Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs. PLoS Medicine. 2020; 17(8):e1003305.
Novel phenotype-disease matching tool for rare genetic diseases. Genetics in Medicine. 2019; 21(2):339-346.
Genome-wide signatures of transcription factor activity: connecting transcription factors, disease, and small molecules. PLoS Computational Biology. 2013; 9(9):e1003198.
ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. Nucleic Acids Research (NAR). 2009; 37(Web Server issue):W305-W311.
Disease candidate gene identification and prioritization using protein interaction networks. BMC Bioinformatics. 2009; 10:73.
Improved human disease candidate gene prioritization using mouse phenotype. BMC Bioinformatics. 2007; 8:392.
ACTC1 Variants Result in Isolated and Syndromic Cardiac Phenotypes. Clinical Genetics. 2025; 108(6):713-719.
Abstract 4355964: Probiotic Extracellular Vesicles Stimulate Macrophage Efferocytosis to Limit Ischemia/Reperfusion-Induced Damage by Delivering 5s-rRNA-Derived Short RNA. Circulation. 2025; 152(Suppl_3):a4355964-a4355964.
Replicative stress-induced aging of hematopoietic stem progenitor cells increases oncogenic mutation burden and incidence of myelodysplasia in sickle cell disease mice. Blood. 2025; 146(Supplement 1):11.
Sequencing validates deep learning models for EHR-based detection of Noonan syndrome in pediatric patients. npj Genomic Medicine. 2025; 10(1):56.
Haplotype-based analysis distinguishes maternal-fetal genetic contribution to pregnancy-related outcomes. PLoS Genetics. 2025; 21(3):e1011575.
Probiotic bacteria-released extracellular vesicles enhance macrophage phagocytosis in polymicrobial sepsis by activating the FPR1/2 pathway. Molecular Medicine. 2024; 30(1):216.
Abstract 4118360: Lipocalin10 is Critical for Macrophage Efferocytosis to Repair Myocardial Ischemia/Reperfusion Injury. Circulation. 2024; 150(Suppl_1):a4118360-a4118360.
Estimating prevalence of rare genetic disease diagnoses using electronic health records in a children's hospital. HGG Advances. 2024; 5(4):100341.
A novel method for cell deconvolution using DNA methylation in PCA space. BMC Genomics. 2024; 25(1):798.
Macrophage-enriched Sectm1a promotes efficient efferocytosis to attenuate ischemia/reperfusion-induced cardiac injury. JCI Insight. 2024; 9(5).
Association of maternal prenatal copper concentration with gestational duration and preterm birth: a multicountry meta-analysis. American Journal of Clinical Nutrition. 2024; 119(1):221-231.
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Nature Genetics. 2023; 55(11):1807-1819.
Lipocalin 10 is essential for protection against inflammation-triggered vascular leakage by activating LDL receptor-related protein 2-slingshot homologue 1 signalling pathway. Cardiovascular Research (CVR). 2023; 119(10):1981-1996.
A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth. BMC Medicine. 2023; 21(1):258.
Identification of a heterogeneous and dynamic ciliome during embryonic development and cell differentiation. Development. 2023; 150(8).
Genetic effects on the timing of parturition and links to fetal birth weight. Nature Genetics. 2023; 55(4):559-567.
In Vivo Crispr Screening Identifies Novel Vulnerabilities in ETO2/GLIS2-rearranged Leukemia. Blood. 2022; 140(Supplement 1):3431-3432.
Using deep learning and electronic health records to detect Noonan syndrome in pediatric patients. Genetics in Medicine. 2022; 24(11):2329-2337.
Prevalence of Genetic Diagnoses in a Cohort With Valvar Pulmonary Stenosis. Circulation. Genomic and precision medicine. 2022; 15(4):e003635.
Interrogating the causal effects of maternal circulating CRP on gestational duration and birth weight. . 2022; 2022.05.16.22275164.
Genetic effects on the timing of parturition and links to fetal birth weight. . 2022; 2022.05.04.22274624.
Abstract 386: Lipocalin 10 Protects Against Sepsis-triggered Vascular Leakage Through Activation Of The Ssh1-cofilin Signaling Pathway. Arteriosclerosis, Thrombosis, and Vascular Biology. 2022; 42(Suppl_1):a386-a386.
PDX models of relapsed pediatric AML preserve global gene expression patterns and reveal therapeutic targets. bioRxiv. 2022; 2022.01.31.478534.
Loss of Lipocalin 10 Exacerbates Diabetes-Induced Cardiomyopathy via Disruption of Nr4a1-Mediated Anti-Inflammatory Response in Macrophages. Frontiers in Immunology. 2022; 13:930397.
The Exosome-Associated Tetraspanin CD63 Contributes to the Efficient Assembly and Infectivity of the Hepatitis B Virus. Hepatology Communications. 2021; 5(7):1238-1251.
Sectm1a Facilitates Protection against Inflammation-Induced Organ Damage through Promoting TRM Self-Renewal. Molecular Therapy. 2021; 29(3):1294-1311.
Sectm1a deficiency aggravates inflammation-triggered cardiac dysfunction through disruption of LXRα signalling in macrophages. Cardiovascular Research (CVR). 2021; 117(3):890-902.
DNA-Damage-Induced Alternative Splicing of p53. Cancers. 2021; 13(2).
Synergistic metalloproteinase-based remodeling of matrix by pancreatic tumor and stromal cells. PLoS ONE. 2021; 16(3):e0248111.