Chloe Stutterd

1.1k total citations
18 papers, 283 citations indexed

About

Chloe Stutterd is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Chloe Stutterd has authored 18 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Chloe Stutterd's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and RNA modifications and cancer (4 papers). Chloe Stutterd is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and RNA modifications and cancer (4 papers). Chloe Stutterd collaborates with scholars based in Australia, United States and New Zealand. Chloe Stutterd's co-authors include Richard J. Leventer, Martin B. Delatycki, Miriam Fanjul‐Fernández, George McGillivray, Zornitza Stark, Paul J. Lockhart, Alison Yeung, Tiong Yang Tan, Natasha J. Brown and Dean Phelan and has published in prestigious journals such as Nature Communications, Neurology and European Journal of Human Genetics.

In The Last Decade

Chloe Stutterd

18 papers receiving 279 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chloe Stutterd Australia 9 135 109 64 31 30 18 283
Simone Gana Italy 9 151 1.1× 125 1.1× 50 0.8× 25 0.8× 24 0.8× 34 255
Kristin Petras United States 5 189 1.4× 141 1.3× 80 1.3× 48 1.5× 33 1.1× 7 306
Weiyi Mu United States 10 148 1.1× 141 1.3× 35 0.5× 53 1.7× 19 0.6× 28 346
Zhengjun Jia China 9 112 0.8× 106 1.0× 86 1.3× 13 0.4× 29 1.0× 23 262
Talia Dor Israel 7 84 0.6× 165 1.5× 42 0.7× 63 2.0× 17 0.6× 7 346
Mary O’Driscoll United Kingdom 10 87 0.6× 129 1.2× 95 1.5× 15 0.5× 26 0.9× 20 390
Filip Roelens Belgium 10 141 1.0× 160 1.5× 46 0.7× 53 1.7× 34 1.1× 17 346
Francisca Millan United States 11 250 1.9× 261 2.4× 49 0.8× 50 1.6× 18 0.6× 19 479
Audrey Putoux France 11 215 1.6× 236 2.2× 72 1.1× 14 0.5× 36 1.2× 32 369
Wakaba Endo Japan 12 108 0.8× 151 1.4× 66 1.0× 82 2.6× 43 1.4× 38 365

Countries citing papers authored by Chloe Stutterd

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Chloe Stutterd

This figure shows the co-authorship network connecting the top 25 collaborators of Chloe Stutterd. A scholar is included among the top collaborators of Chloe Stutterd 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 Chloe Stutterd. Chloe Stutterd is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
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
2.
Luke, Joanne, Philippa Dalach, Ravi Savarirayan, et al.. (2022). Investigating disparity in access to Australian clinical genetic health services for Aboriginal and Torres Strait Islander people. Nature Communications. 13(1). 4966–4966. 11 indexed citations
3.
Stutterd, Chloe, Alexa Kidd, Chris Florkowski, et al.. (2021). Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations. American Journal of Medical Genetics Part A. 185(10). 2941–2950. 2 indexed citations
4.
Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations
5.
Brown, Natasha J., Zimeng Ye, Chloe Stutterd, et al.. (2021). Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome. Molecular Case Studies. 7(6). a006127–a006127. 3 indexed citations
6.
Myers, Kenneth A., Carla Marini, Gemma L. Carvill, et al.. (2021). Phenotypic Spectrum of Seizure Disorders in MBD5-Associated Neurodevelopmental Disorder. Neurology Genetics. 7(2). e579–e579. 13 indexed citations
7.
Braden, Ruth, Chloe Stutterd, Kate Pope, et al.. (2021). Speech, Language, and Oromotor Skills in Patients With Polymicrogyria. Neurology. 96(14). e1898–e1912. 6 indexed citations
8.
Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations
9.
Stutterd, Chloe, Katrien Stouffs, Dana Dumitriu, et al.. (2020). Chudley-McCullough Syndrome: A Recognizable Clinical Entity Characterized by Deafness and Typical Brain Malformations. Journal of Child Neurology. 36(2). 152–158. 4 indexed citations
10.
Stutterd, Chloe, Katrien Stouffs, Miriam Fanjul‐Fernández, et al.. (2020). Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing. Brain Communications. 3(1). fcaa221–fcaa221. 22 indexed citations
11.
Tan, Tiong Yang, Sebastian Lunke, Belinda Chong, et al.. (2019). A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis. European Journal of Human Genetics. 27(12). 1791–1799. 35 indexed citations
12.
Stutterd, Chloe, David Francis, George McGillivray, Paul J. Lockhart, & Richard J. Leventer. (2019). Polymicrogyria associated with 17p13.3p13.2 duplication: Case report and review of the literature. European Journal of Medical Genetics. 63(4). 103774–103774. 6 indexed citations
13.
Yiu, Eppie M., Alison Yeung, Jeremy L. Freeman, et al.. (2019). Hyperinsulinaemic hypoglycaemia: A rare association of vanishing white matter disease. JIMD Reports. 51(1). 11–16. 5 indexed citations
14.
Stutterd, Chloe, George McGillivray, Zornitza Stark, et al.. (2018). Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway. European Journal of Medical Genetics. 61(12). 738–740. 11 indexed citations
15.
Stutterd, Chloe, Nicole J. Lake, Heidi Peters, et al.. (2018). Severe Leukoencephalopathy with Clinical Recovery Caused by Recessive BOLA3 Mutations. JIMD Reports. 43. 63–70. 8 indexed citations
16.
Stutterd, Chloe, Peter Diakumis, Melanie Bahlo, et al.. (2017). Neuropathology of childhood‐onset basal ganglia degeneration caused by mutation of VAC14. Annals of Clinical and Translational Neurology. 4(12). 859–864. 18 indexed citations
17.
Downie, Lilian, et al.. (2017). Advances in genomic testing.. PubMed. 46(4). 200–205. 3 indexed citations
18.
Stutterd, Chloe & Richard J. Leventer. (2014). Polymicrogyria: A common and heterogeneous malformation of cortical development. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(2). 227–239. 76 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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