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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: Apr 19, 2024
. (Total: 63627 Documents since 2012)
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Records 1 - 22 (of 22 Records)
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Informed consent [original query]>>Guidelines Related[Product Type]
Ethical challenges in autism genomics: Recommendations for researchers.
Heini M Natri et al. Eur J Med Genet 2023 66(9) 104810
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Webinar report: stakeholder perspectives on informed consent for the use of genomic data by commercial entities.
Baergen Schultz et al. Journal of medical ethics 2023
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Expanded carrier screening for reproductive risk assessment: An evidence-based practice guideline from the National Society of Genetic Counselors.
Katelynn G Sagaser et al. Journal of genetic counseling 2023
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Considerations for Cardiovascular Genetic and Genomic Research With Marginalized Racial and Ethnic Groups and Indigenous Peoples: A Scientific Statement From the American Heart Association.
Mudd-Martin Gia et al. Circulation. Genomic and precision medicine 2021 HCG0000000000000084
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Opportunistic genomic screening. Recommendations of the European Society of Human Genetics.
de Wert Guido et al. European journal of human genetics : EJHG 2020 Nov
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Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH.
Downes Kate et al. Journal of thrombosis and haemostasis : JTH 2020 Oct 18(10) 2751-2758
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Local Coverage Determination (LCD): Genomic Sequence Analysis Panels in the Treatment of Solid Organ Neoplasms (L37810)
The U.S. Centers for Medicare & Medicaid Services
Clinical practice guidance for next-generation sequencing in cancer diagnosis and treatment (Edition 1.0).
Sunami Kuniko et al. Cancer science 2018 Sep 109(9) 2980-2985
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Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Armour Christine M et al. Journal of medical genetics 2018 Mar
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Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer.
Soto José Luis et al. Medicina clinica 2018 Feb
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No. 348-Joint SOGC-CCMG Guideline: Update on Prenatal Screening for Fetal Aneuploidy, Fetal Anomalies, and Adverse Pregnancy Outcomes.
Audibert Francois et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2017 Sep 39(9) 805-817
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AGO Austria recommendation on screening and diagnosis of Lynch syndrome (LS).
Zeimet Alain G et al. Archives of gynecology and obstetrics 2017 May
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Revamping the US Federal Common Rule: Modernizing Human Participant Research Regulations.
Hodge James G et al. JAMA 2017 Feb
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Ethics of genetic testing and research in sport: a position statement from the Australian Institute of Sport.
Vlahovich Nicole et al. British journal of sports medicine 2016 Nov
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Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.
Wilson R Douglas et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obste´trique et gyne´cologie du Canada : JOGC 2016 Aug 38(8) 742-762.e3
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Prenatal Diagnosis Procedures and Techniques to Obtain a Diagnostic Fetal Specimen or Tissue: Maternal and Fetal Risks and Benefits.
Wilson R Douglas et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obste´trique et gyne´cologie du Canada : JOGC 2015 Jul 37(7) 656-70
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The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Boycott Kym et al. J. Med. Genet. 2015 May 7.
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Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
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Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].
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Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.
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Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.
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Recommendations for ethical approaches to genotype-driven research recruitment.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 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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