Anna Lindstrand
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Molecular Biology top 10%
- Congenital heart defects research
Papers in
- Genetics 53
- Genomic variations and chromosomal abnormalities 32
- Genomics and Rare Diseases 20
- Genetics and Neurodevelopmental Disorders 6
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- Congenital heart defects research 9
- Genomics and Chromatin Dynamics 8
- RNA modifications and cancer 6
- Co-authors
- Ann Nordgren (23 shared papers)Wolfgang Hofmeister (9 shared papers)Maria Pettersson (26 shared papers)Daniel Nilsson (25 shared papers)Raquel Vaz (6 shared papers)Jesper Eisfeldt (28 shared papers)Outi Mäkitie (10 shared papers)Claudia M.B. Carvalho (13 shared papers)
- Journals
- Human Mutation (8 papers)Frontiers in Genetics (6 papers)PLoS ONE (5 papers)Clinical Genetics (5 papers)Scientific Reports (3 papers)
- Partner nations
- SwedenUnited StatesFinland
In The Last Decade
Anna Lindstrand
82 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 98
- Genetics 776
- Molecular Biology 769
- Cell Biology 132
- Cancer Research 105
- Pediatrics, Perinatology and Child Health 105
Countries citing papers authored by Anna Lindstrand
This map shows the geographic impact of Anna Lindstrand'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 Lindstrand with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Lindstrand more than expected).
Fields of papers citing papers by Anna Lindstrand
This network shows the impact of papers produced by Anna Lindstrand. 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 Lindstrand. The network helps show where Anna Lindstrand may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Lindstrand, 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 84 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 98 | |
| 2 | 2016 | 93 | |
| 3 | 2015 | 92 | |
| 4 | 2013 | 89 | |
| 5 | 2019 | 71 | |
| 6 | 2014 | 65 | |
| 7 | 2015 | 61 | |
| 8 | 2010 | 56 | |
| 9 | 2009 | 52 | |
| 10 | 2018 | 47 | |
| 11 | 2013 | 45 | |
| 12 | 2016 | 41 | |
| 13 | 2017 | 37 | |
| 14 | 2019 | 32 | |
| 15 | 2022 | 32 | |
| 16 | 2017 | 31 | |
| 17 | 2014 | 29 | |
| 18 | 2017 | 29 | |
| 19 | 2015 | 28 | |
| 20 | 2016 | 25 |
About Anna Lindstrand
Anna Lindstrand is a scholar working on Genetics, Molecular Biology, Plant Science, Cancer Research and Pathology and Forensic Medicine, having authored 84 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Genomics and Rare Diseases (20 papers), Chromosomal and Genetic Variations (14 papers), Congenital heart defects research (9 papers), Genomics and Chromatin Dynamics (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cancer Genomics and Diagnostics (6 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Genetics (776 citations), Molecular Biology (769 citations), Cell Biology (132 citations), Cancer Research (105 citations) and Pediatrics, Perinatology and Child Health (105 citations). Anna Lindstrand has collaborated with scholars based in Sweden, United States and Finland. Frequent co-authors include Ann Nordgren, Wolfgang Hofmeister, Maria Pettersson, Daniel Nilsson, Raquel Vaz, Jesper Eisfeldt, Outi Mäkitie, Claudia M.B. Carvalho, Britt‐Marie Anderlid and Elisabeth Blennow. Their work appears in journals such as Human Mutation, Frontiers in Genetics, PLoS ONE, Clinical Genetics and Scientific Reports.
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.