Frontiers in Genetics

Article	Citations
Compound heterozygous FAM20C gene variants in a patient with severe Raine syndrome: a case report	253
Editorial: Exploiting genetics and genomics to improve the understanding of eye diseases	206
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 Database	193
Editorial: Clinical Evaluation Criteria for Aging and Aging-Related Multimorbidity	159
Transcriptomic analysis of paired healthy human skeletal muscles to identify modulators of disease severity in DMD	138
EDNRA Gene rs1878406 Polymorphism is Associated With Susceptibility to Large Artery Atherosclerotic Stroke	120
Characterisation of the in-vivo miRNA landscape in Drosophila ribonuclease mutants reveals Pacman-mediated regulation of the highly conserved let-7 cluster during apoptotic processes	102
Editorial: Epigenetic mechanisms and epigenetic-based therapies in cardiometabolic and vascular disease	96
Identification of N7-methylguanosine-related IncRNA signature as a potential predictive biomarker for colon adenocarcinoma	93
Editorial: Epigenomics implication for economic traits in domestic animals	91
DNA methylation and mRNA expression of glutathione S-transferase alpha 4 are associated with intracranial aneurysms in a gender-dependent manner	90
Genetic Variation in the ZNF208 Gene at rs8103163 and rs7248488 Is Associated With Laryngeal Cancer in the Northwestern Chinese Han Male	90
Identifying Functions of Proteins in Mice With Functional Embedding Features	87
RET splice site variants in medullary thyroid carcinoma	85
SOCS3 is Related to Cell Proliferation in Neuronal Tissue: An Integrated Analysis of Bioinformatics and Experiments	83
Incorporating genome-wide and transcriptome-wide association studies to identify genetic elements of longissimus dorsi muscle in Huaxi cattle	83
Single nucleotide variants in nuclear pore complex disassembly pathway associated with poor survival in osteosarcoma	75
Transcriptome profiling and analysis of patients with esophageal squamous cell carcinoma from Kazakhstan	70
Integrative analyses of prognosis, tumor immunity, and ceRNA network of the ferroptosis-associated gene FANCD2 in hepatocellular carcinoma	69
A Novel Age-Related Circular RNA Circ-ATXN2 Inhibits Proliferation, Promotes Cell Death and Adipogenesis in Rat Adipose Tissue-Derived Stromal Cells	69
Repression of enhancer RNA PHLDA1 promotes tumorigenesis and progression of Ewing sarcoma via decreasing infiltrating T‐lymphocytes: A bioinformatic analysis	68
Selection Signature Analyses Revealed Genes Associated With Adaptation, Production, and Reproduction in Selected Goat Breeds in Kenya	68
Comparative Transcriptome Analysis Provides Insight into Spatio-Temporal Expression Characteristics and Genetic Regulatory Network in Postnatal Developing Subcutaneous and Visceral Fat of Bama Pig	67
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 An	66
High Expression of CEMIP Correlates Poor Prognosis and the Tumur Microenvironment in Breast Cancer as a Promisingly Prognostic Biomarker	65

Functional identification of two novel variants and a hypomorphic variant in ASS1 from patients with Citrullinemia type I	63
Editorial: Genetic and epigenetic aspects of non-coding RNAs in physiology and disease	62
Editorial: Cytogenomics: Structural Organization and Evolution of Genomes	60
Discovery of novel eGFR-associated multiple independent signals using a quasi-adaptive method	60
An Augmented High-Dimensional Graphical Lasso Method to Incorporate Prior Biological Knowledge for Global Network Learning	59
A novel signature to predict the neoadjuvant chemotherapy response of bladder carcinoma: Results from a territory multicenter real-world study	59
Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family	57
Case Report: Two Novel Frameshift Mutations in SLC20A2 and One Novel Splice Donor Mutation in PDGFB Associated With Primary Familial Brain Calcification	57
Editorial: Machine Learning and Mathematical Models for Single-Cell Data Analysis	56
Construction of a HOXA11-AS-Interacted Network in Keloid Fibroblasts Using Integrated Bioinformatic Analysis and in Vitro Validation	56
Editorial: Finding New Epigenomics and Epigenetics Biomarkers for Complex Diseases and Significant Developmental Events With Machine Learning Methods	55
Editorial: Alternative Polyadenylation in Development and Disease	55
Identification of a Gene Signature to Aid Treatment Decisions by Integrated Analysis of Mutated Genes Between Primary and Metastatic Prostate Cancer	54
Machine learning potential predictor of idiopathic pulmonary fibrosis	52
