| Celebrating the 20th Anniversary of the <i>Journal of Genetic Counseling</i> |
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| Educational Needs of Primary Care Physicians Regarding Direct‐to‐Consumer Genetic Testing |
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| 2012 National Society of Genetic Counselors Presidential Address: Maintaining Our Professional Identity in an Ever‐Expanding Genetics Universe |
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| Informed Choice in Direct‐to‐Consumer Genetic Testing (DTCGT) Websites: A Content Analysis of Benefits, Risks, and Limitations |
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| Baby Boy Singh |
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| What is a “Balanced” Description? Insight from Parents of Individuals with Down Syndrome |
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| “It's Not Like Judgment Day”: Public Understanding of and Reactions to Personalized Genomic Risk Information |
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| Will My Voice Be Heard? |
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| Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited |
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| Learning to Define Myself |
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| “Sometimes, It's Hard to Be a Parent” |
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| Discovering Resilience |
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| Genetic Counseling Through Hope |
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| Evaluating a Session—Punitive vs. Reflective |
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| Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia |
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| Breaking Difficult News in a Cross‐cultural Setting: a Qualitative Study about Latina Mothers of Children with Down Syndrome |
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patients of European descent; Latina, Latino, Spanish‐speaking |
| Taking Advantage of a Unique Opportunity: A Genetic Counseling Fellowship in Lysosomal Storage Disorders |
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| Countertransference in the Genetic Counseling Setting: One Counselor's Personal Journey |
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| Changing My Perspective: What My Husband's Cancer Taught Me About Being a Genetic Counselor |
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| Rebuilding My Fortress |
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| How to Talk with Families About Genetics and Psychiatric Illness |
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| When Work, Family And Friendship Collide |
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| The Incentive |
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| Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors |
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| Defining Moments in Genetic Counselor Professional Development: One Decade Later |
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| Uncomfortably Content: My Journey Back to School |
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| Diagnosis of Fragile X Syndrome: A Qualitative Study of African American Families |
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| A Life Changing Experience and Its Impact on My Professional Development as a Genetic Counsellor |
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| Losing Sight |
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| Counseling Adolescents and the Challenges for Genetic Counselors |
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| A Serendipitous Invitation |
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| Postpartum Depression: Is It Mood Disorder or Medical Condition? |
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| Learning to Say No |
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| Confusion and Strength |
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| 46 Chromosomes and Me |
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| A Genetic Counselor's Story of Birth, Grief, and Survival |
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| Counseling the “Angry Patient”: A Defining Moment of Changing Focus from Myself to the Patient |
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| Zen and the Art of Program Development |
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| My Achilles Heel—When a Patient's Request Pushed my Boundaries |
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| Developing my Preferred Model of Genetic Counselling |
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| A Couple's Devastating Journey & My Development as a Genetic Counselor |
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| Being The Genuine Me |
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| It's Not Always About the “Genetics”: Giving Patients What They Need |
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| Genetic Counseling and Testing for FSHD (Facioscapulohumeral Muscular Dystrophy) in the Israeli Population |
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| Boris Pasche (ed): Cancer Genetics: Cancer Treatment and Research |
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| Erratum to: In Memoriam: Dr. Charles Epstein (1933–2011) |
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| Mothers’ Perspectives on Their Child's Mental Illness as Compared to Other Complex Disorders in Their Family: Insights to Inform Genetic Counseling Practice |
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| Defining the Role of Laboratory Genetic Counselor |
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| Delivering a Pharmacogenetic Service: Is There a Role for Genetic Counselors? |
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| Effects of a Documentary Film on Public Stigma Related to Mental Illness Among Genetic Counselors |
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| Disability Advocacy and Reproductive Choice: Engaging with the Expressivist Objection |
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| Commentary: How Individual and Profession‐level Factors Influence Discussion of Disability in Prenatal Genetic Counseling |
