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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Implementation [original query]>>Guidelines Related[Product Type]
A framework for the evaluation and reporting of incidental findings in clinical genomic testing.
Carolyn M Brown et al. Eur J Hum Genet 2024
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Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction of CYP2C9, HLA-A and HLA-B with anti-epileptic drugs.
Lisanne E N Manson et al. Eur J Hum Genet 2024
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EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer.
Trudi McDevitt et al. Eur J Hum Genet 2024
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International Atherosclerosis Society Roadmap for Familial Hypercholesterolaemia.
Gerald F Watts et al. Glob Heart 2024 19(1) 12
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Improving care for rare genetic neurodevelopmental disorders: a systematic review and critical appraisal of clinical practice guidelines using AGREE II.
Mirthe J Klein Haneveld et al. Genet Med 2024 101071
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An analysis of the impact of annual cancer genetic testing guideline updates on a past patient population.
Jordan Johnson et al. J Genet Couns 2023
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AGA Clinical Practice Update on Risk Stratification for Colorectal Cancer Screening and Post-Polypectomy Surveillance: Expert Review.
Rachel B Issaka et al. Gastroenterology 2023
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Consensus recommendations on holistic care in hereditary ATTR amyloidosis: an international Delphi survey of patient advocates and multidisciplinary healthcare professionals.
Laura Obici et al. BMJ Open 2023 13(9) e073130
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CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase.
Victoria M Pratt et al. J Mol Diagn 2023
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Nutrition management of PKU with pegvaliase therapy: update of the web-based PKU nutrition management guideline recommendations.
Amy Cunningham et al. Orphanet J Rare Dis 2023 18(1) 155
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International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia.
Gerald F Watts et al. Nat Rev Cardiol 2023
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Recommendations for Next-Generation Sequencing Germline Variant Confirmation: A Joint Report of the Association for Molecular Pathology and National Society of Genetic Counselors.
Kristy R Crooks et al. J Mol Diagn 2023
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Machine Learning in Laboratory Medicine: Recommendations of the IFCC Working Group.
Stephen R Master et al. Clin Chem 2023
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Closing the Testing Gap: Standardization of Comprehensive Biomarker Testing for Metastatic Non-Small-Cell Lung Cancer in a Large Community Oncology Practice.
David M Waterhouse et al. JCO Oncol Pract 2023 OP2200817
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Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2D6, CYP2C19, CYP2B6, SLC6A4, and HTR2A Genotypes and Serotonin Reuptake Inhibitor Antidepressants.
Chad A Bousman et al. Clinical pharmacology and therapeutics 2023
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Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction between CYP2D6, CYP3A4 and CYP1A2 and antipsychotics.
Lianne Beunk et al. European journal of human genetics : EJHG 2023
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Human Genetics Society of Australasia Position Statement: Use of Polygenic Scores in Clinical Practice and Population Health.
Mary-Anne Young et al. Twin research and human genetics : the official journal of the International Society for Twin Studies 2023 1-9
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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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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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Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene-CanVar and the NHS England Haematological Oncology Working Group.
Beverley Speight et al. British journal of haematology 2023
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Benefits and Challenges in Implementation of Artificial Intelligence in Colonoscopy: World Endoscopy Organization Position Statement.
Yuichi Mori et al. Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society 2023
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EBCC-13 manifesto: Balancing pros and cons for contralateral prophylactic mastectomy.
Schmidt Marjanka K et al. European journal of cancer (Oxford, England : 1990) 2023 18179-91
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Consensus on diagnosis and management of Hereditary Angioedema in the Middle East: A Delphi initiative.
Maurer Marcus et al. The World Allergy Organization journal 2023 16(1) 100729
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Patient centered guidelines for the laboratory diagnosis of Gaucher disease type 1.
Dardis A et al. Orphanet journal of rare diseases 2022 17(1) 442
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Dutch pharmacogenetics working group (DPWG) guideline for the gene-drug interaction of CYP2D6 and COMT with atomoxetine and methylphenidate.
Nijenhuis Marga et al. European journal of human genetics : EJHG 2022
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Dutch pharmacogenetics working group (DPWG) guideline for the gene-drug interaction between UGT1A1 and irinotecan.
Hulshof Emma C et al. European journal of human genetics : EJHG 2022
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Guidelines to Establish an Equitable Mobile Health Ecosystem.
Fortuna Karen L et al. Psychiatric services (Washington, D.C.) 2022 appips202200011
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Considerations on the use of carrier screening testing in human reproduction: comparison between recommendations from the Italian Society of Human Genetics and other international societies.
Capalbo Antonio et al. Journal of assisted reproduction and genetics 2022
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The time is now: Achieving FH paediatric screening across Europe - The Prague Declaration.
Bedlington Nicole et al. GMS health innovation and technologies 2022 16Doc04
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Joint EANM/SNMMI guideline on radiomics in nuclear medicine : Jointly supported by the EANM Physics Committee and the SNMMI Physics, Instrumentation and Data Sciences Council.
Hatt M et al. European journal of nuclear medicine and molecular imaging 2022
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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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