Christopher Scheller
Impact in
- Hematology top 5%
- Acute Myeloid Leukemia Research
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Genetic Mapping and Diversity in Plants and Animals
Papers in
- Genetics 4
- Genetic Associations and Epidemiology 4
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 1
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- Lipid metabolism and biosynthesis 1
- Journals
- Nature Communications (2 papers)Nature (2 papers)CHEST Journal (1 paper)Nature Genetics (1 paper)Genome Medicine (1 paper)
- Partner nations
- United StatesFinland
In The Last Decade
Christopher Scheller
7 papers receiving 2.1k citations
Christopher Scheller's Hit Papers
Peers
Comparison fields: 5 of 103
- Hematology 328
- Genetics 820
- Genetics 220
- Cancer Research 222
- Molecular Biology 681
Countries citing papers authored by Christopher Scheller
This map shows the geographic impact of Christopher Scheller'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 Christopher Scheller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Scheller more than expected).
Fields of papers citing papers by Christopher Scheller
This network shows the impact of papers produced by Christopher Scheller. 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 Christopher Scheller. The network helps show where Christopher Scheller may publish in the future.
No co-authors to show.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Hit paper breakdown → | 2021 | 1281 |
| 2 | Inherited causes of clonal haematopoiesis in 97,691 whole genomes Hit paper breakdown → | 2020 | 544 |
| 3 | 2020 | 161 | |
| 4 | 2018 | 86 | |
| 5 | 2021 | 22 | |
| 6 | 2021 | 22 | |
| 7 | 2019 | 5 |
About Christopher Scheller
Christopher Scheller is a scholar working on Genetics, Biochemistry, Molecular Biology, Hematology and Cancer Research, having authored 7 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), RNA modifications and cancer (2 papers), Genomics and Rare Diseases (2 papers), Acute Myeloid Leukemia Research (1 paper), Lipid metabolism and biosynthesis (1 paper), RNA Research and Splicing (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Hematology (328 citations), Genetics (820 citations), Genetics (220 citations), Cancer Research (222 citations) and Molecular Biology (681 citations). Christopher Scheller has collaborated with scholars based in United States and Finland. Their work appears in journals such as Nature Communications, Nature, CHEST Journal, Nature Genetics and Genome Medicine.
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.