211 results on '"Quillin, John"'
Search Results
2. Addressing disparities in the uptake of genetic counseling and testing in African American women; rationale, design and methods
3. An exploration of cultural competency training and genetic counselors' racial biases.
4. Awareness and acceptability of population-based screening for pathogenic BRCA variants: Do race and ethnicity matter?
5. Common Hereditary Cancer Syndromes
6. The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease
7. High-Risk Palliative Care Patients’ Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking
8. Gendered and Non-Gendered Language in Genetic Counseling Patient Interactions
9. Cancer Genetic Counseling and Testing in an Era of Rapid Change
10. Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America
11. Practical Considerations for Implementing Research Recruitment Etiquette
12. Talking (or Not) about Family Health History in Families of Latino Young Adults
13. Assessing Cancer Genetic Counselors’ Decision-Making in Addressing Lifestyle Behavior Changes
14. Evaluating the Impact of a New Educational Tool on Understanding of Polygenic Risk Scores and Beliefs Regarding Alcohol Use Disorder
15. Phone Script and Interview Guide
16. Prevalence of Racial Bias in Genetic Counseling
17. Halleck - Mainstream Hereditary Cancer Testing for Ovarian Cancer Patients
18. Investigating the Understanding and Attitudes of Recommended Guidelines for Cancer Prevention Behaviors Among People Who Have Hereditary Cancer Testing
19. Lifestyle Risk Factors Among People Who Have Had Cancer Genetic Testing
20. Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America.
21. Reaching Hard to Reach Populations with Hard to Communicate Messages: Efficacy of a Breast Health Research Champion Training Program
22. Tolerance for Ambiguity Could Influence Awareness of Breast Cancer Genetic Testing and Inform Health Education
23. Duration of an Intervention's Impact on Perceived Breast Cancer Risk
24. Patient-reported hereditary breast and ovarian cancer in a primary care practice
25. Genetic Counselors’ Current Use of Personal Health Records-Based Family Histories in Genetic Clinics and Considerations for Their Future Adoption
26. Genetic Risk, Perceived Risk, and Cancer Worry in Daughters of Breast Cancer Patients
27. The effect of a school-based educational intervention on gender differences in reported family cancer history
28. CDH1 variants leading to gastric cancer risk management decision‐making experiences in emerging adults: ‘I am not ready yet’
29. Spiritual Coping, Family History, and Perceived Risk for Breast Cancer—Can We Make Sense of it?
30. Gail Model Risk Assessment and Risk Perceptions
31. Social Work and Genetics
32. Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force
33. Universal Mismatch Repair Protein Screening in Upper Tract Urothelial Carcinoma
34. Reducing Disparities in Receipt of Genetic Counseling for Underserved Women at Risk of Hereditary Breast and Ovarian Cancer
35. Black Women’s Confidence in the Genetic Information Nondiscrimination Act
36. Building Genetic Medicine: Breast Cancer, Technology and the Comparative Politics of Health Care
37. Bioarchaeology: The Contextual Analysis of Human Remains
38. Recontacting patients for multigene panel testing in hereditary cancer: Efficacy and insights
39. Theology, Disability and the New Genetics: Why Science Needs the Church: Edited by John Swinton and Brian Brock. T&T Clark, London, 2007, 264 pp., $130.00 hardback, $34.95 paperback
40. The Role of Palliative Medicine in Assessing Hereditary Cancer Risk
41. Missed opportunities: Oncologists and palliative care specialists may be the last chance to explore hereditary cancer among cancer in-patients before information and DNA is lost.
42. High-Risk Palliative Care Patients’ Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking
43. Direct-to-Consumer Genetic Testing and Orphan Drug Development
44. Engaging Patients to Understand Their Family History for Cancer: A Case Study About Recruiting in a Safety-Net Women’s Clinic
45. Family Ties: The Role of Family Context in Family Health History Communication About Cancer
46. Lifestyle Risk Factors Among People Who Have Had Cancer Genetic Testing
47. Getting Youth to Check it Out!®: A New Approach to Teaching Self-screening
48. What Women Think: Cancer Causal Attributions in a Diverse Sample of Women
49. Knowledge, Attitudes, and Behaviors Questionnaire
50. Peer-to-peer communication, cancer prevention, and the internet: Workgroup discussion of peer-to-peer communication about primary and secondary prevention, Society of Behavioral Medicine, San Diego, CA, March 26, 2008
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.