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Author Details
Full Name
Nancy Press
Affiliation
Oregon Health and Science University
ORCID
Career Start Year
1993
Papers
59
H Index
29
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
24946153
The translational potential of research on the ethical, legal, and social implications of genomics.
Genet Med
2015
25660437
Decision making among Veterans with incidental pulmonary nodules: a qualitative analysis.
Respir Med
2015
24321254
Essential elements of personalized medicine.
Urol Oncol
2014
24350704
Breastfeeding infants with phenylketonuria in the United States and Canada.
Breastfeed Med
2014
23580131
Trust is the basis for effective suicide risk screening and assessment in veterans.
J Gen Intern Med
2013
23907645
Recommendations for returning genomic incidental findings? We need to talk!
Genet Med
2013
23952851
What the heck is a "nodule"? A qualitative study of veterans with pulmonary nodules.
Ann Am Thorac Soc
2013
23535584
Patient experiences with full electronic access to health records and clinical notes through the My HealtheVet Personal Health Record Pilot: qualitative study.
J Med Internet Res
2013
22001361
Predictors of recruited melanoma families into a behavioral intervention project.
Contemp Clin Trials
2012
23117904
Communication by nurses in the intensive care unit: qualitative analysis of domains of patient-centered care.
Am J Crit Care
2012
22581585
Life-sustaining treatment decisions in the ICU for patients with ESLD: a prospective investigation.
Res Nurs Health
2012
22241094
IRB perspectives on the return of individual results from genomic research.
Genet Med
2012
22233466
Who is attending? End-of-life decision making in the intensive care unit.
J Palliat Med
2012
20809355
Personal attributions for melanoma risk in melanoma-affected patients and family members.
J Behav Med
2011
21709145
Genetic screening.
Epidemiol Rev
2011
20395690
Debating clinical utility.
Public Health Genomics
2010
20119933
Using a family systems approach to investigate cancer risk communication within melanoma families.
Psychooncology
2010
19208375
Genetic assessment of breast cancer risk in primary care practice.
Am J Med Genet A
2009
19661809
Breast cancer risk communication: assessment of primary care physicians by standardized patients.
Genet Med
2009
18570105
Translational genomics: seeking a shared vision of benefit.
Am J Bioeth
2008
17318844
Genetic information: Special or not? Responses from focus groups with members of a health maintenance organization.
Am J Med Genet A
2007
18037976
Performance of the U.S. Office of Management and Budget's Revised Race and Ethnicity Categories in Asian Populations*.
Int J Intercult Relat
2007
18020937
Anticipating dissemination of cancer genomics in public health: a theoretical approach to psychosocial and behavioral challenges.
Ann Behav Med
2007
16545004
Predictors of belief that genetic test information about hemochromatosis should be shared with family members.
Genet Test
2006
17003399
Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.
JAMA
2006
16723994
Genetics as a tool to improve cancer outcomes: ethics and policy.
Nat Rev Cancer
2006
16451774
Ethical obligations and counseling challenges in cancer genetics.
J Natl Compr Canc Netw
2006
16594854
Effects of counseling Ashkenazi Jewish women about breast cancer risk.
Cultur Divers Ethnic Minor Psychol
2006
15775750
Qualitative research: thoughts on how to do it; how to judge it; when to use it.
Genet Med
2005
16247294
Patient acceptability of genotypic testing for hemochromatosis in primary care.
Genet Med
2005
15955410
'That's like chopping off a finger because you're afraid it might get broken': disease and illness in women's views of prophylactic mastectomy.
Soc Sci Med
2005
15475668
Effects of individual and family functioning on interest in genetic testing.
Community Genet
2004
15265355
Oregon physicians' responses to requests for assisted suicide: a qualitative study.
J Palliat Med
2004
15455364
Ethical issues in identifying and recruiting participants for familial genetic research.
Am J Med Genet A
2004
12589228
Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults.
Am J Med Sci
2003
14509483
Oregon physicians' perceptions of patients who request assisted suicide and their families.
J Palliat Med
2003
12568824
Achieving utility with family history: colorectal cancer risk.
Am J Prev Med
2003
12181100
Genetic test evaluation: information needs of clinicians, policy makers, and the public.
Am J Epidemiol
2002
12811026
Genetics in primary care: a USA faculty development initiative.
Community Genet
2002
11778984
Categorizing genetic tests to identify their ethical, legal, and social implications.
Am J Med Genet
2001
11329986
Misleading presentation of breast cancer in popular magazines.
Eff Clin Pract
2001
11241466
Women's interest in genetic testing for breast cancer susceptibility may be based on unrealistic expectations.
Am J Med Genet
2001
10915332
If you care about women's health, perhaps you should care about the risks of direct marketing of tamoxifen to consumers.
Eff Clin Pract
2000
10986947
Collective fear, individualized risk: the social and cultural context of genetic testing for breast cancer.
Nurs Ethics
2000
10075000
Screening for cystic fibrosis carrier state.
Obstet Gynecol
1999
10414820
'Because of the risks': how US pregnant women account for refusing prenatal screening.
Soc Sci Med
1999
10359538
BRCA1 and BRCA2: a small part of the puzzle.
J Natl Cancer Inst
1999
9714010
Characteristics of women who refuse an offer of prenatal diagnosis: data from the California maternal serum alpha fetoprotein blood test experience.
Am J Med Genet
1998
9669792
Hereditary hemochromatosis: gene discovery and its implications for population-based screening.
JAMA
1998
9727731
Hemochromatosis: genetics helps to define a multifactorial disease.
Clin Genet
1998
1 - 50 of 59
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