Frontiers in Genetics

Papers
(The TQCC of Frontiers in Genetics is 8. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-11-01 to 2025-11-01.)
ArticleCitations
Transcriptome Sequencing Identifies PLAUR as an Important Player in Patients With Dermatomyositis-Associated Interstitial Lung Disease270
Genomic Analysis of Visceral Fat Accumulation in Holstein Cows188
Subject clustering by IF-PCA and several recent methods154
RET splice site variants in medullary thyroid carcinoma136
Fetal Congenital Heart Disease Caused by Compound Heterozygous Mutations in the DNAH9 Gene: A Case Report136
Retraction: Cytokinin and abiotic stress tolerance -what has been accomplished and the way forward?129
Whole genome sequencing and functional annotation of Fusarium oxysporum f. sp. lentis to unravel virulence and secondary metabolite biosynthesis gene clusters120
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in PARD6G-AS1 promotor in a case with arthrogryposis118
BANSMDA: a computational model for predicting potential microbe-disease associations based on bilinear attention networks and sparse autoencoders112
The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study110
Erratum: Heterologous expression of Arabidopsis AtARA6 in soybean enhances salt tolerance95
Identification and Validation of an Immune and Ferroptosis-Combined Index for Non–Small Cell Lung Cancer92
Editorial: Epigenetic mechanisms and epigenetic-based therapies in cardiometabolic and vascular disease92
Bioinformatics revealed biomarkers for diagnosis in kidney stones92
Erratum: A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation79
Clinical characteristics and follow-up of complex arrhythmias associated with RYR2 gene mutations in children79
Consumer-oriented (patient and family) outcomes from nursing in genomics: a scoping review of the literature (2012–2022)78
MiRNA-Seq reveals key MicroRNAs involved in fat metabolism of sheep liver78
A Novel SPG7 Gene Pathogenic Variant in a Cypriot Family With Autosomal Recessive Spastic Ataxia75
Genetically Determined Circulating Levels of Cytokines and the Risk of Rheumatoid Arthritis72
Comprehensive Genetic Analysis of Tuberculosis and Identification of Candidate Biomarkers72
Composition and Dynamics of H1N1 and H7N9 Influenza A Virus Quasispecies in a Co-infected Patient Analyzed by Single Molecule Sequencing Technology71
A combined transcriptomics and proteomics approach reveals S100A4 as a potential biomarker for Graves’ orbitopathy71
miR-224-5p and miR-545-5p Levels Relate to Exacerbations and Lung Function in a Pilot Study of X-Linked MicroRNA Expression in Cystic Fibrosis Monocytes70
Imputation of Ancient Whole Genome Sus scrofa DNA Introduces Biases Toward Main Population Components in the Reference Panel70
Comprehensive analysis of molecular features, prognostic values, and immune landscape association of m6A-regulated immune-related lncRNAs in smoking-associated lung squamous cell carcinoma69
A transmembrane protein family gene signature for overall survival prediction in osteosarcoma69
Genetically predicted 1091 blood metabolites and 309 metabolite ratios in relation to risk of type 2 diabetes: a Mendelian randomization study66
Editorial: Multi-omics studies and applications in precision medicine64
Identifying Functions of Proteins in Mice With Functional Embedding Features63
Scaffolded and annotated nuclear and organelle genomes of the North American brown alga Saccharina latissima63
MK2-mediated AKT/MYC signaling activation promotes epithelial-mesenchymal transition in lung adenocarcinoma63
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing62
COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts61
Comprehensive Analysis of the Transcriptome-Wide m6A Methylation in Mouse Pachytene Spermatocytes and Round Spermatids60
Genomic and physiological mechanisms of high-altitude adaptation in Ethiopian highlanders: a comparative perspective60
Investigating Doxorubicin’s mechanism of action in cervical cancer: a convergence of transcriptomic and metabolomic perspectives60
Development and validation of a TRP-related gene signature for overall survival prediction in lung adenocarcinoma59
Development of a risk model to predict prognosis in breast cancer based on cGAS-STING-related genes58
Prioritizing potential circRNA biomarkers for bladder cancer and bladder urothelial cancer based on an ensemble model58
Transcriptome sequencing reveals novel molecular features of SLE severity57
Genetic and clinical landscape of Duchenne muscular dystrophy in Guatemala: insights from a national study57
