Hamish S. Scott
Impact in
- Hematology top 0.5%
- Acute Myeloid Leukemia Research
-
- Adrenal Hormones and Disorders
- Hormonal Regulation and Hypertension
Papers in
- Hematology 85
- Acute Myeloid Leukemia Research 67
- Chronic Myeloid Leukemia Treatments 24
- Genetics 50
- Myeloproliferative Neoplasms: Diagnosis and Treatment 28
- Genetics and Neurodevelopmental Disorders 17
- Co-authors
- Gordon Smyth (17 shared papers)Stylianos E. Antonarakis (52 shared papers)Jean Luc Michaud (1 shared paper)Pärt Peterson (20 shared papers)Jun Kudoh (17 shared papers)Kai J. E. Krohn (12 shared papers)John J. Hopwood (20 shared papers)Gregory J. Goodall (3 shared papers)
- Journals
- Blood (34 papers)Genomics (16 papers)Human Mutation (14 papers)Leukemia (12 papers)Human Genetics (11 papers)
- Partner nations
- AustraliaUnited StatesSwitzerland
In The Last Decade
Hamish S. Scott
323 papers receiving 17.7k citations
Hamish S. Scott's Hit Papers
Peers
Comparison fields: 5 of 176
- Hematology 2.5k
- Endocrinology, Diabetes and Metabolism 3.0k
- Immunology 3.8k
- Genetics 3.7k
- Cancer Research 1.8k
Countries citing papers authored by Hamish S. Scott
This map shows the geographic impact of Hamish S. Scott'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 Hamish S. Scott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hamish S. Scott more than expected).
Fields of papers citing papers by Hamish S. Scott
This network shows the impact of papers produced by Hamish S. Scott. 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 Hamish S. Scott. The network helps show where Hamish S. Scott may publish in the future.
Co-authors
The 25 scholars most cited alongside Hamish S. Scott, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 337 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Use of within-array replicate spots for assessing differential expression in microarray experiments Hit paper breakdown → | 2005 | 1167 |
| 2 | Positional cloning of the APECED gene Hit paper breakdown → | 1997 | 1158 |
| 3 | 1997 | 601 | |
| 4 | A network-biology perspective of microRNA function and dysfunction in cancer Hit paper breakdown → | 2016 | 570 |
| 5 | Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia Hit paper breakdown → | 2011 | 500 |
| 6 | 2007 | 421 | |
| 7 | 1997 | 277 | |
| 8 | 2004 | 257 | |
| 9 | 2013 | 255 | |
| 10 | 1999 | 244 | |
| 11 | 2000 | 235 | |
| 12 | 2005 | 232 | |
| 13 | 2011 | 231 | |
| 14 | 2008 | 222 | |
| 15 | 2008 | 215 | |
| 16 | 1998 | 210 | |
| 17 | 2000 | 197 | |
| 18 | 2001 | 197 | |
| 19 | 2015 | 183 | |
| 20 | 2007 | 181 |
About Hamish S. Scott
Hamish S. Scott is a scholar working on Hematology, Genetics, Genetics, Endocrinology, Diabetes and Metabolism and Molecular Biology, having authored 337 papers that have together received 18.2k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (67 papers), Adrenal Hormones and Disorders (32 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (28 papers), T-cell and B-cell Immunology (27 papers), Chronic Myeloid Leukemia Treatments (24 papers), Lysosomal Storage Disorders Research (20 papers), Cancer Genomics and Diagnostics (17 papers) and Genetics and Neurodevelopmental Disorders (17 papers). The work is most often cited by research in Hematology (2.5k citations), Endocrinology, Diabetes and Metabolism (3.0k citations), Immunology (3.8k citations), Genetics (3.7k citations) and Cancer Research (1.8k citations). Hamish S. Scott has collaborated with scholars based in Australia, United States and Switzerland. Frequent co-authors include Gordon Smyth, Stylianos E. Antonarakis, Jean Luc Michaud, Pärt Peterson, Jun Kudoh, Kai J. E. Krohn, John J. Hopwood, Gregory J. Goodall, Cameron P. Bracken and Maarit Heino. Their work appears in journals such as Blood, Genomics, Human Mutation, Leukemia and Human Genetics.
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.