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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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All of Us Reports and Publications Database|Home|PHGKB
All of Us Reports and Publications Database
All of Us Publications Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 22, 2024
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Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry.
Lan Jiang, et al. medRxiv 2024 0 0.
Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications.
Marie C Sadler, et al. medRxiv 2024 0 0.
Functional Analysis of G6PD Variants Associated With Low G6PD Activity in the All of Us Research Program.
Powell NR, et al. MEDRXIV April 14, 2024.
Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry
Srushti LJ, et al. MEDRXIV March 13, 2024
PheWAS analysis on large-scale biobank data with PheTK.
Tam C Tran, et al. medRxiv 2024 0 0.
Influence of Health Insurance Type on the Access of Cancer Patients to Ramucirumab Therapy Using All of Us Database
Tibi S, et al, Preprints 2024, 2024020902
To weight or not to weight? Studying the effect of selection bias in three large EHR-linked biobanks
Salvatore M, et al, MEDRXIV, February 13, 2024
PheWAS analysis on large-scale biobank data with PheTK
Tran TC, et al, MEDRXIV, February 13, 2024
Effects of Preanalytical Sample Collection and Handling on Comprehensive Metabolite Measurements in Human Urine Biospecimens
Braisted J, et al. MEDRXIV, January 25, 2024
Improving genetic risk modeling of dementia from real-world data in underrepresented populations
Chang T, et al. MEDRXIV, February 6, 2024
Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer’s
Fu M, et al. MEDRXIV, February 5, 2024
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank
Manigbas CA, et al. MEDRXIV, January 23, 2024
Joint Association of Polygenic Risk and Social Determinants of Health with Coronary Heart Disease in the United States
Norland K, et al. MEDRXIV, January 11, 2024
Genetic and Survey Data Improves Performance of Machine Learning Model for Long COVID
Wei WQ, et al. Research Square, December 19, 2023
The Role of Social Determinants of Health and Social Position in Mental Health: An Examination of the Moderating Effects of Race, Ethnicity, and Gender on Depression through the All of Us Dataset
Kammer-Kerwick M, et al. MEDRXIV November 16, 2023
Wearable Device-Measured Daily Step Count is an Independent Predictor of Postoperative Surgical Complications Among All of Us Research Participants
Gehl CJ, et al. MEDRXIV December 9 2023
Genomic analysis identifies risk factors in restless legs syndrome
Akcimen F, et al. MEDRXIV. December 20 2023
Comorbid psychiatric disease significantly mediates increased rates of alcohol use disorder among patients with inflammatory and pigmentary skin disorders: a case-control study in the All of Us Research Program
Kamal K, et al. Research Square, December 7, 2023
Landscape of racial and ethnic health disparities in the All of Us Research Program
Lam V, et al. Research Square, November 17, 2023
Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score
Rosenthal EA, et al. MEDRXIV, October 24, 2023
Machine Learning Enables Single-Score Assessment of MASLD Presence and Severity
Chen R, et al. MEDRXIV, October 25, 2023
Analysis of 245,368 diverse individuals from the NIH All of Us Cohort identifies incomplete penetrance of the VEXAS-defining UBA1 p.M41L somatic mutation
Corty RW, et al. MEDRXIV November 8, 2023
Predicted loss of function alleles in Bassoon (BSN) are associated with obesity.
Na Zhu, et al. medRxiv 2023 0 0.
Sharing and Reusing Computable Phenotype Definitions
Visweswaran S, et al.MEDRXIV, September 18, 2023
Polygenic Susceptibility to Diabetes and Poor Glycemic Control in Stroke Survivors
Demarais ZS, et al. MEDRXIV, September 18, 2023
Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threats
Steinfeldt J, et al. MEDRXIV, September 26, 2023
Multi-ancestry Polygenic Mechanisms of Type 2 Diabetes Elucidate Disease Processes and Clinical Heterogeneity
Smith K, et al. MEDRXIV, September 29, 2023
Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes
Schroeder P, et al. MEDRXIV, September 29, 2023
Harnessing consumer wearable digital biomarkers for individualized recognition of postpartum depression using the All of Us Research Program dataset
Hurwitz E, et al. MEDRXIV, October 14, 2023
Subtyping Social Determinants of Health in All of Us: Network Analysis and Visualization Approach.
Suresh K Bhavnani, et al. medRxiv 2023 0 0.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 23, 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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