Maria Judit Molnar

11PUBLICATIONS
34CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Obstetrics and gynaecologyNeurology and neuromuscular diseasesGenetics not elsewhere classifiedEpidemiological methods
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Publications (11)

|Jul 28, 2026
Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.

|Nov 27, 2025
Mitochondrial DNA Deletions and Plasma GDF-15 Protein Levels Are Linked to Hormonal Dysregulation and Multi-Organ Involvement in Female Reproductive Endocrine Disorders.

Vera Varhegyi, Barnabas Banfi, Domonkos Trager

|Dec 02, 2023
The improvement of motor symptoms in Huntington's disease during cariprazine treatment.

Reka Csehi, Viktor Molnar, Mariann Fedor

|Jul 03, 2023
AI-based tools for the diagnosis and treatment of rare neurological disorders.

Maria J Molnar, Viktor Molnar

|Feb 11, 2023
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene.

Fanni Annamária Boros, László Szpisjak, Renáta Bozó

|Jun 25, 2022
Genetic landscape of early-onset dementia in Hungary.

Dora Csaban, Anett Illes, Toth-Bencsik Renata

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Frequent Collaborators

1 joint publications

Dorottya Csuka

1 joint publications

Ágnes Szilágyi

1 joint publications

Renáta Bozó

1 joint publications

Dénes Zádori