Mikael Lindlöf
- Co-authors
- Albert de la ChapelleH KääriäinenEeva‐Marja SankilaPerttì AulaAnna‐Elina LehesjokiAntti UutelaHannu KalimoHannu Somer
- Topics
- Muscle Physiology and Disorders (9 papers)Neurogenetic and Muscular Disorders Research (5 papers)Chronic Myeloid Leukemia Treatments (4 papers)
- Cited by
- GeneticsMolecular Biology
- Partner nations
- FinlandUnited StatesSweden
In The Last Decade
Mikael Lindlöf
21 papers receiving 383 citations
Peers
Comparison fields: 5 of 56
- Molecular Biology 252
- Genetics 113
- Genetics 108
- Cellular and Molecular Neuroscience 56
- Physiology 56
Countries citing papers authored by Mikael Lindlöf
This map shows the geographic impact of Mikael Lindlöf'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 Mikael Lindlöf with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mikael Lindlöf more than expected).
Fields of papers citing papers by Mikael Lindlöf
This network shows the impact of papers produced by Mikael Lindlöf. 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 Mikael Lindlöf. The network helps show where Mikael Lindlöf may publish in the future.
Co-authorship network of co-authors of Mikael Lindlöf
This figure shows the co-authorship network connecting the top 25 collaborators of Mikael Lindlöf. A scholar is included among the top collaborators of Mikael Lindlöf 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 Mikael Lindlöf. Mikael Lindlöf is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 12 | |
| 2 | 1 | |
| 3 | 28 | |
| 4 | 16 | |
| 5 | 16 | |
| 6 | 37 | |
| 7 | 1 | |
| 8 | 1 | |
| 9 | Karyotype and BCR studies after bone marrow transplantation for chronic myeloid leukaemia. | 1 |
| 10 | 7 | |
| 11 | 17 | |
| 12 | 8 | |
| 13 | 2 | |
| 14 | Gene deletions in X-linked muscular dystrophy. | 68 |
| 15 | 17 | |
| 16 | Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq. | 18 |
| 17 | 10 | |
| 18 | 21 | |
| 19 | 67 | |
| 20 | 43 |
About Mikael Lindlöf
Mikael Lindlöf is a scholar working on Genetics, Hematology and Genetics, having authored 21 papers that have together received 392 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (9 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Chronic Myeloid Leukemia Treatments (4 papers). The work is most often cited by research in Genetics (108 citations), Genetics (113 citations) and Molecular Biology (252 citations). Mikael Lindlöf has collaborated with scholars based in Finland, United States and Sweden. Frequent co-authors include Albert de la Chapelle, H Kääriäinen, Eeva‐Marja Sankila, Perttì Aula, Anna‐Elina Lehesjoki, Antti Uutela, Hannu Kalimo, Hannu Somer, H. Lang and Helena Kääriäinen. Their work appears in journals such as Blood, PEDIATRICS and Journal of the Neurological Sciences.
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.