Frontiers in Genetics

Papers
(The TQCC of Frontiers in Genetics is 7. 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 2021-01-01 to 2025-01-01.)
ArticleCitations
Compound heterozygous FAM20C gene variants in a patient with severe Raine syndrome: a case report234
Transcriptome Characterization of Short Distance Transport Stress in Beef Cattle Blood184
Editorial: Exploiting genetics and genomics to improve the understanding of eye diseases180
A Nomogram for Predicting the Risk of Bone Metastasis in Newly Diagnosed Head and Neck Cancer Patients: A Real-World Data Retrospective Cohort Study From SEER Database173
Case report: A novel missense variant in melanopsin associates with delayed sleep phenotype: Whole genome sequencing study120
Editorial: Clinical Evaluation Criteria for Aging and Aging-Related Multimorbidity119
Comprehensive analysis of karyopherin alpha family expression in lung adenocarcinoma: Association with prognostic value and immune homeostasis113
Transcriptomic analysis of paired healthy human skeletal muscles to identify modulators of disease severity in DMD93
EDNRA Gene rs1878406 Polymorphism is Associated With Susceptibility to Large Artery Atherosclerotic Stroke92
Bioinformatics analysis of the common targets of miR-223-3p, miR-122-5p, and miR-93-5p in polycystic ovarian syndrome90
Development of a Prognostic Signature Based on Single-Cell RNA Sequencing Data of Immune Cells in Intrahepatic Cholangiocarcinoma89
Characterisation of the in-vivo miRNA landscape in Drosophila ribonuclease mutants reveals Pacman-mediated regulation of the highly conserved let-7 cluster during apoptotic processes87
Whole-Genome Sequencing and Genomic Variant Analysis of Kazakh Individuals84
Editorial: Epigenetic mechanisms and epigenetic-based therapies in cardiometabolic and vascular disease77
Identification of N7-methylguanosine-related IncRNA signature as a potential predictive biomarker for colon adenocarcinoma75
Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin75
Editorial: Epigenomics implication for economic traits in domestic animals72
Genetic Variation in the ZNF208 Gene at rs8103163 and rs7248488 Is Associated With Laryngeal Cancer in the Northwestern Chinese Han Male70
DNA methylation and mRNA expression of glutathione S-transferase alpha 4 are associated with intracranial aneurysms in a gender-dependent manner69
Construction of a prognostic model based on eight ubiquitination-related genes via machine learning and potential therapeutics analysis for cervical cancer67
RET splice site variants in medullary thyroid carcinoma66
Identifying Functions of Proteins in Mice With Functional Embedding Features66
Weaning Induces Stress-Dependent DNA Methylation and Transcriptional Changes in Piglet PBMCs66
Incorporating genome-wide and transcriptome-wide association studies to identify genetic elements of longissimus dorsi muscle in Huaxi cattle65
SOCS3 is Related to Cell Proliferation in Neuronal Tissue: An Integrated Analysis of Bioinformatics and Experiments65
Single nucleotide variants in nuclear pore complex disassembly pathway associated with poor survival in osteosarcoma63
Transcriptome profiling and analysis of patients with esophageal squamous cell carcinoma from Kazakhstan63
RNA Sequencing of Cardiac in a Rat Model Uncovers Potential Target LncRNA of Diabetic Cardiomyopathy60
Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved59
Integrative analyses of prognosis, tumor immunity, and ceRNA network of the ferroptosis-associated gene FANCD2 in hepatocellular carcinoma58
Genes in pediatric pulmonary arterial hypertension and the most promising BMPR2 gene therapy58
A Novel Age-Related Circular RNA Circ-ATXN2 Inhibits Proliferation, Promotes Cell Death and Adipogenesis in Rat Adipose Tissue-Derived Stromal Cells57
Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population56
Repression of enhancer RNA PHLDA1 promotes tumorigenesis and progression of Ewing sarcoma via decreasing infiltrating T‐lymphocytes: A bioinformatic analysis56
Selection Signature Analyses Revealed Genes Associated With Adaptation, Production, and Reproduction in Selected Goat Breeds in Kenya55
Effects of Simulated Microgravity on the Proteome and Secretome of the Polyextremotolerant Black Fungus Knufia chersonesos54
Novel immune-related prognostic model and nomogram for breast cancer based on ssGSEA54
Schizophrenia Plays a Negative Role in the Pathological Development of Myocardial Infarction at Multiple Biological Levels53
