Frontiers in Genetics

Papers
(The median citation count of Frontiers in Genetics is 4. 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 2022-08-01 to 2026-08-01.)
ArticleCitations
Subject clustering by IF-PCA and several recent methods188
RET splice site variants in medullary thyroid carcinoma171
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in PARD6G-AS1 promotor in a case with arthrogryposis129
Editorial: Epigenetic mechanisms and epigenetic-based therapies in cardiometabolic and vascular disease125
Geographical distribution of ALDH2 rs671 polymorphism in Chinese angina pectoris patients120
Panoramic analysis of the biological function and clinical value of SLC38A2 in human cancers: a study based on pan-cancer and single-cell analysis119
Moral judgment of genetic technologies: validation of the genetic technologies questionnaire in the German-speaking population117
The potential impact of GLS and PDHA1 on tumor immunity and immunotherapy response in LUSC104
Editorial: Forensic investigative genetic genealogy and fine-scale structure of human populations101
Editorial: New insights in cellular and molecular biology of cancer stem cells99
Editorial: High-throughput sequencing-based investigation of chronic disease markers and mechanisms, volume II98
Association between arthropathies and postpartum hemorrhage: a bidirectional Mendelian randomization study97
Regulatory role of N6-Methyladenosine on skeletal muscle development in Hu sheep95
Editorial: Genetic and epigenetic aspects of non-coding RNAs in physiology and disease93
Metabolic reprogramming and prognostic modeling in pancreatic cancer: insights from WGCNA93
Editorial: Genetics of reproduction for livestock species91
Editorial: Computational methods to analyze RNA data for human diseases89
Editorial: Prediction and explanation in biomedicine using network-based approaches86
A comprehensive splicing characterization of COL4A5 mutations and prognostic significance in a single cohort with X-linked alport syndrome83
Early-Life Exposure of Pigs to Topsoil Alters miRNA and mRNA Expression in Peripheral Blood Mononuclear Cells82
FGF/FGFR-related lncRNAs based classification predicts prognosis and guides therapy in gastric cancer80
Skin-specific transgenic overexpression of ovine β-catenin in mice79
Development and validation of a chromatin regulator prognostic signature in colon adenocarcinoma78
Identification of discriminant features from stationary pattern of nucleotide bases and their application to essential gene classification78
Mutational signatures representative transcriptomic perturbations in hepatocellular carcinoma78
Two machine learning-derived nomogram for predicting the occurrence and severity of acute graft-versus-host disease: a retrospective study based on serum biomarkers78
Construction of a prognostic model related to copper dependence in breast cancer by single-cell sequencing analysis76
Neoepitope load, T cell signatures and PD-L2 as combined biomarker strategy for response to checkpoint inhibition immunotherapy76
Editorial: The ethics and challenges of studying the genetics of marginalized populations75
Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases74
An immune infiltration-related long non-coding RNAs signature predicts prognosis for hepatocellular carcinoma74
Construction of ceRNA network based on RNA-seq for identifying prognostic lncRNA biomarkers in Perthes disease72
Systemic inflammatory regulators and preeclampsia: a two-sample bidirectional Mendelian randomization study66
From genetic data to kinship clarity: employing machine learning for detecting incestuous relations65
KLF4 loss in hepatocellular carcinoma: Improving prognostic prediction and correlating immune infiltrates64
Bioinformatics revealed biomarkers for diagnosis in kidney stones63
Bioinformatics analysis reveals the landscape of immune cell infiltration and novel immune-related biomarkers in moyamoya disease62
Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis61
Comprehensive analysis of molecular features, prognostic values, and immune landscape association of m6A-regulated immune-related lncRNAs in smoking-associated lung squamous cell carcinoma60
Epigenome-wide DNA methylation profiling in comparison between pathological and physiological hypertrophy of human cardiomyocytes60
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 stress59
Potential immunomodulatory effects of the extract from Artemisia frigida Willd on loaches infested with Aeromonas hydrophila revealed by microRNA analysis59
Genome-wide identification and expression analysis of WRKY family genes under soft rot in Chinese cabbage59
