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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Mar 27, 2024
. (Total: 63367 Documents since 2012)
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Evidence[original query]>>Guidelines Related[Product Type]
Transition from pediatric to adult care in patients with Turner syndrome in Italy: a consensus statement by the TRAMITI project.
T Aversa et al. J Endocrinol Invest 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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The Clinical Utility of FLT3 Mutation Testing in Acute Leukemia: A Canadian Consensus.
Julie Bergeron et al. Curr Oncol 2023 30(12) 10410-10436
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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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Evidence-based consensus guidelines for ALS genetic testing and counseling.
Jennifer Roggenbuck et al. Ann Clin Transl Neurol 2023
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Canadian Consensus Recommendations on the Management of KRAS G12C-Mutated NSCLC.
Parneet K Cheema et al. Curr Oncol 2023 30(7) 6473-6496
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Screening for Lipid Disorders in Children and Adolescents: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2023 330(3) 253-260
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Evidence and Recommendation for Guanidinoacetate Methyltransferase Deficiency Newborn Screening.
Margie A Ream et al. Pediatrics 2023
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Guidelines and Recommendations for Laboratory Analysis in the Diagnosis and Management of Diabetes Mellitus.
David B Sacks et al. Clin Chem 2023
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Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Jeffrey S Dungan et al. Genet Med 2023 100874
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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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Integrating Precision Medicine into Medical Dermatology Clinical Practice: An Expert Consensus Panel.
Danny Zakria et al. J Drugs Dermatol 2023 22(6) 588-593
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Consensus clinical management guidelines for acid sphingomyelinase deficiency (Niemann-Pick disease types A, B and A/B).
Tarekegn Geberhiwot et al. Orphanet J Rare Dis 2023 18(1) 85
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2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes-2023.
Nuha A ElSayed et al. Diabetes care 2022 46(Suppl 1) S19-S40
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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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Bempedoic acid in the management of lipid disorders and cardiovascular risk. 2023 position paper of the international lipid expert panel (ILEP).
Maciej Banach et al. Progress in cardiovascular diseases 2023
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Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG).
Melissa T Carter et al. Journal of medical genetics 2023
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A practical guideline of genomics-driven drug discovery in the era of global biobank meta-analysis.
Shinichi Namba et al. Cell genomics 2023 2(10) 100190
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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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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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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.
Erik Boot et al. Genetics in medicine : official journal of the American College of Medical Genetics 2023 100344
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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.
Sólveig Óskarsdóttir et al. Genetics in medicine : official journal of the American College of Medical Genetics 2023 100338
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How guideline development has informed clinical research for organic acidurias (et vice versa).
Forny Patrick et al. Journal of inherited metabolic disease 2023
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Mismatch Repair and Microsatellite Instability Testing for Immune Checkpoint Inhibitor Therapy: ASCO Endorsement of College of American Pathologists Guideline.
Vikas Praveen et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2023 JCO2202462
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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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European Respiratory Society Statement on Familial Pulmonary Fibrosis.
Borie Raphael et al. The European respiratory journal 2022
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Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Dungan Jeffrey S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 27, 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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