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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: May 09, 2024
. (Total: 63814 Documents since 2012)
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Carpal Tunnel Syndrome and Transthyretin Amyloidosis in the All of Us Research Program.
Naman S Shetty et al. Mayo Clin Proc 2024
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A scoping review of web-based, interactive, personalized decision-making tools available to support breast cancer treatment and survivorship care.
Kaitlyn M Wojcik et al. J Cancer Surviv 2024
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A Scoping Review of Personalized, Interactive, Web-Based Clinical Decision Tools Available for Breast Cancer Prevention and Screening in the United States.
Dalya Kamil et al. MDM Policy Pract 2024 9(1) 23814683241236511
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Health-Related quality of life and DNA Methylation-Based aging biomarkers among survivors of childhood cancer.
Noel-Marie Plonski et al. J Natl Cancer Inst 2024
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Describing patterns of familial cancer risk in subfertile men using population pedigree data.
Joemy M Ramsay et al. Hum Reprod 2024
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Sex Differences in Diagnosis, Treatment, and Cardiovascular Outcomes in Homozygous Familial Hypercholesterolemia.
Janneke W C M Mulder et al. JAMA Cardiol 2024
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Utilizing Human Genetics to Develop Chemoprevention for Cancer-Too Good an Opportunity to be Missed.
Ulrike Peters et al. Cancer Prev Res (Phila) 2024 17(1) 7-12
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Mediating Factors in the Association of Maternal Educational Level With Pregnancy Outcomes: A Mendelian Randomization Study.
Tormod Rogne et al. JAMA Netw Open 2024 7(1) e2351166
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Lung cancer in patients who have never smoked - an emerging disease.
Jaclyn LoPiccolo et al. Nat Rev Clin Oncol 2024
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Using phylogenomic analysis, we identified leading indicators that would have generated EWS ahead of significant increases in COVID-19 hospitalisations in the UK between August 2020 and March 2022. Our results also show that EWS lead time is sensitive to the threshold set for the number of false positive (FP) EWS.
TT Hoang et al, EBiomedicine, January 9, 2024
Genomic landscape and actionable mutations of brain metastases derived from non-small cell lung cancer: A systematic review.
Lily J Andrews et al. Neurooncol Adv 2023 5(1) vdad145
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Family history, socioeconomic factors, comorbidities, health behaviors, and the risk of sudden cardiac arrest.
Eujene Jung et al. Sci Rep 2023 13(1) 21341
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Multitarget Stool RNA Test for Colorectal Cancer Screening.
Erica K Barnell et al. JAMA 2023
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Cost-utility analysis and cross-country comparison of pharmacogenomics-guided treatment in colorectal cancer patients participating in the U-PGx PREPARE study.
Vasileios Fragoulakis et al. Pharmacol Res 2023 106949
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Early-Life Adversity Associations With Later Life Epigenetic Aging Profiles in the Multi-Ethnic Study of Atherosclerosis.
Lauren L Schmitz et al. Am J Epidemiol 2023
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Identification of Sociodemographic, Clinical, and Genetic Factors to Aid Alaska Native and American Indian People to Successfully Quit Smoking.
Jaedon P Avey et al. Nicotine Tob Res 2023
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Diagnostic yield of a risk model versus faecal immunochemical test only: a randomised controlled trial in a colorectal cancer screening programme.
Tim L Kortlever et al. Br J Cancer 2023
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The causal effects of education on adult health, mortality and income: evidence from Mendelian randomization and the raising of the school leaving age.
Neil M Davies et al. Int J Epidemiol 2023
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The relation between epidermal growth factor receptor mutations profiles and smoking patterns in patients with lung adenocarcinoma: A cross-sectional study.
Seyedeh Yasamin Parvar et al. Health Sci Rep 2023 6(7) e1369
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A scoping review of smoking cessation pharmacogenetic studies to advance future research across racial, ethnic, and ancestral populations.
Elizabeth C Prom-Wormley et al. Front Genet 2023 141103966
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BRCA mutations detected by tumour next-generation sequencing in non-small cell lung cancer: impact on response to therapy and disease course.
Roi Tschernichovsky et al. Transl Lung Cancer Res 2023 12(5) 1011-1022
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Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Veera M Rajagopal et al. Nat Genet 2023
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Adjusting for population stratification in polygenic risk score analyses: a guide for model specifications in the UK Biobank.
Bochao Danae Lin et al. J Hum Genet 2023
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Cardiovascular Disease Risk Assessment Using Traditional Risk Factors and Polygenic Risk Scores in the Million Veteran Program.
Jason L Vassy et al. JAMA Cardiol 2023
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Genomic Characterization Revealed PM-Associated Mutational Signatures in Lung Cancer Including Activation of APOBEC3B.
Rongrong Fan et al. Environ Sci Technol 2023
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Genetic Associations with Smoking Relapse and Proportion of Follow-up in Smoking Relapse throughout Adulthood in Pre- and Postmenopausal Women.
Stephanie K Jones et al. Cancer Prev Res (Phila) 2023 OF1-OF12
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Genetic and Clinical Factors Underlying a Self-Reported Family History of Heart Disease.
Amanda Jowell et al. European journal of preventive cardiology 2023
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Impact of Molecular Testing Using Next-Generation Sequencing in the Clinical Management of Patients with Non-Small Cell Lung Cancer in a Public Healthcare Hospital.
Javier Simarro et al. Cancers 2023 15(6)
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Hypercholesterolemia in the Malaysian Cohort Participants: Genetic and Non-Genetic Risk Factors.
Nor Azian Abdul Murad et al. Genes 2023 14(3)
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Next-generation sequencing of non-small cell lung cancer at a Quebec health care cancer centre.
Mark Sorin et al. Cancer treatment and research communications 2023 35100696
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 09, 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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