LncRNA-mediated ceRNA network reveals the mechanism of action of Saorilao-4 decoction against pulmonary fibrosis	52
Case Report: Novel ADA2 variants cause atypical adenosine deaminase 2 deficiency	51
Updates on the molecular spectrum of MEFV variants in lebanese patients with Familial Mediterranean Fever	51
Classical and machine learning tools for identifying yellow-seeded Brassica napus by fusion of hyperspectral features	51
Editorial: Systems biology approaches to psychiatric and psychological disorders: unraveling the complexities	50
In silico design of an epitope-based vaccine ensemble for fasliolopsiasis	50
Case report: Discovery of novel CTNNB1 mutations and comparison of clinical characteristics in two patients with NEDSDV	50
The value of a metabolic and immune-related gene signature and adjuvant therapeutic response in pancreatic cancer	50
Retraction: Cytokinin and abiotic stress tolerance -what has been accomplished and the way forward?	49
Vitamin A family suppresses periodontitis by restoring mitochondrial metabolic reprogramming in macrophages through JAK-STAT pathway	49
Characterization of novel human endogenous retrovirus structures on chromosomes 6 and 7	49
Case Report: Identification of a Novel Heterozygous Missense Mutation in COL4A3 Gene Causing Variable Phenotypes in an Autosomal-Dominant Alport Syndrome Family	49
Inferring human miRNA–disease associations via multiple kernel fusion on GCNII	48
Reclassifying TNM stage I/II colorectal cancer into two subgroups with different overall survival, tumor microenvironment, and response to immune checkpoint blockade treatment	48
Fine-Mapping of the Major Histocompatibility Complex Region Linked to Leprosy in Northern China	48
Commentary: Case report: Optic atrophy and nephropathy with m.13513G>A/MT-ND5 mtDNA pathogenic variant	48
An Improved Deep Learning Model: S-TextBLCNN for Traditional Chinese Medicine Formula Classification	47
Features of the metabolic syndrome and subclinical atherosclerosis in patients with cerebrotendinous xanthomatosis: An augmented risk for premature cardiovascular disease	47
Transcriptome Sequencing Identifies PLAUR as an Important Player in Patients With Dermatomyositis-Associated Interstitial Lung Disease	47
Pathogenic germline variants in patients with breast cancer: conversations across generations, practices and patients’ attitude	47
Parental genetic knowledge and attitudes toward childhood with genetic disorders	47
Construction and Verification of a Glycolysis-Associated Gene Signature for the Prediction of Overall Survival in Low Grade Glioma	46
Morphological description and DNA barcoding research of nine Syringa species	46
Annotation of cis-regulatory-associated histone modifications in the genomes of two Thoroughbred stallions	46
A case report of oculopharyngodistal myopathy with 126 CGG repeat expansions in RILPL1	46
A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data	45
Discovering miRNAs Associated With Multiple Sclerosis Based on Network Representation Learning and Deep Learning Methods	45
Prevalence of inherited metabolic disorders among newborns in Zhuzhou, a southern city in China	45
Identifying Candidate Genes for Short Gestation Length Trait in Chinese Qingping Pigs by Whole-Genome Resequencing and RNA Sequencing	45
Coding roles of long non-coding RNAs in breast cancer: Emerging molecular diagnostic biomarkers and potential therapeutic targets with special reference to chemotherapy resistance	45
The Crosstalk Between Immune Infiltration, Circulating Tumor Cells, and Metastasis in Pancreatic Cancer: Identification of HMGB3 From a Multiple Omics Analysis	44
Causal association between inflammatory bowel disease and acute pancreatitis: a two-sample bidirectional mendelian randomization study	44
Long non-coding RNA (LncRNA) and epigenetic factors: their role in regulating the adipocytes in bovine	43
Development and characterization of type I interferon receptor knockout sheep: A model for viral immunology and reproductive signaling	43
MECP2-related disorders while gene-based therapies are on the horizon	43
The host genetics affects gut microbiome diversity in Chinese depressed patients	43

Molecular diagnosis and preimplantation genetic testing for chromosome 1q21.1 recurrent microduplication	42
Differential responses of the intestine and liver transcriptome to high levels of plant proteins in diets for large yellow croaker (Larimichthys crocea)	42
Editorial: Genomics of pathogens and vectors	42
Mechanism of action of lncRNA-NEAT1 in immune diseases	42
