Aniko Gal
26 Üllői Rd
Budapest, BU 1085, Hungary
Budapest, BU 1085, Hungary
Last Updated: 09/26/2026
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Found 39 publications
Mitochondrial DNA Deletions and Plasma GDF-15 Protein Levels Are Linked to Hormonal Dysregulation and Multi-Organ Involvement in Female Reproductive Endocrine Disorders.
Journal: Life (Basel, Switzerland)
Published: October 21, 2025
Discordant findings in genome-wide non-invasive prenatal testing (GW-NIPT) for rare chromosomal abnormalities, adverse pregnancy outcomes, and maternal malignancies: a systematic review and meta-analysis.
Journal: American journal of obstetrics and gynecology
Published: July 10, 2025
Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort.
Journal: Clinical genetics
Published: October 24, 2024
GDF-15 and mtDNA Deletions Are Useful Biomarkers of Mitochondrial Dysfunction in Insulin Resistance and PCOS.
Journal: International journal of molecular sciences
Published: September 02, 2024
Genome-Wide, Non-Invasive Prenatal Testing for rare chromosomal abnormalities: A systematic review and meta-analysis of diagnostic test accuracy.
Journal: PloS one
Published: December 01, 2023
Multilevel evidence of MECP2-associated mitochondrial dysfunction and its therapeutic implications.
Journal: Frontiers in psychiatry
Published: September 24, 2023
MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
Journal: EMBO molecular medicine
Published: April 26, 2023
Answer to Gerber et al. "Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy".
Answer to Gerber et al. "Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy".
Journal: EMBO molecular medicine
Published: May 02, 2022
Genetic landscape of early-onset dementia in Hungary.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 30, 2022
Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease.
Journal: Life (Basel, Switzerland)
Published: March 30, 2021
New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family.
Journal: Frontiers in genetics
Published: November 13, 2020
Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene
Journal: Orvosi hetilap
Published: May 05, 2020
Last Updated: 09/26/2026