Pär Lundin
- Genetics top 1%
- Molecular Biology top 10%
- Plant Science top 5%
- Cancer Research top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Co-authors
- Michael WiglerAnders ZetterbergJennifer TrogeSusanne MånérNicholas E. NavinJames HicksJonathan SebatRobert Lucito
- Topics
- Cancer Genomics and Diagnostics (6 papers)Genomic variations and chromosomal abnormalities (4 papers)Genomics and Rare Diseases (2 papers)
- Partner nations
- SwedenUnited StatesDenmark
In The Last Decade
Pär Lundin
9 papers receiving 2.3k citations
Hit Papers
Peers
Comparison fields: 5 of 105
- Genetics 1.6k
- Molecular Biology 1.3k
- Plant Science 587
- Cancer Research 579
- Pediatrics, Perinatology and Child Health 233
Countries citing papers authored by Pär Lundin
This map shows the geographic impact of Pär Lundin'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 Pär Lundin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pär Lundin more than expected).
Fields of papers citing papers by Pär Lundin
This network shows the impact of papers produced by Pär Lundin. 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 Pär Lundin. The network helps show where Pär Lundin may publish in the future.
Co-authorship network of co-authors of Pär Lundin
This figure shows the co-authorship network connecting the top 25 collaborators of Pär Lundin. A scholar is included among the top collaborators of Pär Lundin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Pär Lundin. Pär Lundin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 54 | |
| 2 | 16 | |
| 3 | 93 | |
| 4 | 18 | |
| 5 | 9 | |
| 6 | 6 | |
| 7 | 367 | |
| 8 | 23 | |
| 9 | Large-Scale Copy Number Polymorphism in the Human Genomebreakdown → | 1763 |
About Pär Lundin
Pär Lundin is a scholar working on Cancer Research, Genetics and Molecular Biology, having authored 9 papers that have together received 2.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (1.6k citations), Cancer Research (579 citations) and Molecular Biology (1.3k citations). Pär Lundin has collaborated with scholars based in Sweden, United States and Denmark. Frequent co-authors include Michael Wigler, Anders Zetterberg, Jennifer Troge, Susanne Månér, Nicholas E. Navin, James Hicks, Jonathan Sebat, Robert Lucito, Barbara J. Trask and Joan Alexander. Their work appears in journals such as Science, Nature Communications and Bioinformatics.
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.