Genetics Research

Papers
(The TQCC of Genetics Research is 0. 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
Molecular Subtype Classification and Mechanistic Investigation Based on Ferroptosis‐Related lncRNAs in Ovarian Cancer5
Comprehensive Analysis of the Mechanism of Anoikis in Hepatocellular Carcinoma3
The Diverse Roles of the Histone‐Like Nucleoid Structuring (H‐NS) Protein in Vibrio parahaemolyticus3
Hypertension, Dyslipidemia, and Adhesive Capsulitis: A Bidirectional Two‐Sample Mendelian Randomization Study of the European Population2
Research Hotspots and Emerging Trends in Osteoporosis Epigenetics2
1
A Cuproptosis‐Related lncRNA Signature Predicts Prognosis and Shapes the Immune Landscape in Primary Lower‐Grade Glioma1
Comprehensive Analysis of Macrophage Dynamics, CCBE1, and Their Implications in Colorectal Cancer Microenvironment: Insights Into Tumor Progression and Therapeutic Opportunities1
The Correlation and Clinicopathological Significance of TNFAIP8L3 and RAC1 Expression in Lung Adenocarcinoma1
Upregulated Expression of SHMT2 Predicts Poor Survival of Lung Adenocarcinoma1
Two Novel FBN2 Variants Causing Congenital Contractural Arachnodactyly1
Lifestyle Modify Optic Nerve Injury in Mendelian Randomization1
Identification of ECI2 as Potential Prognostic Biomarkers Based on a Fatty Acid Metabolism‐Related Gene Model in Clear Cell Renal Cell Carcinoma1
Analysis of Bladder Cancer Staging Prediction Using Deep Residual Neural Network, Radiomics, and RNA-Seq from High-Definition CT Images1
Identification and Validation of Mitophagy‐Related Biomarkers in Colorectal Cancer: An Integrated Analysis of Single‐Cell Transcriptome and Mendelian Randomization1
Genetic Insights Into Type 2 Diabetes Mellitus Susceptibility: A Case‐Control Study of the ADIPOQ rs1501299 Polymorphism in the Population of Noakhali Re0
HRD‐Driven Reprogramming of Macrophage Function and Spatial Architecture in High‐Grade Serous Ovarian Cancer0
Investigating the Causality and Pathogenesis of Primary Sclerosing Cholangitis in Colorectal Cancer Through Mendelian Randomization and Bioinformatics0
Exploring Genetic Markers for Cold–Heat Patterns: Integrating Traditional Medicine With Modern Genomic Research0
Correction to “ BRCA1 Exon 11 Mutations in Breast Cancer: A Study From Pakistan”0
Identification of Ferroptosis‐Related Genes Associated With Cryptorchidism via Bioinformatics and Experimental Verification0
Association of the rs688 Polymorphism in the Gene Encoding Low‐Density Lipoprotein Receptor in Bangladeshi Population With Coronary Artery Disease0
Investigating the Causal Relationship and Shared Genetic Basis Between Major Depression Disorder and Eight Types of Gastrointestinal Diseases0
Association Between rs920778 Polymorphisms and Cancer Risk: An Updated Meta‐Analysis0
Identification and Validation of Cytotoxicity‐Related Features to Predict Prognostic and Immunotherapy Response in Patients with Clear Cell Renal Cell Carcinoma0
Elucidating the Role of THPO and Related Molecular Markers in Lymph Node Metastasis and Prognosis of Gastric Cancer: Insights From TCGA Data Analysis0
Biological Context–Informed and Population‐Stratified Strategies Improve Genetic Diagnosis of CCDC22 ‐Related Disorder0
Predicting the Impact of Deleterious Single‐Nucleotide Polymorphisms in the p47ING1a Isoform of Human ING1 Gene0
Molecular Profiling of Germline Variants in the DNA Mismatch Repair Genes in Chinese Colorectal Cancer Patients0
0
Methylation Landscapes of Cartilage in Hip Osteoarthritis0
Impact of Extracellular Matrix‐Related Genes on the Tumor Microenvironment and Prognostic Indicators in Esophageal Cancer: A Comprehensive Analytical Study0
