Published in J Nurs Scholarsh on December 09, 2010
Advancing genomic research and reducing health disparities: what can nurse scholars do? J Nurs Scholarsh (2013) 0.76
Building Genetic Competence Through Partnerships and Interactive Models. J Nurs Educ (2016) 0.75
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health. Ann Intern Med (2009) 2.58
Disclosing genetic test results to family members. J Nurs Scholarsh (2005) 2.45
An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countries. Eur J Hum Genet (2007) 2.21
Informed consent and genomic incidental findings: IRB chair perspectives. J Empir Res Hum Res Ethics (2011) 1.72
Challenges assessing clinical endpoints in early Huntington disease. Mov Disord (2010) 1.66
Genetic counsellors: a registration system to assure competence in practice in the United kingdom. Community Genet (2003) 1.56
Nurses transforming health care using genetics and genomics. Nurs Outlook (2010) 1.54
A profile of the genetic counsellor and genetic nurse profession in European countries. J Community Genet (2011) 1.46
Experiences of UK patients with hepatitis C virus infection accessing phlebotomy: A qualitative analysis. Nurs Health Sci (2014) 1.41
Direct-to-consumer genomic testing: systematic review of the literature on user perspectives. Eur J Hum Genet (2012) 1.38
Can I get a retweet please? Health research recruitment and the Twittersphere. J Adv Nurs (2013) 1.34
Toward a biopsychosocial model for 21st-century genetics. Fam Process (2005) 1.33
Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease. Am J Med Genet B Neuropsychiatr Genet (2008) 1.29
Risk reduction and health promotion behaviors following genetic testing for adult-onset disorders. Genet Test (2007) 1.23
Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting. Patient Educ Couns (2012) 1.17
Addressing the issue of e-learning and online genetics for health professionals. Nurs Health Sci (2007) 1.15
Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing? J Genet Couns (2010) 1.14
Feasibility of combining e-health for patients with e-learning for students using synchronous technologies. J Adv Nurs (2006) 1.13
Genomics in nursing education. J Nurs Scholarsh (2005) 1.12
Psychological factors that impact on women's experiences of first-time motherhood: a qualitative study of the transition. Midwifery (2008) 1.11
Genetic testing and counselling in Europe: health professionals current educational provision, needs assessment and potential strategies for the future. Eur J Hum Genet (2007) 1.10
The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice. J Community Genet (2013) 1.10
Educational gaming in the health sciences: systematic review. J Adv Nurs (2008) 1.08
Incidental findings in genetic research and clinical diagnostic tests: a systematic review. Am J Med Genet A (2012) 1.07
Experiences of teens living in the shadow of Huntington Disease. J Genet Couns (2008) 1.07
Life trajectories, genetic testing, and risk reduction decisions in 18-39 year old women at risk for hereditary breast and ovarian cancer. J Genet Couns (2008) 1.06
Perception, experience, and response to genetic discrimination in Huntington disease: the international RESPOND-HD study. Am J Med Genet B Neuropsychiatr Genet (2010) 1.05
Costs and difficulties of recruiting patients to provide e-health support: pilot study in one primary care trust. BMC Med Inform Decis Mak (2012) 1.05
A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases. Prog Neurobiol (2013) 1.03
Communication, encouragement, and cancer screening in families with and without mutations for hereditary nonpolyposis colorectal cancer: a pilot study. Genet Med (2009) 1.03
The emotional experiences of family carers in Huntington disease. J Adv Nurs (2009) 1.03
What counts as effective genetic counselling for presymptomatic testing in late-onset disorders? A study of the consultand's perspective. J Genet Couns (2013) 1.01
Relevance of genomics to healthcare and nursing practice. J Nurs Scholarsh (2013) 1.00
Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users' perspective. Eur J Hum Genet (2012) 0.99
Individual genetic and genomic research results and the tradition of informed consent: exploring US review board guidance. J Med Ethics (2012) 0.95
Fetal sex determination using cell-free fetal DNA: service users' experiences of and preferences for service delivery. Prenat Diagn (2012) 0.94
Genomic health care: is the future now? Nurs Health Sci (2008) 0.93
Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature. J Community Genet (2013) 0.90
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009. NIH Consens State Sci Statements (2009) 0.90
Couples' attributions for work function changes in prodromal Huntington disease. J Genet Couns (2010) 0.90
Living without a diagnosis: the parental experience. Genet Test Mol Biomarkers (2010) 0.89
Living with genetic test results for hereditary breast and ovarian cancer. J Nurs Scholarsh (2009) 0.88
A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs. J Genet Couns (2013) 0.88
Brief report: Predictors of parenting stress among parents of children with biochemical genetic disorders. J Pediatr Psychol (2004) 0.88
Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies. Acta Obstet Gynecol Scand (2010) 0.87
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology. Eur J Hum Genet (2013) 0.87
Family carer personal concerns in Huntington disease. J Adv Nurs (2011) 0.87
