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Challenges in determining the malignant potential of atypical neurofibromas (aNF) using histopathologic features and the potential need for CDKN2A/2B testing: a case report

Genetics in the diagnosis and treatment of cardiovascular diseases

Silent players, loud impact: unveiling the therapeutic potentials of LncRNAs

New approaches and prospects of immunotherapy and gene therapy for prostate cancer

Exploring the comorbidity between internalizing/externalizing dimensions and cognitive disengagement syndrome through twin studies: a narrative review

Molecular basis of neurocognitive dysfunction and psychosis in Alpha-Mannosidosis

An investigation of the anthropometric measurements in males with 47,XXY (Klinefelter Syndrome) from birth to five years of age and the impact of early hormonal treatment (EHT)

Tumor-associated antigen targets for novel immune-based strategies in prostate cancer

Personalised genomic medicine is shaping the future of healthcare

Pathogenic and likely pathogenic germline variation in patients with myeloid malignancies and their unrelated HLA-matched hematopoietic stem cell donors

Multifaceted nature of young-onset diabetes - can genomic medicine improve the precision of diagnosis and management?

What have genetic studies of rare sequence variants taught us about the aetiology of schizophrenia?