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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 18, 2024
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Surveillance[original query]>>Guidelines Related[Product Type]
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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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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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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Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline.
Kratz Christian Peter et al. Geburtshilfe und Frauenheilkunde 2022 82(1) 42-49
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Medical guidelines for Li-Fraumeni syndrome 2019, version 1.1.
Kumamoto Tadashi et al. International journal of clinical oncology 2021
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Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe.
Marmolejo David Humberto et al. European journal of medical genetics 2021 104350
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Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2020 for the Clinical Practice of Hereditary Colorectal Cancer.
Tomita Naohiro et al. International journal of clinical oncology 2021
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European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender.
Seppälä T T et al. The British journal of surgery 2021 108(5) 484-498
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International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers.
Amar Laurence et al. Nature reviews. Endocrinology 2021
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Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Tischkowitz Marc et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
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Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2021 325(19) 1965-1977
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Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
M Tishkowitz et al, Genetics in Medicine, May 11, 2021
Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.
Fortuno Cristina et al. Human mutation 2020 Dec
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Hereditary diffuse gastric cancer: updated clinical practice guidelines.
Blair Vanessa R et al. The Lancet. Oncology 2020 Aug 21(8) e386-e397
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Practical Guidance to Implementing Quality Management Systems in Public Health Laboratories Performing Next-Generation Sequencing: Personnel, Equipment, and Process Management (Phase 1).
Hutchins Rebecca J et al. Journal of clinical microbiology 2019 57(8)
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Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.
Vears Danya F et al. Twin research and human genetics : the official journal of the International Society for Twin Studies 2020 Jun 23(3) 184-189
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Guidelines for the management of hereditary colorectal cancer from the BSG /ACPGBI/UKCGG
British Society Gastroenterology, October 2019
Contemporary prognostic indicators for prostate cancer incorporating International Society of Urological Pathology recommendations.
Egevad Lars et al. Pathology 2018 Jan 50(1) 60-73
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Endoscopic management of Lynch syndrome and of familial risk of colorectal cancer: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.
van Leerdam Monique E et al. Endoscopy 2019 Oct
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Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.
Durno Carol et al. The American journal of gastroenterology 2017 112(5) 682-690
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Local Coverage Determination (LCD): Bladder/Urothelial Tumor Markers (L36975)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Diagnostic and Therapeutic Colonoscopy (L36868)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Diagnostic and Therapeutic Colonoscopy (L34213)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Biomarker Testing (Prior to Initial Biopsy) for Prostate Cancer Diagnosis (L37733)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Biomarker Testing for Neuroendocrine Tumors/Neoplasms (L37851)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Genomic Sequence Analysis Panels in the Treatment of Hematolymphoid Diseases (L37606)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Foodborne Gastrointestinal Panels Identified by Multiplex Nucleic Acid Amplification (NAATs) (L37709)
The U.S. Centers for Medicare & Medicaid Services
Endoscopic management of polyposis syndromes: European Society of Gastrointestinal Endoscopy (ESGE) guideline.
van Leerdam Monique E et al. Endoscopy 2019 Jul
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Adenovirus in solid organ transplant recipients: Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice.
Florescu Diana F et al. Clinical transplantation 2019 Mar e13527
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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
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National Center on Birth Defects and Developmental Disabilities
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