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U01DK085526

Funded outputs count: 93
Funder award ID: U01DK085526
OpenAlex ID: G1181497844
Genetic architecture and biology of youth-onset type 2 diabetes
2024 · Soo Heon Kwak, Shylaja Srinivasan, et al. · Nature Metabolism · 35
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Bivariate quantitative Bayesian LASSO for detecting association of rare haplotypes with two correlated continuous phenotypes
2023 · Ibrahim Hossain Sajal, Swati Biswas · Frontiers in Genetics · 1
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Control for population stratification in genetic association studies based on GWAS summary statistics
2022 · Shijia Yan, Qiuying Sha, et al. · Genetic Epidemiology · 4
Genetic determinants of metabolic biomarkers and their associations with cardiometabolic traits in Hispanic/Latino adolescents
2021 · Daeeun Kim, Anne E. Justice, et al. · Pediatric Research
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APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups
2021 · Shiwali Goyal, Yosuke Tanigawa, et al. · Lipids in Health and Disease · 37
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Monogenic Diabetes in Youth With Presumed Type 2 Diabetes: Results From the Progress in Diabetes Genetics in Youth (ProDiGY) Collaboration
2021 · Jennifer N. Todd, Jeffrey W. Kleinberger, et al. · Diabetes Care · 42
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Identifying the Lipidomic Effects of a Rare Loss-of-Function Deletion in ANGPTL3
2021 · Nicholas B. Blackburn, Peter J. Meikle, et al. · Circulation Genomic and Precision Medicine · 5
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The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium
2021 · Shylaja Srinivasan, Ling Chen, et al. · Diabetes · 81
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A weighted empirical Bayes risk prediction model using multiple traits
2020 · Gengxin Li, Lin Hou, et al. · Statistical Applications in Genetics and Molecular Biology · 1
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Genotype phasing in pedigrees using whole-genome sequence data
2020 · August N. Blackburn, Lucy Blondell, et al. · European Journal of Human Genetics · 8
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Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes
2019 · Xiaochen Yuan, Swati Biswas · Genetic Epidemiology · 6
Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway
2019 · Nicholas B. Blackburn, Laura F. Michael, et al. · Journal of Lipid Research · 25
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
2019 · Broad Genomics Platform, Jason Flannick, et al. · Nature · 303
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General retrospective mega‐analysis framework for rare variant association tests
2018 · Li‐Chu Chien, Yen‐Feng Chiu · Genetic Epidemiology
GxGrare: gene-gene interaction analysis method for rare variants from high-throughput sequencing data
2018 · Minseok Kwon, Sangseob Leem, et al. · BMC Systems Biology · 11
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A rapid epistatic mixed-model association analysis by linear retransformations of genomic estimated values
2018 · Chao Ning, Dan Wang, et al. · Bioinformatics · 31
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Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees
2017 · Goo Jun, Alisa Manning, et al. · Proceedings of the National Academy of Sciences · 35
Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
2017 · Stefan Konigorski, Yuan Wang, et al. · Genetic Epidemiology · 1
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Two‐phase designs for joint quantitative‐trait‐dependent and genotype‐dependent sampling in post‐GWAS regional sequencing
2017 · Osvaldo Espin‐Garcia, Radu V. Craiu, et al. · Genetic Epidemiology · 4
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A comparison of graph- and kernel-based –omics data integration algorithms for classifying complex traits
2017 · Kang K. Yan, Hongyu Zhao, et al. · BMC Bioinformatics · 34
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FOXP3 mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome
2017 · Jessica L Hwang, Soo‐Young Park, et al. · Pediatric Diabetes · 38
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A Partial Loss-of-Function Variant in AKT2 Is Associated With Reduced Insulin-Mediated Glucose Uptake in Multiple Insulin-Sensitive Tissues: A Genotype-Based Callback Positron Emission Tomography Study
2017 · Aino Latva-Rasku, Miikka-Juhani Honka, et al. · Diabetes · 46
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Analysis of population-specific pharmacogenomic variants using next-generation sequencing data
2017 · Eunyong Ahn, Taesung Park · Scientific Reports · 23
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Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution
2017 · Reedik Mägi, Momoko Horikoshi, et al. · Human Molecular Genetics · 279
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Robust Rare-Variant Association Tests for Quantitative Traits in General Pedigrees
2017 · Yunxuan Jiang, Karen N. Conneely, et al. · Statistics in Biosciences · 1
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