Items created by Benjamin, Caroline

2018

Carrieri, Daniele, Howard, Heidi C, Benjamin, Caroline, Clarke, Angus J, Dheensa, Sandi, Doheny, Shane, Hawkins, Naomi, Halbersma-Konings, Tanya F, Jackson, Leigh et al (2018) Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. European Journal of Human Genetics . ISSN 1018-4813

Calzone, Kathleen A, Kirk, Maggie, Tonkin, Emma, Badzek, Laurie, Benjamin, Caroline and Middleton, Anna (2018) Increasing nursing capacity in genomics: Overview of existing global genomics resources. Nurse Education Today, 69 . pp. 53-59. ISSN 0260-6917

Calzone, Kathleen A, Kirk, Maggie, Tonkin, Emma, Badzek, Laurie, Benjamin, Caroline and Middleton, Anna (2018) The Global Landscape of Nursing and Genomics. Journal Of Nursing Scholarship, 50 (3). pp. 249-256. ISSN 1527-6546

Sirchia, Fabio, Carrieri, Daniele, Dheensa, Sandi, Benjamin, Caroline, Kayserili, Hülya, Cordier, Christophe, van El, Carla G, Turnpenny, Peter D, Melegh, Bela et al (2018) Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe. European Journal of Human Genetics . ISSN 1018-4813

2017

Middleton, Anna, Mendes, Alvaro, Benjamin, Caroline and Howard, Heidi Carmen (2017) Direct-to-consumer genetic testing: where and how does genetic counseling fit? Personalized Medicine, 14 (3). pp. 249-257. ISSN 1741-0541

2016

Benjamin, Caroline, Boudioni, Markella, Ward, Helen, Marston, Elliot, Lindenmeyer, Antje, Bangee, Munirah ORCID: 0000-0001-8548-6692, Cook Lucas, Julie ORCID: 0000-0002-6391-5430, LEAVEY, RALPH, Caulfield, Mark et al (2016) Project Report - NHS Genomic Medicine Centres: Process and Participant Materials used in the 100,000 Genomes Project. Project Report. Genomics England, Dawson Hall, Charterhouse Square, London EC1M 6BQ.

2015

Benjamin, Caroline, Thomas, Lois Helene ORCID: 0000-0001-5218-6546, Skirton, Heather, Gustafson, Shanna, Coupe, Jacqueline ORCID: 0000-0002-2025-5620, Patch, Christine, Belk, Rachel, Tishkovskaya, Svetlana ORCID: 0000-0003-3087-6380, Calzone, Kathleen et al (2015) Interventions to improve patient access to and utilisation of genetic and genomic counselling services. Cochrane Database of Systematic Reviews, 11 .

Benjamin, Caroline, Houghton, Catherine, Foo, Claire, Edgar, Chris, Mannion, Gail, Birch, Jan, Ellis, Ian and Weber, Astrid (2015) A prospective cohort study assessing clinical referral management & workforce allocation within a UK regional medical genetics service. European Journal of Human Genetics, 23 (8). pp. 996-1003. ISSN 1018-4813

2014

Skirton, Heather, Cordier, Christophe, Ingvoldstad, Charlotta, Taris, Nicolas and Benjamin, Caroline (2014) The role of the genetic counsellor: a systematic review of research evidence. European Journal of Human Genetics, 23 . pp. 452-458. ISSN 1018-4813

Middleton, Anna, Patch, Chris, Wiggins, Jennifer, Barnes, Kathy, Crawford, Gill, Benjamin, Caroline and Bruce, Anita (2014) Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland). European Journal of Human Genetics, 22 (8). pp. 955-956. ISSN 1018-4813

2013

Benjamin, Caroline, Birch, Jan, Bradley, Aoife and Mannion, Gail (2013) Genetics: examining your competency of practice on a regular basis. Nursing standard (Royal College of Nursing (Great Britain) : 1987), 28 (14). pp. 37-43. ISSN 0029-6570

2011

Nippert, Irmgard, Harris, Hilary J., Julian-Reynier, Claire, Kristoffersson, Ulf, Kate, Leo P., Anionwu, Elizabeth, Benjamin, Caroline, Challen, Kirsty, Schmidtke, Jörg et al (2011) Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1. Journal of Community Genetics, 2 (1). pp. 1-11. ISSN 1868-310X

2010

Challen, Kirsty, Harris, Hilary, Kristoffersson, Ulf, Nippert, Irmgard, Schmidtke, Joerg, Kate, Leo P., Benjamin, Caroline, Anionwu, Elizabeth, Plass, Anne-Marie et al (2010) General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices. Journal of Community Genetics, 1 (2). pp. 83-90. ISSN 1868-310X

2009

Benjamin, Caroline, Anionwu, Elizabeth N., Kristoffersson, Ulf, ten Kate, Leo P., Plass, Anne Marie C., Nippert, Irmgard, Julian-Reynier, Claire, Harris, Hilary J., Schmidtke, Joerg et al (2009) Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden. MIDWIFERY, 25 (5). pp. 483-499. ISSN 0266-6138

