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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Mar 28, 2024
. (Total: 63390 Documents since 2012)
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Data sharing[original query]>>Evidence Synthesis [Product Type]
A systematic review of knowledge, attitude and practice of pharmacogenomics in pediatric oncology patients.
Claire Moore et al. Pharmacol Res Perspect 2023 11(6) e01150
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A Rapid Review on the Value of Biobanks Containing Genetic Information.
Elisabet Rodriguez Llorian et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2023
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Recommendations for next generation sequencing data reanalysis of unsolved cases with suspected Mendelian disorders: A systematic review and meta-analysis.
Dai Pei et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
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Predicting clinical outcomes using artificial intelligence and machine learning in neonatal intensive care units: a systematic review.
McAdams Ryan M et al. Journal of perinatology : official journal of the California Perinatal Association 2022
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Research and Application of Artificial Intelligence Based on Electronic Health Records of Patients With Cancer: Systematic Review.
Yang Xinyu et al. JMIR medical informatics 2022 10(4) e33799
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Digital Health Policy and Programs for Hospital Care in Vietnam: Scoping Review.
Tran Duc Minh et al. Journal of medical Internet research 2022 24(2) e32392
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Machine learning applications in tobacco research: a scoping review.
Fu Rui et al. Tobacco control 2021
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How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies.
Klapwijk Jasmijn E et al. Clinical genetics 2021
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Ethical, Legal, and Social Issues (ELSI) of Responsible Data Sharing Involving Children in Genomics: A Systematic Literature Review of Reasons.
Rahimzadeh Vasiliki et al. AJOB empirical bioethics 2020 Sep 1-13
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Responsible data sharing in international health research: a systematic review of principles and norms.
Kalkman Shona et al. BMC medical ethics 2019 Mar 20(1) 21
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Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries.
de Vries Jantina et al. BMC medical ethics 2017 Feb 18(1) 8
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Expanding Access to Large-Scale Genomic Data While Promoting Privacy: A Game Theoretic Approach.
Wan Zhiyu et al. American journal of human genetics 2017 Jan
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A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Garrison Nanibaa' A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Nov
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Anonymizing patient genomic data for public sharing association studies.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 28, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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