Construction of ceRNA network based on RNA-seq for identifying prognostic lncRNA biomarkers in Perthes disease57
BCR::ABL1-negative myeloproliferative neoplasms in the era of next-generation sequencing57
Editorial: Recent advances in nutrigenomics: Making strides towards precision nutrition56
Potential immunomodulatory effects of the extract from Artemisia frigida Willd on loaches infested with Aeromonas hydrophila revealed by microRNA analysis55
Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database55
Gene set-based identification of two immune subtypes of diffuse large B cell lymphoma for guiding immune checkpoint blocking therapy55
Identification of the ubiquitin–proteasome pathway domain by hyperparameter optimization based on a 2D convolutional neural network54
A Novel Age-Related Circular RNA Circ-ATXN2 Inhibits Proliferation, Promotes Cell Death and Adipogenesis in Rat Adipose Tissue-Derived Stromal Cells54
Fusion Gene Detection Using Whole-Exome Sequencing Data in Cancer Patients54
Genome-wide identification of acyl-CoA binding proteins and possible functional prediction in legumes52
CPIELA: Computational Prediction of Plant Protein–Protein Interactions by Ensemble Learning Approach From Protein Sequences and Evolutionary Information52
The role of lncRNA H19 in tumorigenesis and drug resistance of human Cancers51
Identification of a New Infectious Pancreatic Necrosis Virus (IPNV) Variant in Atlantic Salmon (Salmo salar L.) that can Cause High Mortality Even in Genetically Resistant Fish51
DEAD-Box Helicase 27 Triggers Epithelial to Mesenchymal Transition by Regulating Alternative Splicing of Lipoma-Preferred Partner in Gastric Cancer Metastasis51
SupCAM: Chromosome cluster types identification using supervised contrastive learning with category-variant augmentation and self-margin loss51
Dissecting Immunosuppressive Cell Communication Patterns Reveals JunB Proto-Oncogene (JUNB) Shaping a Non-Inflamed Tumor Microenvironment50
Prenatal Exposures to Common Phthalates and Prevalent Phthalate Alternatives and Infant DNA Methylation at Birth50
N6-Methyladenosine-Related lncRNAs Are Novel Prognostic Markers and Predict the Immune Landscape in Acute Myeloid Leukemia50
Salinity stress endurance of the plants with the aid of bacterial genes49
Set of 15 SNP-SNP Markers for Detection of Unbalanced Degraded DNA Mixtures and Noninvasive Prenatal Paternity Testing49
MECP2-related disorders while gene-based therapies are on the horizon49
Development of an exosome-related and immune microenvironment prognostic signature in colon adenocarcinoma49
miR-145-5p Inhibits Neuroendocrine Differentiation and Tumor Growth by Regulating the SOX11/MYCN Axis in Prostate cancer49
Role of cytokinins in seed development in pulses and oilseed crops: Current status and future perspective49
Whole Genome Sequencing and Morphological Trait-Based Evaluation of UPOV Option 2 for DUS Testing in Rice48
Geographical distribution of ALDH2 rs671 polymorphism in Chinese angina pectoris patients48
A Genome-Wide Analysis of StTGA Genes Reveals the Critical Role in Enhanced Bacterial Wilt Tolerance in Potato During Ralstonia solanacearum Infection48
Evaluation of low-density SNP panels and imputation for cost-effective genomic selection in four aquaculture species48
Panoramic analysis of the biological function and clinical value of SLC38A2 in human cancers: a study based on pan-cancer and single-cell analysis47
Moral judgment of genetic technologies: validation of the genetic technologies questionnaire in the German-speaking population47
Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program47
The potential impact of GLS and PDHA1 on tumor immunity and immunotherapy response in LUSC46
Genetic analysis of digital image derived morphometric traits of black tiger shrimp (Penaeus monodon) by incorporating G × E investigations46
Systemic inflammatory regulators and preeclampsia: a two-sample bidirectional Mendelian randomization study45
Identification of a novel locus C2 controlling canary yellow flesh color in watermelons45
Updating test-day milk yield factors for use in genetic evaluations and dairy production systems: a comprehensive review45
Causal Association Between Periodontitis and Type 2 Diabetes: A Bidirectional Two-Sample Mendelian Randomization Analysis45
Identification of core genes as potential biomarkers for predicting progression and prognosis in glioblastoma44
Editorial: Gene Regulation Explored by Systems Biology in Livestock Science44
