Devon Lamb Thrush
Impact in
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- Metabolism and Genetic Disorders
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- BRCA gene mutations in cancer 2
- Genetic Syndromes and Imprinting 2
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- Congenital heart defects research 3
- Co-authors
- Julie M. Gastier‐Foster (13 shared papers)Caroline Astbury (12 shared papers)Robert E. Pyatt (10 shared papers)Shalini C. Reshmi (9 shared papers)Sayaka Hashimoto (4 shared papers)Sarah Smith (1 shared paper)David H. Miller (1 shared paper)A. E. Harding (1 shared paper)
- Journals
- European Journal of Medical Genetics (4 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)European Journal of Human Genetics (1 paper)Muscle & Nerve (1 paper)Journal of the American College of Cardiology (1 paper)
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Devon Lamb Thrush
19 papers receiving 337 citations
Peers
Comparison fields: 5 of 51
- Clinical Biochemistry 31
- Genetics 122
- Molecular Biology 212
- Cellular and Molecular Neuroscience 54
- Neurology 15
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
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 66 | |
| 2 | 1995 | 63 | |
| 3 | 2011 | 50 | |
| 4 | 2014 | 41 | |
| 5 | 1987 | 30 | |
| 6 | 2012 | 18 | |
| 7 | 2012 | 18 | |
| 8 | 2013 | 17 | |
| 9 | 2013 | 16 | |
| 10 | 2013 | 9 | |
| 11 | 2010 | 8 | |
| 12 | 2020 | 7 | |
| 13 | 2014 | 6 | |
| 14 | 2013 | 6 | |
| 15 | 2019 | 4 | |
| 16 | 2013 | 3 | |
| 17 | 2016 | 3 | |
| 18 | 2013 | 1 | |
| 19 | 2012 | 1 | |
| 20 | 2025 | 0 |
About Devon Lamb Thrush
Devon Lamb Thrush is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Cardiology and Cardiovascular Medicine, having authored 20 papers that have together received 367 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (4 papers), Congenital heart defects research (3 papers), Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), BRCA gene mutations in cancer (2 papers), Autism Spectrum Disorder Research (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Clinical Biochemistry (31 citations), Genetics (122 citations), Molecular Biology (212 citations), Cellular and Molecular Neuroscience (54 citations) and Neurology (15 citations). Devon Lamb Thrush has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Julie M. Gastier‐Foster, Caroline Astbury, Robert E. Pyatt, Shalini C. Reshmi, Sayaka Hashimoto, Sarah Smith, David H. Miller, A. E. Harding, Brian Harding and N. Alsanjari. Their work appears in journals such as European Journal of Medical Genetics, Journal of Neurology Neurosurgery & Psychiatry, European Journal of Human Genetics, Muscle & Nerve and Journal of the American College of Cardiology.
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.