Exploring Deleterious Nonsynonymous SNPs in the ACADM Gene: Insights Into Medium‐Chain Acyl‐CoA Dehydrogenase Deficiency (MCADD) via In Silico Analysis0
STOML2 Alleviates Osteoarthritis by Regulating Mitochondrial Energy Metabolism and Oxidative Stress0
EMP3 Expression in HER2‐Enriched Breast Cancer is Linked to PI3K/AKT Signaling and Indicates Poor Prognosis0
0
Clinical and Genetic Profiles of 11 Chinese Patients With Angelman Syndrome0
A Truncating Variant in the ERCC6 Gene With Three Different Phenotypes: Significant Effects of Modifier Genes0
Causal Association Between 12 Micronutrients and Common Chronic Respiratory Diseases: A Bidirectional Two‐Sample Mendelian Randomization Study0
Early Onset High Myopia and Severe Anisometropia Associated With Familial Exudative Vitreoretinopathy of Irregular Dominant Inheritance in 11 Chinese Families: Analysis of Refraction Features and Path0
Fujian Province β‐Thalassemia: A Molecular and Hematological Study in Southeastern China0
In Silico Identification and Functional Impact of Deleterious Nonsynonymous Single‐Nucleotide Polymorphisms (nsSNPs) in Type 2 Diabetes–Associated Genes in South Asian Populations0
Corrigendum to “Association Between rs920778 Polymorphisms and Cancer Risk: An Updated Meta‐Analysis”0
Compound Heterozygous ATM Variants Cause Adolescent‐Onset Cerebellar and Extrapyramidal Disease Without Telangiectasia in a Consanguineous Pakistani Family0
Common Genetic Variants in TRIO Are Associated With Autism in Chinese Han Population0
PANoptosis‐Related Diagnostic Biomarkers in Non‐Neovascular Age‐Related Macular Degeneration: An Integrative Transcriptomic and Experimental Study0
A Preliminary Study on Transcriptional Regulation of SNP Site C‐1888T in the Promoter Region of Human PLUNC Gene and Nasopharyngeal Carcinoma Susceptibility0
CDC20 Regulates the Progression of Clear Cell Renal Cell Carcinoma via the Wnt/β‐Catenin Signaling Pathway0
Association of IRX6 rs6499755 and HAAO rs3816183 Polymorphisms With Hypospadias Susceptibility in Northern0
The Evolution of Gene Sequencing Technologies: Unveiling Genetic Architecture of Nonsyndromic Orofacial Clefts0
BRCA1 Exon 11 Mutations in Breast Cancer: A Study From Pakistan0
Genomic Structural Equation Modeling Combined With Post‐GWAS Analysis Identifies Two Risk Gene Loci and Functionally Sensitive Genes Associated With Cardiac Conduction Block0
Single‐Cell Transcriptomics and Integrated Bioinformatic Analysis Reveal Critical Biomarkers and Immune Infiltration Characteristics in Osteoarthritis0
Frequency and Distribution of Incidental Chromosomal Abnormalities Detected by Peripheral Blood Karyotyping: A Retrospective Study0
Comprehensive Genetic Testing for Clinical Decision‐Making in a Patient With Congenital Hyperinsulinism0
Development of a Multilayered Prognostic Model for Wilms’ Tumor Based on Characteristic Lymphocyte Genes0
Identification of Genetic Diagnostic Markers for Systemic Lupus Erythematosus0
Lipids and Lipid‐Lowering Drugs With Risk of Intervertebral Disc Degeneration: A Mendelian Randomization Study0
Investigating the Prognostic and Oncogenic Roles of Membrane‐Associated Ring‐CH‐Type Finger 9 in Colorectal Cancer0
Unveiling Hidden Genetic Architectures: Molecular Diagnostic Yield of Whole Exome Sequencing in 50 Children With Autism Spectrum Disorder Negative for Copy Number Variations0
Identification of Coagulation and Fibrinolysis‐Associated Biomarkers With Implications for Preeclampsia0
Pivotal Role of FBXW4 in Glioma Progression and Prognosis0
49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes0
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