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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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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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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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“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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Stratified Cancer Screening: The Practicalities of Implementation

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

2013

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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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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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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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Understanding the outcomes of multi-centre clinical trials: A qualitative study of health professional experiences and views

Social science & medicine (1982), 2012-02, Vol.74 (4), p.574-581

2012

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The experiences of research participants offered genetic test results as a result of taking part in a population based ovarian cancer research study?

Hereditary cancer in clinical practice, 2012-01, Vol.10 (Suppl 2), p.A15-A15

2012

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Women's Understanding of Their Risk of Developing Breast/Ovarian Cancer Before and After Genetic Counseling

Journal of genetic counseling, 1998-08, Vol.7 (4), p.345-364

1998

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Recall of numerical risk estimates and counsellees' perceptions of the importance of risk information following genetic counselling for breast and ovarian cancer

Psychology, health & medicine, 1997-06, Vol.2 (2), p.149-159

1997

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Providing letters to patients. Patients find summary letters useful [letter]

BMJ. British medical journal (International ed.), 1998-06, Vol.316 (7147), p.1830

Hallowell, N

International edition, 1998

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Advising on the management of genetic risk: Offering choice or prescribing action?

Health, risk & society, 1999-11, Vol.1 (3), p.267-280

Hallowell, Nina

1999

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Healthcare professionals’ and researchers’ understanding of cancer genetics activities: a qualitative interview study: Table 1

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: Sociological Perspectives on the New Genetics

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

HALLOWELL, N

1999

Volltextzugriff (PDF)

Genetic Counseling, Reproductive Behavior and Future Reproductive Intentions of People with Neurofibromatosis Type 1 (NF1)

Journal of genetic counseling, 1998-08, Vol.7 (4), p.331-344

1998

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Family Communication and Genetic Counseling: The Case of Hereditary Breast and Ovarian Cancer

Journal of genetic counseling, 1997-03, Vol.6 (1), p.45-60

1997

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Negotiating present and future selves: managing the risk of hereditary ovarian cancer by prophylactic surgery

Health (London, England : 1997), 2002-10, Vol.6 (4), p.423-443

2002

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Providing letters to patients. Patients find summary letters useful

BMJ (Online), 1998-06, Vol.316 (7147), p.1830

Hallowell, N

1998

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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

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

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

Stratified Cancer Screening: The Practicalities of Implementation

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

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

Varieties of suffering: Living with the risk of ovarian cancer

Understanding the outcomes of multi-centre clinical trials: A qualitative study of health professional experiences and views

The experiences of research participants offered genetic test results as a result of taking part in a population based ovarian cancer research study?

Women's Understanding of Their Risk of Developing Breast/Ovarian Cancer Before and After Genetic Counseling

Recall of numerical risk estimates and counsellees' perceptions of the importance of risk information following genetic counselling for breast and ovarian cancer

Providing letters to patients. Patients find summary letters useful [letter]

Advising on the management of genetic risk: Offering choice or prescribing action?

Healthcare professionals’ and researchers’ understanding of cancer genetics activities: a qualitative interview study: Table 1

Doing the right thing : genetic risk and responsibility: Sociological Perspectives on the New Genetics

Genetic Counseling, Reproductive Behavior and Future Reproductive Intentions of People with Neurofibromatosis Type 1 (NF1)

Family Communication and Genetic Counseling: The Case of Hereditary Breast and Ovarian Cancer

Negotiating present and future selves: managing the risk of hereditary ovarian cancer by prophylactic surgery

Providing letters to patients. Patients find summary letters useful

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