Gene Expression Profiling of Glioblastoma to Recognize Potential Biomarker Candidates53
Bioinformatics Analysis of Expression Profiles and Prognostic Values of the Signal Transducer and Activator of Transcription Family Genes in Glioma53
Estimated Breeding Values of Beef Sires Can Predict Performance of Beef-Cross-Dairy Progeny53
Expression and Diagnostic Value of miR-497 and miR-1246 in Hepatocellular Carcinoma53
Comparative Transcriptome Analysis Provides Insight into Spatio-Temporal Expression Characteristics and Genetic Regulatory Network in Postnatal Developing Subcutaneous and Visceral Fat of Bama Pig51
Causal Effects of Circulating Cytokines on the Risk of Psoriasis Vulgaris: A Mendelian Randomization Study51
Causal Association Between Periodontitis and Type 2 Diabetes: A Bidirectional Two-Sample Mendelian Randomization Analysis50
High Expression of CEMIP Correlates Poor Prognosis and the Tumur Microenvironment in Breast Cancer as a Promisingly Prognostic Biomarker50
Functional identification of two novel variants and a hypomorphic variant in ASS1 from patients with Citrullinemia type I50
Association of PTPN22 SNP1858 (rs2476601) and Gene SNP1123 (rs2488457) Polymorphism With Primary Immune Thrombocytopenia Susceptibility: A Meta-Analysis of Case-Control Studies and Trial Sequential An50
Editorial: Genetic and epigenetic aspects of non-coding RNAs in physiology and disease49
Editorial: Cytogenomics: Structural Organization and Evolution of Genomes48
Discovery of novel eGFR-associated multiple independent signals using a quasi-adaptive method48
A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study47
Multiple-Tissue and Multilevel Analysis on Differentially Expressed Genes and Differentially Correlated Gene Pairs for HFpEF46
Identification and analysis of hub genes of hypoxia-immunity in type 2 diabetes mellitus46
Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family46
The Alteration of m6A Modification at the Transcriptome-Wide Level in Human Villi During Spontaneous Abortion in the First Trimester46
An Augmented High-Dimensional Graphical Lasso Method to Incorporate Prior Biological Knowledge for Global Network Learning46
Case Report: Two Novel Frameshift Mutations in SLC20A2 and One Novel Splice Donor Mutation in PDGFB Associated With Primary Familial Brain Calcification45
Identification and validation of novel prognostic biomarkers and therapeutic targets for non-small cell lung cancer45
Identification of potential key genes for immune infiltration in childhood asthma by data mining and biological validation45
Construction of a HOXA11-AS-Interacted Network in Keloid Fibroblasts Using Integrated Bioinformatic Analysis and in Vitro Validation44
Identification of Neoantigens and Construction of Immune Subtypes in Prostate Adenocarcinoma44
Biological and Clinicopathological Characteristics of OPN in Cervical Cancers44
Editorial: Machine Learning and Mathematical Models for Single-Cell Data Analysis43
Editorial: Finding New Epigenomics and Epigenetics Biomarkers for Complex Diseases and Significant Developmental Events With Machine Learning Methods43
Editorial: Alternative Polyadenylation in Development and Disease43
Identification of a Gene Signature to Aid Treatment Decisions by Integrated Analysis of Mutated Genes Between Primary and Metastatic Prostate Cancer42
PHDMF: A Flexible and Scalable Personal Health Data Management Framework Based on Blockchain Technology42
X-box Binding Protein 1 is a Potential Immunotherapy Target in Ovarian Cancer41
LncRNA-mediated ceRNA network reveals the mechanism of action of Saorilao-4 decoction against pulmonary fibrosis41
Fine-Mapping of the Major Histocompatibility Complex Region Linked to Leprosy in Northern China41
A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk41
Inferring human miRNA–disease associations via multiple kernel fusion on GCNII41
Case Report: Identification of a Novel Heterozygous Missense Mutation in COL4A3 Gene Causing Variable Phenotypes in an Autosomal-Dominant Alport Syndrome Family41
Identification and Validation of Prognostic Factors of Lipid Metabolism in Obstructive Sleep Apnea40
Immune-related gene IL17RA as a diagnostic marker in osteoporosis40
Commentary: Case report: Optic atrophy and nephropathy with m.13513G>A/MT-ND5 mtDNA pathogenic variant40
Prioritizing potential circRNA biomarkers for bladder cancer and bladder urothelial cancer based on an ensemble model40
Unraveling T Cell Responses for Long Term Protection of SARS-CoV-2 Infection40
