Michael J. Lyons
Impact in
- Developmental Neuroscience top 10%
- Williams Syndrome Research
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genomics and Rare Diseases
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 4
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- RNA modifications and cancer 4
- Chromatin Remodeling and Cancer 3
- Congenital heart defects research 3
- Co-authors
- Kenton R. Holden (11 shared papers)Wendy J. Introne (5 shared papers)Emily Chen (5 shared papers)Joan M. Stoler (5 shared papers)Tracy L. Trotter (5 shared papers)Susan A. Berry (5 shared papers)Robert J. Hopkin (5 shared papers)Timothy A. Geleske (5 shared papers)
- Journals
- PEDIATRICS (5 papers)Journal of Child Neurology (4 papers)Genetics in Medicine (2 papers)Journal of Medical Genetics (2 papers)Pediatric Neurology (2 papers)
- Partner nations
- United StatesItalyCanada
In The Last Decade
Michael J. Lyons
37 papers receiving 697 citations
Peers
Comparison fields: 5 of 84
- Developmental Neuroscience 49
- Genetics 302
- Neurology 115
- Clinical Biochemistry 38
- Molecular Biology 301
Countries citing papers authored by Michael J. Lyons
This map shows the geographic impact of Michael J. Lyons'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 Michael J. Lyons with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael J. Lyons more than expected).
Fields of papers citing papers by Michael J. Lyons
This network shows the impact of papers produced by Michael J. Lyons. 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 Michael J. Lyons. The network helps show where Michael J. Lyons may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael J. Lyons, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 117 | |
| 2 | 2020 | 70 | |
| 3 | 1997 | 56 | |
| 4 | 2020 | 55 | |
| 5 | 2017 | 52 | |
| 6 | 2005 | 44 | |
| 7 | 2010 | 40 | |
| 8 | 2009 | 27 | |
| 9 | 2014 | 24 | |
| 10 | 2021 | 24 | |
| 11 | 2014 | 22 | |
| 12 | 2015 | 19 | |
| 13 | 2019 | 18 | |
| 14 | 2008 | 18 | |
| 15 | 2011 | 18 | |
| 16 | 2011 | 17 | |
| 17 | 2015 | 14 | |
| 18 | 2010 | 13 | |
| 19 | 2016 | 11 | |
| 20 | 2022 | 10 |
About Michael J. Lyons
Michael J. Lyons is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Neurology, having authored 41 papers that have together received 737 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (4 papers), Genomics and Rare Diseases (4 papers), Chromatin Remodeling and Cancer (3 papers), Congenital heart defects research (3 papers), Prenatal Screening and Diagnostics (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Developmental Neuroscience (49 citations), Genetics (302 citations), Neurology (115 citations), Clinical Biochemistry (38 citations) and Molecular Biology (301 citations). Michael J. Lyons has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Kenton R. Holden, Wendy J. Introne, Emily Chen, Joan M. Stoler, Tracy L. Trotter, Susan A. Berry, Robert J. Hopkin, Timothy A. Geleske, Angela E. Scheuerle and Rizwan Hamid. Their work appears in journals such as PEDIATRICS, Journal of Child Neurology, Genetics in Medicine, Journal of Medical Genetics and Pediatric Neurology.
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.