Establishment and Validation of a Ferroptosis-Related Gene Signature to Predict Overall Survival in Lung Adenocarcinoma44
A comprehensive pan-cancer analysis of the expression characteristics, prognostic value, and immune characteristics of TOP1MT44
Editorial: Forensic investigative genetic genealogy and fine-scale structure of human populations44
Corrigendum: A novel ferroptosis-related LncRNA pair prognostic signature predicts immune landscapes and treatment responses for gastric cancer patients43
Editorial: New insights in cellular and molecular biology of cancer stem cells43
Conduction and validation of a novel mitotic spindle assembly related signature in hepatocellular carcinoma: prognostic prediction, tumor immune microenvironment and drug susceptibility43
Genetic tests as the strongest motivator of cooperation between participants and biobanks–Findings from cross-sectional study43
Development and validation of sex-associated markers using whole-genome re-sequencing in frog Quasipaa spinosa43
Genetic analysis of a bronze age individual from Ulug-depe (Turkmenistan)43
Editorial: High-throughput sequencing-based investigation of chronic disease markers and mechanisms, volume II42
Association between arthropathies and postpartum hemorrhage: a bidirectional Mendelian randomization study42
Corrigendum: Unravelling the genetic framework associated with grain quality and yield-related traits in maize (Zea mays L.)42
Regulatory role of N6-Methyladenosine on skeletal muscle development in Hu sheep42
Genome-wide identification and expression analysis of WRKY family genes under soft rot in Chinese cabbage42
Evaluating the Causal Effects of TIMP-3 on Ischaemic Stroke and Intracerebral Haemorrhage: A Mendelian Randomization Study42
From genetic data to kinship clarity: employing machine learning for detecting incestuous relations41
Editorial: Genetic and epigenetic aspects of non-coding RNAs in physiology and disease41
Metabolic reprogramming and prognostic modeling in pancreatic cancer: insights from WGCNA40
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome40
Identification and validation of diagnostic genes associated with neutrophil extracellular traps of type 2 diabetes mellitus39
Utilization of hypoxia-derived gene signatures to predict clinical outcomes and immune checkpoint blockade therapy responses in prostate cancer39
Transcriptional Regulation of Pine Male and Female Cone Initiation and Development: Key Players Identified Through Comparative Transcriptomics39
Effect modification by sex of genetic associations of vitamin C related metabolites in the Canadian Longitudinal study on aging39
Effectiveness of Ultrasound Imaging in Assessing the Palpation Skills of Rotating Physicians39
Causal role of gut microbiota, serum metabolites, immunophenotypes in myocarditis: a mendelian randomization study38
A comprehensive splicing characterization of COL4A5 mutations and prognostic significance in a single cohort with X-linked alport syndrome38
A de novo TNNI3K variant aggravates the pathogenicity of DMD-associated early-onset cardiomyopathy: a case report38
Editorial: Prediction and explanation in biomedicine using network-based approaches38
Annotation of cis-regulatory-associated histone modifications in the genomes of two Thoroughbred stallions38
Editorial: Computational methods to analyze RNA data for human diseases38
Editorial: Genetics of reproduction for livestock species38
Case Report: Report of Two Cases of Interstitial Lung Disease Caused by Novel Compound Heterozygous Variants in the ABCA3 Gene38
Early-Life Exposure of Pigs to Topsoil Alters miRNA and mRNA Expression in Peripheral Blood Mononuclear Cells38
Workplace genetic testing: which employees are likely to participate, what are their concerns with employer sponsorship, and which design features could reduce barriers and increase participation?38
Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder37
Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype37
FGF/FGFR-related lncRNAs based classification predicts prognosis and guides therapy in gastric cancer37
Development and validation of a chromatin regulator prognostic signature in colon adenocarcinoma37
Development of a Novel Immune-Related Gene Signature to Predict Prognosis and Immunotherapeutic Efficiency in Gastric Cancer37
Mitochondrial Genetic Diversity, Population Structure and Detection of Antillean and Amazonian Manatees in Colombia: New Areas and New Techniques37
Skin-specific transgenic overexpression of ovine β-catenin in mice37
