functioning in Families Having a Child with a Genetic Condition
Knowledge and Attitudes Towards Genetic Testing: A Two Year Follow‐Up Study in Patients with Asthma, Diabetes Mellitus and Cardiovascular Disease
Sharing <i>GJB2</i>/<i>GJB6</i> Genetic Test Information with Family Members
Psychological Follow‐up of Presymptomatic Genetic Testing for Spinocerebellar Ataxia Type 2 (SCA2) in Cuba
When You Care Enough to Do Your Very Best: Genetic Counselor Experiences of Compassion Fatigue
Clinical Characterization and Risk Profile of Individuals Seeking Genetic Counseling for Hereditary Breast Cancer in Brazil
Knowledge and Expectations of Women Undergoing Cancer Genetic Risk Assessment: A Qualitative Analysis of Free‐Text Questionnaire Comments
Probability Biases in Genetic Problem Solving: A Comparison of Undergraduates, Genetic Counseling Graduate Students, and Genetic Counselors
2006 National Society of Genetic Counselors Presidential Address: Join Me on the NSGC Journey
Report from the UK and Eire Association of Genetic Nurses and Counsellors (AGNC) Supervision Working Group on Genetic Counselling Supervision
Editorial on Supervision
Reflections on the Experience of Counseling Supervision by a Team of Genetic Counselors from the UK
Bayesian Risk Assessment in Genetic Testing for Autosomal Dominant Disorders with Age‐Dependent Penetrance
What Is It Like To Be in the Minority? Ethnic and Gender Diversity in the Genetic Counseling Profession ethnic minority
Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families
Cancer Genetic Counseling: Communication and Counselees’ Post‐Visit Satisfaction, Cognitions, Anxiety, and Needs Fulfillment
Attitudes Toward Fragile X Mutation Carrier Testing from Women Identified in a General Population Survey
Presented Abstracts from the Twenty‐Fifth Annual Education Conference of the National Society of Genetic Counselors (Nashville, Tennessee, November 2006)
Knowledge About Genetics Among African Americans African Americans
Risk Perception, Worry and Satisfaction Related to Genetic Counseling for Hereditary Cancer
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
The Effect of Disruptions During Counseling on Recall of Genetic Risk Information: The Case of Cystic Fibrosis
Assessing the Informational Needs of Adolescents with a Genetic Condition: What Do They Want to Know?
Characterization of the Practice and Attitudes of Genetic Counselors with Doctoral Degrees
Increasing Utilization of Cancer Genetic Counseling Services Using a Patient Navigator Model
Spiritual Assessment in Genetic Counseling