Development and validation of a TRP-related gene signature for overall survival prediction in lung adenocarcinoma59
Prioritizing potential circRNA biomarkers for bladder cancer and bladder urothelial cancer based on an ensemble model57
Genetic and clinical landscape of Duchenne muscular dystrophy in Guatemala: insights from a national study57
Editorial: Multi-omics studies and applications in precision medicine56
ARGem: a new metagenomics pipeline for antibiotic resistance genes: metadata, analysis, and visualization55
Genetic analysis of a bronze age individual from Ulug-depe (Turkmenistan)54
Identifying mitochondrial genes and potential biological functions in pre-eclampsia: bioinformatics and experimental insights54
BANSMDA: a computational model for predicting potential microbe-disease associations based on bilinear attention networks and sparse autoencoders52
LRRC56 deficiency cause motile ciliopathies in humans and mice52
HNF1β, LHX1, and GGNBP2 deletion contributed to kidney and reproductive dysfunction in 17q12 deletion syndrome: evidence from a case report51
A combined transcriptomics and proteomics approach reveals S100A4 as a potential biomarker for Graves’ orbitopathy50
A transcriptomic atlas at bulk and single-cell levels identifies novel transcriptional and splicing regulators of ECM homeostasis in osteoarthritis50
Application of next-generation sequencing to determine mutations in candidate genes for congenital eye malformations in the Mexican indigenous population49
Diagnostic and prognostic value of polygene methylation detection in ascites48
Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype47
Gene set-based identification of two immune subtypes of diffuse large B cell lymphoma for guiding immune checkpoint blocking therapy47
A microarray data analysis investigating the pathogenesis and potential biomarkers of autophagy and ferroptosis in intervertebral disc degeneration47
stGuide advances label transfer in spatial transcriptomics through attention-based supervised graph representation learning47
Erratum: Omics approaches to understanding the efficacy and safety of disease-modifying treatments in multiple sclerosis46
Analysis and validation of novel biomarkers related to palmitoylation in adenomyosis46
Erratum: Heterologous expression of Arabidopsis AtARA6 in soybean enhances salt tolerance46
A high-density genetic map and QTL fine mapping for growth- and sex-related traits in red swamp crayfish (Procambarus clarkii)46
Corrigendum: Unravelling the genetic framework associated with grain quality and yield-related traits in maize (Zea mays L.)45
Corrigendum: A novel ferroptosis-related LncRNA pair prognostic signature predicts immune landscapes and treatment responses for gastric cancer patients45
Erratum: A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation45
Retraction: Cytokinin and abiotic stress tolerance -what has been accomplished and the way forward?45
An intronic micro-deletion impacts the transcription and translation of PKD1 gene45
Development of a prognostic model for children with neuroblastoma based on necroptosis-related genes44
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome44
TRPV4 mRNA is elevated in the caudate nucleus with NPH but not in Alzheimer’s disease43
Integrated multi-omic data reveal the potential molecular mechanisms of the nutrition and flavor in Liancheng white duck meat43
Polygenic risk score and phenome-wide association study of the Epstein-Barr virus antibody response43
Genetic tests as the strongest motivator of cooperation between participants and biobanks–Findings from cross-sectional study43
Identification of copy number variants contributing to hallux valgus43
The alternative transcription and expression characterization of Dmc1 in autotetraploid Carassius auratus42
Concordance between genome-wide cfDNA screening and diagnostic test results for large copy-number variants: a multi-site study from the Global Expanded NIPT Consortium42
Identification and validation of diagnostic genes associated with neutrophil extracellular traps of type 2 diabetes mellitus42
Proteome changes of dairy calves rumen epithelium from birth to postweaning42
A pathogenesis-related protein 1 of Cucurbita moschata responds to powdery mildew infection42
The draft genome of the microscopic Nemertoderma westbladi sheds light on the evolution of Acoelomorpha genomes42
Decoding thalassemia and sickle cell disease: advances in molecular technologies for comprehensive variant detection41
Identification of core genes as potential biomarkers for predicting progression and prognosis in glioblastoma41
