A systematic literature review of individuals' perspectives on privacy and genetic information in the United States

EW Clayton, CM Halverson, NA Sathe, BA Malin - PloS one, 2018 - journals.plos.org
Concerns about genetic privacy affect individuals' willingness to accept genetic testing in
clinical care and to participate in genomics research. To learn what is already known about …

Dietary patterns in early childhood and the risk of childhood overweight: the GECKO Drenthe birth cohort

O Sirkka, M Fleischmann, M Abrahamse-Berkeveld… - Nutrients, 2021 - mdpi.com
Limited and inconsistent evidence exists on the associations between dietary patterns and
overweight during childhood. The present study describes dietary patterns of three-year-old …

Mapping the human genome: an assessment of media coverage and public reaction

ES Tambor, BA Bernhardt, J Rodgers… - Genetics in …, 2002 - nature.com
Purpose: To assess public reactions to the June 26, 2000, announcement that scientists had
nearly finished mapping the human genome. Methods: We conducted a random-digit …

Attitudes toward genetic testing and fetal diagnosis, 1990-1996

E Singer, AD Corning, T Antonucci - Journal of Health and Social Behavior, 1999 - JSTOR
With few exceptions, existing research on attitudes toward genetic testing and prenatal
diagnosis is based on small studies using nonprobability samples of specialized …

Parental attitudes and beliefs regarding the genetic testing of children

E Campbell, LF Ross - Public Health Genomics, 2005 - karger.com
Objectives: To explore parental attitudes and beliefs about genetic testing of children for
conditions that present throughout the life cycle. Methods: Twelve semi-structured focus …

Involving hard-to-reach ethnic minorities in low-budget health research: lessons from a health survey among Moluccans in the Netherlands

AJ Bodewes, AE Kunst - BMC research notes, 2016 - Springer
Background There is little evidence on which strategies are effective in recruiting minority
groups in low-budget health surveys. We evaluated different recruitment strategies for their …

Genetics services in a social, ethical and policy context: a collaboration between consumers and providers

DC Wertz, R Gregg - Journal of Medical Ethics, 2000 - jme.bmj.com
We report a unique, collaborative effort by users and providers of genetic services to arrive
at outlines for optimal ethics and clinical practice. Using focus groups of consumers (users) …

[图书][B] An examination of African American college students' knowledge and attitudes regarding sickle cell disease and sickle cell disease carrier testing: A mixed …

KA Stewart - 2007 - search.proquest.com
Abstract Approximately, 80,000 Americans are affected by sickle cell disease (SCD) and it is
the most common inherited blood disorder in the United States. SCD is most prevalent …

Archived specimens: a platform for discussion

DC Wertz - Public Health Genomics, 2000 - karger.com
To facilitate discussion, this paper describes various types of collections of specimens, their
uses in research, types of identifiers, requirements for informed consent, third-party access …

Experience and Perceptions of a Family Health History Risk Assessment Tool among Multi-Ethnic Asian Breast Cancer Patients

S Yoon, H Goh, SM Fung, S Tang, D Matchar… - Journal of Personalized …, 2021 - mdpi.com
A family health history-based risk assessment is particularly valuable for guiding cancer
screening and treatment strategies, yet an optimal implementation depends upon end-users' …