Study on the mechanism of KIF18B affecting the malignant progression of glioblastoma cells	42
Effects of ulcerative colitis and Crohn’s disease on neurodegenerative diseases: A Mendelian randomization study	41
A de novo TNNI3K variant aggravates the pathogenicity of DMD-associated early-onset cardiomyopathy: a case report	41
Identification of biomarkers and target drugs for melanoma: a topological and deep learning approach	41
The relationship of miR-155 host gene polymorphism in the susceptibility of cancer: a systematic review and meta-analysis	41
Exploring the genetic causal association of TIMP3 on CKD and kidney function: a two-sample mendelian randomization	41
STsisal: a reference-free deconvolution pipeline for spatial transcriptomics data	41
Patient-Specific Cell Communication Networks Associate With Disease Progression in Cancer	40
PSG7 indicates that age at diagnosis is associated with papillary thyroid carcinoma: A study based on the cancer genome atlas data	40
Editorial: RNA editing and modification in development and diseases	40
Identification of a 5-lncRNA-Based Signature for Immune Characteristics and Prognosis of Lung Squamous Cell Carcinoma and Verification of the Function of lncRNA SPATA41	40
Editorial: Reproductive genomics	40
Utilization of hypoxia-derived gene signatures to predict clinical outcomes and immune checkpoint blockade therapy responses in prostate cancer	40
Super enhancer-driven core transcriptional regulatory circuitry crosstalk with cancer plasticity and patient mortality in triple-negative breast cancer	40
The frequency of somatic mutations in cancer predicts the phenotypic relevance of germline mutations	40
Type 2 diabetes and glycemic traits are not causal factors of delirium: A two-sample mendelian randomization analysis	39
Transcriptomic analysis of the upper lip and primary palate development in mice	39
Evaluating the Causal Effects of TIMP-3 on Ischaemic Stroke and Intracerebral Haemorrhage: A Mendelian Randomization Study	39
A novel LUAD prognosis prediction model based on immune checkpoint-related lncRNAs	39
Mapping of a QTL associated with sucrose content in peanut kernels using BSA-seq	38
Melatonin Regulates the Periodic Growth of Cashmere by Upregulating the Expression of Wnt10b and β-catenin in Inner Mongolia Cashmere Goats	38
Editorial: Population and ancestry specific variation in disease susceptibility	38
Mitochondrial non-coding RNA in nasopharyngeal carcinoma: Clinical diagnosis and functional analysis	38
Causal role of gut microbiota, serum metabolites, immunophenotypes in myocarditis: a mendelian randomization study	38
Development of a prognostic model for children with neuroblastoma based on necroptosis-related genes	38
NcRNA-mediated upregulation of CAMK2N1 is associated with poor prognosis and tumor immune infiltration of gastric cancer	38
The Genetics of Adverse Drug Outcomes in Type 2 Diabetes: A Systematic Review	38
Identification of the Functions and Prognostic Values of RNA Binding Proteins in Bladder Cancer	37
Comprehensive Analysis of RNA-Seq in Endometriosis Reveals Competing Endogenous RNA Network Composed of circRNA, lncRNA and mRNA	37
Comprehensive Analysis of the Correlation Between Pyroptosis-Related LncRNAs and Tumor Microenvironment, Prognosis, and Immune Infiltration in Hepatocellular Carcinoma	37
The Genetic Structure and East-West Population Admixture in Northwest China Inferred From Genome-Wide Array Genotyping	37
Identification of a Genome Instability-Associated LncRNA Signature for Prognosis Prediction in Colon Cancer	37
Applicability of single-step genomic evaluation with a random regression model for reproductive traits in turkeys (Meleagris gallopavo)	37
Prenatal and postnatal diagnosis of Phelan–McDermid syndrome: A report of 21 cases from a medical center and review of the literature	37
ACP-DA: Improving the Prediction of Anticancer Peptides Using Data Augmentation	37
Editorial: The role of extracellular vesicles in diseases: Shedding light on their role in cell-to-cell communication	36
Causal Relationship Between Parathyroid Hormone and the Risk of Osteoarthritis: A Mendelian Randomization Study	36
Editorial: Reproduction in aquatic animals	36
Hereditary orotic aciduria identified by newborn screening	36
Improving PARP inhibitor efficacy in high-grade serous ovarian carcinoma: A focus on the immune system	36
Identification and validation of diagnostic genes associated with neutrophil extracellular traps of type 2 diabetes mellitus	36
Editorial: New insights in cellular and molecular biology of cancer stem cells	36
