Author

Maria Judit Molnar

Semmelweis University - Cited by 2,799 - neurology - psychiatry - personalized medicine - genetics

Biography

Dr. Maria Judit Molnar is a renowned researcher and author in the field of Molecular Neurology functioning at the Department of Molecular Neurology Clinic and Research Center, Semmelweis University, Budapest, Hungary.
Title
Cited by
Year
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
B Zurek, K Ellwanger, LELM Vissers, R Schüle, M Synofzik, A Töpf, ...European journal of human genetics 29 (9), 1325-1331, 2021202
44
2021
Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial
J Diaz-Manera, PS Kishnani, H Kushlaf, S Ladha, T Mozaffar, V Straub, ...The Lancet Neurology 20 (12), 1012-1026, 2021202
40
2021
Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double …
B Schoser, M Roberts, BJ Byrne, S Sitaraman, H Jiang, P Laforêt, ...The Lancet Neurology 20 (12), 1027-1037, 202
21
2021
Rare and complex urology: clinical overview of ERN eUROGEN
L Oomen, E Leijte, DE Shilhan, M Battye, D Waltregny, F Van der Aa, ...European Urology 81 (2), 204-212, 2022202
14
2022
Safety and efficacy of leriglitazone for preventing disease progression in men with adrenomyeloneuropathy (ADVANCE): a randomised, double-blind, multi-centre, placebo …
W Köhler, M Engelen, F Eichler, R Lachmann, A Fatemi, J Sampson, ...The Lancet Neurology 22 (2), 127-13, 2023202
6
2023
Mapping of European activities on the integration of sex and gender factors in neurology and neuroscience
NB Hentzen, MT Ferretti, A Santuccione Chadha, J Jaarsma, M De Visser, ...European Journal of Neurology 29 (9), 272-279, 2022202
5
2022
Gender issues during the times of COVID‐19 pandemic
W Grisold, E Moro, MT Ferretti, AH Aamodt, G Arabia, ER Lebedeva, ...European journal of neurology 28 (10), e73, 2021202
5
2021
Polymyositis and rhabdomyolysis caused by hepatocellular carcinoma-Case report and literature review
D Bárdos, MJ Molnár, I Dudás, S Tuza, A Szijártó, O HahnAnnals of Medicine and Surgery 65, 102269, 2021202
4
2021
Solving unsolved rare neurological diseases—a Solve-RD viewpoint
R Schüle, D Timmann, CE Erasmus, J Reichbauer, M Wayand, ...European Journal of Human Genetics 29 (9), 1332-1336, 2021202
4
2021
The role of the rare variants in the genes encoding the alpha-ketoglutarate dehydrogenase in Alzheimer’s disease
D Csaban, K Pentelenyi, R Toth-Bencsik, A Illes, Z Grosz, A Gezsi, ...Life 11 (4), 21, 2021202
3
2021
How to approach a neurogenetics diagnosis in different European countries: The European Academy of Neurology Neurogenetics Panel survey
M Mancuso, H Houlden, MJ Molnar, A Filla, M Breza, H Graessner, ...European journal of neurology 9 (7), 1885-1891, 0
2
2022
New insights of phospholipase A2 associated neurodegeneration phenotype based on the long-term follow-up of a large Hungarian family
New insights of phospholipase A associated neurodegeneration phenotype based on the long-term follow-up of a large Hungarian familyR Toth-Bencsik, P Balicza, ET Varga, A Lengyel, G Rudas, A Gal, ...Frontiers in Genetics 1, 68904, 010
2
2021
Genetic landscape of early-onset dementia in Hungary
D Csaban, A Illes, TB Renata, P Balicza, K Pentelenyi, V Molnar, A Gezsi, ...Neurological Sciences 43 (9), 589-5300, 0
2
2022
A nyelvjáráshoz fűződő földrajzi és nyelvi szempontú attitűdvizsgálat pécsi gimnazisták körében= Geographical and Linguistic Attitude Survey of Dialects Among Grammar School …
M MolnárModern Geográfia 7 (), 87-2, 2022202
1
2022
Real-Life Clinical Experience With Cariprazine: A Systematic Review of Case Studies
R Csehi, ZB Dombi, B Sebe, MJ MolnárFrontiers in Psychiatry 3, 827744, 2022202
1
2022
Hungarian genomic data warehouse supporting the healthy ageing research
V Várhegyi, V Molnár, A Gézsi, P Sárközy, P Antal, MJ MolnárOrvosi Hetilap 62 (27), 079-088, 20220
1
2021
Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease
A Gal, Z Grosz, B Borsos, I Szatmari, A Sebők, L Jávor, V Harmath, ...Life (6), 507, 20220
1
2021
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene
FA Boros, L Szpisjak, R Bozó, E Kelemen, D Zádori, A Salamon, J Danis, ...International Journal of Molecular Sciences 24 (3), 267, 2023202
1
2023

Referred From: https://scholar.google.com/citations?user=JAbZ8kcAAAAJ&hl=en

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Citations 2799
h-index 30
i10-index 72
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