Byron Lam

871 citations
32 papers · 632 · h-index 15

Impact in

  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
  • Physiology top 10%
    • Calcium signaling and nucleotide metabolism

Papers in

    • Genetics and Neurodevelopmental Disorders 16
    • Genomics and Rare Diseases 14
    • Cellular transport and secretion 4

Byron Lam

31 papers receiving 615 citations

Peers

Byron Lam
Comparison fields: 5 of 71
  • Genetics 237
  • Physiology 24
  • Clinical Biochemistry 24
  • Cell Biology 61
  • Aging 6
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Citations per field
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Countries citing papers authored by Byron Lam

Since Specialization
Citations

This map shows the geographic impact of Byron 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 Byron Lam with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Byron Lam more than expected).

Fields of papers citing papers by Byron Lam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Byron 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 Byron Lam. The network helps show where Byron Lam may publish in the future.

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All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201980
2 201954
3 202050
4 201943
5 202042
6 201941
7 202136
8 202032
9 202228
10 202027
11 201925
12 202325
13 202119
14 202118
15 202316
16 202213
17 202211
18 20239
19 20239
20 20227

About Byron Lam

Byron Lam is a scholar working on Genetics, Cell Biology, Cellular and Molecular Neuroscience, Molecular Biology and Physiology, having authored 32 papers that have together received 632 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (16 papers), Genomics and Rare Diseases (14 papers), Cellular transport and secretion (4 papers), Hereditary Neurological Disorders (3 papers), Developmental Biology and Gene Regulation (2 papers), Epilepsy research and treatment (1 paper), RNA and protein synthesis mechanisms (1 paper) and Family and Disability Support Research (1 paper). The work is most often cited by research in Genetics (237 citations), Physiology (24 citations), Clinical Biochemistry (24 citations), Cell Biology (61 citations) and Aging (6 citations). Byron Lam has collaborated with scholars based in United States, Italy and Saudi Arabia. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Brain, Orphanet Journal of Rare Diseases and Human Molecular 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.

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