Comparative transcriptome analyses of immune responses to LPS in peripheral blood mononuclear cells from the giant panda, human, mouse, and monkey41
Investigating Doxorubicin’s mechanism of action in cervical cancer: a convergence of transcriptomic and metabolomic perspectives40
Regulation of autophagy, lipid metabolism, and neurodegenerative pathology by heparan sulfate proteoglycans40
Updating test-day milk yield factors for use in genetic evaluations and dairy production systems: a comprehensive review39
The prognostic significance of β-Catenin expression in patients with nasopharyngeal carcinoma: A systematic review and meta-analysis39
Exploring the immunological landscape of osteomyelitis through mendelian randomization analysis39
Clinical characteristics and follow-up of complex arrhythmias associated with RYR2 gene mutations in children38
A comprehensive pan-cancer analysis of the expression characteristics, prognostic value, and immune characteristics of TOP1MT38
MK2-mediated AKT/MYC signaling activation promotes epithelial-mesenchymal transition in lung adenocarcinoma38
Editorial: Insights in human and medical genomics 202438
Effect modification by sex of genetic associations of vitamin C related metabolites in the Canadian Longitudinal study on aging38
CircRNAs in osteoarthritis: research status and prospect38
GViT-GP: injecting the genomic relationship matrix as an inductive bias into a vision transformer via cross-attention for genomic prediction38
Exploring prognostic genes related to lactylation and programmed cell death in pancreatic ductal adenocarcinoma: a comprehensive study combining bulk transcriptomics and experimental verification38
Moss-pathogen interactions: a review of the current status and future opportunities38
Cuproptosis-related LncRNAs signature as biomarker of prognosis and immune infiltration in pancreatic cancer38
Genome-wide identification of acyl-CoA binding proteins and possible functional prediction in legumes38
Unveiling the genetic basis of Fusarium wilt resistance in chickpea using GWAS analysis and characterization of candidate genes38
SupCAM: Chromosome cluster types identification using supervised contrastive learning with category-variant augmentation and self-margin loss38
MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity37
Editorial: Recent advances in nutrigenomics: Making strides towards precision nutrition37
Transcriptome sequencing reveals novel molecular features of SLE severity37
Conduction and validation of a novel mitotic spindle assembly related signature in hepatocellular carcinoma: prognostic prediction, tumor immune microenvironment and drug susceptibility37
Editorial: Functional screening for cancer drug discovery: from experimental approaches to data integration37
Influenza A viruses in gulls in landfills and freshwater habitats in Minnesota, United States36
Proteomic changes of the bovine blood plasma in response to heat stress in a tropically adapted cattle breed36
Construction of a survival nomogram for gastric cancer based on the cancer genome atlas of m6A-related genes36
COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts36
Development of a risk model to predict prognosis in breast cancer based on cGAS-STING-related genes36
Exploration and identification of six novel ferroptosis-related hub genes as potential gene signatures for peripheral nerve injury36
Utilization of hypoxia-derived gene signatures to predict clinical outcomes and immune checkpoint blockade therapy responses in prostate cancer36
Development and validation of sex-associated markers using whole-genome re-sequencing in frog Quasipaa spinosa36
Molecular characterization of a rare heterozygous APOA5 variant in a Chinese family with moderate hypertriglyceridemia36
Capturing heart valve development with Gene Ontology35
Mitochondrial DNA heteroplasmy analysis in keratoconus patients from China35
Genomics-informed elucidation of trait-phenotype relationships and MABB approaches deliver major gene blast resistance in the aromatic rice landrace Mushk Budji35
Genome-wide association analysis of tan spot disease resistance in durum wheat accessions from Tunisia35
The multifaceted role of FAM13A in pulmonary diseases35
Prognostic significance of CKAP2L expression in patients with clear cell renal cell carcinoma35
A de novo TNNI3K variant aggravates the pathogenicity of DMD-associated early-onset cardiomyopathy: a case report35
Genetically predicted 1091 blood metabolites and 309 metabolite ratios in relation to risk of type 2 diabetes: a Mendelian randomization study35
