Derek Lim
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Developmental Biology top 10%
Papers in
- Genetics 30
- Genomics and Rare Diseases 13
- Genetic Syndromes and Imprinting 8
- Genetics and Neurodevelopmental Disorders 7
- Connective tissue disorders research 3
- Genomic variations and chromosomal abnormalities 2
- Ocular Disorders and Treatments 2
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- Tuberous Sclerosis Complex Research 4
- Co-authors
- Eamonn Richard Maher (14 shared papers)Louise J. Tee (3 shared papers)John R.W. Yates (1 shared paper)Shanaz S. Pasha (1 shared paper)Christopher Geoffrey Woods (1 shared paper)Wolf Reik (1 shared paper)Esther Meyer (1 shared paper)Fatimah Rahman (1 shared paper)
- Journals
- Journal of Medical Genetics (6 papers)The American Journal of Human Genetics (5 papers)Nature Communications (3 papers)Clinical Epigenetics (2 papers)Human Mutation (2 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Derek Lim
38 papers receiving 2k citations
Derek Lim's Hit Papers
Peers
Comparison fields: 5 of 86
- Genetics 1.2k
- Developmental Biology 23
- Psychiatry and Mental health 185
- Molecular Biology 437
- Pediatrics, Perinatology and Child Health 80
Countries citing papers authored by Derek Lim
This map shows the geographic impact of Derek Lim'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 Derek Lim with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Derek Lim more than expected).
Fields of papers citing papers by Derek Lim
This network shows the impact of papers produced by Derek Lim. 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 Derek Lim. The network helps show where Derek Lim may publish in the future.
Co-authors
The 25 scholars most cited alongside Derek Lim, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 417 |
| 2 | 2009 | 228 | |
| 3 | 2010 | 149 | |
| 4 | 2010 | 137 | |
| 5 | 2017 | 113 | |
| 6 | 2014 | 106 | |
| 7 | 2010 | 96 | |
| 8 | 2018 | 95 | |
| 9 | 2010 | 73 | |
| 10 | 2018 | 65 | |
| 11 | 2019 | 64 | |
| 12 | 2019 | 63 | |
| 13 | 2015 | 56 | |
| 14 | 2009 | 53 | |
| 15 | 2019 | 51 | |
| 16 | 2019 | 49 | |
| 17 | 2021 | 44 | |
| 18 | 2013 | 39 | |
| 19 | 2011 | 34 | |
| 20 | 2018 | 33 |
About Derek Lim
Derek Lim is a scholar working on Genetics, Physiology, Pathology and Forensic Medicine, Psychiatry and Mental health and Molecular Biology, having authored 38 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetic Syndromes and Imprinting (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Tuberous Sclerosis Complex Research (4 papers), Connective tissue disorders research (3 papers), Epilepsy research and treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Ocular Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (1.2k citations), Developmental Biology (23 citations), Psychiatry and Mental health (185 citations), Molecular Biology (437 citations) and Pediatrics, Perinatology and Child Health (80 citations). Derek Lim has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Eamonn Richard Maher, Louise J. Tee, John R.W. Yates, Shanaz S. Pasha, Christopher Geoffrey Woods, Wolf Reik, Esther Meyer, Fatimah Rahman, Fiona MacDonald and Gail A. Kirby. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Nature Communications, Clinical Epigenetics and Human Mutation.
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.