Robert Lyle
Impact in
- Genetics top 2%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Developmental Neuroscience top 5%
Papers in
-
- Epigenetics and DNA Methylation 31
- Genomics and Phylogenetic Studies 5
- Genetics 25
- Genomic variations and chromosomal abnormalities 8
- Genetic Associations and Epidemiology 7
- Co-authors
- Stylianos E. Antonarakis (28 shared papers)Samuel Deutsch (9 shared papers)Alexandre Reymond (13 shared papers)Emmanouil T. Dermitzakis (7 shared papers)Gregor D. Gilfillan (7 shared papers)Michele De Palma (2 shared papers)Mario Leonardo Squadrito (2 shared papers)Kristina Gervin (20 shared papers)
- Journals
- Clinical Epigenetics (8 papers)BMC Genomics (6 papers)The American Journal of Human Genetics (4 papers)Genomics (4 papers)Human Mutation (3 papers)
- Partner nations
- NorwaySwitzerlandUnited States
In The Last Decade
Robert Lyle
107 papers receiving 7k citations
Robert Lyle's Hit Papers
Peers
Comparison fields: 5 of 127
- Genetics 1.4k
- Developmental Neuroscience 151
- Molecular Biology 2.9k
- Cancer Research 564
- Public Health, Environmental and Occupational Health 1.1k
Countries citing papers authored by Robert Lyle
This map shows the geographic impact of Robert Lyle'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 Robert Lyle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Lyle more than expected).
Fields of papers citing papers by Robert Lyle
This network shows the impact of papers produced by Robert Lyle. 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 Robert Lyle. The network helps show where Robert Lyle may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Lyle, 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 110 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Chromosome 21 and Down syndrome: from genomics to pathophysiology Hit paper breakdown → | 2004 | 539 |
| 2 | Endogenous RNAs Modulate MicroRNA Sorting to Exosomes and Transfer to Acceptor Cells Hit paper breakdown → | 2014 | 520 |
| 3 | 2005 | 423 | |
| 4 | 1994 | 267 | |
| 5 | 2008 | 237 | |
| 6 | 2005 | 231 | |
| 7 | 2016 | 228 | |
| 8 | 2000 | 225 | |
| 9 | 2012 | 184 | |
| 10 | 2002 | 181 | |
| 11 | 2002 | 177 | |
| 12 | 2007 | 160 | |
| 13 | 2012 | 153 | |
| 14 | 2014 | 144 | |
| 15 | 2006 | 142 | |
| 16 | 2008 | 142 | |
| 17 | 2012 | 136 | |
| 18 | 1995 | 135 | |
| 19 | 2015 | 135 | |
| 20 | 2019 | 135 |
About Robert Lyle
Robert Lyle is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Cancer Research, having authored 110 papers that have together received 7.1k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (31 papers), Down syndrome and intellectual disability research (12 papers), Assisted Reproductive Technology and Twin Pregnancy (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic Associations and Epidemiology (7 papers), Maternal Mental Health During Pregnancy and Postpartum (6 papers), Genomics and Phylogenetic Studies (5 papers) and MicroRNA in disease regulation (5 papers). The work is most often cited by research in Genetics (1.4k citations), Developmental Neuroscience (151 citations), Molecular Biology (2.9k citations), Cancer Research (564 citations) and Public Health, Environmental and Occupational Health (1.1k citations). Robert Lyle has collaborated with scholars based in Norway, Switzerland and United States. Frequent co-authors include Stylianos E. Antonarakis, Samuel Deutsch, Alexandre Reymond, Emmanouil T. Dermitzakis, Gregor D. Gilfillan, Michele De Palma, Mario Leonardo Squadrito, Kristina Gervin, Jane Hewitt and Caroline Baer. Their work appears in journals such as Clinical Epigenetics, BMC Genomics, The American Journal of Human Genetics, Genomics and Human Mutation.
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.