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Publication Venue For
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Oxygen availability influences the incidence of testicular teratoma in Dnd1Ter/+ mice..
14:1179256.
2023
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Leveraging Optimized Transcriptomic and Personalized Stem Cell Technologies to Better Understand Syncytialization Defects in Preeclampsia.
13.
2022
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A novel approach to characterize phenotypic variation in GSD IV: Reconceptualizing the clinical continuum..
13:992406.
2022
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Decosus: An R Framework for Universal Integration of Cell Proportion Estimation Methods..
13:802838.
2022
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Development of a clinically validated in vitro functional assay to assess pathogenicity of novel GAA variants in patients with Pompe disease identified via newborn screening..
13:1001154.
2022
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Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data..
13:897210.
2022
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Genetic determinants of apixaban plasma levels and their relationship to bleeding and thromboembolic events..
13:982955.
2022
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Histone Demethylase AMX-1 Regulates Fertility in a p53/CEP-1 Dependent Manner..
13:929716.
2022
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Improvement of Genomic Predictions in Small Breeds by Construction of Genomic Relationship Matrix Through Variable Selection..
13:814264.
2022
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Case Report: Infant With Congenital Adrenal Hyperplasia and 47,XXY..
12:808006.
2021
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Corrigendum: Genome-Wide Variants Associated With Longitudinal Survival Outcomes Among Individuals With Coronary Artery Disease..
12:726466.
2021
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Extensive Variation in Drought-Induced Gene Expression Changes Between Loblolly Pine Genotypes..
12:661440.
2021
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Genome Wide Association Study of Beef Traits in Local Alpine Breed Reveals the Diversity of the Pathways Involved and the Role of Time Stratification..
12:746665.
2021
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Genome-Wide Variants Associated With Longitudinal Survival Outcomes Among Individuals With Coronary Artery Disease..
12:661497.
2021
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Human and Machine Intelligence Together Drive Drug Repurposing in Rare Diseases..
12:707836.
2021
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Revisiting Secondary Information Related to Pharmacogenetic Testing..
12:741395.
2021
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Toxicological Study and Genetic Basis of BTEX Susceptibility in Drosophila melanogaster..
11:594179.
2020
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VisTCR: An Interactive Software for T Cell Repertoire Sequencing Data Analysis..
11:771.
2020
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Comparative Genomic Analysis Reveals the Mechanism Driving the Diversification of Plastomic Structure in Taxaceae Species..
10:1295.
2019
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Pleiotropic Meta-Analysis of Age-Related Phenotypes Addressing Evolutionary Uncertainty in Their Molecular Mechanisms..
10:433.
2019
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The Landscape of SNCA Transcripts Across Synucleinopathies: New Insights From Long Reads Sequencing Analysis..
10:584.
2019
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Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome..
9:173.
2018
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Lack of Association of a Functional Polymorphism in the Serotonin Receptor Gene With Body Mass Index and Depressive Symptoms in a Large Meta-Analysis of Population Based Studies..
9:423.
2018
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To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes..
9:298.
2018
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Corrigendum: Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases..
8:226.
2017
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Interpreting Gene Expression Effects of Disease-Associated Variants: A Lesson from SNCA rs356168..
8:133.
2017
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Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases..
7:179.
2016
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Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures..
7:188.
2016
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Changes in expression of the long non-coding RNA FMR4 associate with altered gene expression during differentiation of human neural precursor cells..
6:263.
2015
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Corrigendum: Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example..
6:231.
2015
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Genetics of aging, health, and survival: dynamic regulation of human longevity related traits..
6:122.
2015
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A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism..
5:33.
2014
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Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis..
5:401.
2014
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Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example..
5:254.
2014
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EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children..
4:268.
2013
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How lifespan associated genes modulate aging changes: lessons from analysis of longitudinal data..
4:3.
2013
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How the quality of GWAS of human lifespan and health span can be improved..
4:125.
2013
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The genetic basis for survivorship in coronary artery disease..
4:191.
2013
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Why does melanoma metastasize into the brain? Genes with pleiotropic effects might be the key..
4:75.
2013
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On the aggregation of multimarker information for marker-set and sequencing data analysis: Genotype collapsing vs. Similarity collapsing.
2.
2012
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Germline copy number variation and ovarian cancer survival..
3:142.
2012
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Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach..
3:203.
2012
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Regular Multivitamin Supplement Use, Single Nucleotide Polymorphisms in ATIC, SHMT2, and SLC46A1, and Risk of Ovarian Carcinoma..
3:33.
2012