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| 37620596 | Principles and methods for transferring polygenic risk scores across global populations. | Nat Rev Genet | 2024 |
| 37620596 | Principles and methods for transferring polygenic risk scores across global populations. | Nat Rev Genet | 2024 |
| 36929942 | Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions. | J Natl Cancer Inst | 2023 |
| 38036788 | Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. | Nat Genet | 2023 |
| 37944514 | Inferring disease architecture and predictive ability with LDpred2-auto. | Am J Hum Genet | 2023 |
| 37643728 | A Bayesian method for estimating gene-level polygenicity under the framework of transcriptome-wide association study. | Stat Med | 2023 |
| 37873378 | Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank. | medRxiv | 2023 |
| 37873338 | Admix-kit: An Integrated Toolkit and Pipeline for Genetic Analyses of Admixed Populations. | bioRxiv | 2023 |
| 37961486 | Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank. | Res Sq | 2023 |
| 37464048 | Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region. | Nat Med | 2023 |
| 37198491 | Polygenic scoring accuracy varies across the genetic ancestry continuum. | Nature | 2023 |
| 36945630 | Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain. | medRxiv | 2023 |
| 36941441 | Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals. | Nat Genet | 2023 |
| 36747759 | Impact of cross-ancestry genetic architecture on GWAS in admixed populations. | bioRxiv | 2023 |
| 36546757 | Optimized high-throughput screening of non-coding variants identified from genome-wide association studies. | Nucleic Acids Res | 2023 |
| 36993726 | Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms. | bioRxiv | 2023 |
| 36929942 | Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions. | J Natl Cancer Inst | 2023 |
| 36540975 | Session Introduction: Overcoming health disparities in precision medicine. | Pac Symp Biocomput | 2023 |
| 37293101 | Cell type deconvolution of bulk blood RNA-Seq to reveal biological insights of neuropsychiatric disorders. | bioRxiv | 2023 |
| 37224807 | Impact of cross-ancestry genetic architecture on GWASs in admixed populations. | Am J Hum Genet | 2023 |
| 37099718 | twas_sim, a Python-based tool for simulation and power analysis of transcriptome-wide association analysis. | Bioinformatics | 2023 |
| 37490908 | Genotype error due to low-coverage sequencing induces uncertainty in polygenic scoring. | Am J Hum Genet | 2023 |
| 37546999 | Calibrated prediction intervals for polygenic scores across diverse contexts. | medRxiv | 2023 |
| 37490908 | Genotype error due to low-coverage sequencing induces uncertainty in polygenic scoring. | Am J Hum Genet | 2023 |
| 37961486 | Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank. | Res Sq | 2023 |
| 37546999 | Calibrated prediction intervals for polygenic scores across diverse contexts. | medRxiv | 2023 |
| 37944514 | Inferring disease architecture and predictive ability with LDpred2-auto. | Am J Hum Genet | 2023 |
| 37643728 | A Bayesian method for estimating gene-level polygenicity under the framework of transcriptome-wide association study. | Stat Med | 2023 |
| 37873378 | Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank. | medRxiv | 2023 |
| 37873338 | Admix-kit: An Integrated Toolkit and Pipeline for Genetic Analyses of Admixed Populations. | bioRxiv | 2023 |
| 38036788 | Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. | Nat Genet | 2023 |
| 36993726 | Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms. | bioRxiv | 2023 |
| 36945630 | Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain. | medRxiv | 2023 |
| 37464048 | Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region. | Nat Med | 2023 |
| 37099718 | twas_sim, a Python-based tool for simulation and power analysis of transcriptome-wide association analysis. | Bioinformatics | 2023 |
| 37198491 | Polygenic scoring accuracy varies across the genetic ancestry continuum. | Nature | 2023 |
| 37293101 | Cell type deconvolution of bulk blood RNA-Seq to reveal biological insights of neuropsychiatric disorders. | bioRxiv | 2023 |
| 37224807 | Impact of cross-ancestry genetic architecture on GWASs in admixed populations. | Am J Hum Genet | 2023 |
| 36546757 | Optimized high-throughput screening of non-coding variants identified from genome-wide association studies. | Nucleic Acids Res | 2023 |
| 36747759 | Impact of cross-ancestry genetic architecture on GWAS in admixed populations. | bioRxiv | 2023 |
| 36540975 | Session Introduction: Overcoming health disparities in precision medicine. | Pac Symp Biocomput | 2023 |
| 36941441 | Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals. | Nat Genet | 2023 |
| 34931067 | Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification. | Nat Genet | 2022 |
| 35396471 | Unlocking capacities of genomics for the COVID-19 response and future pandemics. | Nat Methods | 2022 |
| 35519825 | Powerful eQTL mapping through low-coverage RNA sequencing. | HGG Adv | 2022 |
| 35754340 | Drug-Induced Epigenomic Plasticity Reprograms Circadian Rhythm Regulation to Drive Prostate Cancer toward Androgen Independence. | Cancer Discov | 2022 |
| 36085083 | Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. | Genome Med | 2022 |
| 36071171 | Genetic determinants of chromatin reveal prostate cancer risk mediated by context-dependent gene regulation. | Nat Genet | 2022 |
| 35931050 | Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies. | Am J Hum Genet | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |