Sandra Moore
Impact in
- Genetics top 0.5%
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Chronic Lymphocytic Leukemia Research
- Hematology top 1%
- Chronic Myeloid Leukemia Treatments
- Acute Myeloid Leukemia Research
- Platelet Disorders and Treatments
Papers in
- Genetics 6
- Myeloproliferative Neoplasms: Diagnosis and Treatment 6
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- Acute Myeloid Leukemia Research 3
- Chronic Myeloid Leukemia Treatments 2
- Co-authors
- Benjamin H. Lee (7 shared papers)D. Gary Gilliland (5 shared papers)Ross L. Levine (4 shared papers)Thomas Mercher (4 shared papers)Maricel Gozo (3 shared papers)Elizabeth McDowell (3 shared papers)Gerlinde Wernig (3 shared papers)Yana Pikman (2 shared papers)
- Journals
- Blood (4 papers)Cell stem cell (1 paper)European Journal of Human Genetics (1 paper)Oncogene (1 paper)Journal of Clinical Investigation (1 paper)
- Partner nations
- United StatesGermanySwitzerland
In The Last Decade
Sandra Moore
11 papers receiving 1.8k citations
Sandra Moore's Hit Papers
Peers
Comparison fields: 5 of 66
- Genetics 1.3k
- Hematology 1.0k
- Rheumatology 399
- Molecular Biology 887
- Oncology 238
Countries citing papers authored by Sandra Moore
This map shows the geographic impact of Sandra Moore'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 Sandra Moore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Moore more than expected).
Fields of papers citing papers by Sandra Moore
This network shows the impact of papers produced by Sandra Moore. 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 Sandra Moore. The network helps show where Sandra Moore may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Moore, 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 | MPLW515L Is a Novel Somatic Activating Mutation in Myelofibrosis with Myeloid Metaplasia Hit paper breakdown → | 2006 | 1071 |
| 2 | 2008 | 318 | |
| 3 | 2008 | 108 | |
| 4 | 2009 | 80 | |
| 5 | 2005 | 76 | |
| 6 | 2009 | 61 | |
| 7 | 2015 | 58 | |
| 8 | 2010 | 33 | |
| 9 | 2007 | 11 | |
| 10 | 2022 | 4 | |
| 11 | 2004 | 1 |
About Sandra Moore
Sandra Moore is a scholar working on Genetics, Hematology, Molecular Biology, Rheumatology and Oncology, having authored 11 papers that have together received 1.8k indexed citations. Recurring topics across this work include Myeloproliferative Neoplasms: Diagnosis and Treatment (6 papers), Eosinophilic Disorders and Syndromes (4 papers), Acute Myeloid Leukemia Research (3 papers), Chronic Myeloid Leukemia Treatments (2 papers), Cytokine Signaling Pathways and Interactions (2 papers), Galectins and Cancer Biology (1 paper), Protein Degradation and Inhibitors (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Genetics (1.3k citations), Hematology (1.0k citations), Rheumatology (399 citations), Molecular Biology (887 citations) and Oncology (238 citations). Sandra Moore has collaborated with scholars based in United States, Germany and Switzerland. Frequent co-authors include Benjamin H. Lee, D. Gary Gilliland, Ross L. Levine, Thomas Mercher, Maricel Gozo, Elizabeth McDowell, Gerlinde Wernig, Yana Pikman, Daniel J. DeAngelo and Todd R. Golub. Their work appears in journals such as Blood, Cell stem cell, European Journal of Human Genetics, Oncogene and Journal of Clinical Investigation.
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.