Andrea H. Németh
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- Genetic Neurodegenerative Diseases 29
- Cancer Research top 5%
- Molecular Biology top 5%
- Mitochondrial Function and Pathology 19
- Extracellular vesicles in disease 10
- Retinal Development and Disorders 9
- DNA Repair Mechanisms 6
- Neurology top 2%
- Neurological disorders and treatments 12
- Parkinson's Disease Mechanisms and Treatments 6
- Neurology top 5%
- Neurological disorders and treatments 12
- Parkinson's Disease Mechanisms and Treatments 6
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- Genomics and Rare Diseases 8
- Co-authors
- Edit I. BuzásXabier OsteikoetxeaBarbara W. SódarKatalin Szabó-TaylorKrisztina PálócziÁgnes KittelÉva PállingerKrisztina V Vukman
- Partner nations
- United KingdomHungaryUnited States
In The Last Decade
Andrea H. Németh
91 papers receiving 3.1k citations
Hit Papers
Peers
Comparison fields: 5 of 140
- Cellular and Molecular Neuroscience 768
- Cancer Research 558
- Molecular Biology 2.1k
- Neurology 442
- Neurology 231
Countries citing papers authored by Andrea H. Németh
This map shows the geographic impact of Andrea H. Németh'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 Andrea H. Németh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrea H. Németh more than expected).
Fields of papers citing papers by Andrea H. Németh
This network shows the impact of papers produced by Andrea H. Németh. 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 Andrea H. Németh. The network helps show where Andrea H. Németh may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Andrea H. Németh, 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 | 2023 | 5 | |
| 2 | 2023 | 11 | |
| 3 | 2023 | 1 | |
| 4 | 2023 | 10 | |
| 5 | 2022 | 4 | |
| 6 | 2021 | 0 | |
| 7 | 2020 | 9 | |
| 8 | 2019 | 21 | |
| 9 | 2016 | 41 | |
| 10 | 2016 | 46 | |
| 11 | 2015 | 43 | |
| 12 | 2015 | 152 | |
| 13 | 2014 | 38 | |
| 14 | 2014 | 13 | |
| 15 | 2014 | 19 | |
| 16 | 2008 | 71 | |
| 17 | 2005 | 4 | |
| 18 | Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 | 2002 | 3 |
| 19 | Identification and characterisation of the gene for chorea-acanthocytosis. | 2001 | 1 |
| 20 | Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene. | 1999 | 1 |
About Andrea H. Németh
Andrea H. Németh is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 93 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (29 papers), Mitochondrial Function and Pathology (19 papers), Neurological disorders and treatments (12 papers), Extracellular vesicles in disease (10 papers), Retinal Development and Disorders (9 papers), Genomics and Rare Diseases (8 papers), DNA Repair Mechanisms (6 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (768 citations), Cancer Research (558 citations) and Molecular Biology (2.1k citations). Andrea H. Németh has collaborated with scholars based in United Kingdom, Hungary and United States. Frequent co-authors include Edit I. Buzás, Xabier Osteikoetxea, Barbara W. Sódar, Katalin Szabó-Taylor, Krisztina Pálóczi, Ágnes Kittel, Éva Pállinger, Krisztina V Vukman, Lilla Turiák and László Drahos. Their work appears in journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.
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.