Reclassifying TNM stage I/II colorectal cancer into two subgroups with different overall survival, tumor microenvironment, and response to immune checkpoint blockade treatment40
Pathogenic germline variants in patients with breast cancer: conversations across generations, practices and patients’ attitude40
Features of the metabolic syndrome and subclinical atherosclerosis in patients with cerebrotendinous xanthomatosis: An augmented risk for premature cardiovascular disease40
Congenital Bilateral Absence of the Vas Deferens39
Inference of gene-environment interaction from heterogeneous case-parent trios39
An Improved Deep Learning Model: S-TextBLCNN for Traditional Chinese Medicine Formula Classification39
Type 2 diabetes and glycemic traits are not causal factors of delirium: A two-sample mendelian randomization analysis39
iPoLNG—An unsupervised model for the integrative analysis of single-cell multiomics data39
Transcriptome Sequencing Identifies PLAUR as an Important Player in Patients With Dermatomyositis-Associated Interstitial Lung Disease38
Parental genetic knowledge and attitudes toward childhood with genetic disorders38
Construction and Verification of a Glycolysis-Associated Gene Signature for the Prediction of Overall Survival in Low Grade Glioma38
Discovering miRNAs Associated With Multiple Sclerosis Based on Network Representation Learning and Deep Learning Methods38
Identifying Candidate Genes for Short Gestation Length Trait in Chinese Qingping Pigs by Whole-Genome Resequencing and RNA Sequencing37
CDAE: A Cascade of Denoising Autoencoders for Noise Reduction in the Clustering of Single-Particle Cryo-EM Images36
Coding roles of long non-coding RNAs in breast cancer: Emerging molecular diagnostic biomarkers and potential therapeutic targets with special reference to chemotherapy resistance36
Refined Contact Map Prediction of Peptides Based on GCN and ResNet36
A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data36
The Crosstalk Between Immune Infiltration, Circulating Tumor Cells, and Metastasis in Pancreatic Cancer: Identification of HMGB3 From a Multiple Omics Analysis36
Elevated exposures to persistent endocrine disrupting compounds impact the sperm methylome in regions associated with autism spectrum disorder36
Comprehensive Analysis of Inhibitor of Apoptosis Protein Expression and Prognostic Significance in Non–Small Cell Lung Cancer36
Prevalence of inherited metabolic disorders among newborns in Zhuzhou, a southern city in China36
Nontrivial Replication of Loci Detected by Multi-Trait Methods36
The MID1 Protein: A Promising Therapeutic Target in Huntington’s Disease36
Causal association between inflammatory bowel disease and acute pancreatitis: a two-sample bidirectional mendelian randomization study36
Long non-coding RNA (LncRNA) and epigenetic factors: their role in regulating the adipocytes in bovine35
GeNetOntology: identifying affected gene ontology terms via grouping, scoring, and modeling of gene expression data utilizing biological knowledge-based machine learning35
MECP2-related disorders while gene-based therapies are on the horizon35
The host genetics affects gut microbiome diversity in Chinese depressed patients35
Epigenetics and immune cells in medulloblastoma35
Long Non Coding RNA Based Regulation of Cerebrovascular Endothelium34
MoGCN: A Multi-Omics Integration Method Based on Graph Convolutional Network for Cancer Subtype Analysis34
Significance of Tumor Mutation Burden Combined With Immune Infiltrates in the Progression and Prognosis of Advanced Gastric Cancer34
Development and characterization of type I interferon receptor knockout sheep: A model for viral immunology and reproductive signaling34
AttnTAP: A Dual-input Framework Incorporating the Attention Mechanism for Accurately Predicting TCR-peptide Binding34
Cloning and Functional Characterization of a Pericarp Abundant Expression Promoter (AhGLP17-1P) From Peanut (Arachis hypogaea L.)34
Genomic and Chemical Diversity of Commercially Available High-CBD Industrial Hemp Accessions34
Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana34
Effect of the Expression of ELOVL5 and IGFBP6 Genes on the Metastatic Potential of Breast Cancer Cells34
Identification of Immune-Related Key Genes in Ovarian Cancer Based on WGCNA34
Prognostic significance and immune landscape of a fatty acid metabolism-related gene signature in colon adenocarcinoma34
Effects of ulcerative colitis and Crohn’s disease on neurodegenerative diseases: A Mendelian randomization study33
