Carolyn Ellaway

4.5k total citations
81 papers, 2.6k citations indexed

About

Carolyn Ellaway is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Carolyn Ellaway has authored 81 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 28 papers in Molecular Biology and 22 papers in Cognitive Neuroscience. Recurrent topics in Carolyn Ellaway's work include Genetics and Neurodevelopmental Disorders (44 papers), Autism Spectrum Disorder Research (22 papers) and Family and Disability Support Research (18 papers). Carolyn Ellaway is often cited by papers focused on Genetics and Neurodevelopmental Disorders (44 papers), Autism Spectrum Disorder Research (22 papers) and Family and Disability Support Research (18 papers). Carolyn Ellaway collaborates with scholars based in Australia, United States and France. Carolyn Ellaway's co-authors include Helen Leonard, John Christodoulou, Sarah Williamson, Nicholas de Klerk, Jenny Downs, David Ravine, Carol Bower, Kingsley Wong, Bruce Bennetts and Crystal L. Laurvick and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Carolyn Ellaway

76 papers receiving 2.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Carolyn Ellaway Australia 29 1.8k 1.1k 959 510 294 81 2.6k
Jonathan Picker United States 24 1.3k 0.7× 670 0.6× 1.0k 1.0× 129 0.3× 115 0.4× 47 2.1k
Peter Huppke Germany 26 2.0k 1.1× 1.3k 1.2× 1.2k 1.3× 443 0.9× 74 0.3× 52 2.8k
Xinhua Bao China 24 864 0.5× 341 0.3× 1.1k 1.1× 133 0.3× 276 0.9× 130 2.0k
Mårten Kyllerman Sweden 34 759 0.4× 291 0.3× 1.2k 1.3× 118 0.2× 517 1.8× 88 3.1k
Aglaia Vignoli Italy 27 859 0.5× 490 0.5× 477 0.5× 158 0.3× 45 0.2× 116 2.2k
Isabelle Gourfinkel‐An France 21 883 0.5× 447 0.4× 955 1.0× 105 0.2× 96 0.3× 45 2.3k
Ryoichi Sakuta Japan 22 408 0.2× 256 0.2× 841 0.9× 87 0.2× 436 1.5× 59 1.7k
Helle Hjalgrim Denmark 23 658 0.4× 670 0.6× 486 0.5× 244 0.5× 31 0.1× 56 1.7k
Domenica Battaglia Italy 27 702 0.4× 288 0.3× 563 0.6× 105 0.2× 101 0.3× 115 2.3k
Danielle M. Andrade Canada 30 717 0.4× 414 0.4× 769 0.8× 33 0.1× 116 0.4× 111 2.5k

Countries citing papers authored by Carolyn Ellaway

Since Specialization
Citations

This map shows the geographic impact of Carolyn Ellaway'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 Carolyn Ellaway with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carolyn Ellaway more than expected).

Fields of papers citing papers by Carolyn Ellaway

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carolyn Ellaway. 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 Carolyn Ellaway. The network helps show where Carolyn Ellaway may publish in the future.

Co-authorship network of co-authors of Carolyn Ellaway

This figure shows the co-authorship network connecting the top 25 collaborators of Carolyn Ellaway. A scholar is included among the top collaborators of Carolyn Ellaway based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Carolyn Ellaway. Carolyn Ellaway is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Nicholls, Kathy, Charles Denaro, Michel Tchan, et al.. (2024). Fabry‐specific treatment in Australia: time to align eligibility criteria with international best practices. Internal Medicine Journal. 54(6). 882–890.
2.
Selvanathan, Arthavan, Nancy van Doorn, Susan Thompson, et al.. (2023). Diagnosis and management of children with McArdle Syndrome (GSD V) in New South Wales. JIMD Reports. 64(5). 327–336. 2 indexed citations
3.
Christodoulou, John, Michelle A. Farrar, Dominic Tilden, et al.. (2023). The collective burden of childhood dementia: a scoping review. Brain. 146(11). 4446–4455. 9 indexed citations
4.
Christodoulou, John, et al.. (2023). Multidisciplinary Management of Rett Syndrome: Twenty Years’ Experience. Genes. 14(8). 1607–1607. 12 indexed citations
5.
Tolun, Adviye Ayper, et al.. (2023). Keeping you on your toes: Smith–Lemli–Opitz Syndrome is an easily missed cause of developmental delays. SHILAP Revista de lepidopterología. 11(2). e6920–e6920. 4 indexed citations
6.
Smith, Nicholas, Alexandra Johnson, Kaustuv Bhattacharya, et al.. (2023). Characterizing Common Phenotypes Across the Childhood Dementia Disorders: A Cross-sectional Study From Two Australian Centers. Pediatric Neurology. 149. 75–83. 2 indexed citations
7.
Ellaway, Carolyn, et al.. (2022). Gene Editing and Rett Syndrome: Does It Make the Cut?. The CRISPR Journal. 5(4). 490–499. 5 indexed citations
8.
Fennell, Andrew, Samuel F. Berkovic, Carolyn Ellaway, et al.. (2022). The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American Journal of Medical Genetics Part A. 188(12). 3432–3447. 12 indexed citations
9.
Ellaway, Carolyn, et al.. (2022). Efficacy and safety of cannabidivarin treatment of epilepsy in girls with Rett syndrome: A phase 1 clinical trial. Epilepsia. 63(7). 1736–1747. 23 indexed citations
10.
Riley, Lisa G., Mark J. Cowley, Velimir Gayevskiy, et al.. (2020). The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease. Genetics in Medicine. 22(7). 1254–1261. 45 indexed citations
11.
Moravej, Hossein, Ruqaiah Altassan, Jaak Jaeken, et al.. (2019). Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients. JIMD Reports. 51(1). 76–81. 10 indexed citations
12.
13.
Šimaitė, Deimantė, Maolian Gong, Franz Rüschendorf, et al.. (2014). Recessive Mutations in PCBD1 Cause a New Type of Early-Onset Diabetes. Diabetes. 63(10). 3557–3564. 39 indexed citations
14.
Downs, Jenny, Kingsley Wong, Madhur Ravikumara, et al.. (2014). Experience of Gastrostomy Using a Quality Care Framework. Medicine. 93(28). e328–e328. 29 indexed citations
15.
Ryan, Monique M., Carolyn Ellaway, David Ketteridge, et al.. (2007). Dietary L-Tyrosine Supplementation in Nemaline Myopathy. Journal of Child Neurology. 23(6). 609–613. 41 indexed citations
16.
Young, Deidra J., Ami Bebbington, Alison Anderson, et al.. (2007). The diagnosis of autism in a female: could it be Rett syndrome?. European Journal of Pediatrics. 167(6). 661–669. 56 indexed citations
17.
Hall, Sonĵa E., et al.. (2006). The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(2). 177–183. 56 indexed citations
18.
Ellaway, Carolyn, Jennifer Peat, Katrina Williams, Helen Leonard, & John Christodoulou. (2001). Medium-term open label trial of L-carnitine in Rett syndrome. Brain and Development. 23. S85–S89. 32 indexed citations
19.
Leonard, Helen, Emma J. Glasson, Sue Fyfe, et al.. (1999). A population‐based approach to the investigation of osteopenia in Rett syndrome. Developmental Medicine & Child Neurology. 41(5). 323–328. 10 indexed citations
20.
Ellaway, Carolyn & John Christodoulou. (1999). Rett syndrome: Clinical update and review of recent genetic advances. Journal of Paediatrics and Child Health. 35(5). 419–426. 22 indexed citations

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.

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