|
| 37358516 | Spatial Single-Cell Technologies for Exploring Gastrointestinal Tissue Transcriptome. | | 2023 |
| 37473732 | SiftCell: A robust framework to detect and isolate cell-containing droplets from single-cell RNA sequence reads. | | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 35347136 | Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Nat Commun | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 36284674 | STtools: A Comprehensive Software Pipeline for Ultra-high Resolution Spatial Transcriptomics Data. | Bioinform Adv | 2022 |
| 35939579 | Germline Mutations in <i>CIDEB</i> and Protection against Liver Disease. | N Engl J Med | 2022 |
| 36192399 | Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Nat Commun | 2022 |
| 36417511 | Identification of the niche and mobilization mechanism for tissue-protective multipotential bone marrow ILC progenitors. | Science advances | 2022 |
| 36450978 | Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 34459872 | FIVEx: an interactive eQTL browser across public datasets. | Bioinformatics | 2022 |
| 35100255 | Meta-imputation of transcriptome from genotypes across multiple datasets by leveraging publicly available summary-level data. | PLoS Genet | 2022 |
| 34662886 | Exome sequencing and analysis of 454,787 UK Biobank participants. | Nature | 2021 |
| 33632709 | Genetic architectures of proximal and distal colorectal cancer are partly distinct. | Gut | 2021 |
| 34115981 | Microscopic examination of spatial transcriptome using Seq-Scope. | Cell | 2021 |
| 34115965 | Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. | Am J Hum Genet | 2021 |
| 33674754 | Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. | Mol Psychiatry | 2021 |
| 34108472 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. | Nat Commun | 2021 |
| 33619501 | Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease. | medRxiv | 2021 |
| 34214102 | Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. | PLoS One | 2021 |
| 34210852 | Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity. | Science | 2021 |
| 33989384 | Sparse allele vectors and the savvy software suite. | Bioinformatics | 2021 |
| 33655273 | A catalog of associations between rare coding variants and COVID-19 outcomes. | medRxiv | 2021 |
| 33760063 | muCNV: Genotyping Structural Variants for Population-level Sequencing. | Bioinformatics | 2021 |
| 33103450 | Holistic characterization of single-hepatocyte transcriptome responses to high-fat diet. | American Journal of Physiology - Endocrinology and Metabolism | 2021 |
| 32966749 | Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans. | Am J Respir Crit Care Med | 2021 |
| 33320851 | Integrating comprehensive functional annotations to boost power and accuracy in gene-based association analysis. | PLoS Genet | 2020 |
| 31665830 | Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico. | Pediatr Pulmonol | 2020 |
| 31980570 | Ancestry-agnostic estimation of DNA sample contamination from sequence reads. | Genome Res | 2020 |
| 32459537 | Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth. | Am J Respir Crit Care Med | 2020 |
| 32327564 | Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand <i>KITLG/SCF</i> and Gene-By-Air-Pollution Interaction. | Genetics | 2020 |
| 33046696 | Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium. | Nat Commun | 2020 |
| 33339817 | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. | Nat Commun | 2020 |
| 32511326 | Type 2 and interferon inflammation strongly regulate SARS-CoV-2 related gene expression in the airway epithelium. | bioRxiv | 2020 |
| 32846134 | Single-Cell Transcriptome Analysis of Colon Cancer Cell Response to 5-Fluorouracil-Induced DNA Damage. | Cell Rep | 2020 |
| 33057163 | Author Correction: Multiplexed droplet single-cell RNA-sequencing using natural genetic variation. | Nat Biotechnol | 2020 |
| 31537649 | Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. | J Am Soc Nephrol | 2019 |
| 30510241 | Discovery of common and rare genetic risk variants for colorectal cancer. | Nat Genet | 2019 |
| 30204848 | emeraLD: rapid linkage disequilibrium estimation with massive datasets. | Bioinformatics | 2019 |
| 31529278 | Comparative Disease Burden in Patients with Rheumatoid Arthritis, Psoriatic Arthritis, or Axial Spondyloarthritis: Data from Two Corrona Registries. | Rheumatology and Therapy | 2019 |
| 31092822 | Hydro-Seq enables contamination-free high-throughput single-cell RNA-sequencing for circulating tumor cells. | Nat Commun | 2019 |
| 30820706 | Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. | Hum Genet | 2019 |
| 31182850 | Using and producing publicly available genomic data to accelerate discovery in nephrology. | Nature Reviews Nephrology | 2019 |
| 31015462 | Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. | Nat Commun | 2019 |
| 31118516 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. | Nature | 2019 |
| 31254090 | Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. | Hum Genet | 2019 |
| 31363178 | Author Correction: Using and producing publicly available genomic data to accelerate discovery in nephrology. | Nature Reviews Nephrology | 2019 |