Wayne K. Lam
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Clinical Biochemistry top 5%
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 2
-
- Congenital heart defects research 3
- Genomics and Chromatin Dynamics 3
- Advanced biosensing and bioanalysis techniques 1
- Co-authors
- Eamonn Richard Maher (2 shared papers)Wolf Reik (2 shared papers)Maureen Cleary (2 shared papers)Sarah C. Bowdin (1 shared paper)Louise J. Tee (1 shared paper)Anthony A. Fryer (1 shared paper)Fiona MacDonald (1 shared paper)Edward M. Blair (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Neurology (1 paper)The American Journal of Human Genetics (1 paper)Toxicology Letters (1 paper)
- Partner nations
- United KingdomUnited StatesIreland
In The Last Decade
Wayne K. Lam
17 papers receiving 1.2k citations
Wayne K. Lam's Hit Papers
Peers
Comparison fields: 5 of 82
- Genetics 649
- Clinical Biochemistry 81
- Pediatrics, Perinatology and Child Health 182
- Molecular Biology 564
- Psychiatry and Mental health 95
Countries citing papers authored by Wayne K. Lam
This map shows the geographic impact of Wayne K. 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 K. 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 K. Lam more than expected).
Fields of papers citing papers by Wayne K. Lam
This network shows the impact of papers produced by Wayne K. 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 K. Lam. The network helps show where Wayne K. Lam may publish in the future.
Co-authors
The 25 scholars most cited alongside Wayne K. 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
| # | Work | ||
|---|---|---|---|
| 1 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 402 |
| 2 | 2008 | 198 | |
| 3 | 2014 | 134 | |
| 4 | 2017 | 111 | |
| 5 | 2018 | 91 | |
| 6 | 2000 | 58 | |
| 7 | 2019 | 50 | |
| 8 | 2001 | 37 | |
| 9 | 2011 | 35 | |
| 10 | 2019 | 35 | |
| 11 | 2010 | 27 | |
| 12 | 1996 | 26 | |
| 13 | 2022 | 8 | |
| 14 | Tolerance and Safety of Energy-Dense Enteral Formulae for Young Children | 2003 | 7 |
| 15 | 2023 | 5 | |
| 16 | 2024 | 3 | |
| 17 | 2025 | 1 | |
| 18 | 2024 | 0 |
About Wayne K. Lam
Wayne K. Lam is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 18 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (4 papers), Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Chromatin Dynamics (3 papers), Genetic Syndromes and Imprinting (2 papers), Tracheal and airway disorders (2 papers) and Advanced biosensing and bioanalysis techniques (1 paper). The work is most often cited by research in Genetics (649 citations), Clinical Biochemistry (81 citations), Pediatrics, Perinatology and Child Health (182 citations), Molecular Biology (564 citations) and Psychiatry and Mental health (95 citations). Wayne K. Lam has collaborated with scholars based in United Kingdom, United States and Ireland. Frequent co-authors include Eamonn Richard Maher, Wolf Reik, Maureen Cleary, Sarah C. Bowdin, Louise J. Tee, Anthony A. Fryer, Fiona MacDonald, Edward M. Blair, Tim James Cole and Christine Oley. Their work appears in journals such as European Journal of Human Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Neurology, The American Journal of Human Genetics and Toxicology Letters.
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.