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| Information Related to Prenatal Genetic Counseling: Interpretation by Adolescents, Effects on Risk Perception and Ethical Implications |
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| Talking about Disability in Prenatal Genetic Counseling: A Report of Two Interactive Workshops |
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| Commentary on “Life as a Pregnant Genetic Counselor: Take Two” |
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| Life as a Pregnant Genetic Counselor: Take Two |
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| What Information Do Cancer Genetic Counselees Prioritize? |
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| Trends in Telehealth versus On‐site Clinical Genetics Appointments in Manitoba: A Comparative Study |
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| Presented Abstracts from the Thirtieth Annual Education Conference of the National Society of Genetic Counselors (San Diego, CA, October 2011) |
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| Family Physicians’ Awareness and Knowledge of the Genetic Information Non‐Discrimination Act (GINA) |
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| Transition to the Clinical Doctorate: Attitudes of the Genetic Counseling Training Program Directors in North America |
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| Introduction to the Special Issue: Toward Diversity and Cultural Competence in Genetic Counseling |
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| Are Genetic Counselors and GLBT Patients “on the Same Page”? an Investigation of Attitudes, Practices, and Genetic Counseling Experiences |
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| Reading Between the Lines: A Comparison of Responders and Non‐responders to a Family History Questionnaire and Implications for Cancer Genetic Counselling |
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| Forming State Collaborations to Diversify the Nation's Health Workforce: The Experience of the Sullivan Alliance to Transform the Health Professions |
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| Barriers to and Motivations for Physician Referral of Patients to Cancer Genetics Clinics |
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| Iona College Community Centered Family Health History Project: Lessons Learned from Student Focus Groups |
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| Influence of Genetic Risk Information on Parental Role Identity in Adolescent Girls and Young Women from Families with Fragile X Syndrome |
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| At‐Risk Marriages after Compulsory Premarital Testing and Counseling for β‐Thalassemia and Sickle Cell Disease in Saudi Arabia, 2005–2006 |
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| Effectiveness of Pre‐counseling Genetic Education Workshops at a Large Urban Community Health Center Serving Low‐Income Chinese American Women |
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Chinese American; Chinese-speaking populations |
| Sources of Uncertainty About Daughters’ Breast Cancer Risk that Emerge During Genetic Counseling Consultations |
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| Providers’ Perceptions and Practices Regarding <b><i>BRCA1/2</i></b> Genetic Counseling and Testing in African American Women |
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| Waiting for the next Shoe to Drop: The Experience of Parents of Children with Fanconi Anemia |
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| In Memoriam: Dr. Charles Epstein (1993–2011) |
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| Effect of Pre‐test Genetic Counseling for Deaf Adults on Knowledge of Genetic Testing |
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| Using a Family History Intervention to Improve Cancer Risk Perception in a Black Community |
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African American; Black; racial/ethnic |
| Predictors of Heart‐Focused Anxiety in Patients Undergoing Genetic Investigation and Counseling of Long QT Syndrome or Hypertrophic Cardiomyopathy: A One Year Follow‐up |
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| Enriching the Genetic Counseling Recruitment Pipeline: A National Cross‐Sectional Study of Public High School Counselors |
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minorities; ethnic minorities |
| Concurrent Use of Cultural Health Practices and Western Medicine During Pregnancy: Exploring the Mexican Experience in the United States |
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| Primary Care Physicians’ Awareness, Experience and Opinions of Direct‐to‐Consumer Genetic Testing |
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| Attitudes and Beliefs of African‐Americans Toward Genetics, Genetic Testing, and Sickle Cell Disease Education and Awareness |
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African‐Americans |
| Presymptomatic Testing for Neurogenetic Diseases in Brazil: Assessing Who Seeks and Who Follows through with Testing |
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many European samples studied previously |
| In Memoriam: Dr. Charles J. Epstein (1933–2011) |
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| Diversity and General Student Scholarship Recipient Essays: 2010 National Society of Genetic Counselors Membership Committee |
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"minority cultural/ethnic backgrounds"; "students who are from communities underrepresented in the N |
| Clinical Use of the Surgeon General's “My Family Health Portrait” (MFHP) Tool: Opinions of Future Health Care Providers |
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| A Survey of Ethical and Professional Challenges Experienced by Spanish Health‐Care Professionals that Provide Genetic Counseling Services |
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| Personality Traits Associated with Genetic Counselor Compassion Fatigue: The Roles of Dispositional Optimism and Locus of Control |
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| Awareness and Preferences Regarding <i>BRCA1/2</i> Genetic Counseling and Testing Among Latinas and Non‐Latina White Women at Increased Risk for Hereditary Breast and Ovarian Cancer |
