| Efficacy of the Health Belief Model for Predicting Intention to Pursue Genetic Testing for Colorectal Cancer |
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| Women's Perceptions of the Personal and Family Impact of Genetic Cancer Risk Assessment: Focus Group Findings |
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| Examining the Relationship Between Genetic Counselors’ Attitudes Toward Deaf People and the Genetic Counseling Session |
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| Prenatal Testing for Down Syndrome: Comparison of Screening Practices in the UK and USA |
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| The Genome Book: A Must‐Have Guide to Your DNA for Maximum Health by April Lynch with Vickie Venne MS CGC. Sunrise River Press, North Branch, MN 55056, April 2009, 239 pp., $14.95 |
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| Genetic Counselors’ Perceived Responsibilities Regarding Reproductive Issues for Patients at Risk for Huntington Disease |
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| Doris Teichler Zallen, To Test or Not To Test: A Guide to Genetic Screening and Risk |
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| Primary Care Providers’ Responses to Patient‐Generated Family History |
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| A Transnational Approach: A Commentary on Lost in Translation: Limitations of a Universal Approach in Genetic Counseling |
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| Decisions to Seek Healthcare Based on Family Health History Among Urban Appalachian Women |
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Appalachian |
| Women's Decision Making about Risk‐Reducing Strategies in the Context of Hereditary Breast and Ovarian Cancer: A Systematic Review |
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| Lost in Translation: Limitations of a Universal Approach in Genetic Counseling |
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| Billing for Medical Genetics and Genetic Counseling Services: A National Survey |
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| Perceptions of High‐Risk Care and Barriers to Care Among Women at Risk for Hereditary Breast and Ovarian Cancer following Genetic Counseling in the Community Setting |
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| Presented Abstracts from the Twenty‐Eighth Annual Education Conference of the National Society of Genetic Counselors (Atlanta, Georgia, November 2009) |
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| Unprepared, Understaffed, and Unplanned: Thoughts on the Practical Implications of Discovering New Breast and Ovarian Cancer Causing Genes |
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| Provision of Genetic Services for Hearing Loss: Results from a National Survey and Comparison to Insights Obtained from Previous Focus Group Discussions |
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| A Balancing Act—Telehealth Cancer Genetics and Practitioners’ Experiences of a Triadic Consultation |
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| “Testing Times, Challenging Choices”: An Australian Study of Prenatal Genetic Counseling |
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| Attitudes and Practice of Genetic Counselors Regarding Anonymous Testing for BRCA1/2 |
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| Response to Robert G. Resta Commentary (Unprepared, Understaffed, and Unplanned: Thoughts on the Practical Implications of Discovering New Breast and Ovarian Cancer Causing Genes) |
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| Genetic Counselors’ Religiosity & Spirituality: Are Genetic Counselors Different from the General Population? |
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| A Remembrance of Dr. George Tiller |
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| Grandmothers as Gems of Genetic Wisdom: Exploring South African Traditional Beliefs About the Causes of Childhood Genetic Disorders |
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| Perceptions of the Concept of Mutation among Family Members of Patients Receiving Outpatient Genetic Services and University Students |
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| Introduction to Commentaries |
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| George Tiller's Legacy for Genetic Counseling |
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| A Cross Sectional Study Exploring Factors Impacting Recruitment of African American College Students into the Genetic Counseling Profession |
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| Recontacting Patients Who have Tested Negative for <i>BRCA1</i> and <i>BRCA2</i> Mutations: How, Who and Why? |
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| Role of the Disease in the Psychological Impact of Pre‐Symptomatic Testing for SCA2 and FAP ATTRV30M: Experience with the Disease, Kinship and Gender of the Transmitting Parent |
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| Agency and Choice in Genetic Counseling: Acknowledging Patients’ Concerns |
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| Challenges Faced by Genetics Service Providers’ Practicing in a Culturally and Linguistically Diverse Population: An Australian Experience |
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| A Collaborative Approach to Genetic Testing: A Community Hospital's Experience |
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| Parents’ Perceptions of Autism Spectrum Disorder Etiology and Recurrence Risk and Effects of their Perceptions on Family Planning: Recommendations for Genetic Counselors |