Decipering the Molecular Mechanism of ACE2 Regulating A549 Cells	36
Editorial: Epigenetics of metabolism, immunology and aging	36
Subject clustering by IF-PCA and several recent methods	35
A Multilayer Interactome Network Constructed in a Forest Poplar Population Mediates the Pleiotropic Control of Complex Traits	35
Discovery and Verification of an Immune-Related Gene Pairs Signature for Predicting Prognosis in Head and Neck Squamous Cell Carcinoma	35
Editorial: Genetics of reproduction for livestock species	35
Case Report: Report of Two Cases of Interstitial Lung Disease Caused by Novel Compound Heterozygous Variants in the ABCA3 Gene	35
Editorial: RNA Biology in Cardiovascular Disease	35
Editorial: Identifying genetics-based mechanisms and treatments for neurodevelopmental and psychiatric disorders through data integration	35
Method for Identifying Essential Proteins by Key Features of Proteins in a Novel Protein-Domain Network	35
Creation and Worldwide Utilisation of New COVID-19 Online Information Hub for Genetics Health Professionals, Patients and Families	35
A Panel of E2F Target Gene Signature Predicting the Prognosis of Hepatocellular Carcinoma	35
Case Report: Variegate porphyria disclosed by post-gastric bypass complications and causing predominant painful sensorimotor axonal peripheral neuropathy	34
Single-cell transcriptome analysis for cancer and biology of the pancreas: A review on recent progress	34
Is an SV caller compatible with sequencing data? An online recommendation tool to automatically recommend the optimal caller based on data features	34
Identification of Potential Core Genes for the Rupture of Intracranial Aneurysms by a Bioinformatics Analysis	34
Exploring the role of tumor stemness and the potential of stemness-related risk model in the prognosis of intrahepatic cholangiocarcinoma	33
Light at the end of the tunnel: Clinical features and therapeutic prospects of KRAS mutant subtypes in non-small-cell lung cancer	33
Chromosome-level genome assembly of Fragaria pentaphylla using PacBio and Hi-C technologies	33
Gibberellin Induced Transcriptome Profiles Reveal Gene Regulation of Loquat Flowering	33
A Novel Risk Model Identified Based on Pyroptosis-Related lncRNA Predicts Overall Survival and Associates With the Immune Landscape of GC Patients	33
Identification and functional characteristics of a novel splicing heterozygote variant of COL2A1 associated with Stickler syndrome type I	33
Nanomaterials in Animal Husbandry: Research and Prospects	33
Genetically predicted major depression causally increases the risk of temporomandibular joint disorders	33
Copy Number Variations Analysis Identifies QPRT as a Candidate Gene Associated With Susceptibility for Solitary Functioning Kidney	32
Editorial: Plant transcription factors associated with abiotic stress tolerance in crops and wild-relatives	32
Assessments of TP53 and CTNNB1 gene hotspot mutations in circulating tumour DNA of hepatitis B virus-induced hepatocellular carcinoma	32
Whole Exome Sequencing Identifies Genes Associated With Non-Obstructive Azoospermia	32
Editorial: Statistical Methods, Computing and Resources for Genome-Wide Association Studies	32
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 Pathway	32
Genome-wide association mapping of quantitative trait loci for chalkiness-related traits in rice (Oryza sativa L.)	32
A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels	32
A Genome-Wide Analysis of StTGA Genes Reveals the Critical Role in Enhanced Bacterial Wilt Tolerance in Potato During Ralstonia solanacearum Infection	32
Prenatal diagnosis in a fetuses with a clenched hands, overlapping fingers, and clubfoot due to MED12 deficiency in three affected siblings: A case report	32

Genetically predicted 1091 blood metabolites and 309 metabolite ratios in relation to risk of type 2 diabetes: a Mendelian randomization study	32
Identification of a novel locus C2 controlling canary yellow flesh color in watermelons	32
Are inflammatory bowel diseases associated with an increased risk of COVID-19 susceptibility and severity? A two-sample Mendelian randomization study	32
The EIF2AK4/rs4594236 AG/GG Genotype Is a Hazard Factor of Immunoglobulin Therapy Resistance in Southern Chinese Kawasaki Disease Patients	32
Unraveling the therapeutic mechanisms of dichloroacetic acid in lung cancer through integrated multi-omics approaches: metabolomics and transcriptomics	31
The association between vitamin D and uterine fibroids: A mendelian randomization study	31
Relationship between the image characteristics of artificial intelligence and EGFR gene mutation in lung adenocarcinoma	31
