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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|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 02, 2024
. (Total: 63767 Documents since 2012)
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Biopsy-based transcriptomics in the diagnosis of kidney transplant rejection.
Tristan de Nattes et al. Curr Opin Nephrol Hypertens 2024
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Challenges and best practices in omics benchmarking.
Thomas G Brooks et al. Nat Rev Genet 2024
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Predicting response to enzalutamide and abiraterone in metastatic prostate cancer using whole-omics machine learning.
Anouk C de Jong et al. Nature communications 2023 14(1) 1968
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Diagnostic classification of childhood cancer using multiscale transcriptomics.
Federico Comitani et al. Nature medicine 2023
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Emergence of nutrigenomics and dietary components as a complementary therapy in cancer prevention.
Shambhavi Srivastava et al. Environmental science and pollution research international 2022 29(60) 89853-89873
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Defining genomic, transcriptomic, proteomic, epigenetic, and phenotypic biomarkers with prognostic capability in male breast cancer: a systematic review.
Subarnarekha Chatterji et al. The Lancet. Oncology 2023 24(2) e74-e85
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Advancing CAR T cell therapy through the use of multidimensional omics data.
Jingwen Yang et al. Nature reviews. Clinical oncology 2023
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Harnessing the Power of Electronic Health Records and Genomics for Drug Discovery.
Krebs Kristi et al. Annual review of pharmacology and toxicology 2023 6365-76
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Multimodal single-cell and whole-genome sequencing of small, frozen clinical specimens.
Wang Yiping et al. Nature genetics 2023
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Prediction Performance of Feature Selectors and Classifiers on Highly Dimensional Transcriptomic Data for Prediction of Weight Loss in Filipino Americans at Risk for Type 2 Diabetes.
Chang Lisa et al. Biological research for nursing 2023 10998004221147513
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Single-cell transcriptomics for the assessment of cardiac disease.
Miranda Antonio M A et al. Nature reviews. Cardiology 2022
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An immune dysfunction score for stratification of patients with acute infection based on whole-blood gene expression.
Cano-Gamez Eddie et al. Science translational medicine 2022 14(669) eabq4433
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Spatial genomics maps the structure, nature and evolution of cancer clones.
Lomakin Artem et al. Nature 2022
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Mapping, clustering, and analysis of research in psychiatric genomics.
Yadav Sabita et al. Psychiatric genetics 2022
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Transcriptomics-based network medicine approach identifies metformin as a repurposable drug for atrial fibrillation
JC Lal et al, Cell Reports Med, October 11, 2022
A comprehensive genomic and transcriptomic dataset of triple-negative breast cancers.
Chen Qingwang et al. Scientific data 2022 9(1) 587
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Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.
Yin Xianyong et al. American journal of human genetics 2022
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Immune Checkpoint Blockade Outcome in Small-Cell Lung Cancer and Its Relationship With Retinoblastoma Mutation Status and Function.
Dowlati Afshin et al. JCO precision oncology 2022 6e2200257
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Transcriptome variation in human tissues revealed by long-read sequencing.
Glinos Dafni A et al. Nature 2022
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Large-Scale Multi-Omics Studies Provide New Insights into Blood Pressure Regulation.
Kamali Zoha et al. International journal of molecular sciences 2022 23(14)
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Cross-Platform Omics Prediction procedure: a statistical machine learning framework for wider implementation of precision medicine.
Wang Kevin Y X et al. NPJ digital medicine 2022 5(1) 85
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An introduction to spatial transcriptomics for biomedical research
CG Williams et al, Genome Medicine, June 27, 2022
Transcriptomics Meta-Analysis Predicts Two Robust Human Biomarkers for Severe Infection with SARS-CoV-2
J Clancy et al, MEDRXIV, June 6, 2022
An Artificial Intelligence-guided signature reveals the shared host immune response in MIS-C and Kawasaki disease
P Ghosh et al, Nature Comms, May 2022
Single-cell transcriptomics reveal a unique memory-like NK cell subset that accumulates with ageing and correlates with disease severity in COVID-19
C Guo et al, Genome Medicine, May 3, 2022
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
X Hu et al, AJHG, April 5, 2022
A guide for the diagnosis of rare and undiagnosed disease: beyond the exome.
Marwaha Shruti et al. Genome medicine 2022 14(1) 23
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RNA profiles reveal signatures of future health and disease in pregnancy
M Rasmussen et al, Nature, January 7, 2022
Osteoarthritis year in review: genetics, genomics, epigenetics.
Young David A et al. Osteoarthritis and cartilage 2021
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The BrAID study protocol: integration of machine learning and transcriptomics for brugada syndrome recognition.
Morales M A et al. BMC cardiovascular disorders 2021 21(1) 494
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 02, 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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