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What Precision Medicine Can Learn from Rare Genetic Disease Research and Translation

Dados Bibliográficos

ID15744768
AutoresHolly K Tabor (0000-0003-1005-5008, Center for Clinical Research (United States), autor correspondente), Aaron J Goldenberg (0000-0002-0314-0303, Case Western Reserve University)
Ano2018
Volume20
Fascículo9
PáginasE834-840
Data de publicação2018-09-01
Peer ReviewedSim
Open AccessSim
TipoARTICLE
PeriódicoThe AMA Journal of Ethic (JOURNAL)
Identificadores do periódicoISSN: 2376-6980 • E-ISSN: 2376-6980
EditoraAmerican Medical Association (PUBLISHER • US)
DOI10.1001/amajethics.2018.834
PMID30242814
OpenAlexW2892378636
IdiomaEN
Citações recebidas3
Referências citadas1

The goal of this article is to examine the intersections of precision health and rare diseases. Specifically, we propose 3 lessons from the last decade of applying genomics to rare diseases: (1) precision can end one odyssey and start another; (2) precise interventions can exacerbate health disparities and create other ethical dilemmas; and (3) democratization of data will transform research and translation. By studying experiences of patients with rare diseases, researchers, clinicians, and policymakers can anticipate similar challenges in precision medicine and hopefully mitigate potential harms or injustices

Biology · Disease · Drug · Drug development · Engineering ethics · Gene · Intensive care medicine · Pathology · Precision medicine · Rare disease · Translation (biology · Translational medicine · BRCA gene mutations in cancer · Cancer Genomics and Diagnostics · Engineering · Genomics and Rare Diseases · Medicine · Genetics · Pharmacology

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    Open Access•Holly K Tabor, Aaron J Goldenberg•The AMA Journal of Ethic•2018

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Obras citantes distintas3
Citações por ano0,38
Intervalo de citações2018 - 2024 (7)
Velocidade de citaçãorecent
Altamente citadoNão
Tipos de citaçãoNeutras: 3
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