Devon Lamb Thrush
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Metabolism and Genetic Disorders
Papers in ⓘ
- Genetics 12
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 2
- Neurogenetic and Muscular Disorders Research 2
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- Congenital heart defects research 3
- 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)Brian Harding (1 shared paper)N. Alsanjari (1 shared paper)Sarah Smith (1 shared paper)
- Journals
- European Journal of Medical Genetics (4 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)Muscle & Nerve (1 paper)Autism Research (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Devon Lamb Thrush
19 papers receiving 312 citations
Peers
Comparison fields: 5 of 49
- Genetics 141
- Clinical Biochemistry 29
- Molecular Biology 218
- Cellular and Molecular Neuroscience 54
- Genetics 25
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 | 59 | |
| 2 | 1995 | 54 | |
| 3 | 2011 | 46 | |
| 4 | 2014 | 39 | |
| 5 | 1987 | 27 | |
| 6 | 2012 | 17 | |
| 7 | 2012 | 16 | |
| 8 | 2013 | 16 | |
| 9 | 2013 | 14 | |
| 10 | 2013 | 9 | |
| 11 | 2010 | 8 | |
| 12 | 2014 | 6 | |
| 13 | 2013 | 6 | |
| 14 | 2020 | 5 | |
| 15 | 2019 | 4 | |
| 16 | 2016 | 3 | |
| 17 | 2013 | 3 | |
| 18 | 2012 | 1 | |
| 19 | 2013 | 1 |
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 19 papers that have together received 334 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Congenital heart defects research (3 papers), Autism Spectrum Disorder Research (2 papers), Genetic Syndromes and Imprinting (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Genetics (141 citations), Clinical Biochemistry (29 citations), Molecular Biology (218 citations), Cellular and Molecular Neuroscience (54 citations) and Genetics (25 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, Shalini C. Reshmi, Robert E. Pyatt, Sayaka Hashimoto, Brian Harding, N. Alsanjari, Sarah Smith, David H. Miller and F Scaravilli. Their work appears in journals such as European Journal of Medical Genetics, Journal of Neurology Neurosurgery & Psychiatry, Muscle & Nerve, Autism Research and European Journal of Human Genetics.
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.