Transcriptome Analysis Reveals Hub Genes Regulating Autophagy in Patients With Severe COVID-1937
EMILIN2 is associated with prognosis and immunotherapy in clear cell renal cell carcinoma36
Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis36
Moss-pathogen interactions: a review of the current status and future opportunities36
Editorial: Functional screening for cancer drug discovery: from experimental approaches to data integration36
Two machine learning-derived nomogram for predicting the occurrence and severity of acute graft-versus-host disease: a retrospective study based on serum biomarkers36
The prognostic significance of β-Catenin expression in patients with nasopharyngeal carcinoma: A systematic review and meta-analysis36
Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype36
Mutational signatures representative transcriptomic perturbations in hepatocellular carcinoma36
Editorial: Population and ancestry specific variation in disease susceptibility36
Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey35
Identification of Novel Compound Heterozygous Variants of the PNPLA6 Gene in Boucher–Neuhäuser Syndrome35
Identification of resistance gene analogs of the NBS-LRR family through transcriptome probing and in silico prediction of the expressome of Dalbergia sissoo under dieback disease stress35
Construction of a survival nomogram for gastric cancer based on the cancer genome atlas of m6A-related genes35
Epigenome-wide DNA methylation profiling in comparison between pathological and physiological hypertrophy of human cardiomyocytes35
Construction and validation of a novel coagulation-related 7-gene prognostic signature for gastric cancer35
Hereditary orotic aciduria identified by newborn screening35
Comprehensive Characterization of Pyroptosis Patterns with Implications in Prognosis and Immunotherapy in Low-Grade Gliomas35
The Alteration of m6A Modification at the Transcriptome-Wide Level in Human Villi During Spontaneous Abortion in the First Trimester35
Erratum: Omics approaches to understanding the efficacy and safety of disease-modifying treatments in multiple sclerosis35
Identification of a Novel Immune-Related lncRNA CTD-2288O8.1 Regulating Cisplatin Resistance in Ovarian Cancer Based on Integrated Analysis35
Association Between a TLR2 Gene Polymorphism (rs3804099) and Proteinuria in Kidney Transplantation Recipients35
Chromosomal Diversification in Ancistrus Species (Siluriformes: Loricariidae) Inferred From Repetitive Sequence Analysis34
Exploration and identification of six novel ferroptosis-related hub genes as potential gene signatures for peripheral nerve injury34
Capturing heart valve development with Gene Ontology34
Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl34
MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity33
Identification of discriminant features from stationary pattern of nucleotide bases and their application to essential gene classification33
Novel causative RYR2 indel variant with exon and intron involvement inducing exon 13 skipping in a family exhibiting catecholaminergic polymorphic ventricular tachycardia33
ARGem: a new metagenomics pipeline for antibiotic resistance genes: metadata, analysis, and visualization33
Refined expression quantitative trait locus analysis on adenocarcinoma at the gastroesophageal junction reveals susceptibility and prognostic markers33
Multi-task learning for predicting SARS-CoV-2 antibody escape33
Prognostic significance of CKAP2L expression in patients with clear cell renal cell carcinoma32
Construction of a prognostic model related to copper dependence in breast cancer by single-cell sequencing analysis32
Multi-Size Deep Learning Based Preoperative Computed Tomography Signature for Prognosis Prediction of Colorectal Cancer32
Trait-specific Selection Signature Detection Reveals Novel Loci of Meat Quality in Large White Pigs32
Neoepitope load, T cell signatures and PD-L2 as combined biomarker strategy for response to checkpoint inhibition immunotherapy32
Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)32
Editorial: The ethics and challenges of studying the genetics of marginalized populations32
KLF4 loss in hepatocellular carcinoma: Improving prognostic prediction and correlating immune infiltrates32
Characterization of novel human endogenous retrovirus structures on chromosomes 6 and 732
Perthes Disease in a Child With Osteogenesis Imperfecta From a Rare Genetic Variant: A Case Report32
stGuide advances label transfer in spatial transcriptomics through attention-based supervised graph representation learning32
Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency32
Editorial: Genetic advancements for improving the plant tolerance to biotic and abiotic stresses31
An immune infiltration-related long non-coding RNAs signature predicts prognosis for hepatocellular carcinoma31
Integrated multi-omic data reveal the potential molecular mechanisms of the nutrition and flavor in Liancheng white duck meat31
AttnTAP: A Dual-input Framework Incorporating the Attention Mechanism for Accurately Predicting TCR-peptide Binding31
A high-density genetic map and QTL fine mapping for growth- and sex-related traits in red swamp crayfish (Procambarus clarkii)31
Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases31
TRPV4 mRNA is elevated in the caudate nucleus with NPH but not in Alzheimer’s disease31
Mitochondrial DNA heteroplasmy analysis in keratoconus patients from China31
Genetic basis of phenotypic diversity in C. stenophylla: a stepping stone for climate-adapted coffee cultivar development31
VTP-Identifier: Vesicular Transport Proteins Identification Based on PSSM Profiles and XGBoost31
Genome-Wide Identification of mRNAs, lncRNAs, and Proteins, and Their Relationship With Sheep Fecundity31
Phenotypic and Genetic Complexity in Pediatric Movement Disorders31
Identifying novel genetic loci associated with polycystic ovary syndrome based on its shared genetic architecture with type 2 diabetes31
Analysis and validation of novel biomarkers related to palmitoylation in adenomyosis30
Identification of genomic regions of wheat associated with grain Fe and Zn content under drought and heat stress using genome-wide association study30
Long Non Coding RNA Based Regulation of Cerebrovascular Endothelium30
Cuproptosis-related LncRNAs signature as biomarker of prognosis and immune infiltration in pancreatic cancer30
Regulation of autophagy, lipid metabolism, and neurodegenerative pathology by heparan sulfate proteoglycans30
HNF1β, LHX1, and GGNBP2 deletion contributed to kidney and reproductive dysfunction in 17q12 deletion syndrome: evidence from a case report30
Influenza A viruses in gulls in landfills and freshwater habitats in Minnesota, United States30
Skills Capacity Building For Health Care Services and Research Through the Sickle Pan African Research Consortium30
Amino Acid Metabolism-Related lncRNA Signature Predicts the Prognosis of Breast Cancer30
Correction: Multi-omics integration uncovers key transcriptional regulators in triple-negative breast cancer spatial heterogeneity30
A syndrome differentiation model of TCM based on multi-label deep forest using biomedical text mining30
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndrome30
Exposure to endosulfan can cause long term effects on general biology, including the reproductive system of mice30
The Role of the APC/C and Its Coactivators Cdh1 and Cdc20 in Cancer Development and Therapy30
Exploring the immunological landscape of osteomyelitis through mendelian randomization analysis30
Genome-wide association analysis of tan spot disease resistance in durum wheat accessions from Tunisia30
Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort29
Evolutionary Genomics Reveals Multiple Functions of Arylalkylamine N-Acetyltransferase in Fish29
Multiple Cases of Bacterial Sequence Erroneously Incorporated Into Publicly Available Chloroplast Genomes29
Integrated Bioinformatics Analysis Identifies Heat Shock Factor 2 as a Prognostic Biomarker Associated With Immune Cell Infiltration in Hepatocellular Carcinoma29
Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy29
Immune Classification and Immune Landscape Analysis of Triple-Negative Breast Cancer29
Keloid Biomarkers and Their Correlation With Immune Infiltration29
Population Structure of Curraleiro Pé-Duro Cattle and its Relationship With the Serological Profile Against Pathogens of Economic and Zoonotic Interest29
Genetic Variation and the Distribution of Variant Types in the Horse29
Molecular mechanism of ferroptosis and its role in the occurrence and treatment of diabetes29
Identification of key genes for heart failure in dilated cardiomyopathy in different populations28
A pathogenesis-related protein 1 of Cucurbita moschata responds to powdery mildew infection28
Hypoxia-Induced miR-378a-3p Inhibits Osteosarcoma Invasion and Epithelial-to-Mesenchymal Transition via BYSL Regulation28
Coding roles of long non-coding RNAs in breast cancer: Emerging molecular diagnostic biomarkers and potential therapeutic targets with special reference to chemotherapy resistance28
Identification of copy number variants contributing to hallux valgus28
