Frontiers in genetics
Journal
Overview
publication venue for
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Destabilized 3'UTR elements therapeutically degrade ERBB2 mRNA in drug-resistant ERBB2+ cancer models..
14.
2023
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Clinical and molecular significance of the RNA m6A methyltransferase complex in prostate cancer..
13.
2023
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APOL1 variant-expressing endothelial cells exhibit autophagic dysfunction and mitochondrial stress..
13.
2022
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Longitudinal Study of DNA Methylation and Epigenetic Clocks Prior to and Following Test-Confirmed COVID-19 and mRNA Vaccination..
13.
2022
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Further Evidence That OPG rs2073618 Is Associated With Increased Risk of Musculoskeletal Symptoms in Patients Receiving Aromatase Inhibitors for Early Breast Cancer..
12.
2021
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A Dual Systems Genetics Approach Identifies Common Genes, Networks, and Pathways for Type 1 and 2 Diabetes in Human Islets..
12.
2021
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Origin Sample Prediction and Spatial Modeling of Antimicrobial Resistance in Metagenomic Sequencing Data..
12.
2021
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Role of Endothelial and Mesenchymal Cell Transitions in Heart Failure and Recovery Thereafter..
11.
2021
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A Machine Learning Approach to Predicting Autism Risk Genes: Validation of Known Genes and Discovery of New Candidates..
11.
2020
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Genome-Wide Association Study Reveals a Novel Association Between MYBPC3 Gene Polymorphism, Endurance Athlete Status, Aerobic Capacity and Steroid Metabolism..
11.
2020
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Epigenetic Delay in the Neurodevelopmental Trajectory of DNA Methylation States in Autism Spectrum Disorders..
10.
2019
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Transcriptional Analysis of Lennert Lymphoma Reveals a Unique Profile and Identifies Novel Therapeutic Targets..
10.
2019
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A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids..
10.
2019
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Targeted, High-Resolution RNA Sequencing of Non-coding Genomic Regions Associated With Neuropsychiatric Functions..
10.
2019
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Genetic Risk for Psychiatric Disorders and Telomere Length..
9.
2018
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EM Adaptive LASSO-A Multilocus Modeling Strategy for Detecting SNPs Associated with Zero-inflated Count Phenotypes..
7.
2016
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Exome sequencing of a colorectal cancer family reveals shared mutation pattern and predisposition circuitry along tumor pathways..
6.
2015
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Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index..
5.
2014
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The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study..
5.
2014
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Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk..
5.
2014
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G protein-linked signaling pathways in bipolar and major depressive disorders..
4.
2013
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Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos..
3.
2012
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Editorial: RNA-Mediated Epigenetic and Transcriptional Regulation..
13.
2022
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Editorial: Methods for Single-Cell and Microbiome Sequencing Data..
13.
2022
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Editorial: Statistical and Computational Methods for Microbiome Multi-Omics Data..
11.
2020
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Editorial: Bioinformatics Analysis of Single Cell Sequencing Data and Applications in Precision Medicine..
10.
2020
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Non-human Primate Models to Investigate Mechanisms of Infection-Associated Fetal and Pediatric Injury, Teratogenesis and Stillbirth.
2021
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Duplex Telomere-Binding Proteins in Fungi With Canonical Telomere Repeats: New Lessons in the Rapid Evolution of Telomere Proteins.
2021
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Getting the Entire Message: Progress in Isoform Sequencing.
2019
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Epigenetic Modifications in Acute Myeloid Leukemia: Prognosis, Treatment, and Heterogeneity.
2019
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Telomere DNA recognition in Saccharomycotina yeast: potential lessons for the co-evolution of ssDNA and dsDNA-binding proteins and their target sites.
2015
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Multi-Substrate Specificity and the Evolutionary Basis for Interdependence in tRNA Editing and Methylation Enzymes.
2019
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Dysregulation of antiviral helicase pathways in systemic lupus erythematosus.
2014
Identity
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