Annotation of cis-regulatory-associated histone modifications in the genomes of two Thoroughbred stallions35
Novel causative RYR2 indel variant with exon and intron involvement inducing exon 13 skipping in a family exhibiting catecholaminergic polymorphic ventricular tachycardia35
Refined expression quantitative trait locus analysis on adenocarcinoma at the gastroesophageal junction reveals susceptibility and prognostic markers35
Correction: Multi-omics integration uncovers key transcriptional regulators in triple-negative breast cancer spatial heterogeneity35
Editorial: Population and ancestry specific variation in disease susceptibility34
EMILIN2 is associated with prognosis and immunotherapy in clear cell renal cell carcinoma34
BCR::ABL1-negative myeloproliferative neoplasms in the era of next-generation sequencing34
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?33
Molecular mechanism of ferroptosis and its role in the occurrence and treatment of diabetes33
Identification of genomic regions of wheat associated with grain Fe and Zn content under drought and heat stress using genome-wide association study33
Whole Genome Sequencing and Morphological Trait-Based Evaluation of UPOV Option 2 for DUS Testing in Rice33
Identification of a novel locus C2 controlling canary yellow flesh color in watermelons33
Construction and validation of a novel coagulation-related 7-gene prognostic signature for gastric cancer33
The association of metabolic syndrome with telomere length as a marker of cellular aging: a systematic review and meta-analysis33
Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy33
Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder33
Pangenome-wide analysis of cyclic nucleotide-gated channel (CNGC) gene family in citrus Spp. Revealed their intraspecies diversity and potential roles in abiotic stress tolerance32
Federated, governed, and interoperable? The emerging architecture of public human genomic data infrastructures: a European perspective32
Hereditary orotic aciduria identified by newborn screening32
The genetic architecture of human skin pigmentation: evolution and adaptation across global populations32
Genomic and physiological mechanisms of high-altitude adaptation in Ethiopian highlanders: a comparative perspective32
MSFN: a multi-omics stacked fusion network for breast cancer survival prediction32
Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database32
Coding roles of long non-coding RNAs in breast cancer: Emerging molecular diagnostic biomarkers and potential therapeutic targets with special reference to chemotherapy resistance32
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndrome32
Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype31
Characterization of novel human endogenous retrovirus structures on chromosomes 6 and 731
Identifying novel genetic loci associated with polycystic ovary syndrome based on its shared genetic architecture with type 2 diabetes31
Elective genomic screening: results of the implementation of a whole genome sequencing program at a medical check-up unit in Spain31
Genetic analysis of digital image derived morphometric traits of black tiger shrimp (Penaeus monodon) by incorporating G × E investigations31
MECP2-related disorders while gene-based therapies are on the horizon31
Imagining an ethics for synthetic biology31
Salinity stress endurance of the plants with the aid of bacterial genes31
Development of an exosome-related and immune microenvironment prognostic signature in colon adenocarcinoma31
Genetics and marker-assisted breeding for sex expression in cucumber31
Exposure to endosulfan can cause long term effects on general biology, including the reproductive system of mice31
Whole genome sequencing and functional annotation of Fusarium oxysporum f. sp. lentis to unravel virulence and secondary metabolite biosynthesis gene clusters31
AttnTAP: A Dual-input Framework Incorporating the Attention Mechanism for Accurately Predicting TCR-peptide Binding31
Causal role of gut microbiota, serum metabolites, immunophenotypes in myocarditis: a mendelian randomization study30
A transmembrane protein family gene signature for overall survival prediction in osteosarcoma30
The role of lncRNA H19 in tumorigenesis and drug resistance of human Cancers30
Identification of key genes for heart failure in dilated cardiomyopathy in different populations30
Multi-task learning for predicting SARS-CoV-2 antibody escape30
MiRNA-Seq reveals key MicroRNAs involved in fat metabolism of sheep liver30
Consumer-oriented (patient and family) outcomes from nursing in genomics: a scoping review of the literature (2012–2022)30