NR4A1 as a potential therapeutic target in colon adenocarcinoma: a computational analysis of immune infiltration and drug response	31
Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma weakening	31
Development of a risk model to predict prognosis in breast cancer based on cGAS-STING-related genes	31
Integrative Analysis Reveals Potentially Functional N6-Methylandenosine-Related Long Noncoding RNAs in Colon Adenocarcinoma	31
Comprehensive analysis of mitophagy-related genes in diagnosis and heterogeneous endothelial cells in chronic rhinosinusitis: based on bulk and single-cell RNA sequencing data	31
Case Report: Neuroblastoma Breakpoint Family Genes Associate With 1q21 Copy Number Variation Disorders	31
Immune-related gene signature associates with immune landscape and predicts prognosis accurately in patients with skin cutaneous melanoma	30
CLGBO: An Algorithm for Constructing Highly Robust Coding Sets for DNA Storage	30
Correlation of GDFT combined with rehabilitation therapy in DNA damage repair of esophageal cancer cells	30
Editorial: Current progress in genomic and genetic research on human viral diseases	30
Editorial: Computational and integrative approaches for developmental biology and molecular evolution	30
A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy	30
Development and validation of a prognostic prediction model for iron metabolism-related genes in patients with pancreatic adenocarcinoma	30
The top 100 most cited articles on mucopolysaccharidoses: a bibliometric analysis	30
Convergence Analysis of Rust Fungi and Anther Smuts Reveals Their Common Molecular Adaptation to a Phytoparasitic Lifestyle	30
Editorial: Non-Genetic Heterogeneity in Development and Disease	30
Construction of a novel prognostic signature based on the composition of tumor-infiltrating immune cells in clear cell renal cell carcinoma	30
Development and validation of a chromatin regulator prognostic signature in colon adenocarcinoma	30
Editorial: Population genetics and conservation of aquatic species	30
Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A1	30
Rare primary dyslipidaemias associated with low LDL and HDL cholesterol values in Portugal	30
Editorial: Prediction and explanation in biomedicine using network-based approaches	29
Case report: Preimplantation genetic testing for infantile GM1 gangliosidosis	29
Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence	29
A Novel Purine and Uric Metabolism Signature Predicting the Prognosis of Hepatocellular Carcinoma	29
A comprehensive analysis of G-protein-signaling modulator 2 as a prognostic and diagnostic marker for pan-cancer	29
Whole-Genome Sequencing of Sinocyclocheilus maitianheensis Reveals Phylogenetic Evolution and Immunological Variances in Various Sinocyclocheilus Fishes	29
Structural Features of the Nucleosomal DNA Modulate the Functional Binding of a Transcription Factor and Productive Transcription	29
Editorial: Genetic Pleiotropy in Complex Traits and Diseases	29
Gamma irradiation-induced genetic variability and its effects on the phenotypic and agronomic traits of groundnut (Arachis hypogaeaL.)	29
Clinical and molecular delineation of classical-like Ehlers–Danlos syndrome through a comprehensive next-generation sequencing-based screening system	29
Genome-wide identification and expression analysis of GRAS transcription factors under cold stress in diploid and triploid Eucalyptus	28
Genomic selection for resistance to one pathogenic strain of Vibrio splendidus in blue mussel Mytilus edulis	28
Mutation in the COL2A1 gene is associated with acetabular dysplasia	28
Editorial: The genetics and epigenetics of mental health	28
Based on bioinformatics, SESN2 negatively regulates ferroptosis induced by ischemia reperfusion via the System Xc−/GPX4 pathway	28
Identification of key genes underlying radiosensitivity and radioresistance in endometrial cancer through integrated bioinformatics analysis	28
Behind the scenes with genomics researchers	28
LINC01614 is a promising diagnostic and prognostic marker in HNSC linked to the tumor microenvironment and oncogenic function	28
Mendelian randomization and multiomics comprehensively reveal the causal relationship and potential mechanism between atrial fibrillation and gastric cancer	28
Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report	28
Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy	27
Novel Variant Expands the Clinical Spectrum of CUX2-Associated Developmental and Epileptic Encephalopathies	27