Editorial: Genomics of pathogens and vectors33
miR-145-5p Inhibits Neuroendocrine Differentiation and Tumor Growth by Regulating the SOX11/MYCN Axis in Prostate cancer33
DeCban: Prediction of circRNA-RBP Interaction Sites by Using Double Embeddings and Cross-Branch Attention Networks33
Exploring the genetic causal association of TIMP3 on CKD and kidney function: a two-sample mendelian randomization33
Gender bias and menstrual blood in stem cell research: A review of pubmed articles (2008–2020)33
FGF/FGFR-related lncRNAs based classification predicts prognosis and guides therapy in gastric cancer32
Editorial: Reproductive genomics32
Case report: Analysis of novel compound heterozygous TPP1 variants in a Chinese patient with neuronal ceroid lipofuscinosis type 232
Utilization of hypoxia-derived gene signatures to predict clinical outcomes and immune checkpoint blockade therapy responses in prostate cancer32
Identification of a 5-lncRNA-Based Signature for Immune Characteristics and Prognosis of Lung Squamous Cell Carcinoma and Verification of the Function of lncRNA SPATA4132
Patient-Specific Cell Communication Networks Associate With Disease Progression in Cancer32
A novel LUAD prognosis prediction model based on immune checkpoint-related lncRNAs31
Relationship between irregular diet and risk of esophageal cancer: A meta-analysis31
Ethical Implications of e-Health Applications in Early Preventive Healthcare31
Editorial: RNA editing and modification in development and diseases31
Progress in the Study of Non-Coding RNAs in Multidifferentiation Potential of Dental-Derived Mesenchymal Stem Cells31
Genomic insight into COVID-19 severity in MAFLD patients: a single-center prospective cohort study31
Microsatellite markers of the major histocompatibility complex genomic region of domestic camels31
The frequency of somatic mutations in cancer predicts the phenotypic relevance of germline mutations31
Transcriptomic analysis of the upper lip and primary palate development in mice31
Network Analyses Predict Small RNAs That Might Modulate Gene Expression in the Testis and Epididymis of Bos indicus Bulls31
PSG7 indicates that age at diagnosis is associated with papillary thyroid carcinoma: A study based on the cancer genome atlas data31
Super enhancer-driven core transcriptional regulatory circuitry crosstalk with cancer plasticity and patient mortality in triple-negative breast cancer31
WVMDA: Predicting miRNA–Disease Association Based on Weighted Voting31
Editorial: Population and ancestry specific variation in disease susceptibility31
Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients30
Type 2 Diabetes and Glycemic Traits Are Not Causal Factors of Osteoarthritis: A Two-Sample Mendelian Randomization Analysis30
Editorial: Reproduction in aquatic animals30
Integrated Bioinformatics Analysis Identifies Heat Shock Factor 2 as a Prognostic Biomarker Associated With Immune Cell Infiltration in Hepatocellular Carcinoma30
Editorial: New insights in cellular and molecular biology of cancer stem cells30
Exploring the causal link among statin drugs and the osteoarthritis risk based on Mendelian randomization research30
Identification and validation of diagnostic genes associated with neutrophil extracellular traps of type 2 diabetes mellitus30
Improving PARP inhibitor efficacy in high-grade serous ovarian carcinoma: A focus on the immune system30
Hereditary orotic aciduria identified by newborn screening30
Editorial: The role of extracellular vesicles in diseases: Shedding light on their role in cell-to-cell communication30
Causal Relationship Between Parathyroid Hormone and the Risk of Osteoarthritis: A Mendelian Randomization Study30
Decipering the Molecular Mechanism of ACE2 Regulating A549 Cells30
Editorial: Epigenetics of metabolism, immunology and aging30
Expression patterns of platinum resistance-related genes in lung adenocarcinoma and related clinical value models30
Subject clustering by IF-PCA and several recent methods29
Editorial: Identifying genetics-based mechanisms and treatments for neurodevelopmental and psychiatric disorders through data integration29
A Panel of E2F Target Gene Signature Predicting the Prognosis of Hepatocellular Carcinoma29
Creation and Worldwide Utilisation of New COVID-19 Online Information Hub for Genetics Health Professionals, Patients and Families29
Method for Identifying Essential Proteins by Key Features of Proteins in a Novel Protein-Domain Network29
