All of Us Reports and Publications Database

All of Us Publications Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

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Striving Towards Equity in Cardiovascular Genomics Research. Javier Jurado Vélez, et al. Curr Atheroscler Rep 2025 0 0. (1) 34 Similar articles in PubMed
Coding Variants of the Genitourinary Development Gene WNT9B Carry High Risk for Prostate Cancer. William D Dupont, et al. JCO Precis Oncol 2025 0 0. e2400569 Similar articles in PubMed
Using polygenic risk scores and APOE e4 to evaluate the risk for Alzheimer’s disease in European ancestry populations Dongbing Lai, et al. Alzheimers Dement 2025 0 0. e089048
Genome Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program. Kyoung A Viola Lee, et al. Ophthalmology 2025 0 0. Similar articles in PubMed
Polygenic overlap with granulocyte counts identifies novel loci for clozapine metabolism and clozapine-induced agranulocytosis. Elise Koch, et al. Neuropsychopharmacology 2025 0 0. Similar articles in PubMed
A clinical algorithm to identify people with the glucose-6-phosphate dehydrogenase p.Val68Met variant at risk for diabetes undertreatment Pershad Y, et al.MEDRXIV, January 17, 2025
Rare Variant Analyses in Ancestrally Diverse Cohorts Reveal Novel ADHD Risk Genes Jung S, et al. MEDRXIV, January 17, 2025
Characterization of the Phenotypic Consequences of the Duffy-Null Genotype. Micah R Hysong, et al. Blood Adv 2025 0 0. Similar articles in PubMed
Subcontinental Genetic Diversity in the All of Us Research Program: Implications for Biomedical Research Gouveia MH, et al. BIORXIV, January 10, 2025
Unsupervised Ensemble Learning for Efficient Integration of Pre-trained Polygenic Risk Scores Gao C, et al. MEDRXIV, January 6, 2025
Genomic insights into Neolithic founding paternal lineages around the Qinghai-Xizang Plateau using integrated YanHuang resource. Mengge Wang, et al. iScience 2025 0 0. (12) 111456 Similar articles in PubMed
Targeted Variant Assessments of Human Endogenous Retroviral Regions in Whole Genome Sequencing Data Reveal Retroviral Variants Associated with Papillary Thyroid Cancer. Erik Stricker, et al. Microorganisms 2025 0 0. (12) Similar articles in PubMed
A semi-empirical Bayes approach for calibrating weak instrumental bias in sex-specific Mendelian randomization studies Huang YJ, et al. MEDRXIV, January 2, 2025
Alcohol Use Disorder Polygenic Score Compared With Family History and ADH1B. Dongbing Lai, et al. JAMA Netw Open 2025 0 0. (12) e2452705 Similar articles in PubMed
Intersection of rare pathogenic variants from TCGA in the All of Us Research Program v6. Blaine A Bates, et al. HGG Adv 2025 0 0. 100405 Similar articles in PubMed
Impact of population screening for Lynch syndrome insights from the All of Us data. Jiheum Park, et al. Nat Commun 2025 0 0. (1) 523 Similar articles in PubMed
Precision Medicine for Pulmonary Vascular Disease: The Future Is Now (2023 Grover Conference Series). Lindsay M Forbes, et al. Pulm Circ 2025 0 0. (1) e70027 Similar articles in PubMed
Meta-EA: a gene-specific combination of available computational tools for predicting missense variant effects. Panagiotis Katsonis, et al. Nat Commun 2025 0 0. (1) 159 Similar articles in PubMed
Integrating electronic health records and GWAS summary statistics to predict the progression of autoimmune diseases from preclinical stages. Chen Wang, et al. Nat Commun 2025 0 0. (1) 180 Similar articles in PubMed
The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup Huang YJ, et al. MEDRXIV, December 20, 2024
Genetics in Medicine Open to us all. Bo Yuan, et al. Genet Med Open 2024 0 0. (1) 100772 Similar articles in PubMed
SurVIndel2: improving copy number variant calling from next-generation sequencing using hidden split reads. Ramesh Rajaby, et al. Nat Commun 2024 0 0. (1) 10473 Similar articles in PubMed
Rare disease genomics and precision medicine. Juhyeon Hong, et al. Genomics Inform 2024 0 0. (1) 28 Similar articles in PubMed
Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts. Mart Kals, et al. EClinicalMedicine 2024 0 0. 102956 Similar articles in PubMed
Integrated exposomic analysis of lipid phenotypes: Leveraging GE.db in environment by environment interaction studies. Andre Luis Garao Rico, et al. Pac Symp Biocomput 2024 0 0. 535-550 Similar articles in PubMed
Estimation of genetic admixture proportions via haplotypes. Seyoon Ko, et al. Comput Struct Biotechnol J 2024 0 0. 4384-4395 Similar articles in PubMed
Polygenic scores and social determinants of health: Their correlations and potential biases. Daniel J Schaid, et al. HGG Adv 2024 0 0. (1) 100389 Similar articles in PubMed
Using genomic databases to determine the frequency and population-based heterogeneity of autosomal recessive conditions. William B Hannah, et al. Genet Med Open 2024 0 0. 101881 Similar articles in PubMed
A missense variant effect map for the human tumor-suppressor protein CHK2. Marinella Gebbia, et al. Am J Hum Genet 2024 0 0. (12) 2675-2692 Similar articles in PubMed
Health equity innovation in precision medicine: data stewardship and agency to expand representation in clinicogenomics. Patrick J Silva, et al. Health Res Policy Syst 2024 0 0. (1) 170 Similar articles in PubMed

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