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 2021-11-01 to 2025-11-01.)
ArticleCitations
Comprehensive Analysis of the Mechanism of Anoikis in Hepatocellular Carcinoma2
Causal Association Between 12 Micronutrients and Common Chronic Respiratory Diseases: A Bidirectional Two‐Sample Mendelian Randomization Study1
Identification of ECI2 as Potential Prognostic Biomarkers Based on a Fatty Acid Metabolism‐Related Gene Model in Clear Cell Renal Cell Carcinoma1
Upregulated Expression of SHMT2 Predicts Poor Survival of Lung Adenocarcinoma1
1
The Correlation and Clinicopathological Significance of TNFAIP8L3 and RAC1 Expression in Lung Adenocarcinoma1
Analysis of Bladder Cancer Staging Prediction Using Deep Residual Neural Network, Radiomics, and RNA-Seq from High-Definition CT Images1
In Silico Identification and Functional Impact of Deleterious Nonsynonymous Single‐Nucleotide Polymorphisms (nsSNPs) in Type 2 Diabetes–Associated Genes in South Asian Populations0
Identification and Validation of Cytotoxicity‐Related Features to Predict Prognostic and Immunotherapy Response in Patients with Clear Cell Renal Cell Carcinoma0
Pivotal Role of FBXW4 in Glioma Progression and Prognosis0
Investigating the Causality and Pathogenesis of Primary Sclerosing Cholangitis in Colorectal Cancer Through Mendelian Randomization and Bioinformatics0
Association of IRX6 rs6499755 and HAAO rs3816183 Polymorphisms With Hypospadias Susceptibility in Northern Chinese Han Population0
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49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes0
Impact of Extracellular Matrix‐Related Genes on the Tumor Microenvironment and Prognostic Indicators in Esophageal Cancer: A Comprehensive Analytical Study0
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
Corrigendum to “Association Between rs920778 Polymorphisms and Cancer Risk: An Updated Meta‐Analysis”0
Identification of Coagulation and Fibrinolysis‐Associated Biomarkers With Implications for Preeclampsia0
Elucidating the Role of THPO and Related Molecular Markers in Lymph Node Metastasis and Prognosis of Gastric Cancer: Insights From TCGA Data Analysis0
Fujian Province β‐Thalassemia: A Molecular and Hematological Study in Southeastern China0
Association Between rs920778 Polymorphisms and Cancer Risk: An Updated Meta‐Analysis0
BRCA1 Exon 11 Mutations in Breast Cancer: A Study From Pakistan0
A Preliminary Study on Transcriptional Regulation of SNP Site C‐1888T in the Promoter Region of Human PLUNC Gene and Nasopharyngeal Carcinoma Susceptibility0
Investigating the Prognostic and Oncogenic Roles of Membrane‐Associated Ring‐CH‐Type Finger 9 in Colorectal Cancer0
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