Publications by Dr Nina Hallowell - ePrints

Browsing publications by Dr Nina Hallowell.

Newcastle Authors	Title	Year
Dr Nina Hallowell Dr Pauline McCormack	Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis	2019
Professor Madeleine Murtagh Dr Mwenza Blell Dr Olly Butters Dr Lorraine Cowley Dr Nina Hallowell et al.	Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure	2018
Jan Lecouturier Michael Clarke Dr Gail Errington Dr Nina Hallowell Professor Madeleine Murtagh et al.	Treating childhood intermittent distance exotropia: a qualitative study of decision making	2015
Dr Nina Hallowell	How do index patients participating in genetic screening programmes for familial hypercholesterolemia (FH) interpret their DNA results? A UK-based qualitative interview study	2013
Dr Nina Hallowell	Looking different, feeling different: women's reactions to risk-reducing breast and ovarian surgery	2012
Dr Nina Hallowell	Understanding the outcomes of multi-centre clinical trials: A qualitative study of health professional experiences and views	2012
Dr Nina Hallowell	A family perspective of the value of a diagnosis for Intellectual Disability: experiences from a genetic research study	2011
Dr Nina Hallowell	Challenges of maintaining research protocol fidelity in a clinical care setting: A qualitative study of the experiences and views of patients and staff participating in a randomized controlled trial	2011
Dr Nina Hallowell	Patients' experience of intensifying insulin therapy during the Treating to Targe in Type 2 Diabetes (4-T) trial: qualitative interview study	2011
Dr Nina Hallowell	An investigation of cancer genetics patients'motivations for their particiption in research	2010
Dr Nina Hallowell	Initiating insulin as part of the Treat to Target in Type 2 Diabetes (4-T) trial: A interview study of patients' and health professionals' experiences	2010
Dr Nina Hallowell	Lay and professional understandings of research and clinical activities in cancer genetics and their implications for informed consent	2010
Dr Nina Hallowell	A comparison of male attenders and nonattendees at a familial cancer clinic	2009
Dr Nina Hallowell	Attendance of men at the familial cancer clinic: What they value from the consultation	2009
Dr Nina Hallowell	Distinguishing research in clinical care in cancer genetics: theoretical justifications and practical strategies	2009
Dr Nina Hallowell	Healthcare professionals' and researchers' undertanding of cancer genetics activities: a qualitative interview study	2009
Dr Nina Hallowell	Treatment focused DNA-testing for breast/ovarian cancer: some implications for the practice of oncology	2009
Dr Nina Hallowell	"We should change ourselves, but we can't": accounts of food and eating practices amongst British Pakistanis and Indians with type 2 diabetes	2008
Dr Nina Hallowell	Consent to genetic testing: A family affair?	2008
Dr Nina Hallowell	Encounters with medical professionals: a crisis of trust or matter of respect?	2008
Dr Nina Hallowell	Ethics and Research Governance: the views of researchers, healthcare professionals and other stakeholders	2008
Dr Nina Hallowell	Genetic research on rare familial disorders: consent and the blured boundaries between clinical service and research	2008
Dr Nina Hallowell	Is consent sufficient? A case study of qualitative research with men with intellectual disabilties	2008
Dr Nina Hallowell	Recall of participation in cancer genetics research projects	2008
Dr Nina Hallowell	Contextualising accounts of illness: notions of responsibility and blame in white and South Asian respondents' accounts of diabetes causation	2007
Dr Nina Hallowell	"I can't do any serious exercise": barriers to physical activity amongst people of Pakistani and Indian origin with Type 2 diabetes	2006
Dr Nina Hallowell	Diabetes service provision: a qualitative study of the experiences and views of Pakistani and Indian patients with type 2 diabetes	2006
Dr Nina Hallowell	Guilt, blame and responsibility: Men's understanding of their role in the transmission of BRCA1/2 mutations within their family	2006
Dr Nina Hallowell	Seeking ethial approval: opening up the lines of communication	2006
Dr Nina Hallowell	Varieties of suffering: living with the risk of ovarian cancer	2006
Dr Nina Hallowell	Family communication about predictive BRCA 1/2 genetic testing: patterns, priorities and problems	2005
Dr Nina Hallowell	Men's decision-making about predictive BRCA 1/2 testing: the role of family	2005
Dr Nina Hallowell	Perceptions and experiences of taking oral hypoglycaemic agents amongst people of Pakistani and Indian origin: qualitative study	2005
Dr Nina Hallowell	Accommodating risk: women's responses to BRCA1/2 genetic testing following a cancer diagnosis.	2004
Dr Nina Hallowell	Can there be moral experts?	2004
Dr Nina Hallowell	High risk premenapausal women's experiences of undergoing prophylactic oophorectomy: a descriptive study.	2004
Dr Nina Hallowell	Reflections on Research: the realities of doing research in the social sciences	2004
Dr Nina Hallowell	Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information	2003
Dr Nina Hallowell	Ethics and evidence	2003
Dr Nina Hallowell	Genetic testing for women previously diagnosed with breast/ovarian cancer: examining the impact of BRCA and BRCA2 mutation searching	2002
Dr Nina Hallowell	Negotiating present and future selves: decision-making about prophylactic surgery for hereditary ovarian cancer	2002
Dr Nina Hallowell	Surveillance or surgery? A description of the factors that influence high-risk premenopausal women's decisions about prophylactic oophorectomy	2001
Dr Nina Hallowell	A qualitative study of the information needs of high-risk women undergoing prophylactic oophorectomy	2000
Dr Nina Hallowell	Reconstructing the body or reconstructing the woman? Perceptions of prophylactic mastectomy for hereditary breast cancer risk	2000
Dr Nina Hallowell	Advising on the management of genetic risk: offering choice or prescribing action?	1999
Dr Nina Hallowell	Controlling dangerous bodies: the dilemma faced by women at genetic risk of breast or ovarian cancer	1999
Dr Nina Hallowell	Doing the right thing: genetic risk and responsibility	1999
Dr Nina Hallowell	"You don't want to lose your ovaries because you think 'I might become a man'.": women's perceptions of prophylactic surgery as a cancer risk management option.	1998
Dr Nina Hallowell	Genetic counseling, reproductive behavior and future reproductive intentions of people with Neurofibromatosis type 1 (NF1)	1998
Dr Nina Hallowell	The value of written summaries of genetic consultations	1998
Dr Nina Hallowell	Women's understanding of their risk of developing breast/ovarian cancer before and after genetic counseling	1998
Dr Nina Hallowell	"Talking about chance": the presentation of risk information during genetic counseling for breast and ovarian cancer	1997
Dr Nina Hallowell	Family communication and genetic counseling: the case of hereditary breast and ovarian cancer	1997
Dr Nina Hallowell	Recall of numerical risk estimates and counsellees' perceptions of the importance of risk information following genetic counselling for breast and ovarian cancer	1997
Dr Nina Hallowell	Understanding Life's Lottery: an evaluation of studies of genetic risk awareness.	1997
Dr Nina Hallowell	Women's need for information before attending genetic counselling for familial breast or ovarian cancer: a questionnaire, interview and observational study	1997
Dr Nina Hallowell	Counseling families with hereditary breast and ovarian cancer: a psychosocial perspective	1995
Dr Nina Hallowell	Up and down the ontological tree: categories and semantic generalisation	1995
Dr Nina Hallowell	Attentional bias to threat: roles of trait anxiety, stressful events and awareness	1994