4.1 Article

Genomic Data in the Electronic Medical Record: Perspectives From a Biobank Community Advisory Board

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Biochemistry & Molecular Biology

Public Knowledge of and Attitudes Toward Genetics and Genetic Testing

Susanne B. Haga et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS (2013)

Article Medicine, General & Internal

The Mayo Clinic Biobank: A Building Block for Individualized Medicine

Janet E. Olson et al.

MAYO CLINIC PROCEEDINGS (2013)

Article Health Care Sciences & Services

Experiences of patients with chronic gastrointestinal conditions: in their own words

Jennifer B. McCormick et al.

HEALTH AND QUALITY OF LIFE OUTCOMES (2012)

Article Multidisciplinary Sciences

Sequencing set to alter clinical landscape

Erika Check Hayden

NATURE (2012)

Editorial Material Multidisciplinary Sciences

The Ultimate Genetic Test

Radoje Drmanac

SCIENCE (2012)

Editorial Material Multidisciplinary Sciences

Whole-Genome Sequencing: The New Standard of Care?

Liam R. Brunham et al.

SCIENCE (2012)

Article Genetics & Heredity

Study Newsletters, Community and Ethics Advisory Boards, and Focus Group Discussions Provide Ongoing Feedback for a Large Biobank

Catherine A. McCarty et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)

Article Biochemistry & Molecular Biology

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research

Flavia M. Facio et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2011)

News Item Multidisciplinary Sciences

GENOMES ON PRESCRIPTION

Brendan Maher

NATURE (2011)

Article Genetics & Heredity

Genomic research and wide data sharing: Views of prospective participants

Susan Brown Trinidad et al.

GENETICS IN MEDICINE (2010)

Article Ethics

GLAD YOU ASKED: PARTICIPANTS' OPINIONS OF RE-CONSENT FOR DBGAP DATA SUBMISSION

Evette J. Ludman et al.

JOURNAL OF EMPIRICAL RESEARCH ON HUMAN RESEARCH ETHICS (2010)

Article Genetics & Heredity

Public and Biobank Participant Attitudes toward Genetic Research Participation and Data Sharing

A. A. Lemke et al.

PUBLIC HEALTH GENOMICS (2010)

Article Genetics & Heredity

Public Opinion about the Importance of Privacy in Biobank Research

David J. Kaufman et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2009)

Article Genetics & Heredity

Assessing the Understanding of Biobank Participants

K. E. Ormond et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)

Article Biochemistry & Molecular Biology

The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine

Leslie G. Biesecker et al.

GENOME RESEARCH (2009)

Article Ethics

Patients' Views on Identifiability of Samples and Informed Consent for Genetic Research

Sara Chandros Hull et al.

AMERICAN JOURNAL OF BIOETHICS (2008)

Article Oncology

Informed consent for biorepositories: Assessing prospective participants' understanding and opinions

Laura M. Beskow et al.

CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2008)

Article Genetics & Heredity

DNA data sharing: research participants' perspectives

Amy L. McGuire et al.

GENETICS IN MEDICINE (2008)

Article Public, Environmental & Occupational Health

Genetic research and donation of tissue samples to biobanks.: What do potential sample donors in the Swedish general public think?

Asa Kettis-Lindblad et al.

EUROPEAN JOURNAL OF PUBLIC HEALTH (2006)