|
| 36214830 | Mendelian Randomization Analysis Reveals a Complex Genetic Interplay among Atopic Dermatitis, Asthma, and Gastroesophageal Reflux Disease. | Am J Respir Crit Care Med | 2023 |
| 36214830 | Mendelian Randomization Analysis Reveals a Complex Genetic Interplay among Atopic Dermatitis, Asthma, and Gastroesophageal Reflux Disease. | Am J Respir Crit Care Med | 2023 |
| 38076879 | Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets. | medRxiv | 2023 |
| 37689782 | Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. | Nat Commun | 2023 |
| 37418489 | Regularized sequence-context mutational trees capture variation in mutation rates across the human genome. | PLoS Genet | 2023 |
| 37205563 | Mendelian randomization analyses clarify the effects of height on cardiovascular diseases. | medRxiv | 2023 |
| 37205500 | Evaluation of the Performance of the RECODe Equation with the Addition of Polygenic Risk Scores for Adverse Cardiovascular Outcomes in Individuals with Type II Diabetes. | medRxiv | 2023 |
| 37425708 | Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program. | medRxiv | 2023 |
| 37165871 | Evaluating the Contribution of Cell Type-Specific Alternative Splicing to Variation in Lipid Levels. | Circ Genom Precis Med | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 38076879 | Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets. | medRxiv | 2023 |
| 37689782 | Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. | Nat Commun | 2023 |
| 37425708 | Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program. | medRxiv | 2023 |
| 37418489 | Regularized sequence-context mutational trees capture variation in mutation rates across the human genome. | PLoS Genet | 2023 |
| 37205563 | Mendelian randomization analyses clarify the effects of height on cardiovascular diseases. | medRxiv | 2023 |
| 37205500 | Evaluation of the Performance of the RECODe Equation with the Addition of Polygenic Risk Scores for Adverse Cardiovascular Outcomes in Individuals with Type II Diabetes. | medRxiv | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 37165871 | Evaluating the Contribution of Cell Type-Specific Alternative Splicing to Variation in Lipid Levels. | Circ Genom Precis Med | 2023 |
| 35166671 | Body mass index and adipose distribution have opposing genetic impacts on human blood traits. | Elife | 2022 |
| 36376295 | Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. | Nat Commun | 2022 |
| 35848019 | Polygenic Risk Scores in Alzheimer's Disease Genetics: Methodology, Applications, Inclusion, and Diversity. | J Alzheimers Dis | 2022 |
| 35710981 | Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease. | Nat Genet | 2022 |
| 35654975 | A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. | Nat Genet | 2022 |
| 35653334 | A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. | PLoS Genet | 2022 |
| 35705896 | TSABL: Trait Specific Annotation Based Locus predictor. | BMC Genomics | 2022 |
| 36229773 | Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach. | BMC Bioinformatics | 2022 |
| 35894642 | ColocQuiaL: a QTL-GWAS colocalization pipeline. | Bioinformatics | 2022 |
| 35482673 | A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program. | PLoS Genet | 2022 |
| 35666730 | Characterization of the genome and silk-gland transcriptomes of Darwin's bark spider (Caerostris darwini). | PLoS One | 2022 |
| 35915156 | Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. | Nat Med | 2022 |
| 35186008 | Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci. | Front Genet | 2022 |
| 35166671 | Body mass index and adipose distribution have opposing genetic impacts on human blood traits. | Elife | 2022 |
| 35129650 | Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetes. | Diabetologia | 2022 |
| 35285134 | Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. | J Thromb Haemost | 2022 |
| 35710981 | Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease. | Nat Genet | 2022 |
| 35653334 | A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. | PLoS Genet | 2022 |
| 35705896 | TSABL: Trait Specific Annotation Based Locus predictor. | BMC Genomics | 2022 |
| 35666730 | Characterization of the genome and silk-gland transcriptomes of Darwin's bark spider (Caerostris darwini). | PLoS One | 2022 |
| 35654975 | A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. | Nat Genet | 2022 |
| 35482673 | A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program. | PLoS Genet | 2022 |
| 35848019 | Polygenic Risk Scores in Alzheimer's Disease Genetics: Methodology, Applications, Inclusion, and Diversity. | J Alzheimers Dis | 2022 |
| 36229773 | Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach. | BMC Bioinformatics | 2022 |
| 35894642 | ColocQuiaL: a QTL-GWAS colocalization pipeline. | Bioinformatics | 2022 |
| 35915156 | Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. | Nat Med | 2022 |
| 36376295 | Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. | Nat Commun | 2022 |
| 35129650 | Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetes. | Diabetologia | 2022 |
| 35285134 | Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. | J Thromb Haemost | 2022 |
| 35186008 | Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci. | Front Genet | 2022 |
| 33397451 | Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual. | Genome Biol | 2021 |
| 33853351 | Association Between Genetic Variation in Blood Pressure and Increased Lifetime Risk of Peripheral Artery Disease. | Arterioscler Thromb Vasc Biol | 2021 |