Characterization of depression in prodromal Huntington disease in the neurobiological predictors of HD (PREDICT-HD) study. J Psychiatr Res (2013) 0.86
Huntington disease: families' experiences of healthcare services. J Adv Nurs (2010) 0.86
Informed consent to healthcare interventions in people with learning disabilities--an integrative review. J Adv Nurs (2008) 0.85
Informed decision making regarding antenatal screening for fetal abnormality in the United Kingdom: a qualitative study of parents and professionals. Nurs Health Sci (2013) 0.85
EuroGentest patient information leaflets: a free resource available in over 20 languages. Eur J Hum Genet (2009) 0.85
Palliative day care: a qualitative study of service users' experiences in the United Kingdom. Nurs Health Sci (2011) 0.85
Increasing participation in genomic research and biobanking through community-based capacity building. J Genet Couns (2014) 0.85
Using meta-ethnography to understand the emotional impact of caring for people with increasing cognitive impairment. Nurs Health Sci (2013) 0.84
Use of educational games in the health professions: a mixed-methods study of educators' perspectives in the UK. Nurs Health Sci (2010) 0.83
Ethics, policy, and educational issues in genetic testing. J Nurs Scholarsh (2006) 0.83
Perception, experience, and response to genetic discrimination in Huntington's disease: the Australian results of The International RESPOND-HD study. Genet Test Mol Biomarkers (2013) 0.83
A systematic review of factors influencing uptake of invasive fetal genetic testing by pregnant women of advanced maternal age. Midwifery (2013) 0.83
A systematic review of the impact of foreign postings on accompanying spouses of military personnel. Nurs Health Sci (2012) 0.83
Knowledge of genetics and the role of the nurse in genetic health care: a survey of Italian nurses. J Adv Nurs (2012) 0.83
Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles. Genet Test Mol Biomarkers (2011) 0.82
Couples' coping in prodromal Huntington disease: a mixed methods study. J Genet Couns (2012) 0.81
Reproductive empowerment: the main motivator and outcome of carrier testing. J Health Psychol (2011) 0.81
End-of-life care discussions with nonmalignant respiratory disease patients: a systematic review. J Palliat Med (2013) 0.80
Perceptions of young people about decision making in the acute healthcare environment. Paediatr Nurs (2007) 0.80
Exploring supportive care for individuals affected by Huntington disease and their family caregivers in a community setting. J Clin Nurs (2008) 0.79
Development of the HD-Teen Inventory. Clin Nurs Res (2011) 0.79
Genetic testing and screening. Am J Nurs (2002) 0.78
A new scale to measure family members' perception of community health care services for persons with Huntington disease. J Eval Clin Pract (2010) 0.78
Storytellers as partners in developing a genetics education resource for health professionals. Nurse Educ Today (2011) 0.77
Pregnancy as foreground in cystic fibrosis carrier testing decisions in primary care. Genet Test Mol Biomarkers (2009) 0.77
The Department of Health-supported genetic counsellor training post scheme in England: a unique initiative? J Community Genet (2012) 0.77
Adaption and adjustment of military spouses to overseas postings: an online forum study. Nurs Health Sci (2014) 0.77
The use of genealogy databases for risk assessment in genetic health service: a systematic review. J Community Genet (2012) 0.77
An iterative consensus-building approach to revising a genetics/genomics competency framework for nurse education in the UK. J Adv Nurs (2013) 0.76
The importance of patient engagement. Genet Test Mol Biomarkers (2013) 0.76
U.S. genetics nurses in advanced practice. J Nurs Scholarsh (2006) 0.75
Development of the Huntington disease work function scale. J Occup Environ Med (2012) 0.75
Nursing research linking genetics and health. Res Theory Nurs Pract (2003) 0.75
Building Genetic Competence Through Partnerships and Interactive Models. J Nurs Educ (2016) 0.75
Genetic association studies in nursing practice and scholarship. J Nurs Scholarsh (2008) 0.75
Critical care outreach--a meaningful evaluation. Nurs Crit Care (2007) 0.75
A review assessing the current treatment strategies for postnatal psychological morbidity with a focus on post-traumatic stress disorder. Midwifery (2012) 0.75
Counseling adolescents and the challenges for genetic counselors. J Genet Couns (2011) 0.75
Advancing social research relationships in postnatal support settings. Public Health Nurs (2013) 0.75
Social Change: A Framework for Inclusive Leadership Development in Nursing Education. J Nurs Educ (2016) 0.75
The role of genetic/genomic factors in health, illness and care provision. Nurs Stand (2013) 0.75
International collaboration on genomics education for nurses. J Contin Educ Nurs (2005) 0.75
From Nightingale and Mendel to genomics in health care for children. J Pediatr Nurs (2008) 0.75
Student experience highlights need for good communication. Nurs Stand (2010) 0.75
Development of an evidence-based information booklet to support parents of children without a diagnosis. J Genet Couns (2012) 0.75
Informed consent for blood tests in people with a learning disability. J Adv Nurs (2012) 0.75
Genetic counseling: a survey to explore knowledge and attitudes of Italian nurses and midwives. Nurs Health Sci (2012) 0.75
Academic and Institutional Review Board Collaboration to Ensure Ethical Conduct of Doctor of Nursing Practice Projects. J Nurs Educ (2015) 0.75