Tracy Dudding‐Byth
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
- Genetics 12
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 3
- Genetic and rare skin diseases. 1
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- Epigenetics and DNA Methylation 2
- Co-authors
- Cheryl Shoubridge (2 shared papers)Benjamin Kamien (3 shared papers)Anna Hackett (4 shared papers)Michael Field (4 shared papers)Kathryn Friend (2 shared papers)William T. Gibson (1 shared paper)Rodney J. Scott (2 shared papers)Michelle C. Ward (1 shared paper)
- Journals
- European Journal of Medical Genetics (2 papers)Human Mutation (2 papers)Clinical Genetics (2 papers)Australian and New Zealand Journal of Obstetrics and Gynaecology (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Tracy Dudding‐Byth
17 papers receiving 280 citations
Peers
Comparison fields: 5 of 56
- Genetics 132
- Aging 4
- Molecular Biology 130
- Pediatrics, Perinatology and Child Health 31
- Health Informatics 2
Countries citing papers authored by Tracy Dudding‐Byth
This map shows the geographic impact of Tracy Dudding‐Byth'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 Tracy Dudding‐Byth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tracy Dudding‐Byth more than expected).
Fields of papers citing papers by Tracy Dudding‐Byth
This network shows the impact of papers produced by Tracy Dudding‐Byth. 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 Tracy Dudding‐Byth. The network helps show where Tracy Dudding‐Byth may publish in the future.
Co-authors
The 25 scholars most cited alongside Tracy Dudding‐Byth, 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 | 2015 | 41 | |
| 2 | 2018 | 35 | |
| 3 | 2016 | 33 | |
| 4 | 2018 | 32 | |
| 5 | 2017 | 26 | |
| 6 | 2018 | 23 | |
| 7 | 2017 | 19 | |
| 8 | A powerful team: the family physician advocating for patients with a rare disease. | 2015 | 17 |
| 9 | 2019 | 14 | |
| 10 | 2021 | 10 | |
| 11 | 2024 | 8 | |
| 12 | 2021 | 7 | |
| 13 | 2015 | 6 | |
| 14 | 2022 | 4 | |
| 15 | 2023 | 3 | |
| 16 | 2022 | 3 | |
| 17 | 2023 | 1 | |
| 18 | 2025 | 0 |
About Tracy Dudding‐Byth
Tracy Dudding‐Byth is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Surgery, having authored 18 papers that have together received 282 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (3 papers), Autism Spectrum Disorder Research (2 papers), Epigenetics and DNA Methylation (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Genetics (132 citations), Aging (4 citations), Molecular Biology (130 citations), Pediatrics, Perinatology and Child Health (31 citations) and Health Informatics (2 citations). Tracy Dudding‐Byth has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Cheryl Shoubridge, Benjamin Kamien, Anna Hackett, Michael Field, Kathryn Friend, William T. Gibson, Rodney J. Scott, Michelle C. Ward, Gemma Poke and Louise Christie. Their work appears in journals such as European Journal of Medical Genetics, Human Mutation, Clinical Genetics, Australian and New Zealand Journal of Obstetrics and Gynaecology and Human Molecular 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.