Genetic basis of phenotypic diversity in C. stenophylla: a stepping stone for climate-adapted coffee cultivar development30
Scaffolded and annotated nuclear and organelle genomes of the North American brown alga Saccharina latissima30
A syndrome differentiation model of TCM based on multi-label deep forest using biomedical text mining30
Role of cytokinins in seed development in pulses and oilseed crops: Current status and future perspective30
Editorial: Genetic advancements for improving the plant tolerance to biotic and abiotic stresses30
Evaluation of low-density SNP panels and imputation for cost-effective genomic selection in four aquaculture species30
Neutrophil in the suppressed immune microenvironment: Critical prognostic factor for lung adenocarcinoma patients with KEAP1 mutation29
Clinical and genetic analysis in Chinese families with synpolydactyly, and cellular localization of HOXD13 with different length of polyalanine tract29
Systematic pharmacology-based strategy to investigate the mechanism of beta-sitosterol for the treatment of rheumarthritis29
An efficient five-lncRNA signature for lung adenocarcinoma prognosis, with AL606489.1 showing sexual dimorphism29
Kalpra: A kernel approach for longitudinal pathway regression analysis integrating network information with an application to the longitudinal PsyCourse Study29
Neurobehavioral characteristics of mice with SETD5 mutations as models of IDD23 and KBG syndromes29
Comprehensive analysis of transcriptome characteristics and identification of TLK2 as a potential biomarker in dermatofibrosarcoma protuberans29
Assessing genomics confidence and learning needs in Australian nurses and midwives: an educational program evaluation29
The role of small extracellular vesicle non-coding RNAs in kidney diseases29
A layer-wise fusion network incorporating self-supervised learning for multimodal MR image synthesis29
Inquiring the inter-relationships amongst grain-filling, grain-yield, and grain-quality of Japonica rice at high latitudes of China29
Multi-omic data integration for the study of production, carcass, and meat quality traits in Nellore cattle28
Developing genomic tools to assist turnip rape [Brassica rapa (L.) subsp.oleifera (DC.) Metzg.] breeding28
Population genomic analysis reveals genetic divergence and adaptation in Brachymystax lenok28
Functional analysis of MEIS2 splice site variant c.438 + 1G>T in a congenital heart patient28
Evidence for a genetic contribution to the ossification of spinal ligaments in Ossification of Posterior Longitudinal Ligament and Diffuse idiopathic skeletal hyperostosis: A narrative review28
Comparative transcriptome analysis, unfolding the pathways regulating the seed-size trait in cultivated lentil (Lens culinaris Medik.)28
STS-BN: An efficient Bayesian network method for detecting causal SNPs28
Genetic diversity and haplotype distribution patterns analysis of cytb and RAG2 sequences in Rana hanluica from southern China28
A comprehensive pan-cancer analysis unveiling the oncogenic effect of plant homeodomain finger protein 14 (PHF14) in human tumors28
Analysis of RPGR gene mutations in 41 Chinese families affected by X-linked inherited retinal dystrophy28
Identifying metabolism-related genes in liver cancer through weighted gene co-expression network analysis and machine learning28
Case Report: A rare chromosomal imbalance with dup 7q36.3-qter and del 7pter-p22.3 arising from parental pericentric inversion27
Clinical and Genetic Analysis of a Patient With Coexisting 17a-Hydroxylase/17,20-Lyase Deficiency and Moyamoya Disease27
Genome-wide association analysis of resistance to bacterial cold-water disease in an important rainbow trout aquaculture breeding population27
Lessons from a phenotypically normal infant with uniparental isodisomy of chromosome 21: a Case Report and review27
The application of clinical variable-based nomogram in predicting overall survival in malignant phyllodes tumors of the breast27
Editorial: Utilization of pharmacogenomics in clinical practice27
Screening and functional analysis of the differential peptides from the placenta of patients with healthy pregnancy and preeclampsia using placental peptidome26
Integration of single-cell and bulk RNA-seq to establish a predictive signature based on the differentiation trajectory of M2 macrophages in lung adenocarcinoma26
Delta-catenin attenuates medulloblastoma cell invasion by targeting EMT pathway26
Risk model of hepatocellular carcinoma based on cuproptosis-related genes26
The risk of various types of cardiovascular diseases in mutation positive familial hypercholesterolemia; a review26
