Quality of life in rare genetic conditions: a systematic review of the literature.

Ambivalence toward undergoing invasive prenatal testing: an exploration of its origins.

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

Commentary on "My Story: A Genetic Counselor's Journey from Provider to Patient"

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

International perspectives on genetic counseling and testing for breast cancer risk.

Uncertainty and perceived personal control among parents of children with rare chromosome conditions: the role of genetic counseling.

BRCA1/2 testing in hereditary breast and ovarian cancer families III: risk perception and screening.

Genetic susceptibility testing for Alzheimer disease: motivation to obtain information and control as precursors to coping with increased risk.

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.

The relationship of nondirectiveness to genetic counseling: report of a workshop at the 2003 NSGC Annual Education Conference.

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

Truth-telling and Turner Syndrome: the importance of diagnostic disclosure.

Genetic susceptibility testing from a stress and coping perspective.

Living with Marfan syndrome: coping with stigma.

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

Community involvement in developing policies for genetic testing: assessing the interests and experiences of individuals affected by genetic conditions.

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

BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention.

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

Living with achondroplasia: attitudes toward population screening and correlation with quality of life.

Ethical issues in psychiatric genetics research: points to consider.

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

Issues surrounding prenatal genetic testing for achondroplasia.

The decision to continue: the experiences and needs of parents who receive a prenatal diagnosis of holoprosencephaly.