Wayne Lam
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 5
- RNA modifications and cancer 2
- Genetics 13
- Genetic Syndromes and Imprinting 4
- Connective tissue disorders research 3
- BRCA gene mutations in cancer 2
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Johanna A. Joyce (2 shared papers)Paul N. Schofield (2 shared papers)Wolf Reik (2 shared papers)Eamonn R. Maher (1 shared paper)Sachiko Oh‐ishi (1 shared paper)Dian Donnai (1 shared paper)Izuho Hatada (1 shared paper)Trevor Cole (1 shared paper)
- Journals
- Journal of Medical Genetics (4 papers)European Journal of Human Genetics (2 papers)The Journal of Urology (2 papers)BMJ Open (1 paper)Familial Cancer (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Wayne Lam
21 papers receiving 705 citations
Peers
Comparison fields: 5 of 74
- Genetics 352
- Pediatrics, Perinatology and Child Health 143
- Molecular Biology 466
- Cell Biology 89
- Endocrinology, Diabetes and Metabolism 77
Countries citing papers authored by Wayne Lam
This map shows the geographic impact of Wayne Lam'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 Wayne Lam with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wayne Lam more than expected).
Fields of papers citing papers by Wayne Lam
This network shows the impact of papers produced by Wayne Lam. 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 Wayne Lam. The network helps show where Wayne Lam may publish in the future.
Co-authors
The 25 scholars most cited alongside Wayne Lam, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 124 | |
| 2 | 1999 | 123 | |
| 3 | 2014 | 88 | |
| 4 | 1997 | 73 | |
| 5 | 2009 | 70 | |
| 6 | 2007 | 50 | |
| 7 | 2017 | 44 | |
| 8 | 2016 | 37 | |
| 9 | 2010 | 21 | |
| 10 | 2008 | 16 | |
| 11 | 2005 | 13 | |
| 12 | 2020 | 10 | |
| 13 | 2008 | 8 | |
| 14 | 2007 | 6 | |
| 15 | 2023 | 6 | |
| 16 | 1998 | 6 | |
| 17 | 2020 | 6 | |
| 18 | 2011 | 5 | |
| 19 | 2009 | 4 | |
| 20 | 2023 | 3 |
About Wayne Lam
Wayne Lam is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Epidemiology, having authored 22 papers that have together received 715 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (4 papers), Connective tissue disorders research (3 papers), Skin and Cellular Biology Research (2 papers), BRCA gene mutations in cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Genetics (352 citations), Pediatrics, Perinatology and Child Health (143 citations), Molecular Biology (466 citations), Cell Biology (89 citations) and Endocrinology, Diabetes and Metabolism (77 citations). Wayne Lam has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Johanna A. Joyce, Paul N. Schofield, Wolf Reik, Eamonn R. Maher, Sachiko Oh‐ishi, Dian Donnai, Izuho Hatada, Trevor Cole, Tsunehiro Mukai and E.R. Maher. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, The Journal of Urology, BMJ Open and Familial Cancer.
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.