Insights into the evolution and regulation of miRNAs from the view of their DNA replication temporal domains26
Biosensing circulating MicroRNAs in autoinflammatory skin diseases: Focus on Hidradenitis suppurativa26
Analysis of common genetic variation across targets of microRNAs dysregulated both in ASD and epilepsy reveals negative correlation26
Editorial: Progress in understanding the immunogenetic basis of disease susceptibility and outcomes26
A deletion variant Arg616 of androgen receptor in a Chinese family with complete androgen insensitivity syndrome26
A GHKNN model based on the physicochemical property extraction method to identify SNARE proteins26
Genetic Alchemy unveiled: MicroRNA-mediated gene therapy as the Artisan craft in the battlefront against hepatocellular carcinoma—a comprehensive chronicle of strategies and innovations26
bk-5214S2L, an allelic variant of bk-5, as high-quality silage maize genetic resource26
Phylogenomics as an effective approach to untangle cross-species hybridization event: A case study in the family Nymphaeaceae26
Identification of cuproptosis-associated IncRNAs signature and establishment of a novel nomogram for prognosis of stomach adenocarcinoma25
Genome-wide identification and expression analysis of EPF/EPFL gene family in Populus trichocarpa25
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant25
Mucosal DNA methylome alteration in Crohn’s disease: surgical and non-surgical groups25
KLK2 single-nucleotide polymorphism rs198977 is associated with increased susceptibility and hyperleukocytosis in AML25
Transcriptional data analysis reveals the association between infantile hemangiomas and venous malformations25
Identification of the lncRNA–miRNA‒mRNA regulatory network for middle cerebral artery occlusion-induced ischemic stroke25
Methylation-related genes involved in renal carcinoma progression25
Construction of a ceRNA network in polycystic ovary syndrome (PCOS) driven by exosomal lncRNA25
Identification and functional analysis of a novel CSNK2A1 frameshift variant in stillbirth25
Polyketide synthases mutation in tuberculosis transmission revealed by whole genomic sequence, China, 2011–201925
Detection of BRCA1/2 pathogenic variants in patients with breast and/or ovarian cancer and their families. Analysis of 3,458 cases from Lower Silesia (Poland) according to the diagnostic algorithm of 25
Genetic association of LOC100130476 rs80213143 with susceptibility and renal involvement in systemic lupus erythematosus25
Editorial: Genetic modulation of gut microbiome: effects on neurological health and aging24
Microfibrillar-associated protein 2 is a prognostic marker that correlates with the immune microenvironment in glioma24
Revealing the key modules and potential prognostic markers of gastric cancer transformation based on weighted gene co-expression networks24
The African Goat Improvement Network: a scientific group empowering smallholder farmers24
Epitranscriptomic regulation of endothelial plasticity under hemodynamic forces: insights from the KLF2/4–METTL3–H19 pathway24
Perfluorooctanesulfonic acid contributes to primary open-angle glaucoma in a FABP4-Dependent manner: a novel mechanism for environmental risk of glaucoma24
Long-read sequencing reveals absence of 5mC in Ogataea parapolymorpha DL-1 genome and introduces telomere-to-telomere assembly24
MicroRNA-21 and microRNA-148a affects PTEN, NO and ROS in canine leishmaniasis24
Correction: SPDL1 overexpression is associated with the 18F-FDG PET/CT metabolic parameters, prognosis, and progression of esophageal cancer24
Genetic diversity assessment of the indigenous goat population of Benin using microsatellite markers24
Low expression of the metabolism-related gene SLC25A21 predicts unfavourable prognosis in patients with acute myeloid leukaemia24
Identification of a prognostic risk-scoring model and risk signatures based on glycosylation-associated cluster in breast cancer24
Editorial: Current trends and future perspectives about liquid biopsy24
Identification of immune-related signature for the prognosis and benefit of immunotherapy in triple-negative breast cancer24
Identifying genetic variants associated with amphotericin B (AMB) resistance in Aspergillus fumigatus via k-mer-based GWAS24
The prognostic value and clinical significance of mitophagy-related genes in hepatocellular carcinoma24
Identification of novel immune ferroptosis-related genes associated with clinical and prognostic features in breast cancer23
Prognosis analysis of necroptosis-related genes in colorectal cancer based on bioinformatic analysis23
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