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Z. Grosz · SciRah

Researcher profile · Semantic Scholar

Z. Grosz

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Z. Grosz — researcher profile on SciRah

h-index: 9
Works: 31
Citations: 271

Most-cited papers

Efficacy of nusinersen in type 1, 2 and 3 spinal muscular atrophy: Real world data from Hungarian patients.
L. Szabó, A. Gergely, Rita Jakus, A. Fogarasi +8 more
2020European journal of paediatric neurology55 citations Open access
Semantic Scholar
Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
P. Balicza, Z. Grosz, Michael A. Gonzalez, Renáta Bencsik +7 more
2016Journal of Neurological Sciences39 citations
Semantic Scholar
Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients.
Gyorgy Mate Milley, E. Varga, Z. Grosz, C. Nemes +5 more
2018Neuromuscular Disorders27 citations
Semantic Scholar
Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment
M. Molnár, V. Molnar, M. Fedor, R. Csehi +3 more
2022Frontiers in Psychiatry22 citations Open access
Semantic Scholar
Broadening the phenotype of the TWNK gene associated Perrault syndrome
Bálint Fekete, Klára Pentelényi, G. Rudas, A. Gál +6 more
2019BMC Medical Genetics22 citations Open access
Semantic Scholar
NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement
P. Balicza, Z. Grosz, V. Molnar, Anett Illés +6 more
2018Frontiers in Genetics20 citations Open access
Semantic Scholar
The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials
Anett Illés, Dóra Csabán, Z. Grosz, P. Balicza +6 more
2019Frontiers in Genetics15 citations Open access
Semantic Scholar
Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability
P. Balicza, Renáta Bencsik, A. Lengyel, A. Gál +6 more
2020Neurology: Genetics13 citations Open access
Semantic Scholar
The improvement of motor symptoms in Huntington’s disease during cariprazine treatment
R. Csehi, Viktor Molnar, M. Fedor, Vivien Zsumbera +5 more
2023Orphanet Journal of Rare Diseases11 citations Open access
Semantic Scholar
Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients.
Gyorgy Mate Milley, E. Varga, Z. Grosz, B. Bereznai +6 more
2016Neuromuscular Disorders9 citations
Semantic Scholar
Genetic landscape of early-onset dementia in Hungary
Dóra Csabán, Anett Illés, Tóth Renáta, P. Balicza +8 more
2022Neurological Sciences7 citations Open access
Semantic Scholar
The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer’s Disease
Dóra Csabán, Klára Pentelényi, Renata Toth-Bencsik, Anett Illés +3 more
2021Life7 citations Open access
Semantic Scholar
Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease
A. Gál, Z. Grosz, Beáta Borsos, I. Szatmári +11 more
2021Life5 citations Open access
Semantic Scholar
Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort
Idris János Jimoh, P. Balicza, Tamás Szlepák, Dóra Csabán +7 more
2025Clinical Genetics4 citations Open access
Semantic Scholar
[The transition of children with rare diseases from pediatric to adult care].
M. Molnár, Judit Cs Sági, L. Szabó, Z. Grosz
2022Orvosi Hetilap4 citations Open access
Semantic Scholar
Elevated Urinary Titin in Adult Spinal Muscular Atrophy: A Multicenter, Cross-Sectional Observational Study
Andrea Sipos, Emese Rebeka Ripszám, J. Molnár, Z. Grosz +8 more
2025Neurology International3 citations Open access
Semantic Scholar
[Significance of whole exome sequencing in the diagnostics of rare neurological diseases - own experiences through a case presenting with ataxia].
P. Balicza, Z. Grosz, Renáta Bencsik, Anett Illés +3 more
2018Orvosi Hetilap3 citations Open access
Semantic Scholar
[The long-term follow-up of enzyme replacement treatment in late onset Pompe disease].
M. Molnár, Beáta Boros Oláh, Katalin Várdy Visy, Z. Grosz +7 more
2020Ideggyógyászati Szemle2 citations
Semantic Scholar
Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen’s attitude
P. Balicza, A. Terebessy, Z. Grosz, N. Varga +3 more
2018The EPMA Journal2 citations Open access
Semantic Scholar
[Pompe disease treated with enzyme replacement therapy in pregnancy].
Z. Grosz, K. Várdi, J. Molnár
2020Ideggyógyászati Szemle1 citations
Semantic Scholar
Genetic epidemiology of C9orf72 repeat expansion associated amyotrophic lateral sclerosis in Hungary
Z. Nagy, Adrienn Géresi, Z. Grosz, Barbara Trombitás +8 more
2026Molecular Medicine0 citations Open access
Semantic Scholar
SOD1 Variants in Patients With Amyotrophic Lateral Sclerosis in Central Eastern Europe: From Genetic Testing to SOD1 Targeted Therapy
Magui Khazaal, Paula Stretavská, M. Kuźma-Kozakiewicz, Krzysztof Nieporęcki +17 more
2026European Journal of Neurology0 citations Open access
Semantic Scholar
Nationwide survey and epidemiology of Huntington's disease in Hungary.
A. Gál, Domonkos Traeger, Barbara Trombitás, Lilla Buzai-Kiss +7 more
2026Neuroepidemiology0 citations Open access
Semantic Scholar
The Challenge of Genetic Counselling in Early Onset Parkinsonian Disorders (2621)
M. Molnár, P. Balicza, Dóra Csabán, Viktor Molnar +4 more
2020Neurology0 citations
Semantic Scholar
24th Annual Meeting of the ALPE ADRIA ASSOCIATION OF CARDIOLOGY (AAAC) April 21-23, 2016, Vienna Abstracts
B. Csányi, V. Nagy, L. Haţegan, J. Borbás +15 more
20180 citations
Semantic Scholar
H20 Initiating and setting up a patient advocacy group for huntington’s disease in hungary
Z. Grosz, G. Pék, G. Báthori, J. Molnár
2018Clinical care and clinical services0 citations
Semantic Scholar
Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth patients
E. Varga, Z. Grosz
20160 citations
Semantic Scholar
Genetic Background of the Hereditary Spastic Paraplegia Phenotypes in Hungary (P5.049)
M. Molnár, P. Balicza, Z. Grosz, Michael A. Gonzalez +6 more
2016Neurology0 citations
Semantic Scholar
B28 Combined replication malfunctions in huntington’s disease
Z. Grosz, Danuta Szirmai, Viktória Reményi, Renáta Bencsik +1 more
20160 citations
Semantic Scholar
Neurodegeneration and Brain Iron Accumulation disorders in Hungary: genotype-phenotype analysis (P7.291)
M. Molnár, Z. Grosz, Renáta Bencsik, P. Balicza +4 more
2015Neurology0 citations
Semantic Scholar
Objective Evaluation of Stroke Patients’ Movement
Á. Jobbágy, P. Simon, G. Fazekas, P. Harcos +1 more
20080 citations
Semantic Scholar

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