C. Ciobanu

Genotype–Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review

C. Rusu, A. Ivanov, M. Panzaru, 2023, Genes.

Genetic Polymorphisms in a Familial Hypercholesterolemia Population from North-Eastern Europe

E. Cojocaru, F. Mitu, C. Rusu, 2022, Journal of personalized medicine.

Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation

L. Butnariu, C. Rusu, M. Panzaru, 2022, Genes.

Mitochondrial Dysfunction, Oxidative Stress, and Therapeutic Strategies in Diabetes, Obesity, and Cardiovascular Disease

M. Blaj, C. Vlad, I. Luchian, 2023, Antioxidants.

Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome

C. Rusu, A. Ivanov, L. Caba, 2023, International journal of molecular sciences.