Andrew E. Timms
Impact in
- Developmental Neuroscience top 2%
- Rheumatology top 1%
- Spondyloarthritis Studies and Treatments
Papers in
- Rheumatology 17
- Spondyloarthritis Studies and Treatments 14
- Genetics 27
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 8
- Craniofacial Disorders and Treatments 6
- Co-authors
- Matthew Arthur Brown (18 shared papers)Linda A. Bradbury (12 shared papers)B P Wordsworth (9 shared papers)Andrei Călin (5 shared papers)Steven H. Laval (3 shared papers)Sinead T Brophy (3 shared papers)David R. Beier (7 shared papers)Charles A. Mein (1 shared paper)
- Journals
- The American Journal of Human Genetics (7 papers)Annals of the Rheumatic Diseases (4 papers)Lara D. Veeken (3 papers)Nature Genetics (3 papers)Genetics in Medicine (3 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
Andrew E. Timms
75 papers receiving 4.1k citations
Andrew E. Timms's Hit Papers
Peers
Comparison fields: 5 of 101
- Developmental Neuroscience 167
- Rheumatology 617
- Genetics 1.2k
- Hematology 376
- Pediatrics, Perinatology and Child Health 330
Countries citing papers authored by Andrew E. Timms
This map shows the geographic impact of Andrew E. Timms'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 Andrew E. Timms with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew E. Timms more than expected).
Fields of papers citing papers by Andrew E. Timms
This network shows the impact of papers produced by Andrew E. Timms. 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 Andrew E. Timms. The network helps show where Andrew E. Timms may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew E. Timms, 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 77 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia Hit paper breakdown → | 2011 | 499 |
| 2 | 1998 | 272 | |
| 3 | 2013 | 261 | |
| 4 | 2016 | 223 | |
| 5 | 2001 | 194 | |
| 6 | 2016 | 139 | |
| 7 | 2021 | 138 | |
| 8 | 2019 | 123 | |
| 9 | 2002 | 119 | |
| 10 | 2013 | 114 | |
| 11 | 2004 | 110 | |
| 12 | 2007 | 105 | |
| 13 | 2016 | 104 | |
| 14 | 2018 | 102 | |
| 15 | 2002 | 99 | |
| 16 | 2017 | 95 | |
| 17 | 2016 | 83 | |
| 18 | 2020 | 80 | |
| 19 | 2021 | 73 | |
| 20 | 2019 | 72 |
About Andrew E. Timms
Andrew E. Timms is a scholar working on Rheumatology, Genetics, Pediatrics, Perinatology and Child Health, Nephrology and Hematology, having authored 77 papers that have together received 4.2k indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (14 papers), Spondyloarthritis Studies and Treatments (14 papers), Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Craniofacial Disorders and Treatments (6 papers), Gout, Hyperuricemia, Uric Acid (4 papers), Acute Myeloid Leukemia Research (3 papers) and Retinal Development and Disorders (3 papers). The work is most often cited by research in Developmental Neuroscience (167 citations), Rheumatology (617 citations), Genetics (1.2k citations), Hematology (376 citations) and Pediatrics, Perinatology and Child Health (330 citations). Andrew E. Timms has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Matthew Arthur Brown, Linda A. Bradbury, B P Wordsworth, Andrei Călin, Steven H. Laval, Sinead T Brophy, David R. Beier, Charles A. Mein, Francesco Cucca and Anthony H Barnett. Their work appears in journals such as The American Journal of Human Genetics, Annals of the Rheumatic Diseases, Lara D. Veeken, Nature Genetics and Genetics in 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.