Rosalind A Eeles
Biographic Data
| ID | 3465560 |
|---|---|
| NAME | Rosalind A Eeles |
| GIVEN NAMES | Rosalind A |
| FAMILY NAME | Eeles |
| SIGNATURE | EELES R A |
| AFFILIATIONS | Institute of Cancer Research |
| ORCID | 0000-0002-3698-6241 |
| VERIFIED | Yes |
| TOTAL WORKS | 6 |
| TOTAL CITATIONS | 46 |
| AUTHOR COUNT | 6 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2002 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 4 |
Understanding Barriers to Engagement With a Prostate Cancer Research and Genetic Risk Service Among UK Men of Black African or Black Caribbean Ancestry
INTRODUCTION: Prostate cancer is the second most common cancer worldwide, and there is no national prostate cancer screening programme in the United Kingdom. Men of African ancestry are twice as likely to be diagnosed as men of European ancestry and are diagnosed at a younger age. Despite this, Black men are under-represented in seeking advice about prostate cancer symptoms, screening and genetic research. There is increasing research focused on …
Guilt, blame and responsibility
Men and women who have a family history of breast and/or ovarian cancer may be offered a predictive genetic test to determine whether or not they carry the family specific BRCA1/2 mutation. The sons and daughters of mutation carriers have a 50 per cent chance of inheriting a mutation, which will increase their risk of developing cancer. Little is known about at-risk men's feelings about the part they play in the transmission of BRCA1/2 mutations …
Accommodating risk
Living with chronic risk
This paper investigates how healthy women with a family history of breast/ovarian cancer live with their heightened awareness of risk, and introduces a chronic risk perspective for studying this topic. Healthy women from these at-risk families and individuals suffering from a chronic illness address many of the same issues concerning adaptation to biographical disruption and an uncertain future. We report on risk perception, family history, life …
Family stories and the use of heuristics
The practice of medicine will increasingly be medicine of the family rather than the traditional physician/patient dyad, especially where a genetic condition is involved. This study explores how clients from suspected hereditary breast and ovarian cancer (HBOC) families seeking cancer genetics risk counselling are influenced by family stories and the use of heuristics (inferential shortcuts used to make sense of complicated information) in interp…
Genetic Testing for Breast and Ovarian Cancer Predisposition
The purpose of this study was to explore experiences of cancer in the family and motivation for predictive genetic testing among women at increased risk of developing breast and/or ovarian cancer due to their family history. Fifteen women were interviewed prior to receiving their genetic test results. A grounded theory approach was adopted to analyse the interview transcripts. The findings indicated that experiences of cancer in the family play a…
Guilt, blame and responsibility
Men and women who have a family history of breast and/or ovarian cancer may be offered a predictive genetic test to determine whether or not they carry the family specific BRCA1/2 mutation. The sons and daughters of mutation carriers have a 50 per cent chance of inheriting a mutation, which will increase their risk of developing cancer. Little is known about at-risk men's feelings about the part they play in the transmission of BRCA1/2 mutations …
Accommodating risk
Family stories and the use of heuristics
The practice of medicine will increasingly be medicine of the family rather than the traditional physician/patient dyad, especially where a genetic condition is involved. This study explores how clients from suspected hereditary breast and ovarian cancer (HBOC) families seeking cancer genetics risk counselling are influenced by family stories and the use of heuristics (inferential shortcuts used to make sense of complicated information) in interp…
Genetic Testing for Breast and Ovarian Cancer Predisposition
The purpose of this study was to explore experiences of cancer in the family and motivation for predictive genetic testing among women at increased risk of developing breast and/or ovarian cancer due to their family history. Fifteen women were interviewed prior to receiving their genetic test results. A grounded theory approach was adopted to analyse the interview transcripts. The findings indicated that experiences of cancer in the family play a…
Genetic Testing for Breast and Ovarian Cancer Predisposition
The purpose of this study was to explore experiences of cancer in the family and motivation for predictive genetic testing among women at increased risk of developing breast and/or ovarian cancer due to their family history. Fifteen women were interviewed prior to receiving their genetic test results. A grounded theory approach was adopted to analyse the interview transcripts. The findings indicated that experiences of cancer in the family play a…
Living with chronic risk
This paper investigates how healthy women with a family history of breast/ovarian cancer live with their heightened awareness of risk, and introduces a chronic risk perspective for studying this topic. Healthy women from these at-risk families and individuals suffering from a chronic illness address many of the same issues concerning adaptation to biographical disruption and an uncertain future. We report on risk perception, family history, life …
Family stories and the use of heuristics
The practice of medicine will increasingly be medicine of the family rather than the traditional physician/patient dyad, especially where a genetic condition is involved. This study explores how clients from suspected hereditary breast and ovarian cancer (HBOC) families seeking cancer genetics risk counselling are influenced by family stories and the use of heuristics (inferential shortcuts used to make sense of complicated information) in interp…
Accommodating risk
Guilt, blame and responsibility
Men and women who have a family history of breast and/or ovarian cancer may be offered a predictive genetic test to determine whether or not they carry the family specific BRCA1/2 mutation. The sons and daughters of mutation carriers have a 50 per cent chance of inheriting a mutation, which will increase their risk of developing cancer. Little is known about at-risk men's feelings about the part they play in the transmission of BRCA1/2 mutations …
Understanding Barriers to Engagement With a Prostate Cancer Research and Genetic Risk Service Among UK Men of Black African or Black Caribbean Ancestry
INTRODUCTION: Prostate cancer is the second most common cancer worldwide, and there is no national prostate cancer screening programme in the United Kingdom. Men of African ancestry are twice as likely to be diagnosed as men of European ancestry and are diagnosed at a younger age. Despite this, Black men are under-represented in seeking advice about prostate cancer symptoms, screening and genetic research. There is increasing research focused on …
Medicine (6 works) · BRCA gene mutations in cancer (5 works) · Cancer (5 works) · Internal Medicine (5 works) · Breast cancer (4 works) · Family history (4 works) · Genetic testing (4 works) · Psychology (4 works) · Qualitative research (4 works) · Family medicine (3 works)