Plass, Anne Marie C., Baars, Marieke J.H., Cornel, Martina C., Julian-Reynier, Claire, Nippert, Irmgard, Harris, Hillary, Kristoffersson, Ulf, Schmidtke, Jörg, Anionwu, Elizabeth N. et al (2009) Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union. Genetic Testing and Molecular Biomarkers, 13 (3). pp. 367-376. ISSN 1945-0265

2008

Calefato, Jean-Marc, Nippert, Irma, Harris, Hilary J, Kristoffersson, Ulf, Schmidtke, Jorg, Ten Kate, Leo P, Anionwu, Elizabeth, Benjamin, Caroline, Challen, Kirsty et al (2008) Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale. Genetics in Medicine, 10 (2). pp. 99-106. ISSN 1098-3600

Julian-Reynier, Claire, Nippert, Irma, Calefato, Jean-Marc, Harris, Hilary, Kristoffersson, Ulf, Schmidtke, Joerg, Ten Kate, Leo, Anionwu, Elizabeth, Benjamin, Caroline et al (2008) Genetics in clinical practice: general practitioners' educational priorities in European countries. Genetics in Medicine, 10 (2). pp. 107-113. ISSN 1098-3600

Benjamin, Caroline, Flynn, Maria, Hallett, Christine, Ellis, Ian and Booth, Katie (2008) The use of the life course paradigm and life course charts to explore referral for family history of breast cancer. International Journal of Nursing Studies, 45 (1). pp. 95-109. ISSN 0020-7489

2006

Harris, Rodney, Challen, Kirsty, Benjamin, Caroline and Harris, Hilary (2006) Genetic Education for Non-Geneticist Health Professionals. Community Genetics, 9 (4). pp. 224-226. ISSN 1422-2795

Challen, Kirsty, Harris, Hilary, Benjamin, Caroline and Harris, Rodney (2006) Genetics Teaching for Non-Geneticist Health Care Professionals in the UK. Community Genetics, 9 (4). pp. 251-259. ISSN 1422-2795

2005

Benjamin, Caroline and Gamet, Kimberley (2005) Recognising the limitations of your genetics expertise. Nursing standard, 20 (6). pp. 49-54. ISSN 0029-6570

Challen, Kirsty, Harris, Hilary J, Julian-Reynier, Claire, ten Kate, Leo P, Kristoffersson, Ulf, Nippert, Irmgard, Schmidtke, Jörg, Benjamin, Caroline and Harris, Rodney (2005) Genetic education and nongenetic health professionals: Educational providers and curricula in Europe. Genetics in Medicine, 7 (5). pp. 302-310. ISSN 1098-3600

2003

Benjamin, Caroline, Booth, Katie and Ellis, Ian (2003) A prospective comparison study of different methods of gathering self-reported family history information for breast cancer risk assessment. Journal of Genetic Counseling, 12 (2). pp. 151-170. ISSN 1059-7700

2001

Benjamin, Caroline (2001) Stigma associated with genetic conditions. In: Stigma and Social Exclusion in Healthcare. Routledge. ISBN 978-0-415-22199-3

Benjamin, Caroline and Gibson, J (2001) Will the human genome project have any impact on nursing? Nursing times, 97 (12). p. 17. ISSN 0954-7762

2000

Benjamin, Caroline and Lashwood, A (2000) United Kingdom experience with presymptomatic testing of individuals at 25% risk for Huntington's disease. Clinical Genetics, 58 (1). pp. 41-49. ISSN 0009-9163

1995

Telenius, H, Almqvist, E, Kremer, B, Spence, N, Squitieri, F, Nichol, K, Grandell, U, Starr, E, Benjamin, Caroline et al (1995) Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease. Human molecular genetics, 4 (2). pp. 189-95. ISSN 0964-6906

1994

Benjamin, Caroline, Adam, S, Wiggins, S, Theilmann, J L, Copley, T T, Bloch, M, Squitieri, F, McKellin, W, Cox, S et al (1994) Proceed with care: direct predictive testing for Huntington disease. American journal of human genetics, 55 (4). pp. 606-17. ISSN 0002-9297

1993

Benjamin, Caroline, Colley, A, Donnai, D, Kingston, H, Harris, R and Kerzin-Storrar, L (1993) Neurofibromatosis type 1 (NF1): knowledge, experience, and reproductive decisions of affected patients and families. Journal of medical genetics, 30 (7). pp. 567-74. ISSN 0022-2593

1991

Maher, E R, Iselius, L, Yates, J R, Littler, M, Benjamin, Caroline, Harris, R, Sampson, J, Williams, A, Ferguson-Smith, M A et al (1991) Von Hippel-Lindau disease: a genetic study. Journal of medical genetics, 28 (7). pp. 443-7. ISSN 0022-2593

1990

Maher, E.R., Bentley, E., Yates, J.R.W., Barton, D., Jennings, A., Fellows, I.W., Ponder, M.A., Ponder, B.A.J., Benjamin, Caroline et al (1990) Mapping of Von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis. Journal of the Neurological Sciences, 100 (1-2). pp. 27-30. ISSN 0022510X

Maher, E R, Yates, J R, Harries, R, Benjamin, Caroline, Harris, R, Moore, A T and Ferguson-Smith, M A (1990) Clinical features and natural history of von Hippel-Lindau disease. The Quarterly journal of medicine, 77 (2). pp. 1151-1163. ISSN 0033-5622