Most Cited Articles

Open access

ISSN: 2699-9404

CRISPR–Cas9 Gene Editing: Curing Genetic Diseases by Inherited Epigenetic Modifications

Expert Consensus on the Diagnosis and Treatment of NRG1/2 Gene Fusion Solid Tumors

The Role of the Plasminogen Activator Inhibitor 1 (PAI1) in Ovarian Cancer: Mechanisms and Therapeutic Implications

Laboratory-developed Droplet Digital PCR Assay for Quantification of the JAK2V617F Mutation

The Multifaceted Role of Oxytocinergic System and OXTR Gene

Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives

The Alarming Situation of Highly Pathogenic Avian Influenza Viruses in 2019–2023

Gene Mutations in Gastrointestinal Stromal Tumors: Advances in Treatment and Mechanism Research

Expert Consensus on the Diagnosis and Treatment of FGFR Gene-Altered Solid Tumors

The Role of CRISPR/Cas9 in Revolutionizing Duchenne's Muscular Dystrophy Treatment: Opportunities and Obstacles

Analyzing Cell-free Genomic DNA in Spent Culture Media: Noninvasive Insight into the Blastocysts

Potential Mechanism and Perspectives of Mesenchymal Stem Cell Therapy for Ischemic Stroke: A Review

16S rRNA Sequencing Reveals Alterations of Gut Bacteria in Hirschsprung-Associated Enterocolitis

Human Viral Oncoproteins and Ubiquitin–Proteasome System

Comparing Genomic Profiles of ALK Fusion-Positive and ALK Fusion-Negative Nonsmall Cell Lung Cancer Patients

Genetic Modifications of Developmental Dyslexia and Its Representation Using In Vivo, In Vitro Model

Mesenchymal Stem Cells in Clinical Trials for Immune Disorders

Association of Cytogenetics Aberrations and IGHV Mutations with Outcome in Chronic Lymphocytic Leukemia Patients in a Real-World Clinical Setting

ABO Blood Type and Urinary Bladder Cancer: Phenotype, Genotype, Allelic Association with a Clinical or Histological Stage and Recurrence Rate

Recurrent Cerebral Venous Sinus Thrombosis Occurred in an Acute Lymphoblastic Leukemia Child with Mutated Lipoprotein Lipase Gene during Asparaginase Therapy

Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages

Genomic Landscape Features of Minimally Invasive Adenocarcinoma and Invasive Lung Adenocarcinoma

Prevalence and Associations of Co-occurrence of NFE2L2 Mutations and Chromosome 3q26 Amplification in Lung Cancer

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