Kasper D. Hansen
Impact in
- Molecular Biology top 0.5%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- Gene expression and cancer classification
- RNA Research and Splicing
- Genomics and Phylogenetic Studies
- Cancer Research top 1%
- Cancer-related molecular mechanisms research
Papers in
- Genetics 25
- Genetic Syndromes and Imprinting 11
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 9
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- Epigenetics and DNA Methylation 29
- RNA modifications and cancer 23
- Gene expression and cancer classification 14
- Single-cell and spatial transcriptomics 9
- Genomics and Chromatin Dynamics 9
- Co-authors
- Rafael A. IrizarryAndrew P. FeinbergSandrine DudoitMartin J. AryeeHéctor Corrada BravoChristine Ladd‐AcostaAndrew E. JaffeBen Langmead
- Journals
- Genome biology (11 papers)PLoS Genetics (4 papers)Genome Research (4 papers)Bioinformatics (3 papers)Biostatistics (3 papers)
- Partner nations
- United StatesIcelandGermany
In The Last Decade
Kasper D. Hansen
73 papers receiving 10.5k citations
Hit Papers
Peers
Comparison fields: 5 of 167
- Molecular Biology 8.1k
- Cancer Research 1.5k
- Genetics 2.4k
- Aging 88
- Pediatrics, Perinatology and Child Health 986
Countries citing papers authored by Kasper D. Hansen
This map shows the geographic impact of Kasper D. Hansen'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 Kasper D. Hansen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kasper D. Hansen more than expected).
Fields of papers citing papers by Kasper D. Hansen
This network shows the impact of papers produced by Kasper D. Hansen. 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 Kasper D. Hansen. The network helps show where Kasper D. Hansen may publish in the future.
Co-authors
The 25 scholars most cited alongside Kasper D. Hansen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 1 | |
| 2 | 2024 | 3 | |
| 3 | 2024 | 2 | |
| 4 | 2024 | 1 | |
| 5 | 2023 | 2 | |
| 6 | 2023 | 11 | |
| 7 | 2023 | 25 | |
| 8 | 2022 | 104 | |
| 9 | 2022 | 11 | |
| 10 | 2021 | 9 | |
| 11 | 2021 | 11 | |
| 12 | 2021 | 17 | |
| 13 | 2020 | 6 | |
| 14 | 2019 | 18 | |
| 15 | 2019 | 39 | |
| 16 | 2017 | 61 | |
| 17 | 2016 | 3 | |
| 18 | Preprocessing, normalization and integration of the Illumina HumanMethylationEPIC array with minfi Hit paper breakdown → | 2016 | 508 |
| 19 | Functional normalization of 450k methylation array data improves replication in large cancer studies Hit paper breakdown → | 2014 | 495 |
| 20 | 2012 | 203 |
About Kasper D. Hansen
Kasper D. Hansen is a scholar working on Genetics, Molecular Biology, Medical Laboratory Technology, Cancer Research and Biophysics, having authored 75 papers that have together received 10.6k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (29 papers), RNA modifications and cancer (23 papers), Gene expression and cancer classification (14 papers), Genetic Syndromes and Imprinting (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (9 papers), Single-cell and spatial transcriptomics (9 papers) and Genomics and Chromatin Dynamics (9 papers). The work is most often cited by research in Molecular Biology (8.1k citations), Cancer Research (1.5k citations), Genetics (2.4k citations), Aging (88 citations) and Pediatrics, Perinatology and Child Health (986 citations). Kasper D. Hansen has collaborated with scholars based in United States, Iceland and Germany. Frequent co-authors include Rafael A. Irizarry, Andrew P. Feinberg, Sandrine Dudoit, Martin J. Aryee, Héctor Corrada Bravo, Christine Ladd‐Acosta, Andrew E. Jaffe, Ben Langmead, James Bullard and Elizabeth Purdom. Their work appears in journals such as Genome biology, PLoS Genetics, Genome Research, Bioinformatics and Biostatistics.
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.