The alternative transcription and expression characterization of Dmc1 in autotetraploid Carassius auratus28
Genetics and marker-assisted breeding for sex expression in cucumber28
Pangenome-wide analysis of cyclic nucleotide-gated channel (CNGC) gene family in citrus Spp. Revealed their intraspecies diversity and potential roles in abiotic stress tolerance28
MSFN: a multi-omics stacked fusion network for breast cancer survival prediction28
Bioinformatics analysis reveals the landscape of immune cell infiltration and novel immune-related biomarkers in moyamoya disease28
Outcome of Hydroxyurea Use in SCD and Evaluation of Patients’ Perception and Experience in Nigeria28
Proteome changes of dairy calves rumen epithelium from birth to postweaning28
Development of a prognostic model for children with neuroblastoma based on necroptosis-related genes27
Compound Heterozygous Variants of the CPAMD8 Gene Co-Segregating in Two Chinese Pedigrees With Pigment Dispersion Syndrome/Pigmentary Glaucoma27
Editorial: The functional role of non-coding RNAs in tumor microenvironment and metastasis of genitourinary tumor and its potential application as tumor molecular biomarkers27
Genome-wide association analysis of resistance to bacterial cold-water disease in an important rainbow trout aquaculture breeding population27
The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives27
The association of metabolic syndrome with telomere length as a marker of cellular aging: a systematic review and meta-analysis27
CircRNAs in osteoarthritis: research status and prospect27
Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia27
Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population27
A layer-wise fusion network incorporating self-supervised learning for multimodal MR image synthesis27
Utilization of genetic information for medicines development and equitable benefit sharing27
Case report: Optical genome mapping revealed double rearrangements in a male undergoing preimplantation genetic testing27
Unveiling the genetic basis of Fusarium wilt resistance in chickpea using GWAS analysis and characterization of candidate genes27
Genetic Structure of the Endangered Coral Cladocora caespitosa Matches the Main Bioregions of the Mediterranean Sea27
Proteomic changes of the bovine blood plasma in response to heat stress in a tropically adapted cattle breed27
Pursuing Public Health Benefit Within National Genomic Initiatives: Learning From Different Policies27
Clinical Characteristics, In Silico Analysis, and Intervention of Neonatal-Onset Inflammatory Bowel Disease With Combined Immunodeficiency Caused by Novel TTC7A Variants27
Exploration of biomarkers associated with histone lactylation modification in spinal cord injury27
Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis27
Inflammatory aging clock: A cancer clock to characterize the patients’ subtypes and predict the overall survival in glioblastoma27
Pan-Cancer Analyses Identify the CTC1-STN1-TEN1 Complex as a Protective Factor and Predictive Biomarker for Immune Checkpoint Blockade in Cancer27
The draft genome of the microscopic Nemertoderma westbladi sheds light on the evolution of Acoelomorpha genomes27
A microarray data analysis investigating the pathogenesis and potential biomarkers of autophagy and ferroptosis in intervertebral disc degeneration27
Metabolite profiling and transcriptome analyses provide insight into the regulatory network of graft incompatibility in litchi27
MicroRNA-21 and microRNA-148a affects PTEN, NO and ROS in canine leishmaniasis26
Clinical and Genetic Analysis of a Patient With Coexisting 17a-Hydroxylase/17,20-Lyase Deficiency and Moyamoya Disease26
Corrigendum: Prognostic Values and Clinical Significance of S100 Family Member’s Individualized mRNA Expression in Pancreatic Adenocarcinoma26
Comprehensive Analysis of Sinonasal Inverted Papilloma Expression Profiles Identifies Long Non-Coding RNA AKTIP as a Potential Biomarker26
Long-read sequencing reveals absence of 5mC in Ogataea parapolymorpha DL-1 genome and introduces telomere-to-telomere assembly26
Editorial: Utilization of pharmacogenomics in clinical practice26
Lessons from a phenotypically normal infant with uniparental isodisomy of chromosome 21: a Case Report and review26
Phasor Histone FLIM-FRET Microscopy Maps Nuclear-Wide Nanoscale Chromatin Architecture With Respect to Genetically Induced DNA Double-Strand Breaks26
De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis26
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