Niklas Darín
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Mitochondrial Function and Pathology 41
- ATP Synthase and ATPases Research 15
- Muscle Physiology and Disorders 14
- RNA modifications and cancer 7
-
- Metabolism and Genetic Disorders 26
- Co-authors
- M. Tulinius (37 shared papers)Anders Oldfors (44 shared papers)Elisabeth Holme (12 shared papers)Ali‐Reza Moslemi (10 shared papers)T Hallböök (13 shared papers)Kalliopi Sofou (16 shared papers)Björn Andersson (1 shared paper)Per Mårin (1 shared paper)
- Journals
- Neuromuscular Disorders (14 papers)European Journal of Human Genetics (7 papers)European Journal of Paediatric Neurology (7 papers)Journal of Inherited Metabolic Disease (6 papers)Neurology (5 papers)
- Partner nations
- SwedenNetherlandsNorway
In The Last Decade
Niklas Darín
103 papers receiving 5.0k citations
Niklas Darín's Hit Papers
Peers
Comparison fields: 5 of 125
- Clinical Biochemistry 1.1k
- Genetics 599
- Molecular Biology 3.2k
- Behavioral Neuroscience 119
- Endocrine and Autonomic Systems 157
Countries citing papers authored by Niklas Darín
This map shows the geographic impact of Niklas Darín'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 Niklas Darín with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Niklas Darín more than expected).
Fields of papers citing papers by Niklas Darín
This network shows the impact of papers produced by Niklas Darín. 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 Niklas Darín. The network helps show where Niklas Darín may publish in the future.
Co-authors
The 25 scholars most cited alongside Niklas Darín, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 106 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy Hit paper breakdown → | 2011 | 546 |
| 2 | 1992 | 409 | |
| 3 | 2008 | 284 | |
| 4 | 2001 | 282 | |
| 5 | 2007 | 210 | |
| 6 | 2014 | 175 | |
| 7 | 2000 | 148 | |
| 8 | 2002 | 144 | |
| 9 | 2017 | 132 | |
| 10 | 2000 | 117 | |
| 11 | 2013 | 114 | |
| 12 | 2016 | 111 | |
| 13 | 2006 | 97 | |
| 14 | 2009 | 86 | |
| 15 | 2002 | 84 | |
| 16 | 2014 | 84 | |
| 17 | 2006 | 77 | |
| 18 | 2007 | 73 | |
| 19 | 1998 | 71 | |
| 20 | 2009 | 70 |
About Niklas Darín
Niklas Darín is a scholar working on Molecular Biology, Clinical Biochemistry, Cardiology and Cardiovascular Medicine, Cognitive Neuroscience and Genetics, having authored 106 papers that have together received 5.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (41 papers), Metabolism and Genetic Disorders (26 papers), ATP Synthase and ATPases Research (15 papers), Muscle Physiology and Disorders (14 papers), Sleep and Wakefulness Research (12 papers), Cardiomyopathy and Myosin Studies (12 papers), Neurogenetic and Muscular Disorders Research (11 papers) and RNA modifications and cancer (7 papers). The work is most often cited by research in Clinical Biochemistry (1.1k citations), Genetics (599 citations), Molecular Biology (3.2k citations), Behavioral Neuroscience (119 citations) and Endocrine and Autonomic Systems (157 citations). Niklas Darín has collaborated with scholars based in Sweden, Netherlands and Norway. Frequent co-authors include M. Tulinius, Anders Oldfors, Elisabeth Holme, Ali‐Reza Moslemi, T Hallböök, Kalliopi Sofou, Björn Andersson, Per Mårin, Teiko Amemiya and Sverker Jern. Their work appears in journals such as Neuromuscular Disorders, European Journal of Human Genetics, European Journal of Paediatric Neurology, Journal of Inherited Metabolic Disease and Neurology.
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.