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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
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Records 1 - 24 (of 24 Records)
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Communication[original query]>>Guidelines Related[Product Type]
Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
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Recommendations for the use of pediatric data in artificial intelligence and machine learning ACCEPT-AI.
V Muralidharan et al. NPJ Digit Med 2023 6(1) 166
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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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Guidelines for genetic ancestry inference created through roundtable discussions.
Jennifer K Wagner et al. HGG advances 2023 4(2) 100178
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Optimising tissue acquisition and the molecular testing pathway for patients with non-small cell lung cancer: A UK expert consensus statement.
Navani Neal et al. Lung cancer (Amsterdam, Netherlands) 2022 172142-153
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Portuguese Consensus Recommendations for Next-Generation Sequencing of Lung Cancer, Rare Tumors, and Cancers of Unknown Primary Origin in Clinical Practice.
R Teixeira Manuel et al. Acta medica portuguesa 2022
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Healthcare Transition from Pediatric- to Adult-Focused Care in X-Linked Hypophosphatemia: Review and Expert Consensus.
Dahir Kathryn et al. The Journal of clinical endocrinology and metabolism 2021
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Presenting artificial intelligence, deep learning, and machine learning studies to clinicians and healthcare stakeholders: an introductory reference with a guideline and a Clinical AI Research (CAIR) checklist proposal.
Olczak Jakub et al. Acta orthopaedica 2021 1-13
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Application of a framework to guide genetic testing communication across clinical indications.
Hallquist Miranda L G et al. Genome medicine 2021 13(1) 71
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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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Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin Summary, Number 226.
et al. Obstetrics and gynecology 2020 Oct 136(4) 859-867
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Methods for Development of the European Commission Initiative on Breast Cancer Guidelines: Recommendations in the Era of Guideline Transparency.
Schünemann Holger J et al. Annals of internal medicine 2019 Jul
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Lung transplant referral for individuals with cystic fibrosis: Cystic Fibrosis Foundation consensus guidelines.
Ramos Kathleen J et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2019 May 18(3) 321-333
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Consensus on BCR-ABL1 reporting in chronic myeloid leukaemia in the UK.
Cross Nicholas C P et al. British journal of haematology 2018 Aug
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The International Rare Diseases Research Consortium: Policies and Guidelines to maximize impact.
Lochmüller Hanns, et al. European journal of human genetics : EJHG 2017 12 0. (12) 1293-1302
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Improving molecular testing and personalized medicine in non-small-cell lung cancer in Ontario.
Lim C et al. Current oncology (Toronto, Ont.) 2017 Apr 24(2) 103-110
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Committee Opinion No. 693: Counseling About Genetic Testing and Communication of Genetic Test Results.
et al. Obstetrics and gynecology 2017 Apr 129(4) e96-e101
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Community Health Workers: An Untapped Resource to Promote Genomic Literacy.
Allen Caitlin G et al. Journal of health communication 2016 21(sup2) 25-29
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Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project.
Hart Sarah J et al. Journal of genetic counseling 2016 Feb 25(1) 6-17
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Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalised Nutrition: Part 1 - Fields of Precision Nutrition.
Ferguson Lynnette R et al. Journal of nutrigenetics and nutrigenomics 2016 May 9(1) 12-27
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First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy.
Adams David et al. Current opinion in neurology 2016 Jan
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Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Botkin Jeffrey R et al. Am. J. Hum. Genet. 2015 Jul 2. 97(1) 6-21
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Guidelines for diagnosis and treatment of Hunter Syndrome for clinicians in Latin America.
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Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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