Genetics Research

Papers
(The median citation count 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 2022-01-01 to 2026-01-01.)
ArticleCitations
Comprehensive Analysis of the Mechanism of Anoikis in Hepatocellular Carcinoma3
The Correlation and Clinicopathological Significance of TNFAIP8L3 and RAC1 Expression in Lung Adenocarcinoma2
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
1
A Cuproptosis‐Related lncRNA Signature Predicts Prognosis and Shapes the Immune Landscape in Primary Lower‐Grade Glioma1
Lifestyle Modify Optic Nerve Injury in Mendelian Randomization1
Investigating the Causal Relationship and Shared Genetic Basis Between Major Depression Disorder and Eight Types of Gastrointestinal Diseases0
Comprehensive Genetic Testing for Clinical Decision‐Making in a Patient With Congenital Hyperinsulinism0
Genetic Insights Into Type 2 Diabetes Mellitus Susceptibility: A Case‐Control Study of the ADIPOQ rs1501299 Polymorphism in the Population of Noakhali Region of Bangladesh0
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 Ferroptosis‐Related Genes Associated With Cryptorchidism via Bioinformatics and Experimental Verification0
In Silico Identification and Functional Impact of Deleterious Nonsynonymous Single‐Nucleotide Polymorphisms (nsSNPs) in Type 2 Diabetes–Associated Genes in South Asian Populations0
Exploring Genetic Markers for Cold–Heat Patterns: Integrating Traditional Medicine With Modern Genomic Research0
Investigating the Prognostic and Oncogenic Roles of Membrane‐Associated Ring‐CH‐Type Finger 9 in Colorectal Cancer0
Impact of Extracellular Matrix‐Related Genes on the Tumor Microenvironment and Prognostic Indicators in Esophageal Cancer: A Comprehensive Analytical Study0
Identification and Validation of Cytotoxicity‐Related Features to Predict Prognostic and Immunotherapy Response in Patients with Clear Cell Renal Cell Carcinoma0
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
Clinical and Genetic Profiles of 11 Chinese Patients With Angelman Syndrome0
Fujian Province β‐Thalassemia: A Molecular and Hematological Study in Southeastern China0
Investigating the Causality and Pathogenesis of Primary Sclerosing Cholangitis in Colorectal Cancer Through Mendelian Randomization and Bioinformatics0
Association Between rs920778 Polymorphisms and Cancer Risk: An Updated Meta‐Analysis0
Elucidating the Role of THPO and Related Molecular Markers in Lymph Node Metastasis and Prognosis of Gastric Cancer: Insights From TCGA Data Analysis0
Common Genetic Variants in TRIO Are Associated With Autism in Chinese Han Population0
A Truncating Variant in the ERCC6 Gene With Three Different Phenotypes: Significant Effects of Modifier Genes0
Association of IRX6 rs6499755 and HAAO rs3816183 Polymorphisms With Hypospadias Susceptibility in Northern Chinese Han Population0
Upregulated Expression of SHMT2 Predicts Poor Survival of Lung Adenocarcinoma0
Causal Association Between 12 Micronutrients and Common Chronic Respiratory Diseases: A Bidirectional Two‐Sample Mendelian Randomization Study0
Development of a Multilayered Prognostic Model for Wilms’ Tumor Based on Characteristic Lymphocyte Genes0
Pivotal Role of FBXW4 in Glioma Progression and Prognosis0
Corrigendum to “Association Between rs920778 Polymorphisms and Cancer Risk: An Updated Meta‐Analysis”0
BRCA1 Exon 11 Mutations in Breast Cancer: A Study From Pakistan0
49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes0
Identification of Coagulation and Fibrinolysis‐Associated Biomarkers With Implications for Preeclampsia0
A Preliminary Study on Transcriptional Regulation of SNP Site C‐1888T in the Promoter Region of Human PLUNC Gene and Nasopharyngeal Carcinoma Susceptibility0
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