Anna Walentinsson
Impact in
- Genetics top 10%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Nephrology top 10%
- Chronic Kidney Disease and Diabetes
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 3
- Genetic Mapping and Diversity in Plants and Animals 3
- Genetic Associations and Epidemiology 3
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- Genomics and Chromatin Dynamics 5
- Epigenetics and DNA Methylation 3
- RNA modifications and cancer 3
- Co-authors
- Khalil Helou (6 shared papers)Göran Levan (6 shared papers)Claude Szpirer (4 shared papers)Fredrik L. Ståhl (2 shared papers)Hans Jürgen Hedrich (3 shared papers)Olle Nerman (1 shared paper)G�ran Levan (3 shared papers)Lars Agréus (2 shared papers)
- Journals
- European Heart Journal (3 papers)Genes Chromosomes and Cancer (3 papers)Nature (2 papers)Scientific Reports (2 papers)Mammalian Genome (2 papers)
- Partner nations
- SwedenUnited KingdomUnited States
In The Last Decade
Anna Walentinsson
36 papers receiving 1.1k citations
Anna Walentinsson's Hit Papers
Peers
Comparison fields: 5 of 92
- Genetics 366
- Nephrology 65
- Gastroenterology 37
- Cancer Research 84
- Molecular Biology 396
Countries citing papers authored by Anna Walentinsson
This map shows the geographic impact of Anna Walentinsson'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 Anna Walentinsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Walentinsson more than expected).
Fields of papers citing papers by Anna Walentinsson
This network shows the impact of papers produced by Anna Walentinsson. 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 Anna Walentinsson. The network helps show where Anna Walentinsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Walentinsson, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Rare variant contribution to human disease in 281,104 UK Biobank exomes Hit paper breakdown → | 2021 | 341 |
| 2 | 2018 | 162 | |
| 3 | 2023 | 102 | |
| 4 | 2009 | 53 | |
| 5 | 2001 | 52 | |
| 6 | 2018 | 50 | |
| 7 | 2019 | 41 | |
| 8 | 2001 | 27 | |
| 9 | 2001 | 27 | |
| 10 | 2024 | 25 | |
| 11 | 2018 | 25 | |
| 12 | 2001 | 19 | |
| 13 | 2000 | 18 | |
| 14 | Independent amplification of two gene clusters on chromosome 4 in rat endometrial cancer: identification and molecular characterization. | 2001 | 17 |
| 15 | 2020 | 12 | |
| 16 | 2001 | 12 | |
| 17 | 2008 | 10 | |
| 18 | 2024 | 9 | |
| 19 | 2024 | 8 | |
| 20 | 2023 | 8 |
About Anna Walentinsson
Anna Walentinsson is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Cell Biology and Cancer Research, having authored 36 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Chromatin Dynamics (5 papers), Cardiovascular Function and Risk Factors (4 papers), Genomics and Rare Diseases (3 papers), Epigenetics and DNA Methylation (3 papers), RNA modifications and cancer (3 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers) and Genetic Associations and Epidemiology (3 papers). The work is most often cited by research in Genetics (366 citations), Nephrology (65 citations), Gastroenterology (37 citations), Cancer Research (84 citations) and Molecular Biology (396 citations). Anna Walentinsson has collaborated with scholars based in Sweden, United Kingdom and United States. Frequent co-authors include Khalil Helou, Göran Levan, Claude Szpirer, Fredrik L. Ståhl, Hans Jürgen Hedrich, Olle Nerman, G�ran Levan, Lars Agréus, Maria Lagerstrom Fermer and Karin Klinga‐Levan. Their work appears in journals such as European Heart Journal, Genes Chromosomes and Cancer, Nature, Scientific Reports and Mammalian Genome.
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.