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Hhsn268201800002i

Funded outputs count: 204
Funder award ID: HHSN268201800002I
OpenAlex ID: G2096685756
ScreenDMT reveals metabolites replicably associated with sleep disorders across three human cohorts
2026 · Jonathan M Dreyfuss, Dhruv Dubey, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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DrugTargetWorld: A Synthetic Biobank for Training and Benchmarking AI Scientists
2026 · Margolis, Samuel, Schmiedmayer, Paul, et al. · arXiv (Cornell University)
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The Soifua Manuia reference panel with 2,570 Samoan haplotypes improves genotype imputation quality among Samoans
2026 · Jenna C. Carlson, Mohanraj Krishnan, et al. · Communications Biology · 1
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Longitudinal Repeated Protein Measurements in a Multiethnic Cohort Identify Novel Diabetes Biomarkers That Reveal Unique Disease Pathways
2026 · Zsu-Zsu Chen, Michael Y. Mi, et al. · Diabetes
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Tandem repeat expansions in DAPK1 , ANK3 , and RPL14 are associated with diverse neurodegenerative diseases
2026 · Gabrielle N. Altman, Bharati Jadhav, et al. · medRxiv
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Transcriptomic profiling of pediatric asthma by diseases state and severity
2026 · Jihoon Kim, Jelte Kelchtermans, et al. · Respiratory Research
Multimodal gene prioritization reveals nonlinear regulatory architecture in childhood-onset asthma
2026 · Nan Huang, Michelle F. Ragsac, et al. · medRxiv
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Structural Variant Imputation in Samoans Using a Population-Specific Reference Panel
2026 · Lauren M. Spor, Emily M. Liau, et al. · medRxiv
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Genetic Determinants of Pulmonary Artery Size in over 50,000 Subjects with and without COPD
2026 · Vasile Foris, Kangjin Kim, et al. · medRxiv
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Performance of age-adjusted whole genome sequencing telomere length in idiopathic pulmonary fibrosis
2026 · John S Kim, Brody Receveur, et al. · American Journal of Respiratory and Critical Care Medicine · 1
LANTERN: Leveraging Local Ancestry Tracts to Enhance Rare-Variant Aggregate Association Testing
2026 · Yu Wang, Bjoernar Tuftin, et al. · medRxiv
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Whole Genome Sequence Analysis of Weight Loss in 16 972 Participants With COPD Reveals Novel Risk Loci in DRAIC and RFX3
2026 · Joe W. Chiles, Alison Rocco, et al. · Journal of Cachexia Sarcopenia and Muscle
Age-dependent Transcriptional Programs Distinguish Pediatric from Adult Dilated Cardiomyopathy
2026 · Zoe Leroux, Obed O. Nyarko, et al. · medRxiv
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Local ancestry modulates gene expression: shifting our understanding of genetic regulation and disease association within and across populations
2026 · Hung-Hsin Chen, Yanwei Cai, et al. · medRxiv
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Estimating population structure using epigenome-wide methylation data
2026 · Ziqing Wang, Kent D Taylor, et al. · Briefings in Bioinformatics
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Chromosome X-wide association study in multiple system atrophy identifies sex-differential risk loci
2026 · Anindita Ray, Ruth Chia, et al. · Brain · 1
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Practical utility of sequence-to-omics models for improving the reproducibility of genetic fine-mapping
2026 · Michael D. Sweeney, Hyun Min Kang · bioRxiv (Cold Spring Harbor Laboratory) · 2
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Association Analysis of Mitochondrial Heteroplasmic Variants and Cardiometabolic Traits
2026 · Xianbang Sun, Xue Liu, et al. · medRxiv
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Human Immunodeficiency Virus–Associated Proteomic Signature of Myocardial Fibrosis and Incident Heart Failure
2026 · Tess E Peterson, Virginia S Hahn, et al. · The Journal of Infectious Diseases
Transcriptomic signatures of lipids in blood provide hypotheses of functional mechanisms linked to lipid metabolism and immune-cell regulation
2026 · Jessica I Lundin, Mariaelisa Graff, et al. · Human Molecular Genetics
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Integrating whole genome and transcriptome sequencing to characterize the genetic architecture of isoform variation
2025 · Chunyu Liu, Roby Joehanes, et al. · Nature Communications · 2
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Hi-C informed kernel association test: integrating 3-dimensional genome structure into variant-set association for whole-genome sequencing data
2025 · Yueyang Huang, Riddhik Basu, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
2025 · Silverman, Edwin K., Tracy, Russell P., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations
2025 · Joshua S. Weinstock, Sharjeel A. Chaudhry, et al. · Nature Communications · 2
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Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
2025 · Rich, Stephen S., de Vries, Paul S., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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