Chloe Stutterd
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Ocular Disorders and Treatments
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
Papers in
- Genetics 15
- Genomics and Rare Diseases 9
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 2
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- Fetal and Pediatric Neurological Disorders 3
- Co-authors
- Richard Jacob Leventer (11 shared papers)Miriam Fanjul‐Fernández (5 shared papers)Martin Bruce Delatycki (5 shared papers)George McGillivray (4 shared papers)Zornitza Stark (5 shared papers)Paul J. Lockhart (6 shared papers)Alison Yeung (4 shared papers)Tiong Yang Tan (3 shared papers)
- Journals
- Molecular Genetics and Metabolism (3 papers)Neurology Genetics (3 papers)Human Mutation (3 papers)European Journal of Medical Genetics (3 papers)European Journal of Human Genetics (3 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Chloe Stutterd
42 papers receiving 887 citations
Chloe Stutterd's Hit Papers
Peers
Comparison fields: 5 of 43
- Genetics 252
- Psychiatry and Mental health 130
- Clinical Biochemistry 23
- Pediatrics, Perinatology and Child Health 60
- Cellular and Molecular Neuroscience 29
Countries citing papers authored by Chloe Stutterd
This map shows the geographic impact of Chloe Stutterd'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 Chloe Stutterd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chloe Stutterd more than expected).
Fields of papers citing papers by Chloe Stutterd
This network shows the impact of papers produced by Chloe Stutterd. 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 Chloe Stutterd. The network helps show where Chloe Stutterd may publish in the future.
Co-authors
The 25 scholars most cited alongside Chloe Stutterd, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 95 | |
| 2 | 2014 | 92 | |
| 3 | De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome Hit paper breakdown → | 2024 | 80 |
| 4 | 2020 | 66 | |
| 5 | 2019 | 51 | |
| 6 | 2017 | 46 | |
| 7 | 2020 | 45 | |
| 8 | 2020 | 37 | |
| 9 | 2020 | 29 | |
| 10 | 2020 | 29 | |
| 11 | 2020 | 24 | |
| 12 | 2020 | 23 | |
| 13 | 2024 | 23 | |
| 14 | 2019 | 22 | |
| 15 | 2017 | 20 | |
| 16 | Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications | 2022 | 20 |
| 17 | 2021 | 16 | |
| 18 | 2022 | 16 | |
| 19 | 2022 | 16 | |
| 20 | 2022 | 14 |
About Chloe Stutterd
Chloe Stutterd is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Psychiatry and Mental health, Physiology and Cellular and Molecular Neuroscience, having authored 43 papers that have together received 903 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Epilepsy research and treatment (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Lysosomal Storage Disorders Research (2 papers), Hereditary Neurological Disorders (2 papers) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Genetics (252 citations), Psychiatry and Mental health (130 citations), Clinical Biochemistry (23 citations), Pediatrics, Perinatology and Child Health (60 citations) and Cellular and Molecular Neuroscience (29 citations). Chloe Stutterd has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Richard Jacob Leventer, Miriam Fanjul‐Fernández, Martin Bruce Delatycki, George McGillivray, Zornitza Stark, Paul J. Lockhart, Alison Yeung, Tiong Yang Tan, Dean Phelan and Sebastian Lunke. Their work appears in journals such as Molecular Genetics and Metabolism, Neurology Genetics, Human Mutation, European Journal of Medical 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.