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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 30, 2024
. (Total: 63724 Documents since 2012)
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Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium.
Erica Soster et al. Mol Cytogenet 2024 17(1) 9
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Utilization and Outcomes of Multigene Panel Testing in Patients With Pancreatic Ductal Adenocarcinoma.
Derk C F Klatte et al. JCO Oncol Pract 2024 OP2300447
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Colorectal Cancer Risk between Mendelian and Non-Mendelian Inheritance.
Elizabeth A Hibler et al. Clin Colon Rectal Surg 2024 37(3) 140-145
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Factors Influencing Adherence to the Risk Management Program for Women With a Genetic Predisposition to Breast Cancer: Real-World Data from a French Multicenter Program.
Ke Zhou et al. Oncologist 2024
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Dynamic SARS-CoV-2 surveillance model combining seroprevalence and wastewater concentrations for post-vaccine disease burden estimates
RH Holm et al, Comm Med, April 9, 2024
Genomics reveals heterogeneous Plasmodium falciparum transmission and selection signals in Zambia.
Abebe A Fola et al. Commun Med (Lond) 2024 4(1) 67
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Concerted efforts toward genomic surveillance of viral pathogens in immunocompromised individuals.
Matheus Filgueira Bezerra et al. Lancet Microbe 2024
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Newborn screening for Duchenne muscular dystrophy: the perspectives of stakeholders.
Charli Ji et al. Lancet Reg Health West Pac 2024 45101049
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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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The Italian registry of families at risk for pancreatic cancer (IRFARPC): implementation and evolution of a national program for pancreatic cancer surveillance in high-risk individuals.
Livia Archibugi et al. Fam Cancer 2024
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[Return of Individual Genomic Results to Germline Pathogenic Variant Carriers of Hereditary Cancer in Population Based Cohort Study].
Kinuko Ohneda et al. Gan To Kagaku Ryoho 2024 51(3) 231-236
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Viral genome sequencing to decipher in-hospital SARS-CoV-2 transmission events.
Elisabeth Esser et al. Sci Rep 2024 14(1) 5768
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Prevalence of persistent SARS-CoV-2 in a large community surveillance study.
Mahan Ghafari et al. Nature 2024
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Cost-Effectiveness of Gene-Specific Prevention Strategies for Ovarian and Breast Cancer.
Xia Wei et al. JAMA Netw Open 2024 7(2) e2355324
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Maximizing scarce colonoscopy resources: the crucial role of Stool-Based tests.
Gloria D Coronado et al. J Natl Cancer Inst 2024
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The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
Megan J Puckelwartz et al. Genome Med 2024 16(1) 13
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The 31-Gene Expression Profile Test Outperforms AJCC in Stratifying Risk of Recurrence in Patients with Stage I Cutaneous Melanoma.
Sebastian Podlipnik et al. Cancers (Basel) 2024 16(2)
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Genomic Medicine Guidance: A Point-of-Care App for Heritable Thoracic Aortic Diseases.
Rohan Patil et al. medRxiv 2024
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Planning for Actionable Precision Medicine.
James J Cimino et al. Stud Health Technol Inform 2024 310244-248
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Ten-Year Follow-Up of Women at High Risk for Familial Breast and Ovarian Cancer in Otago and Southland, New Zealand.
Simone Petrich et al. Asian Pac J Cancer Prev 2024 25(1) 3-7
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Families' experiences accessing care after genomic sequencing in the pediatric cancer context: "It's just been a big juggle".
Blake Vuocolo et al. J Genet Couns 2024
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Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders.
Alexandra Santana Almansa et al. Ann Clin Transl Neurol 2024
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Surveillance Compliance and Quality of Life Assessment Among Surgical Patients with Familial Adenomatous Polyposis Syndrome.
Noura Alhassan et al. J Epidemiol Glob Health 2024
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Patient experiences with tissue-based genomic testing during active surveillance for prostate cancer.
Michael S Leapman et al. BJUI Compass 2024 5(1) 142-149
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Clinical Utility of the 31-Gene Expression Profile Test on the Management of Cutaneous Melanoma by Nurse Practitioners and Physician Assistants.
Renata Block et al. J Adv Pract Oncol 2024 14(7) 586-596
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Counselling and management of women with genetic predisposition to gynaecological cancers.
Naushabah Malik et al. Eur J Obstet Gynecol Reprod Biol 2024 29444-48
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Experiences of patients and family members with follow-up care, information needs and provider support after identification of Lynch Syndrome.
Ryan Mooney et al. Hered Cancer Clin Pract 2023 21(1) 28
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Risk-reducing decisions regarding germline BRCA pathogenic variant: focusing on the timing of genetic testing and RRSO.
Akiko Abe et al. J Med Genet 2023
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Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction.
Anja Tüchler et al. Breast 2023 73103615
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Risk of Proctectomy After Ileorectal Anastomosis in Familial Adenomatous Polyposis in the Modern Era.
Sudeep Banerjee et al. Dis Colon Rectum 2023
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 30, 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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