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| 35218565 | Leveraging a surrogate outcome to improve inference on a partially missing target outcome. | Biometrics | 2023 |
| 36350676 | FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. | Nucleic Acids Res | 2023 |
| 36000269 | Differences in set-based tests for sparse alternatives when testing sets of outcomes compared to sets of explanatory factors in genetic association studies. | Biostatistics | 2023 |
| 37749244 | A new method for multiancestry polygenic prediction improves performance across diverse populations. | Nat Genet | 2023 |
| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 37802043 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. | Am J Hum Genet | 2023 |
| 36775193 | Clinicopathologic and Genomic Factors Impacting Efficacy of First-Line Chemoimmunotherapy in Advanced NSCLC. | J Thorac Oncol | 2023 |
| 37260165 | Lung cancer risk discrimination of prediagnostic proteomics measurements compared with existing prediction tools. | J Natl Cancer Inst | 2023 |
| 37247843 | Impact of Aneuploidy and Chromosome 9p Loss on Tumor Immune Microenvironment and Immune Checkpoint Inhibitor Efficacy in NSCLC. | J Thorac Oncol | 2023 |
| 36798290 | Accurate and Efficient Estimation of Local Heritability using Summary Statistics and LD Matrix. | bioRxiv | 2023 |
| 37368928 | Caught in the crossfire: Fears of Chinese-American scientists. | Proc Natl Acad Sci U S A | 2023 |
| 37425772 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. | medRxiv | 2023 |
| 37099174 | Advanced non-small-cell lung cancer treated with first-line pembrolizumab plus chemotherapy: tumor response dynamics as a marker for survival. | Eur Radiol | 2023 |
| 35218565 | Leveraging a surrogate outcome to improve inference on a partially missing target outcome. | Biometrics | 2023 |
| 37802043 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. | Am J Hum Genet | 2023 |
| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 37749244 | A new method for multiancestry polygenic prediction improves performance across diverse populations. | Nat Genet | 2023 |
| 37425772 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. | medRxiv | 2023 |
| 37247843 | Impact of Aneuploidy and Chromosome 9p Loss on Tumor Immune Microenvironment and Immune Checkpoint Inhibitor Efficacy in NSCLC. | J Thorac Oncol | 2023 |
| 37368928 | Caught in the crossfire: Fears of Chinese-American scientists. | Proc Natl Acad Sci U S A | 2023 |
| 37099174 | Advanced non-small-cell lung cancer treated with first-line pembrolizumab plus chemotherapy: tumor response dynamics as a marker for survival. | Eur Radiol | 2023 |
| 37260165 | Lung cancer risk discrimination of prediagnostic proteomics measurements compared with existing prediction tools. | J Natl Cancer Inst | 2023 |
| 36775193 | Clinicopathologic and Genomic Factors Impacting Efficacy of First-Line Chemoimmunotherapy in Advanced NSCLC. | J Thorac Oncol | 2023 |
| 36798290 | Accurate and Efficient Estimation of Local Heritability using Summary Statistics and LD Matrix. | bioRxiv | 2023 |
| 36000269 | Differences in set-based tests for sparse alternatives when testing sets of outcomes compared to sets of explanatory factors in genetic association studies. | Biostatistics | 2023 |
| 36350676 | FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. | Nucleic Acids Res | 2023 |
| 34450659 | Response to Hopkins, Kichenadasse, Logan, et al. | J Natl Cancer Inst | 2022 |
| 35845434 | Simultaneous Detection of Signal Regions Using Quadratic Scan Statistics With Applications to Whole Genome Association Studies. | J Am Stat Assoc | 2022 |
| 35708671 | Association of High Tumor Mutation Burden in Non-Small Cell Lung Cancers With Increased Immune Infiltration and Improved Clinical Outcomes of PD-L1 Blockade Across PD-L1 Expression Levels. | JAMA Oncol | 2022 |
| 35822943 | Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea. | Am J Respir Crit Care Med | 2022 |
| 35441669 | STAAR workflow: a cloud-based workflow for scalable and reproducible rare variant analysis. | Bioinformatics | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 35637906 | Connectivity in eQTL networks dictates reproducibility and genomic properties. | Cell Rep Methods | 2022 |
| 35989709 | Large-Scale Hypothesis Testing for Causal Mediation Effects with Applications in Genome-wide Epigenetic Studies. | J Am Stat Assoc | 2022 |
| 36114182 | Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks. | Nat Commun | 2022 |
| 35915169 | Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. | Nat Genet | 2022 |
| 35300209 | AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos. | HGG Adv | 2022 |
| 34450659 | Response to Hopkins, Kichenadasse, Logan, et al. | J Natl Cancer Inst | 2022 |
| 35216679 | A multi-dimensional integrative scoring framework for predicting functional variants in the human genome. | Am J Hum Genet | 2022 |
| 35190428 | Risk assessment for acute kidney injury and death among new COVID-19 positive adult patients without chronic kidney disease: retrospective cohort study among three US hospitals. | BMJ Open | 2022 |
| 35087136 | Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study. | Sci Rep | 2022 |
| 35845434 | Simultaneous Detection of Signal Regions Using Quadratic Scan Statistics With Applications to Whole Genome Association Studies. | J Am Stat Assoc | 2022 |
| 35708671 | Association of High Tumor Mutation Burden in Non-Small Cell Lung Cancers With Increased Immune Infiltration and Improved Clinical Outcomes of PD-L1 Blockade Across PD-L1 Expression Levels. | JAMA Oncol | 2022 |
| 35441669 | STAAR workflow: a cloud-based workflow for scalable and reproducible rare variant analysis. | Bioinformatics | 2022 |
| 35637906 | Connectivity in eQTL networks dictates reproducibility and genomic properties. | Cell Rep Methods | 2022 |
| 35822943 | Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea. | Am J Respir Crit Care Med | 2022 |
| 35989709 | Large-Scale Hypothesis Testing for Causal Mediation Effects with Applications in Genome-wide Epigenetic Studies. | J Am Stat Assoc | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 35915169 | Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. | Nat Genet | 2022 |
| 36114182 | Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks. | Nat Commun | 2022 |