Hubert Smeets
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
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- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- Hedgehog Signaling Pathway Studies
- Epigenetics and DNA Methylation
Papers in
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- Mitochondrial Function and Pathology 3
- RNA modifications and cancer 2
- Ion channel regulation and function 1
- Co-authors
- I.F.M. de Coo (3 shared papers)Francisca Díaz (2 shared papers)Michele Rana (2 shared papers)Carlos T. Moraes (2 shared papers)Rogier Q. Hintzen (1 shared paper)Wim J. Sluiter (1 shared paper)Alexandra T.M. Hendrickx (1 shared paper)Anneke Maat‐Kievit (1 shared paper)
- Journals
- Human Mutation (2 papers)Annals of Neurology (2 papers)Nucleic Acids Research (1 paper)Frontiers in Pharmacology (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- NetherlandsUnited StatesBelgium
In The Last Decade
Hubert Smeets
9 papers receiving 303 citations
Peers
Comparison fields: 5 of 49
- Clinical Biochemistry 64
- Molecular Biology 251
- Developmental Biology 8
- Cancer Research 30
- Immunology 39
Countries citing papers authored by Hubert Smeets
This map shows the geographic impact of Hubert Smeets'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 Hubert Smeets with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hubert Smeets more than expected).
Fields of papers citing papers by Hubert Smeets
This network shows the impact of papers produced by Hubert Smeets. 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 Hubert Smeets. The network helps show where Hubert Smeets may publish in the future.
Co-authors
The 25 scholars most cited alongside Hubert Smeets, 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 | 2000 | 105 | |
| 2 | 2009 | 70 | |
| 3 | 2015 | 56 | |
| 4 | 2007 | 41 | |
| 5 | 2020 | 23 | |
| 6 | 2003 | 5 | |
| 7 | 2000 | 4 | |
| 8 | DNA microarrays as a method to monitor changes in mitochondria-related gene expression in patients with OXPHOS defects and/or mitochondrial cardiomyopathy | 2001 | 2 |
| 9 | 2021 | 2 |
About Hubert Smeets
Hubert Smeets is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Cardiology and Cardiovascular Medicine and Developmental Biology, having authored 9 papers that have together received 308 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (3 papers), RNA modifications and cancer (2 papers), Metalloenzymes and iron-sulfur proteins (1 paper), Cardiac electrophysiology and arrhythmias (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Immunotherapy and Immune Responses (1 paper), Ion channel regulation and function (1 paper) and T-cell and B-cell Immunology (1 paper). The work is most often cited by research in Clinical Biochemistry (64 citations), Molecular Biology (251 citations), Developmental Biology (8 citations), Cancer Research (30 citations) and Immunology (39 citations). Hubert Smeets has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include I.F.M. de Coo, Francisca Díaz, Michele Rana, Carlos T. Moraes, Rogier Q. Hintzen, Wim J. Sluiter, Alexandra T.M. Hendrickx, Anneke Maat‐Kievit, Liesbeth Spruijt and Kees Schoonderwoerd. Their work appears in journals such as Human Mutation, Annals of Neurology, Nucleic Acids Research, Frontiers in Pharmacology and The American Journal of Human Genetics.
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.