Original Research
Published on 23 Jun 2025
Directional genomic hybridization (dGH™) identifies small inverted duplications in situ
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1604822
- 3,101 views
Type at least 3 characters
16,562 articles
articles
Original Research
Published on 23 Jun 2025
Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1539902
- 2,996 views
- 1 citation
Original Research
Published on 20 Jun 2025
Generalized information criteria for personalized gene network inference
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1583756
- 1,478 views
Original Research
Published on 20 Jun 2025
Integrative bioinformatics analysis of pyroptosis-related genes and immune infiltration patterns in childhood asthma
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1557709
- 2,644 views
Original Research
Published on 20 Jun 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical setting
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1580879
- 3,840 views
Original Research
Published on 20 Jun 2025
Identification of neutrophil extracellular trap-related biomarkers in ulcerative colitis based on bioinformatics and machine learning
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1589999
- 4,038 views
- 1 citation
Methods
Published on 19 Jun 2025
GTMALoc: prediction of miRNA subcellular localization based on graph transformer and multi-head attention mechanism
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1623008
- 1,534 views
Original Research
Published on 19 Jun 2025
Two novel variants in CNNM2 disrupts magnesium efflux leading to neurodevelopmental disorders
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1600877
- 2,606 views
Original Research
Published on 19 Jun 2025
Identification of biomarkers associated with mitochondrial dysfunction and programmed cell death in chronic obstructive pulmonary disease via transcriptomics
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1567173
- 2,787 views
- 2 citations
Case Report
Published on 18 Jun 2025
Case Report: A first case of desmin-related myofibrillar myopathy due to inheritance from a confirmed mosaic asymptomatic carrier
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1597851
- 2,375 views
- 1 citation
Brief Research Report
Published on 18 Jun 2025
Novel causative RYR2 indel variant with exon and intron involvement inducing exon 13 skipping in a family exhibiting catecholaminergic polymorphic ventricular tachycardia
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1581535
- 2,588 views
Case Report
Published on 18 Jun 2025
Case Report: A case of ALS type 6 associated with a FUS gene variant and right limb muscle weakness and atrophy as the initial symptom
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1578249
- 2,440 views
Original Research
Published on 18 Jun 2025
Clinical characteristics and genetic mutation analysis in 18 pediatric patients with Shwachman-Diamond syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1603782
- 2,449 views
Original Research
Published on 18 Jun 2025
A xyloglucan endotransglucosylase/hydrolase gene, IbXTH16, increases cold tolerance in transgenic sweetpotato
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2025.1629260
- 1,713 views
Original Research
Published on 18 Jun 2025
Identification and functional characterization of ABCA4 gene variants in three patients with Stargardt disease or retinitis pigmentosa
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1516872
- 3,699 views
Original Research
Published on 18 Jun 2025
Epigenetic study of the long-term effects of gulf War illness
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1553410
- 2,710 views
- 1 citation
Brief Research Report
Published on 18 Jun 2025
Data simulation to optimize frameworks for genome-wide association studies in diverse populations
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2025.1559496
- 2,736 views
- 1 citation
Original Research
Published on 18 Jun 2025
Identification of three T cell-related genes as diagnostic and prognostic biomarkers for triple-negative breast cancer and exploration of potential mechanisms
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1584334
- 3,087 views
Original Research
Published on 18 Jun 2025
Role of inflammation-related genes as prognostic biomarkers and mechanistic implications in idiopathic pulmonary fibrosis
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1602588
- 2,886 views
Original Research
Published on 18 Jun 2025
Epigenetic mechanisms linking atherosclerosis to ischemic stroke: insights from DNA methylation and transcriptome integration
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1567951
- 2,473 views
Original Research
Published on 18 Jun 2025
Integrative bioinformatics analysis and experimental validation reveals key genes and regulatory mechanisms in the development of gout
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1598835
- 2,778 views
Opinion
Published on 18 Jun 2025
Regulation of term and preterm labor: genetics and epigenetics
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1594030
- 2,044 views
Original Research
Published on 18 Jun 2025
Whole genome sequencing and functional annotation of Fusarium oxysporum f. sp. lentis to unravel virulence and secondary metabolite biosynthesis gene clusters
in Genomics of Plants and Plant-Associated Organisms
Frontiers in Genetics
doi 10.3389/fgene.2025.1585510
- 3,904 views
Original Research
Published on 18 Jun 2025
Application of non-invasive prenatal testing for fetal chromosomal disorders in low-risk pregnancies: a follow-up study in central China
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1574775
- 4,268 views
- 4 citations