Michael J. Lyons
Impact in
- Developmental Neuroscience top 10%
- Williams Syndrome Research
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genomics and Rare Diseases
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 4
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- RNA modifications and cancer 4
- Congenital heart defects research 2
- Epigenetics and DNA Methylation 2
- Co-authors
- Kenton R. Holden (11 shared papers)Timothy A. Geleske (5 shared papers)Joan M. Stoler (5 shared papers)Tracy L. Trotter (5 shared papers)Wendy J. Introne (5 shared papers)Susan A. Berry (5 shared papers)Angela E. Scheuerle (5 shared papers)Emily Chen (5 shared papers)
- Journals
- PEDIATRICS (5 papers)Journal of Child Neurology (4 papers)Journal of Medical Genetics (2 papers)Developmental Medicine & Child Neurology (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United StatesGermanyCanada
In The Last Decade
Michael J. Lyons
37 papers receiving 741 citations
Peers
Comparison fields: 5 of 83
- Developmental Neuroscience 49
- Genetics 308
- Neurology 116
- Clinical Biochemistry 29
- Infectious Diseases 74
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 | 125 | |
| 2 | 2020 | 73 | |
| 3 | 1997 | 60 | |
| 4 | 2020 | 57 | |
| 5 | 2010 | 57 | |
| 6 | 2017 | 55 | |
| 7 | 2005 | 47 | |
| 8 | 2009 | 31 | |
| 9 | 2014 | 25 | |
| 10 | 2014 | 24 | |
| 11 | 2021 | 24 | |
| 12 | 2015 | 22 | |
| 13 | 2011 | 20 | |
| 14 | 2008 | 20 | |
| 15 | 2019 | 19 | |
| 16 | 2011 | 17 | |
| 17 | 2015 | 14 | |
| 18 | 2010 | 13 | |
| 19 | 2016 | 12 | |
| 20 | 2022 | 11 |
About Michael J. Lyons
Michael J. Lyons is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Epidemiology, having authored 41 papers that have together received 804 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (4 papers), RNA modifications and cancer (4 papers), Prenatal Screening and Diagnostics (3 papers), Congenital heart defects research (2 papers), Epigenetics and DNA Methylation (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Developmental Neuroscience (49 citations), Genetics (308 citations), Neurology (116 citations), Clinical Biochemistry (29 citations) and Infectious Diseases (74 citations). Michael J. Lyons has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Kenton R. Holden, Timothy A. Geleske, Joan M. Stoler, Tracy L. Trotter, Wendy J. Introne, Susan A. Berry, Angela E. Scheuerle, Emily Chen, Robert J. Hopkin and Barbara R. DuPont. Their work appears in journals such as PEDIATRICS, Journal of Child Neurology, Journal of Medical Genetics, Developmental Medicine & Child Neurology and Genetics in Medicine.
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.