Specific classification and new therapeutic targets for neuroendocrine prostate cancer: A patient-based, diagnostic study29
Single-cell transcriptome analysis for cancer and biology of the pancreas: A review on recent progress29
Editorial: RNA Biology in Cardiovascular Disease29
Case Report: Report of Two Cases of Interstitial Lung Disease Caused by Novel Compound Heterozygous Variants in the ABCA3 Gene29
Editorial: Genetics of reproduction for livestock species29
Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases29
ATAC-seq reveals the roles of chromatin accessibility in the chondrocytes of Kashin–Beck disease compared with primary osteoarthritis29
Discovery and Verification of an Immune-Related Gene Pairs Signature for Predicting Prognosis in Head and Neck Squamous Cell Carcinoma29
A Multilayer Interactome Network Constructed in a Forest Poplar Population Mediates the Pleiotropic Control of Complex Traits29
Case Report: Variegate porphyria disclosed by post-gastric bypass complications and causing predominant painful sensorimotor axonal peripheral neuropathy28
Chromosome-level genome assembly of Fragaria pentaphylla using PacBio and Hi-C technologies28
Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family28
Exploring the role of tumor stemness and the potential of stemness-related risk model in the prognosis of intrahepatic cholangiocarcinoma28
Genetically predicted 1091 blood metabolites and 309 metabolite ratios in relation to risk of type 2 diabetes: a Mendelian randomization study28
Identification of a novel locus C2 controlling canary yellow flesh color in watermelons28
Light at the end of the tunnel: Clinical features and therapeutic prospects of KRAS mutant subtypes in non-small-cell lung cancer28
Is an SV caller compatible with sequencing data? An online recommendation tool to automatically recommend the optimal caller based on data features28
Genetically predicted major depression causally increases the risk of temporomandibular joint disorders28
Nanomaterials in Animal Husbandry: Research and Prospects28
Exploration and identification of anoikis-related genes in polycythemia vera28
Genome-wide association mapping of quantitative trait loci for chalkiness-related traits in rice (Oryza sativa L.)28
Interaction Between LncRNA and UPF1 in Tumors28
Identification of Potential Core Genes for the Rupture of Intracranial Aneurysms by a Bioinformatics Analysis28
The Causal Effects of Primary Biliary Cholangitis on Thyroid Dysfunction: A Two-Sample Mendelian Randomization Study28
A Novel Risk Model Identified Based on Pyroptosis-Related lncRNA Predicts Overall Survival and Associates With the Immune Landscape of GC Patients28
Editorial: Plant transcription factors associated with abiotic stress tolerance in crops and wild-relatives28
Identification and functional characteristics of a novel splicing heterozygote variant of COL2A1 associated with Stickler syndrome type I28
Gibberellin Induced Transcriptome Profiles Reveal Gene Regulation of Loquat Flowering28
Convergence Analysis of Rust Fungi and Anther Smuts Reveals Their Common Molecular Adaptation to a Phytoparasitic Lifestyle27
Case report: A third variant in the 5′ UTR of TWIST1 creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome27
Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes27
Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma weakening27
Thallium-induced DNA damage, genetic, and epigenetic alterations27
Whole Exome Sequencing Identifies Genes Associated With Non-Obstructive Azoospermia27
Exploring the optimal strategy of imputation from SNP array to whole-genome sequencing data in farm animals27
Relationship between the image characteristics of artificial intelligence and EGFR gene mutation in lung adenocarcinoma27
Rare primary dyslipidaemias associated with low LDL and HDL cholesterol values in Portugal27
Correlation of GDFT combined with rehabilitation therapy in DNA damage repair of esophageal cancer cells27
Editorial: Population genetics and conservation of aquatic species27
A Genome-Wide Analysis of StTGA Genes Reveals the Critical Role in Enhanced Bacterial Wilt Tolerance in Potato During Ralstonia solanacearum Infection27
Are inflammatory bowel diseases associated with an increased risk of COVID-19 susceptibility and severity? A two-sample Mendelian randomization study27
A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels27
Integrating genome-wide association studies and population genomics analysis reveals the genetic architecture of growth and backfat traits in pigs27
