| Care of the Self and Patient Participation in Genetic Discourse: A Foucauldian Reading of the Surgeon General's “My Family Health Portrait” Program |
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| Genetics and Life Insurance Medical Underwriting and Social Policy |
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| Perceptions and Attitudes about <i>HFE</i> Genotyping Among College‐Age Adults |
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| Risk‐Reduction Surgery Decisions in High‐Risk Women Seen for Genetic Counseling |
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| “SLANG”—Sensitive Language and the New Genetics—an Exploratory Study |
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| Psychological Adjustment and Knowledge About Hereditary Hemochromatosis in a Clinic‐Based Sample: A Prospective Study |
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| Sequential Down Syndrome Screening: The Importance of First and Second Trimester Test Correlations when Calculating Risk |
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| Doctor's Expertise and Managing Discrepant Information from Other Sources in Genetic Counseling: A Conversation Analytic Perspective |
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| Genetics and Life Insurance Medical Underwriting and Social Policy |
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| Care of the Self and Patient Participation in Genetic Discourse: A Foucauldian Reading of the Surgeon General's “My Family Health Portrait” Program |
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| Thursdays with Marion: The Therapist's Tale |
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| Communication Analysis of BRCA1 Genetic Counseling |
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| Comparing Knowledge of β‐Thalassemia in Samples of Italians, Italian‐Americans, and Non‐Italian‐Americans |
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Italians, Italian-Americans, Other-Americans |
| Schizophrenia: An Update and Review |
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| Factors Influencing Uptake of Genetic Testing For Colorectal Cancer Risk in an Australian Jewish Population |
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Australian Ashkenazi Jewish community; Australian Jewish individuals; Jewish communities |
| Predictive Genetic Testing for Hereditary Breast and Ovarian Cancer: Psychological Distress and Illness Representations 1 Year Following Disclosure |
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| Who Are the Next Generation of Genetic Counselors? A Survey of Students |
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ethnic minorities |
| Policy Recommendations for Carrier Testing and Predictive Testing in Childhood: A Distinction That Makes a Real Difference |
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| Psychosocial Issues That Face Patients With Charcot-Marie-Tooth Disease: The Role of Genetic Counseling |
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| Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis |
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| Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors |
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| Educating Genetic Counselors in Australia: Developing an International Perspective |
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| An Assessment of Risk Understanding in Hispanic Genetic Counseling Patients |
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| Policy Recommendations for Carrier Testing and Predictive Testing in Childhood: A Distinction That Makes a Real Difference |
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| Educating Genetic Counselors in Australia: Developing an International Perspective |
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| An Assessment of Risk Understanding in Hispanic Genetic Counseling Patients |
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| Psychosocial Issues That Face Patients With Charcot‐Marie‐Tooth Disease: The Role of Genetic Counseling |
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| Women's Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis |
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| Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors |
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| Evaluating Genetic Counseling: Client Expectations, Psychological Adjustment and Satisfaction with Service |
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| Negotiating Responsibility: Case Studies of Reproductive Decision‐Making and Prenatal Genetic Testing in Families Facing Huntington Disease |
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| Racial‐Ethnic Differences in Genetic Amniocentesis Uptake |
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Hispanic; African American; Asian; race-ethnicity |
| Assessment of the Use and Feasibility of Video to Supplement the Genetic Counseling Process: A Cancer Genetic Counseling Perspective |
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| Men's Decision‐Making About Predictive <i>BRCA1/2</i> Testing: The Role of Family |
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| Genetic Evaluation and Counseling of Couples with Recurrent Miscarriage: Recommendations of the National Society of Genetic Counselors |
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| National Society of Genetic Counselors, 24th Annual Education Conference |
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| Disability Rights, Prenatal Diagnosis and Eugenics: A Cross‐Cultural View |
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| Genetic Testing for Cancer: Psychological Approaches for Helping Patients and Families |
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| How do Obstetric Providers Discuss Referrals for Prenatal Genetic Counseling? |
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| Psychodynamic Theory and Counseling in Predictive Testing for Huntington's Disease |
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| Genetic Counseling Outcomes: Perceived Risk and Distress After Counseling for Hereditary Colorectal Cancer |
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| Emotional Responses to APO E Genotype Disclosure for Alzheimer Disease |
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| A Practical Account of Autonomy: Why Genetic Counseling is Especially Well Suited to the Facilitation of Informed Autonomous Decision Making |
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| NSGC Foundations—Then, Now, and Tomorrow |
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| National Society of Genetic Counselors, 24th Annual Education Conference |
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| Facilitating Family Communication About Predictive Genetic Testing: Probands’ Perceptions |
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| Experiences of Prenatal Diagnosis of Spina Bifida or Hydrocephalus in Parents Who Decide to Continue with Their Pregnancy |
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| Consideration of Genetic Counseling as a Career: Implications for Diversifying the Genetic Counseling Field |
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| Cystic Fibrosis Prenatal Screening in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors |
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| (Mis)alignments in Counseling for Huntington's Disease Predictive Testing: Clients’ Responses to Reflective Frames |
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| Evaluating the Impact of Genetic Counseling and Testing with Signal Detection Methods |
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| Differences in Individual Approaches: Communication in the Familial Breast Cancer Consultation and the Effect on Patient Outcomes |
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| The Effect of Experiential Knowledge on Construction of Risk Perception in Hereditary Breast/Ovarian Cancer |
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| Book Review: The Genetic Basis of Human Cancer (2nd ed.), by Berf Vogelstein and Kenneth w. Kinzler |
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