Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. 
 PMID:35241825
                                    
                                
                                    Investigating the Genetic Profile of the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (ALS-FTD) Continuum in Patients of Diverse Race, Ethnicity and Ancestry. 
 PMID:35052416
                                    
                                
                                    Sequencing-based genome-wide association studies reporting standards. 
 PMID:34870259
                                    
                                
                                    Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps. 
 PMID:34782789
                                    
                                
                                    An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci. 
 PMID:34711957
                                    
                                
                                    The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits. 
 PMID:34595549
                                    
                                
                                    Epicardial Adipose Tissue: The Genetics Behind an Emerging Cardiovascular Risk Marker. 
 PMID:34276231
                                    
                                
                                    Health equality, race and pharmacogenomics. 
 PMID:34251046
                                    
                                
                                    Pro12Ala polymorphism of peroxisome proliferator activated receptor gamma 2 may be associated with adverse neurodevelopment in European preterm babies. 
 PMID:34152086
                                    
                                
                                    Automated AI labeling of optic nerve head enables insights into cross-ancestry glaucoma risk and genetic discovery in >280,000 images from UKB and CLSA. 
 PMID:34077762
                                    
                                
                                    The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy. 
 PMID:33983834
                                    
                                
                                    The Need for a Human Pangenome Reference Sequence. 
 PMID:33929893
                                    
                                
                                    How understudied populations have contributed to our understanding of Alzheimer's disease genetics. 
 PMID:33889936
                                    
                                
                                    Human OMICs and Computational Biology Research in Africa: Current Challenges and Prospects. 
 PMID:33794662
                                    
                                
                                    Advancing drug discovery using the power of the human genome. 
 PMID:33748968
                                    
                                
                                    Improving reporting standards for polygenic scores in risk prediction studies. 
 PMID:33692554
                                    
                                
                                    Ethical Principles, Constraints and Opportunities in Clinical Proteomics. 
 PMID:33453411
                                    
                                
                                    Population-Matched Transcriptome Prediction Increases TWAS Discovery and Replication Rate. 
 PMID:33313492
                                    
                                
                                    The Impact of African Ancestry on Prostate Cancer Disparities in the Era of Precision Medicine. 
 PMID:33302594
                                    
                                
                                    Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition. 
 PMID:33256598
                                    
                                
                                    Diversity matters: opportunities in the study of the genetics of psychotic disorders in low- and middle-income countries in Latin America. 
 PMID:33237255
                                    
                                
                                    PPARG (Pro12Ala) genetic variant and risk of T2DM: a systematic review and meta-analysis. 
 PMID:32728045
                                    
                                
                                    Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos. 
 PMID:32699239
                                    
                                
                                    Ancestry effects on type 2 diabetes genetic risk inference in Hispanic/Latino populations. 
 PMID:32580712
                                    
                                
                                    Kir2.1 Interactome Mapping Uncovers PKP4 as a Modulator of the Kir2.1-Regulated Inward Rectifier Potassium Currents. 
 PMID:32541000
                                    
                                
                                    Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. 
 PMID:32514122
                                    
                                
                                    Polygenic risk scores: from research tools to clinical instruments. 
 PMID:32423490
                                    
                                
                                    Polygenic Scores to Assess Atherosclerotic Cardiovascular Disease Risk: Clinical Perspectives and Basic Implications. 
 PMID:32324503
                                    
                                
                                    Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway. 
 PMID:32313116
                                    
                                
                                    Personalised nutrition technologies: a new paradigm for dietetic practice and training in a digital transformation era. 
 PMID:32173947
                                    
                                
                                    Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. 
 PMID:32171239
                                    
                                
                                    Evaluating the promise of inclusion of African ancestry populations in genomics. 
 PMID:32140257
                                    
                                
                                    Machine learning applied to whole-blood RNA-sequencing data uncovers distinct subsets of patients with systemic lupus erythematosus. 
 PMID:31921420
                                    
                                
                                    Structural variation in the sequencing era. 
 PMID:31729472
                                    
                                
                                    Diversity In Precision Medicine And Pharmacogenetics: Methodological And Conceptual Considerations For Broadening Participation. 
 PMID:31686892
                                    
                                
                                    Deconvolution of the Genomic and Epigenomic Interaction Landscape of Triple-Negative Breast Cancer. 
 PMID:31683572
                                    
                                
                                    Risky behaviors and Parkinson disease: A mendelian randomization study. 
 PMID:31527283
                                    
                                
                                    The genetic architecture of Parkinson's disease. 
 PMID:31521533
                                    
                                
                                    Symptom Experience, Management, and Outcomes According to Race and Social Determinants Including Genomics, Epigenomics, and Metabolomics (SEMOARS + GEM): an Explanatory Model for Breast Cancer Treatment Disparity. 
 PMID:31392599
                                    
                                
                                    Rare and common variant discovery in complex disease: the IBD case study. 
 PMID:31363759
                                    
                                
                                    Clinical use of current polygenic risk scores may exacerbate health disparities. 
 PMID:30926966
                                    
                                
                                    Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. 
 PMID:30787307
                                    
                                
                                    African American ancestry contribution to asthma and atopic dermatitis. 
 PMID:30772392
                                    
                                
                                    Predicting Polygenic Risk of Psychiatric Disorders. 
 PMID:30737014
                                    
                                
                                    Host and Microbiome Genome-Wide Association Studies: Current State and Challenges. 
 PMID:30723493
                                    
                                
                                    A scientometric review of genome-wide association studies. 
 PMID:30623105
                                    
                                
                                    Genetics of Obesity in Diverse Populations. 
 PMID:30456705
                                    
                                
                                    The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics. 
 PMID:30311373
                                    
                                
                                    The critical needs and challenges for genetic architecture studies in Africa. 
 PMID:30240950
                                    
                                
                                    Enhancing diversity to reduce health information disparities and build an evidence base for genomic medicine. 
 PMID:30209973
                                    
                                
                                    Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative. 
 PMID:29779563