Journal of Genetic Counseling - 2009

71 articles | Last updated: 2025-12-03 14:12:57
Caucasian
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European
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Other
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Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Efficacy of the Health Belief Model for Predicting Intention to Pursue Genetic Testing for Colorectal Cancer
Women's Perceptions of the Personal and Family Impact of Genetic Cancer Risk Assessment: Focus Group Findings
Examining the Relationship Between Genetic Counselors’ Attitudes Toward Deaf People and the Genetic Counseling Session
Prenatal Testing for Down Syndrome: Comparison of Screening Practices in the UK and USA
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
Genetic Counselors’ Perceived Responsibilities Regarding Reproductive Issues for Patients at Risk for Huntington Disease
Doris Teichler Zallen, To Test or Not To Test: A Guide to Genetic Screening and Risk
Primary Care Providers’ Responses to Patient‐Generated Family History
A Transnational Approach: A Commentary on Lost in Translation: Limitations of a Universal Approach in Genetic Counseling
Decisions to Seek Healthcare Based on Family Health History Among Urban Appalachian Women Appalachian
Women's Decision Making about Risk‐Reducing Strategies in the Context of Hereditary Breast and Ovarian Cancer: A Systematic Review
Lost in Translation: Limitations of a Universal Approach in Genetic Counseling
Billing for Medical Genetics and Genetic Counseling Services: A National Survey
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
Presented Abstracts from the Twenty‐Eighth Annual Education Conference of the National Society of Genetic Counselors (Atlanta, Georgia, November 2009)
Unprepared, Understaffed, and Unplanned: Thoughts on the Practical Implications of Discovering New Breast and Ovarian Cancer Causing Genes
Provision of Genetic Services for Hearing Loss: Results from a National Survey and Comparison to Insights Obtained from Previous Focus Group Discussions
A Balancing Act—Telehealth Cancer Genetics and Practitioners’ Experiences of a Triadic Consultation
“Testing Times, Challenging Choices”: An Australian Study of Prenatal Genetic Counseling
Attitudes and Practice of Genetic Counselors Regarding Anonymous Testing for BRCA1/2
Response to Robert G. Resta Commentary (Unprepared, Understaffed, and Unplanned: Thoughts on the Practical Implications of Discovering New Breast and Ovarian Cancer Causing Genes)
Genetic Counselors’ Religiosity & Spirituality: Are Genetic Counselors Different from the General Population?
A Remembrance of Dr. George Tiller
Grandmothers as Gems of Genetic Wisdom: Exploring South African Traditional Beliefs About the Causes of Childhood Genetic Disorders
Perceptions of the Concept of Mutation among Family Members of Patients Receiving Outpatient Genetic Services and University Students
Introduction to Commentaries
George Tiller's Legacy for Genetic Counseling
A Cross Sectional Study Exploring Factors Impacting Recruitment of African American College Students into the Genetic Counseling Profession
Recontacting Patients Who have Tested Negative for <i>BRCA1</i> and <i>BRCA2</i> Mutations: How, Who and Why?
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
Agency and Choice in Genetic Counseling: Acknowledging Patients’ Concerns
Challenges Faced by Genetics Service Providers’ Practicing in a Culturally and Linguistically Diverse Population: An Australian Experience
A Collaborative Approach to Genetic Testing: A Community Hospital's Experience
Parents’ Perceptions of Autism Spectrum Disorder Etiology and Recurrence Risk and Effects of their Perceptions on Family Planning: Recommendations for Genetic Counselors
A Pilot Study to Assess the Feasibility of a Multicenter Cluster Randomized Trial for the Management of Asymptomatic Persons with a Thrombophilia
Psychosocial Impact of Familial Adenomatous Polyposis on Young Adults: A Qualitative Study
The Effect of BRCA Gene Testing on Family Relationships: A Thematic Analysis of Qualitative Interviews
The Utility of Genetic Counseling Prior to Offering First Trimester Screening Options
The Effectiveness of Family History Questionnaires in Cancer Genetic Counseling
Telephoned <i>BRCA1/2</i> Genetic Test Results: Prevalence, Practice, and Patient Satisfaction
A Comparative Analysis of Ethical and Professional Challenges Experienced by Australian and U.S. Genetic Counselors
Perceptions of Licensure: A Survey of Michigan Genetic Counselors
Development of E‐Info Gene<sup>ca</sup>: A Website Providing Computer‐Tailored Information and Question Prompt Prior to Breast Cancer Genetic Counseling
Cancer Genetics Service Interest in Women with a Limited Family History of Breast Cancer
Diplomates Certified in 2007
Reactions to and Desire for Prognostic Testing in Choroidal Melanoma Patients
High School Biology/Life Science Teachers’ Presentation of Genetic Counseling and Health Care Career Options in Their Classrooms
Risk Perception Among Women at Risk for Hereditary Breast and Ovarian Cancer
A Decade of Genetic Counseling in Frontotemporal Dementia Affected Families: Few Counseling Requests and much Familial Opposition to Testing
Decision‐Making About Inherited Cancer Risk: Exploring Dimensions of Genetic Responsibility
An Investigation of Relationships among Genetic Counselors’ Supervision Skills and Multicultural Counseling Competence
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>
A Systematic Review of the Impact of Genetic Counseling on Risk Perception Accuracy
Genetic Counseling Practice Analysis
Genetic Risk Communication: Experiences of Adolescent Girls and Young Women from Families with Fragile X Syndrome
Issues and Management of Joint Hypermobility: A Guide for the Ehlers‐Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome
Pancreatic Cancer Surveillance Among High‐Risk Populations: Knowledge and Intent
Letter to the Editor
Genetic Library: Grief and Bereavement
Can Population‐Based Carrier Screening Be Left to the Community? Orthodox Jewish community
Diversity in Genetic Counseling: Strategies from the LEND Network
Experiences and Decisions that Motivate Women at Increased Risk of Breast Cancer to Participate in an Experimental Screening Program
Introduction to Diversity Essays
2008 National Society of Genetic Counselors Presidential Address: The NSGC Should Do Something About That… and We Are
Addressing Diversity in the Genetic Counseling Profession
Diversity Through the Eyes of a Minority Student
Cancer Genetic Counselees’ Self‐Reported Psychological Distress, Changes in Life, and Adherence to Recommended Surveillance Programs 3–7 Years Post Counseling Swedish
Professional Ambivalence: Accounts of Ethical Practice in Childhood Genetic Testing
Consumers’ Desire towards Current and Prospective Reproductive Genetic Testing
Living at Risk: The Sibling's Perspective of Early‐Onset Alzheimer's Disease
Evaluation of Group Genetic Counseling for Hereditary Breast and Ovarian Cancer