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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)
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Last data update: Apr 25, 2024
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all[original query]>>Original Studies[Product Type]
Correlation between NGS panel-based mutation results and clinical information in colorectal cancer patients.
Bo Cheng et al. Heliyon 2024 10(7) e29299
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A Study on the Retrospective Reinterpretation of BRCA1 and BRCA2 Variants.
Jin Ju Kim et al. Clin Lab 2024 70(4)
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Assessing the value of incorporating a polygenic risk score with non-genetic factors for predicting breast cancer diagnosis in the UK Biobank.
Jennifer A Collister et al. Cancer Epidemiol Biomarkers Prev 2024
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Uptake of Risk-Reducing Measures, Cascade Testing, and Related Challenges Among Carriers of Breast Cancer-Associated Germline Pathogenic Variants in Mexico.
Fernanda Mesa-Chavez et al. JCO Glob Oncol 2024 10e2300417
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Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants.
Zhenzhen Zhang et al. JAMA Netw Open 2024 7(4) e247421
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Prevalence of Homologous Recombination Deficiency Among Patients With Germline RAD51C/D Breast or Ovarian Cancer.
Sara Torres-Esquius et al. JAMA Netw Open 2024 7(4) e247811
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Prediction of tumor origin in cancers of unknown primary origin with cytology-based deep learning.
Fei Tian et al. Nat Med 2024
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A Machine Learning Algorithm Facilitates Prognosis Prediction and Treatment Selection for Barcelona Clinic Liver Cancer Stage C Hepatocellular Carcinoma.
Ji Won Han et al. Clin Cancer Res 2024
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Predicting the risk of lung cancer using machine learning: A large study based on UK Biobank.
Siqi Zhang et al. Medicine (Baltimore) 2024 103(16) e37879
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Comparing preferences for skin cancer screening: AI-enabled app vs dermatologist.
Susanne Gaube et al. Soc Sci Med 2024 349116871
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Application value of the automated machine learning model based on modified CT index combined with serological indices in the early prediction of lung cancer.
Leyuan Meng et al. Front Public Health 2024 121368217
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Development and Validation of an 18-Gene Urine Test for High-Grade Prostate Cancer
Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants
Somatic Tumor Testing in Prostate Cancer: Experience of a Tertiary-Care Center Including Pathologist-Driven Reflex Testing of Localized Tumors at Diagnosis.
Susan Prendeville et al. Mod Pathol 2024 100489
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Impact of Family History and Germline Genetic Risk Single Nucleotide Polymorphisms on Long-Term Outcomes of Favorable-Risk Prostate Cancer.
Florian Rumpf et al. J Urol 2024 101097JU0000000000003927
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Uptake of screening and risk-reducing recommendations among women with hereditary breast and ovarian cancer syndrome due to pathogenic BRCA1/2 variants evaluated at a large urban comprehensive cancer center.
Hadeel Assad et al. Breast Cancer Res Treat 2024
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A qualitative feasibility study of a prototype patient-centered video intervention to increase uptake of cancer genetic testing among Black Americans.
Katherine Clegg Smith et al. Pilot Feasibility Stud 2024 10(1) 62
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Clinical features of prostate cancer by polygenic risk score.
Christina Spears et al. Fam Cancer 2024
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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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A Semiautonomous Deep Learning System to Reduce False-Positive Findings in Screening Mammography.
Stefano Pedemonte et al. Radiol Artif Intell 2024 e230033
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Conventional and machine-learning based risk score for patients with early-stage hepatocellular carcinoma.
Chun-Ting Ho et al. Clin Mol Hepatol 2024
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Explainable and visualizable machine learning models to predict biochemical recurrence of prostate cancer.
Wenhao Lu et al. Clin Transl Oncol 2024
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The potential of machine learning models to identify malnutrition diagnosed by GLIM combined with NRS-2002 in colorectal cancer patients without weight loss information.
Tiantian Wu et al. Clin Nutr 2024 43(5) 1151-1161
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The Impact of Next-generation Sequencing on Interobserver Agreement and Diagnostic Accuracy of Desmoplastic Melanocytic Neoplasms.
Alice Chen et al. Am J Surg Pathol 2024
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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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Population-based BRCA germline mutation screening in the Han Chinese identifies individuals at risk of BRCA mutation-related cancer: experience from a clinical diagnostic center from greater Shanghai area.
Zhiyuan Wu et al. BMC Cancer 2024 24(1) 411
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Oncologists' perceptions of tumor genomic profiling and barriers to communicating secondary hereditary risks to African American cancer patients.
Michael J Hall et al. BMC Cancer 2024 24(1) 412
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BRCA awareness and testing experience in the UK Jewish population: a qualitative study.
Katrina Sarig et al. J Med Genet 2024
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Hereditary Cancer Syndrome Carriers: Feeling Left in the Corner.
Celia Diez de Los Rios de la Serna et al. Semin Oncol Nurs 2024 151624
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Non-invasive prenatal test identifies circulating cell-free DNA chromosomal abnormalities derived from clonal hematopoiesis in aggressive hematological malignancies.
Valentina Giudice et al. Clin Exp Med 2024 24(1) 69
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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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