Devon Lamb Thrush
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
-
- Congenital heart defects research
- Muscle Physiology and Disorders
- Epigenetics and DNA Methylation
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 3
- Neurogenetic and Muscular Disorders Research 2
- Genetic Syndromes and Imprinting 2
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- Congenital heart defects research 6
- Muscle Physiology and Disorders 2
- Co-authors
- Julie M. Gastier‐Foster (13 shared papers)Caroline Astbury (12 shared papers)Shalini C. Reshmi (9 shared papers)Robert E. Pyatt (10 shared papers)Sayaka Hashimoto (4 shared papers)Nazar Alsanjari (1 shared paper)Sarah Jane Smith (1 shared paper)Brian N Harding (1 shared paper)
- Journals
- European Journal of Medical Genetics (4 papers)The American Journal of Human Genetics (3 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)Journal of the American College of Cardiology (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Devon Lamb Thrush
22 papers receiving 763 citations
Peers
Comparison fields: 5 of 66
- Genetics 433
- Molecular Biology 474
- Cognitive Neuroscience 104
- Clinical Biochemistry 35
- Cellular and Molecular Neuroscience 65
Countries citing papers authored by Devon Lamb Thrush
This map shows the geographic impact of Devon Lamb Thrush'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 Devon Lamb Thrush with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Devon Lamb Thrush more than expected).
Fields of papers citing papers by Devon Lamb Thrush
This network shows the impact of papers produced by Devon Lamb Thrush. 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 Devon Lamb Thrush. The network helps show where Devon Lamb Thrush may publish in the future.
Co-authors
The 25 scholars most cited alongside Devon Lamb Thrush, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 193 | |
| 2 | 2013 | 139 | |
| 3 | 2010 | 109 | |
| 4 | 2010 | 71 | |
| 5 | 1995 | 66 | |
| 6 | 2011 | 54 | |
| 7 | 2014 | 44 | |
| 8 | 1987 | 32 | |
| 9 | 2013 | 19 | |
| 10 | 2012 | 18 | |
| 11 | 2013 | 18 | |
| 12 | 2012 | 16 | |
| 13 | 2010 | 10 | |
| 14 | 2013 | 9 | |
| 15 | 2020 | 9 | |
| 16 | 2014 | 7 | |
| 17 | 2013 | 6 | |
| 18 | 2016 | 6 | |
| 19 | 2019 | 4 | |
| 20 | 2013 | 3 |
About Devon Lamb Thrush
Devon Lamb Thrush is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Cognitive Neuroscience, having authored 23 papers that have together received 836 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (6 papers), Prenatal Screening and Diagnostics (4 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Muscle Physiology and Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (433 citations), Molecular Biology (474 citations), Cognitive Neuroscience (104 citations), Clinical Biochemistry (35 citations) and Cellular and Molecular Neuroscience (65 citations). Devon Lamb Thrush has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Julie M. Gastier‐Foster, Caroline Astbury, Shalini C. Reshmi, Robert E. Pyatt, Sayaka Hashimoto, Nazar Alsanjari, Sarah Jane Smith, Brian N Harding, C. Mark Wiles and Francesco Scaravilli. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, Journal of Neurology Neurosurgery & Psychiatry, Journal of the American College of Cardiology and Neuromuscular Disorders.
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.