Daniel Nilsson
Impact in
- Epidemiology top 1%
- Trypanosoma species research and implications
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 41
- Genomics and Rare Diseases 21
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 4
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- Hereditary Neurological Disorders 6
- Genetic Neurodegenerative Diseases 6
- Co-authors
- Anna Lindstrand (28 shared papers)Björn Andersson (11 shared papers)Måns Ehrenberg (1 shared paper)Johan Elf (1 shared paper)Tanel Tenson (1 shared paper)Jesper Eisfeldt (16 shared papers)Oliver Mühlemann (1 shared paper)Florian Aeschimann (1 shared paper)
- Journals
- PLoS ONE (7 papers)Human Mutation (4 papers)Neurology Genetics (4 papers)Frontiers in Genetics (4 papers)Clinical Genetics (3 papers)
- Partner nations
- SwedenUnited StatesSwitzerland
In The Last Decade
Daniel Nilsson
90 papers receiving 5.2k citations
Daniel Nilsson's Hit Papers
Peers
Comparison fields: 5 of 127
- Epidemiology 1.7k
- Genetics 1k
- Molecular Biology 1.5k
- Clinical Biochemistry 100
- Parasitology 107
Countries citing papers authored by Daniel Nilsson
This map shows the geographic impact of Daniel Nilsson'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 Daniel Nilsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Nilsson more than expected).
Fields of papers citing papers by Daniel Nilsson
This network shows the impact of papers produced by Daniel Nilsson. 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 Daniel Nilsson. The network helps show where Daniel Nilsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Nilsson, 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 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Genome Sequence of Trypanosoma cruzi , Etiologic Agent of Chagas Disease Hit paper breakdown → | 2005 | 1182 |
| 2 | Comparative Genomics of Trypanosomatid Parasitic Protozoa Hit paper breakdown → | 2005 | 655 |
| 3 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 407 |
| 4 | 2003 | 214 | |
| 5 | 2011 | 193 | |
| 6 | Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients Hit paper breakdown → | 2021 | 187 |
| 7 | 2010 | 154 | |
| 8 | 2017 | 149 | |
| 9 | 2012 | 120 | |
| 10 | 2019 | 112 | |
| 11 | 2013 | 110 | |
| 12 | 2014 | 108 | |
| 13 | 2017 | 91 | |
| 14 | 2016 | 78 | |
| 15 | 2007 | 76 | |
| 16 | 2005 | 71 | |
| 17 | 2007 | 60 | |
| 18 | 2010 | 59 | |
| 19 | 2008 | 58 | |
| 20 | 2016 | 57 |
About Daniel Nilsson
Daniel Nilsson is a scholar working on Genetics, Cellular and Molecular Neuroscience, Epidemiology, Molecular Biology and Urology, having authored 92 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (21 papers), Genomic variations and chromosomal abnormalities (17 papers), Trypanosoma species research and implications (12 papers), Hereditary Neurological Disorders (6 papers), Genetic Neurodegenerative Diseases (6 papers), Genomics and Phylogenetic Studies (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genetic factors in colorectal cancer (3 papers). The work is most often cited by research in Epidemiology (1.7k citations), Genetics (1k citations), Molecular Biology (1.5k citations), Clinical Biochemistry (100 citations) and Parasitology (107 citations). Daniel Nilsson has collaborated with scholars based in Sweden, United States and Switzerland. Frequent co-authors include Anna Lindstrand, Björn Andersson, Måns Ehrenberg, Johan Elf, Tanel Tenson, Jesper Eisfeldt, Oliver Mühlemann, Florian Aeschimann, Michal J. Okoniewski and Hasmik Yepiskoposyan. Their work appears in journals such as PLoS ONE, Human Mutation, Neurology Genetics, Frontiers in Genetics and Clinical 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.