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non‐Latina white |
| Exploring the Role of Religiosity and Spirituality in Amniocentesis Decision‐Making Among Latinas |
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Latinas |
| Differences Between African American and White Research Volunteers in Their Attitudes, Beliefs and Knowledge Regarding Genetic Testing for Alzheimer's Disease |
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| Media Coverage of Direct‐to‐Consumer Genetic Testing |
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| Practice Guidelines for Communicating a Prenatal or Postnatal Diagnosis of Down Syndrome: Recommendations of the National Society of Genetic Counselors |
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| Acceptability of Prenatal Diagnosis by a Sample of Parents of Sickle Cell Anemia Patients in Cameroon (Sub‐Saharan Africa) |
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| Pediatric Sub‐specialist Controversies in the Treatment of Congenital Heart Disease in Trisomy 13 or 18 |
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| An Exploration of the Cultural Context of Kinship and Genetics Amongst Arabic‐Australians: Implications for Practice |
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| Unpacking the Blockers: Understanding Perceptions and Social Constraints of Health Communication in Hereditary Breast Ovarian Cancer (HBOC) Susceptibility Families |
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| Distress and Psychosocial Needs of a Heterogeneous High Risk Familial Cancer Population |
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| Where are the Males? Gender Differences in Undergraduates’ Interest in and Perceptions of the Genetic Counseling Profession |
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| RETRACTED ARTICLE: Gender Testing in Sport: The Right of Genetic Diversity and the Right to Not Be Harmed |
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| Extreme Values of Maternal Serum Analytes in Second Trimester Screening: Looking Beyond Trisomy and NTD's |
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| Genetic Twists of Fate Stanley Fields and Mark Johnston |
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| Breast and Ovarian Cancer: The Forgotten Paternal Contribution |
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| Barriers in Identification and Referral to Genetic Counseling for Familial Cancer Risk: The Perspective of Genetic Service Providers |
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| Parents’ Communication with Siblings of Children Affected by an Inherited Genetic Condition |
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| Testing of Collegiate Athletes for Sickle Cell Trait: What We, as Genetic Counselors Should Know |
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| Extended Family Impact of Genetic Testing: The Experiences of X‐linked Carrier Grandmothers |
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| Genetic Testing and Parkinson Disease: Assessment of Patient Knowledge, Attitudes, and Interest |
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| Shock, Adjust, Decide: Reproductive Decision Making in Cystic Fibrosis (CF) Carrier Couples—A Qualitative Study |
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White British population |
| The Use of Family History Questionnaires: An Examination of Genetic Risk Estimates and Genetic Testing Eligibility in the Non‐responder Population |
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| Self Diagnosis of Lynch Syndrome Using Direct to Consumer Genetic Testing: A Case Study |
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| Neurogenetic Syndromes: Behavioral Issues and Their Treatment |
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| The Alpha‐1 Association Genetic Counseling Program: An Innovative Approach to Service |
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| Carole H. Browner and H. Mabel Preloran <i>Neurogenetic Diagnoses: The Power of Hope, and the Limits of Today's Medicine</i> |
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| The Culture of the Elite Athlete: An Enhanced Perspective on the Case of Caster Semenya, and Gender Verification Testing |
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| Teaching About Genetic Testing Issues in the Undergraduate Classroom: A Case Study |
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| Development and Evaluation of a Decision Aid for <i>BRCA</i> Carriers with Breast Cancer |
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| PREVIVORS: Facing the Breast Cancer Gene and Making Life‐Changing Decisions |
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| Validation of a Self‐Concept Scale for Lynch Syndrome in Different Nationalities |
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| ABGC Diplomates Certified in 2010 |
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| Why is Everyone So Anxious?: An Exploration of Stress and Anxiety in Genetic Counseling Graduate Students |
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| Ethical Dilemmas in Genetic Testing: Examples from the Cuban Program for Predictive Diagnosis of Hereditary Ataxias |
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| Presidential Address |
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| A Model of Professional Development for Practicing Genetic Counselors: Adaptation of Communication Skills Training in Oncology |
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| Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven‐Year Period |
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| “You Have to Sit and Explain it All, and Explain Yourself.” Mothers’ Experiences of Support Services for Their Offspring with a Rare Genetic Intellectual Disability Syndrome |
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| Peer Observed Interaction and Structured Evaluation (POISE): A Canadian Experience with Peer Supervision for Genetic Counselors |
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| Communication of Genetic Information by Other Health Professionals: The Role of the Genetic Counsellor in Specialist Clinics |
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