Anders Mälarstig
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Physiology top 1%
- Alzheimer's disease research and treatments
Papers in
- Genetics 71
- Genetic Associations and Epidemiology 65
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 4
- Co-authors
- Anders Hamsten (18 shared papers)Adam S. Butterworth (3 shared papers)Stephen Burgess (2 shared papers)Agneta G Siegbahn (7 shared papers)Simon G. Thompson (1 shared paper)Lars C. Wallentin (5 shared papers)Per Olof Eriksson (10 shared papers)Craig L Hyde (4 shared papers)
- Journals
- Nature Communications (11 papers)Scientific Reports (6 papers)Arteriosclerosis Thrombosis and Vascular Biology (6 papers)Nature Genetics (6 papers)PLoS ONE (5 papers)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Anders Mälarstig
121 papers receiving 13.9k citations
Anders Mälarstig's Hit Papers
Peers
Comparison fields: 5 of 135
- Genetics 5.3k
- Physiology 1.6k
- Psychiatry and Mental health 974
- Hematology 691
- Cardiology and Cardiovascular Medicine 1.2k
Countries citing papers authored by Anders Mälarstig
This map shows the geographic impact of Anders Mälarstig'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 Anders Mälarstig with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anders Mälarstig more than expected).
Fields of papers citing papers by Anders Mälarstig
This network shows the impact of papers produced by Anders Mälarstig. 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 Anders Mälarstig. The network helps show where Anders Mälarstig may publish in the future.
Co-authors
The 25 scholars most cited alongside Anders Mälarstig, 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 128 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | FinnGen provides genetic insights from a well-phenotyped isolated population Hit paper breakdown → | 2023 | 2526 |
| 2 | New insights into the genetic etiology of Alzheimer’s disease and related dementias Hit paper breakdown → | 2022 | 1531 |
| 3 | Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease Hit paper breakdown → | 2009 | 1340 |
| 4 | Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure Hit paper breakdown → | 2020 | 611 |
| 5 | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease Hit paper breakdown → | 2011 | 583 |
| 6 | Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals Hit paper breakdown → | 2020 | 465 |
| 7 | Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets Hit paper breakdown → | 2023 | 446 |
| 8 | Exome-wide association study of plasma lipids in >300,000 individuals Hit paper breakdown → | 2017 | 442 |
| 9 | 2010 | 306 | |
| 10 | 2011 | 301 | |
| 11 | 2009 | 296 | |
| 12 | Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries Hit paper breakdown → | 2021 | 276 |
| 13 | 2017 | 256 | |
| 14 | 2017 | 252 | |
| 15 | 2013 | 248 | |
| 16 | 2016 | 244 | |
| 17 | 2012 | 226 | |
| 18 | 2019 | 205 | |
| 19 | 2016 | 180 | |
| 20 | 2013 | 175 |
About Anders Mälarstig
Anders Mälarstig is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Hematology, Rheumatology and Immunology, having authored 128 papers that have together received 14.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (65 papers), Lipoproteins and Cardiovascular Health (13 papers), Blood Coagulation and Thrombosis Mechanisms (8 papers), Atherosclerosis and Cardiovascular Diseases (8 papers), Dementia and Cognitive Impairment Research (5 papers), BRCA gene mutations in cancer (5 papers), Alzheimer's disease research and treatments (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (5.3k citations), Physiology (1.6k citations), Psychiatry and Mental health (974 citations), Hematology (691 citations) and Cardiology and Cardiovascular Medicine (1.2k citations). Anders Mälarstig has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Anders Hamsten, Adam S. Butterworth, Stephen Burgess, Agneta G Siegbahn, Simon G. Thompson, Lars C. Wallentin, Per Olof Eriksson, Craig L Hyde, Mai-Lis Hellénius and Paul M. Ridker. Their work appears in journals such as Nature Communications, Scientific Reports, Arteriosclerosis Thrombosis and Vascular Biology, 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.