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Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children

Clinical genetics, 2014-02, Vol.85 (2), p.120-126

2014

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Defining personal utility in genomics: A Delphi study

Clinical genetics, 2017-09, Vol.92 (3), p.290-297

2017

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Effects of informed consent for individual genome sequencing on relevant knowledge

Clinical genetics, 2012-11, Vol.82 (5), p.408-415

2012

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PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing

Clinical genetics, 2017-08, Vol.92 (2), p.172-179

2017

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Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life

Clinical genetics, 2015-11, Vol.88 (5), p.425-430

2015

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Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age

Clinical genetics, 2016-03, Vol.89 (3), p.378-384

2016

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Adaptation to living with a genetic condition or risk: a mini-review

Clinical genetics, 2008-11, Vol.74 (5), p.401-407

2008

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Genetic susceptibility testing from a stress and coping perspective

Social science & medicine (1982), 2006-04, Vol.62 (8), p.1880-1890

2006

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Goals of genetic counseling

Clinical genetics, 2001-11, Vol.60 (5), p.323-330

Biesecker, BB

2001

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Family risk and related education and counseling needs: Perceptions of adults with bipolar disorder and siblings of adults with bipolar disorder

American journal of medical genetics. Part A, 2009-03, Vol.149A (3), p.364-371

2009

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The future of genetic counselling: an international perspective

Nature genetics, 1999-06, Vol.22 (2), p.133-137

1999

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Truth-telling and Turner Syndrome: The Importance of Diagnostic Disclosure

The Journal of pediatrics, 2006, Vol.148 (1), p.102-107

2006

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Breast cancer susceptibility genes. BRCA1 and BRCA2

Medicine (Baltimore), 1998-05, Vol.77 (3), p.208-226

1998

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Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients

Genetics in medicine, 2004-11, Vol.6 (6), p.510-516

2004

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Living with achondroplasia in an average-sized world: An assessment of quality of life

American journal of medical genetics, 2003-08, Vol.120A (4), p.447-458

2003

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Community Involvement in Developing Policies for Genetic Testing: Assessing the Interests and Experiences of Individuals Affected by Genetic Conditions

American journal of public health (1971), 2005-01, Vol.95 (1), p.35-41

2005

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Ethical issues in psychiatric genetics research: points to consider

Psychopharmacology, 2003-12, Vol.171 (1), p.27-35

2003

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Living with Marfan syndrome: coping with stigma

Clinical genetics, 2005-07, Vol.68 (1), p.6-14

2005

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Genetic counseling for mental illness: goals resemble counseling goals for other common conditions

Clinical genetics, 2006-01, Vol.69 (1), p.93-94

Biesecker, BB

2006

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Living with Marfan syndrome III. Quality of life and reproductive planning

Clinical genetics, 2002-08, Vol.62 (2), p.110-120

2002

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BRCA1/2 testing in hereditary breast and ovarian cancer families II: Impact on relationships

American journal of medical genetics. Part A, 2005-03, Vol.133A (2), p.165-169

2005

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Living with Marfan syndrome I. Perceptions of the condition

Clinical genetics, 2001-10, Vol.60 (4), p.273-282

2001

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Living with Marfan syndrome II. Medication adherence and physical activity modification

Clinical genetics, 2001-10, Vol.60 (4), p.283-292

2001

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Genetics and alcoholism among at-risk relatives I: Perceptions of cause, risk, and control

American journal of medical genetics, 2004-07, Vol.128A (2), p.144-150

2004

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Future Directions in Genetic Counseling: Practical and Ethical Considerations

Kennedy Institute of Ethics journal, 1998-06, Vol.8 (2), p.145-160

Biesecker, Barbara

1998

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Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children

Defining personal utility in genomics: A Delphi study

Effects of informed consent for individual genome sequencing on relevant knowledge

PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing

Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life

Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age

Adaptation to living with a genetic condition or risk: a mini-review

Genetic susceptibility testing from a stress and coping perspective

Goals of genetic counseling

Family risk and related education and counseling needs: Perceptions of adults with bipolar disorder and siblings of adults with bipolar disorder

The future of genetic counselling: an international perspective

Truth-telling and Turner Syndrome: The Importance of Diagnostic Disclosure

Breast cancer susceptibility genes. BRCA1 and BRCA2

Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients

Living with achondroplasia in an average-sized world: An assessment of quality of life

Community Involvement in Developing Policies for Genetic Testing: Assessing the Interests and Experiences of Individuals Affected by Genetic Conditions

Ethical issues in psychiatric genetics research: points to consider

Living with Marfan syndrome: coping with stigma

Genetic counseling for mental illness: goals resemble counseling goals for other common conditions

Living with Marfan syndrome III. Quality of life and reproductive planning

BRCA1/2 testing in hereditary breast and ovarian cancer families II: Impact on relationships

Living with Marfan syndrome I. Perceptions of the condition

Living with Marfan syndrome II. Medication adherence and physical activity modification

Genetics and alcoholism among at-risk relatives I: Perceptions of cause, risk, and control

Future Directions in Genetic Counseling: Practical and Ethical Considerations

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