Mária Judit Molnár
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 17
- Neurology top 5%
- Neurological diseases and metabolism 19
- Neurology top 5%
- Neurological diseases and metabolism 19
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- Genetic Neurodegenerative Diseases 17
- Hereditary Neurological Disorders 12
- Genetics top 5%
- Genomics and Rare Diseases 9
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- Mitochondrial Function and Pathology 28
- ATP Synthase and ATPases Research 11
- RNA modifications and cancer 8
- Co-authors
- Gábor G. KovácsJ. M. SchröderAnikó GálHerbert BudkaPéter DiószeghyKatalin MajtényiJill R. MurrellBernardino Ghetti
- Cited by
- Clinical BiochemistryNeurology
- Partner nations
- HungaryGermanyUnited States
In The Last Decade
Mária Judit Molnár
134 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 132
- Clinical Biochemistry 233
- Neurology 377
- Neurology 183
- Cellular and Molecular Neuroscience 279
- Genetics 161
Countries citing papers authored by Mária Judit Molnár
This map shows the geographic impact of Mária Judit Molnár's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mária Judit Molnár with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mária Judit Molnár more than expected).
Fields of papers citing papers by Mária Judit Molnár
This network shows the impact of papers produced by Mária Judit Molnár. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mária Judit Molnár. The network helps show where Mária Judit Molnár may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Mária Judit Molnár, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 2 | |
| 2 | 2024 | 8 | |
| 3 | 2023 | 4 | |
| 4 | 2023 | 2 | |
| 5 | 2023 | 3 | |
| 6 | 2022 | 5 | |
| 7 | 2021 | 1 | |
| 8 | 2020 | 18 | |
| 9 | 2019 | 15 | |
| 10 | 2018 | 40 | |
| 11 | [Investigation of CNTF, COMT, DDR1, DISC1, DRD2, DRD3, and DTNBP1 candidate genes in schizophrenia: Results from the Hungarian SCHIZOBANK Consortium]. | 2016 | 7 |
| 12 | [Breast cancer: patient care, rehabilitation, psychooncology]. | 2016 | 1 |
| 13 | 2016 | 24 | |
| 14 | 2016 | 6 | |
| 15 | 2013 | 16 | |
| 16 | [The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients]. | 2012 | 2 |
| 17 | [Genetics and present therapy options in Parkinson's disease: a review]. | 2009 | 3 |
| 18 | INCOME OF HOUSEHOLDS WITH CHILDREN AND CHILD POVERTY | 2009 | 1 |
| 19 | 2009 | 89 | |
| 20 | [Hereditary motor and sensory Lom-neuropathy--first Hungarian case report]. | 2007 | 2 |
About Mária Judit Molnár
Mária Judit Molnár is a scholar working on Neurology, Clinical Biochemistry and Neurology, having authored 142 papers that have together received 1.9k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (28 papers), Neurological diseases and metabolism (19 papers), Genetic Neurodegenerative Diseases (17 papers), Metabolism and Genetic Disorders (17 papers), Hereditary Neurological Disorders (12 papers), ATP Synthase and ATPases Research (11 papers), Genomics and Rare Diseases (9 papers) and RNA modifications and cancer (8 papers). The work is most often cited by research in Clinical Biochemistry (233 citations), Neurology (377 citations) and Neurology (183 citations). Mária Judit Molnár has collaborated with scholars based in Hungary, Germany and United States. Frequent co-authors include Gábor G. Kovács, J. M. Schröder, Anikó Gál, Herbert Budka, Péter Diószeghy, Katalin Majtényi, Jill R. Murrell, Bernardino Ghetti, Salvatore Spina and Zoltán Grosz. Their work appears in journals such as PLoS ONE, Neurology and Scientific Reports.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.