Tim Morgan
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms
Papers in
- Genetics 27
- Connective tissue disorders research 19
- Genomics and Rare Diseases 14
- Dermatological and Skeletal Disorders 6
- Genetics and Neurodevelopmental Disorders 3
- Craniofacial Disorders and Treatments 3
- Genomic variations and chromosomal abnormalities 2
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- Congenital limb and hand anomalies 3
- Co-authors
- Stephen P. Robertson (21 shared papers)David Markie (7 shared papers)Andrew J. Sutherland‐Smith (3 shared papers)Mary Jane Gray (2 shared papers)Gregory M. Sawyer (2 shared papers)Bernd Wollnik (2 shared papers)Julian J. Eaton‐Rye (1 shared paper)Shannon Clarke (1 shared paper)
- Journals
- Human Mutation (3 papers)The American Journal of Human Genetics (3 papers)Genes (2 papers)Nature Genetics (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- New ZealandUnited KingdomAustralia
In The Last Decade
Tim Morgan
31 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 74
- Developmental Biology 67
- Developmental Neuroscience 93
- Genetics 619
- Cell Biology 161
- Pediatrics, Perinatology and Child Health 110
Countries citing papers authored by Tim Morgan
This map shows the geographic impact of Tim Morgan'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 Tim Morgan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tim Morgan more than expected).
Fields of papers citing papers by Tim Morgan
This network shows the impact of papers produced by Tim Morgan. 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 Tim Morgan. The network helps show where Tim Morgan may publish in the future.
Co-authors
The 25 scholars most cited alongside Tim Morgan, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 219 | |
| 2 | 2005 | 165 | |
| 3 | 2011 | 161 | |
| 4 | 2008 | 155 | |
| 5 | 2012 | 92 | |
| 6 | 2017 | 79 | |
| 7 | 2015 | 70 | |
| 8 | 2011 | 56 | |
| 9 | 2016 | 51 | |
| 10 | 2008 | 45 | |
| 11 | 2018 | 40 | |
| 12 | 1998 | 38 | |
| 13 | 2011 | 30 | |
| 14 | 2011 | 30 | |
| 15 | 2017 | 26 | |
| 16 | 2012 | 23 | |
| 17 | 2010 | 21 | |
| 18 | 2016 | 20 | |
| 19 | 2017 | 20 | |
| 20 | 2014 | 14 |
About Tim Morgan
Tim Morgan is a scholar working on Genetics, Developmental Biology, Developmental Neuroscience, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 33 papers that have together received 1.4k indexed citations. Recurring topics across this work include Connective tissue disorders research (19 papers), Genomics and Rare Diseases (14 papers), Dermatological and Skeletal Disorders (6 papers), Congenital limb and hand anomalies (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Craniofacial Disorders and Treatments (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Developmental Biology (67 citations), Developmental Neuroscience (93 citations), Genetics (619 citations), Cell Biology (161 citations) and Pediatrics, Perinatology and Child Health (110 citations). Tim Morgan has collaborated with scholars based in New Zealand, United Kingdom and Australia. Frequent co-authors include Stephen P. Robertson, David Markie, Andrew J. Sutherland‐Smith, Mary Jane Gray, Gregory M. Sawyer, Bernd Wollnik, Julian J. Eaton‐Rye, Shannon Clarke, Martin Rachwalski and Martijn H. Breuning. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, Genes, Nature Genetics 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.