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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 18, 2024
. (Total: 63623 Documents since 2012)
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all[original query]>>Guidelines Related[Product Type]
A focused update to the 2019 NLA scientific statement on use of lipoprotein(a) in clinical practice.
Marlys L Koschinsky et al. J Clin Lipidol 2024
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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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Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
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Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions.
Ali AlMail et al. NPJ Genom Med 2024 9(1) 27
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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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A Guideline for Open-Source Tools to Make Medical Imaging Data Ready for Artificial Intelligence Applications: A Society of Imaging Informatics in Medicine (SIIM) Survey.
Sanaz Vahdati et al. J Imaging Inform Med 2024
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Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.
Danya F Vears et al. Twin Res Hum Genet 2024 1-8
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Clinical Guideline for Preimplantation Genetic Testing in Inherited Cardiac Diseases.
Job A J Verdonschot et al. Circ Genom Precis Med 2024 e004416
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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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Clinical Practice Guidelines on using artificial intelligence and gadgets for mental health and well-being.
Vipul Singh et al. Indian J Psychiatry 2024 66(Suppl 2) S414-S419
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Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic Ancestry Groups in Biomedical Publications
G Feero et al, JAMA, March 12, 2024
Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
Theresa A Grebe et al. Genet Med 2024 101052
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A holistic approach to fragile X syndrome integrated guidance for person-centred care.
Kirsten Johnson et al. J Appl Res Intellect Disabil 2024 37(3) e13214
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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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Incorporating a Prognostic Gene Expression Profile Test into the Management of Cutaneous Squamous Cell Carcinoma: An Expert Consensus Panel Report.
Danny Zakria et al. J Drugs Dermatol 2024 23(2) 54-60
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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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Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium.
M Janatová et al. Klin Onkol 2023 37(6) 431-439
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Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey.
Sophie Allen et al. J Med Genet 2023
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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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Slice Testing - Considerations from Ordering to Reporting: A Joint Report of the Association for Molecular Pathology, College of American Pathologists, and National Society of Genetic Counselors.
Jeffrey A SoRelle et al. J Mol Diagn 2023
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Incorporating a Prognostic Gene Expression Profile Test into the Management of Cutaneous Squamous Cell Carcinoma: An Expert Consensus Panel Report.
Danny Zakria et al. J Drugs Dermatol 2023 22(12) 7691
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Co-design of patient information leaflets for germline predisposition to cancer: recommendations for clinical practice from the UK Cancer Genetics Group (UKCGG), Cancer Research UK (CRUK) funded CanGene-CanVar Programme and the Association of Genetic Nurse Counsellors (AGNC).
Kelly Kohut et al. J Med Genet 2023
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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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NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024.
Mary B Daly et al. J Natl Compr Canc Netw 2023 21(10) 1000-1010
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Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia.
Danya F Vears et al. Eur J Hum Genet 2023
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Expert Consensus on the Long-Term Effectiveness of Medical Nutrition Therapy and Its Impact on the Outcomes of Adults with Phenylketonuria.
Júlio César Rocha et al. Nutrients 2023 15(18)
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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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Evidence-based consensus guidelines for ALS genetic testing and counseling.
Jennifer Roggenbuck et al. Ann Clin Transl Neurol 2023
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 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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