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| A Pilot Study to Assess the Feasibility of a Multicenter Cluster Randomized Trial for the Management of Asymptomatic Persons with a Thrombophilia |
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| Psychosocial Impact of Familial Adenomatous Polyposis on Young Adults: A Qualitative Study |
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| The Effect of BRCA Gene Testing on Family Relationships: A Thematic Analysis of Qualitative Interviews |
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| The Utility of Genetic Counseling Prior to Offering First Trimester Screening Options |
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| The Effectiveness of Family History Questionnaires in Cancer Genetic Counseling |
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| Telephoned <i>BRCA1/2</i> Genetic Test Results: Prevalence, Practice, and Patient Satisfaction |
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| A Comparative Analysis of Ethical and Professional Challenges Experienced by Australian and U.S. Genetic Counselors |
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| Perceptions of Licensure: A Survey of Michigan Genetic Counselors |
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| Development of E‐Info Gene<sup>ca</sup>: A Website Providing Computer‐Tailored Information and Question Prompt Prior to Breast Cancer Genetic Counseling |
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| Cancer Genetics Service Interest in Women with a Limited Family History of Breast Cancer |
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| Diplomates Certified in 2007 |
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| Reactions to and Desire for Prognostic Testing in Choroidal Melanoma Patients |
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| High School Biology/Life Science Teachers’ Presentation of Genetic Counseling and Health Care Career Options in Their Classrooms |
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| Risk Perception Among Women at Risk for Hereditary Breast and Ovarian Cancer |
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| A Decade of Genetic Counseling in Frontotemporal Dementia Affected Families: Few Counseling Requests and much Familial Opposition to Testing |
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| Decision‐Making About Inherited Cancer Risk: Exploring Dimensions of Genetic Responsibility |
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| An Investigation of Relationships among Genetic Counselors’ Supervision Skills and Multicultural Counseling Competence |
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| Alison Stewart, Philippa Brice, Hilary Burton, Paul Pharaoh, Simon Sanderson and Ron Zimmern, <b>Genetics, Health Care and Public Health Genetics. An Introduction to Public Health Genetics.</b> |
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| A Systematic Review of the Impact of Genetic Counseling on Risk Perception Accuracy |
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| Genetic Counseling Practice Analysis |
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| Genetic Risk Communication: Experiences of Adolescent Girls and Young Women from Families with Fragile X Syndrome |
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| Issues and Management of Joint Hypermobility: A Guide for the Ehlers‐Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome |
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| Pancreatic Cancer Surveillance Among High‐Risk Populations: Knowledge and Intent |
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| Letter to the Editor |
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| Genetic Library: Grief and Bereavement |
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| Can Population‐Based Carrier Screening Be Left to the Community? |
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Orthodox Jewish community |
| Diversity in Genetic Counseling: Strategies from the LEND Network |
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| Experiences and Decisions that Motivate Women at Increased Risk of Breast Cancer to Participate in an Experimental Screening Program |
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| Introduction to Diversity Essays |
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| 2008 National Society of Genetic Counselors Presidential Address: The NSGC Should Do Something About That… and We Are |
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| Addressing Diversity in the Genetic Counseling Profession |
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| Diversity Through the Eyes of a Minority Student |
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| Cancer Genetic Counselees’ Self‐Reported Psychological Distress, Changes in Life, and Adherence to Recommended Surveillance Programs 3–7 Years Post Counseling |
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Swedish |
| Professional Ambivalence: Accounts of Ethical Practice in Childhood Genetic Testing |
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| Consumers’ Desire towards Current and Prospective Reproductive Genetic Testing |
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| Living at Risk: The Sibling's Perspective of Early‐Onset Alzheimer's Disease |
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| Evaluation of Group Genetic Counseling for Hereditary Breast and Ovarian Cancer |
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