Development and validation of a prognostic prediction model for iron metabolism-related genes in patients with pancreatic adenocarcinoma27
Neurogenesis Potential Evaluation and Transcriptome Analysis of Fetal Hypothalamic Neural Stem/Progenitor Cells With Prenatal High Estradiol Exposure27
Construction of a novel prognostic signature based on the composition of tumor-infiltrating immune cells in clear cell renal cell carcinoma27
Immune-related gene signature associates with immune landscape and predicts prognosis accurately in patients with skin cutaneous melanoma27
A Circ-0007022/miR-338-3p/Neuropilin-1 Axis Reduces the Radiosensitivity of Esophageal Squamous Cell Carcinoma by Activating Epithelial-To-Mesenchymal Transition and PI3K/AKT Pathway27
Assessments of TP53 and CTNNB1 gene hotspot mutations in circulating tumour DNA of hepatitis B virus-induced hepatocellular carcinoma27
Case Report: Neuroblastoma Breakpoint Family Genes Associate With 1q21 Copy Number Variation Disorders27
Proteome changes of dairy calves rumen epithelium from birth to postweaning27
Editorial: Computational and integrative approaches for developmental biology and molecular evolution27
The top 100 most cited articles on mucopolysaccharidoses: a bibliometric analysis26
Pan-cancer analysis identifies DDX56 as a prognostic biomarker associated with immune infiltration and drug sensitivity26
Editorial: Current progress in genomic and genetic research on human viral diseases26
Gamma irradiation-induced genetic variability and its effects on the phenotypic and agronomic traits of groundnut (Arachis hypogaeaL.)26
Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injury26
Development and validation of a chromatin regulator prognostic signature in colon adenocarcinoma26
Editorial: Non-Genetic Heterogeneity in Development and Disease26
Exploration and identification of six novel ferroptosis-related hub genes as potential gene signatures for peripheral nerve injury26
ctDNA-Profiling-Based UBL Biological Process Mutation Status as a Predictor of Atezolizumab Response Among TP53-Negative NSCLC Patients26
Application of Copy Number Variation Detection to Fetal Diagnosis of Echogenic Intracardiac Focus During Pregnancy26
Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence26
CLGBO: An Algorithm for Constructing Highly Robust Coding Sets for DNA Storage26
A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy26
Genome-wide association analysis of tan spot disease resistance in durum wheat accessions from Tunisia26
Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A126
Mitochondrial non-coding RNA in nasopharyngeal carcinoma: Clinical diagnosis and functional analysis26
Natural Selection of ATP2B1 Underlies Susceptibility to Essential Hypertension26
Whole-Genome Sequencing of Sinocyclocheilus maitianheensis Reveals Phylogenetic Evolution and Immunological Variances in Various Sinocyclocheilus Fishes26
CIEGAN: A Deep Learning Tool for Cell Image Enhancement26
The influence of the pollination compatibility type on the pistil S-RNase expression in European pear (Pyrus communis)25
Editorial: Applied Genetics of Natural Fiber Plants25
A novel natural killer cell-related signatures to predict prognosis and chemotherapy response of pancreatic cancer patients25
Editorial: SARS-CoV-2: From Genetic Variability to Vaccine Design25
LINC01614 is a promising diagnostic and prognostic marker in HNSC linked to the tumor microenvironment and oncogenic function25
Clinical and molecular delineation of classical-like Ehlers–Danlos syndrome through a comprehensive next-generation sequencing-based screening system25
Case report: Preimplantation genetic testing for infantile GM1 gangliosidosis25
Understanding Crassostrea virginica tolerance of Perkinsus marinus through global gene expression analysis25
A Novel Pyroptosis-Related Gene Signature for Predicting Prognosis in Kidney Renal Papillary Cell Carcinoma25
Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon25
A Novel Purine and Uric Metabolism Signature Predicting the Prognosis of Hepatocellular Carcinoma25
Editorial: The genetics and epigenetics of mental health25
Single nucleotide variants in microRNA biosynthesis genes in Mexican individuals25
New Structural and Single Nucleotide Mutations in Type I and Type II Collagens in Taiwanese Children With Type I and Type II Collagenopathies25
De novo Prediction of Moonlighting Proteins Using Multimodal Deep Ensemble Learning25
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