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Author Details
Full Name
Joan Scott
Affiliation
ORCID
Career Start Year
2005
Papers
20
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35642870
Introducing the Blueprint for Change: A National Framework for a System of Services for Children and Youth with Special Health Care Needs.
Pediatrics
2022
35642876
A Blueprint for Change: Guiding Principles for a System of Services for Children and Youth With Special Health Care Needs and Their Families.
Pediatrics
2022
35642873
Progress, Persistence, and Hope: Building a System of Services for CYSHCN and Their Families.
Pediatrics
2022
22402755
Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study.
Genet Med
2012
29768770
Preparing health professionals for individualized medicine.
Per Med
2012
22538255
Preferences for opt-in and opt-out enrollment and consent models in biobank research: a national survey of Veterans Administration patients.
Genet Med
2012
22278220
Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.
J Genet Couns
2012
22411865
New models for large prospective studies: is there a better way?
Am J Epidemiol
2012
21828326
Noninvasive fetal sex determination using cell-free fetal DNA: a systematic review and meta-analysis.
JAMA
2011
19556748
Developing the blueprint for a genetic testing registry.
Public Health Genomics
2010
19346960
Veterans' attitudes regarding a database for genomic research.
Genet Med
2009
19878915
Public opinion about the importance of privacy in biobank research.
Am J Hum Genet
2009
19833988
Public perspectives on informed consent for biobanking.
Am J Public Health
2009
18189289
Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion.
Am J Med Genet C Semin Med Genet
2008
19011407
Subjects matter: a survey of public opinions about a large genetic cohort study.
Genet Med
2008
19061108
Public expectations for return of results from large-cohort genetic research.
Am J Bioeth
2008
18700896
Carrier screening for cystic fibrosis in US genetic testing laboratories: a survey of laboratory directors.
Clin Genet
2008
16964214
Oversight of US genetic testing laboratories.
Nat Biotechnol
2006
15950627
Opinions about new reproductive genetic technologies: hopes and fears for our genetic future.
Fertil Steril
2005
16274615
PGD patients' and providers' attitudes to the use and regulation of preimplantation genetic diagnosis.
Reprod Biomed Online
2005
1 - 20 of 20
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Mildred K Cho
Center for Biomedical Ethics, Stanford University School of Medicine
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E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
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Wylie Burke
The Heart Institute, Cincinnati Children's Hospital Medical Center
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row(s) 1 - 30 of 30
Collaborators
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From the National Institutes of Health
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Berman Institute of Bioethics, Johns Hopkins University
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National Human Genome Research Institute
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Gail Geller
Berman Institute of Bioethics, Johns Hopkins University
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Gail H Javitt
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Berman Institute of Bioethics, Johns Hopkins University
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University of Maryland
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Abt Associates Inc.
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University of Washington School of Medicine.
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Christine D Berg
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Barbara A Bernhardt
Thomas Jefferson University
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Rory Collins
Co-authored papers
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Nancy L Pedersen
Co-authored papers
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Francis S Collins
University of Michigan ann arbor
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David J Doukas
a Tulane University School of Medicine, New Orleans VA Medical Center
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From the Columbia University School of Nursing
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VA Boston Healthcare System
Co-authored papers
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Catherine A McCarty
University of Minnesota Medical School, 1035 University Drive duluth
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National Cancer Institute
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Debra J H Mathews
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John H Evans
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