Integrated genomic analysis defines molecular subgroups in dilated cardiomyopathy and identifies novel biomarkers based on machine learning methods	27
Editorial: Characterization of esophageal cancer molecular signatures and mechanisms using multi-omics analyses	27
GOLM1 is related to the inflammatory/immune nature of uveal melanoma and acts as a promising indicator for prognosis and immunotherapy response	27
Spectrum of genetic variants in bilateral sensorineural hearing loss	27
Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegia	27
Association Between Insulin-like Growth Factor-1 rs35767 Polymorphism and Type 2 Diabetes Mellitus Susceptibility: A Meta-Analysis	27
Comprehensive analyses of the microRNA–messenger RNA–transcription factor regulatory network in mouse and human renal fibrosis	27
Whole Genome Sequencing Reveals Signatures for Artificial Selection for Different Sizes in Japanese Primitive Dog Breeds	27
A Multi-Marker Test for Analyzing Paired Genetic Data in Transplantation	27
Eastern king prawn Penaeus plebejus stock enhancement—Genetic evidence that hatchery bred prawns have survived in the wild after release	27
Identifying Membrane Protein Types Based on Lifelong Learning With Dynamically Scalable Networks	27
HLA Diversity in Saudi Population: High Frequency of Homozygous HLA Alleles and Haplotypes	27
Development and validation of a tumor immune cell infiltration-related gene signature for recurrence prediction by weighted gene co-expression network analysis in prostate cancer	27
Noninvasive Prenatal Screening Based on Second-Trimester Ultrasonographic Soft Markers in Low-Risk Pregnant Women	27
Editorial: Applied Genetics of Natural Fiber Plants	26
Editorial: SARS-CoV-2: From Genetic Variability to Vaccine Design	26
Editorial: The epigenetic control of transposable elements in development and in diseases	26
Empirical validation of ProteinMPNN’s efficiency in enhancing protein fitness	26
i2APP: A Two-Step Machine Learning Framework For Antiparasitic Peptides Identification	26
A novel natural killer cell-related signatures to predict prognosis and chemotherapy response of pancreatic cancer patients	26
Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon	26
Editorial: Emerging talents in genomic assay technology	26
A novel marker integrating multiple genetic alterations better predicts platinum sensitivity in ovarian cancer than HRD score	26
Fusion Gene Detection Using Whole-Exome Sequencing Data in Cancer Patients	26
Immune-Related Molecular Profiling of Thymoma With Myasthenia Gravis	26
A Novel Pyroptosis-Related Gene Signature for Predicting Prognosis in Kidney Renal Papillary Cell Carcinoma	26
Prognostic utility of TME-associated genes in pancreatic cancer	26
Identification of Distinct Molecular Patterns and a Four-Gene Signature in Colon Cancer Based on Invasion-Related Genes	26
Editorial: Computational methods for multi-omics data analysis in cancer precision medicine	26
Survival association of XRCC1 for patients with head and neck squamous cell carcinoma: A systematic review and meta-analysis	25
Genomic surveillance unfolds the SARS-CoV-2 transmission and divergence dynamics in Bangladesh	25
Commentary: Conserved polymorphic sequences protect themselves for future challenges	25
Clinical and genetic features of luscan-lumish syndrome associated with a novel de novo variant of SETD2 gene: Case report and literature review	25
Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiation	25
Case report: Early use of whole exome sequencing unveils HNRNPU-related neurodevelopmental disorder and answers additional clinical questions through reanalysis	25
Feedback Inhibition Might Dominate the Accumulation Pattern of BR in the New Shoots of Tea Plants (Camellia sinensis)	25
Editorial: Aquatic genomics and transcriptomics for evolutionary biology	25
Human Immune System Diseasome Networks and Female Oviductal Microenvironment: New Horizons to be Discovered	25
Living in Temporary Ponds Loading Giant Genomes: The Neotropical Annual Killifish Genus Austrolebias as New Outstanding Evolutionary Model	25
Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant	25
Optical genome mapping identifies a homozygous deletion in the non-coding region of the SCN9A gene in individuals from the same family with congenital insensitivity to pain	25
Pregnancy outcomes and genetic analysis for fetal ventriculomegaly	25
Advances in early detection methods for solid tumors	25
Biochemical and molecular features of tetrahydrobiopterin deficiency in Fujian Province, southeastern China	25
MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity	25