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‘I can't do any serious exercise’: barriers to physical activity amongst people of Pakistani and Indian origin with Type 2 diabetes

Health education research, 2006-02, Vol.21 (1), p.43-54

2006

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Written versus verbal consent: a qualitative study of stakeholder views of consent procedures used at the time of recruitment into a peripartum trial conducted in an emergency setting

BMC medical ethics, 2017-05, Vol.18 (1), p.36-36, Article 36

2017

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An investigation of patients’ motivations for their participation in genetics-related research

Journal of medical ethics, 2010-01, Vol.36 (1), p.37-45

2010

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Broadening the Debate About Post-trial Access to Medical Interventions: A Qualitative Study of Participant Experiences at the End of a Trial Investigating a Medical Device to Support Type 1 Diabetes Self-Management

AJOB empirical bioethics, 2019-04, Vol.10 (2), p.100-112

2019

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Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study

Journal of genetic counseling, 2019-04, Vol.28 (2), p.343-354

2019

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Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study

Journal of genetic counseling, 2019-04, Vol.28 (2), p.343

2019

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Implementing risk-stratified screening for common cancers: a review of potential ethical legal and social issues

Journal of public health (Oxford, England), 2014-06, Vol.36 (2), p.285-291

2014

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A qualitative study of the information needs of high-risk women undergoing prophylactic oophorectomy

Psycho-oncology (Chichester, England), 2000-11, Vol.9 (6), p.486-495

Hallowell, N.

2000

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“I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings

Journal of community genetics, 2018-07, Vol.9 (3), p.305-314

2018

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Accommodating risk: Responses to BRCA1/2 genetic testing of women who have had cancer

Social science & medicine (1982), 2004-08, Vol.59 (3), p.553-565

2004

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Stratified Cancer Screening: The Practicalities of Implementation

Public health genomics, 2013-01, Vol.16 (3), p.94-99

2013

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Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information

Journal of medical ethics, 2003-04, Vol.29 (2), p.74-83

2003

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Participants' experiences of intensifying insulin therapy during the Treating to Target in Type 2 Diabetes (4-T) trial: qualitative interview study

Diabetic medicine, 2011-05, Vol.28 (5), p.543-548

2011

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Diabetes service provision: a qualitative study of the experiences and views of Pakistani and Indian patients with Type 2 diabetes

Diabetic medicine, 2006-09, Vol.23 (9), p.1003-1007

2006

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Healthcare professionals’ and researchers’ understanding of cancer genetics activities: a qualitative interview study

Journal of medical ethics, 2009-02, Vol.35 (2), p.113-119

2009

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Doing the right thing: genetic risk and responsibility

Sociology of health & illness, 1999-09, Vol.21 (5), p.597-621

Hallowell, Nina

1999

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Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research

Journal of medical ethics, 2008-09, Vol.34 (9), p.690-694

2008

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Men's Decision‐Making About Predictive BRCA1/2 Testing: The Role of Family

Journal of genetic counseling, 2005-06, Vol.14 (3), p.207-217

2005

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Treatment-focused DNA testing for newly diagnosed breast cancer patients: some implications for clinical practice

Clinical genetics, 2010-04, Vol.77 (4), p.350-354

2010

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Surveillance or surgery? A description of the factors that influence high risk premenopausal women's decisions about prophylactic oophorectomy

Journal of medical genetics, 2001-10, Vol.38 (10), p.683-691

2001

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Incorporating genomics into breast and prostate cancer screening: assessing the implications

Genetics in medicine, 2013-06, Vol.15 (6), p.423-432

2013

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Risk-reducing surgery for breast and ovarian cancer risks - where are we now?

Hereditary cancer in clinical practice, 2012-01, Vol.10 (Suppl 2), p.A13-A13

2012

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Rehabilitating the sick role: post-surgical experiences of high risk women who undergo risk reducing mastectomy

Hereditary cancer in clinical practice, 2012-01, Vol.10 (Suppl 2), p.A6-A6

2012

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Women's need for information before attending genetic counselling for familial breast or ovarian cancer: a questionnaire, interview, and observational study

BMJ, 1997-01, Vol.314 (7076), p.281-281

International edition, 1997

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Varieties of suffering: Living with the risk of ovarian cancer

Health, risk & society, 2006-03, Vol.8 (1), p.9-26

Hallowell, Nina

2006

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‘I can't do any serious exercise’: barriers to physical activity amongst people of Pakistani and Indian origin with Type 2 diabetes

Written versus verbal consent: a qualitative study of stakeholder views of consent procedures used at the time of recruitment into a peripartum trial conducted in an emergency setting

An investigation of patients’ motivations for their participation in genetics-related research

Broadening the Debate About Post-trial Access to Medical Interventions: A Qualitative Study of Participant Experiences at the End of a Trial Investigating a Medical Device to Support Type 1 Diabetes Self-Management

Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study

Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study

Implementing risk-stratified screening for common cancers: a review of potential ethical legal and social issues

A qualitative study of the information needs of high-risk women undergoing prophylactic oophorectomy

“I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings

Accommodating risk: Responses to BRCA1/2 genetic testing of women who have had cancer

Stratified Cancer Screening: The Practicalities of Implementation

Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information

Participants' experiences of intensifying insulin therapy during the Treating to Target in Type 2 Diabetes (4-T) trial: qualitative interview study

Diabetes service provision: a qualitative study of the experiences and views of Pakistani and Indian patients with Type 2 diabetes

Healthcare professionals’ and researchers’ understanding of cancer genetics activities: a qualitative interview study

Doing the right thing: genetic risk and responsibility

Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research

Men's Decision‐Making About Predictive BRCA1/2 Testing: The Role of Family

Treatment-focused DNA testing for newly diagnosed breast cancer patients: some implications for clinical practice

Surveillance or surgery? A description of the factors that influence high risk premenopausal women's decisions about prophylactic oophorectomy

Incorporating genomics into breast and prostate cancer screening: assessing the implications

Risk-reducing surgery for breast and ovarian cancer risks - where are we now?

Rehabilitating the sick role: post-surgical experiences of high risk women who undergo risk reducing mastectomy

Women's need for information before attending genetic counselling for familial breast or ovarian cancer: a questionnaire, interview, and observational study

Varieties of suffering: Living with the risk of ovarian cancer

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