Emma Burkitt‐Wright

2.1k total citations
18 papers, 386 citations indexed

About

Emma Burkitt‐Wright is a scholar working on Molecular Biology, Neurology and Epidemiology. According to data from OpenAlex, Emma Burkitt‐Wright has authored 18 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Neurology and 6 papers in Epidemiology. Recurrent topics in Emma Burkitt‐Wright's work include Protein Tyrosine Phosphatases (8 papers), Neurofibromatosis and Schwannoma Cases (6 papers) and Peptidase Inhibition and Analysis (5 papers). Emma Burkitt‐Wright is often cited by papers focused on Protein Tyrosine Phosphatases (8 papers), Neurofibromatosis and Schwannoma Cases (6 papers) and Peptidase Inhibition and Analysis (5 papers). Emma Burkitt‐Wright collaborates with scholars based in United Kingdom, France and Italy. Emma Burkitt‐Wright's co-authors include D. Gareth Evans, Shruti Garg, Bronwyn Kerr, Susan Huson, Jonathan Green, Colin R. Lindsay, Amy Burns, Richard Emsley, Fiona Blackhall and Angeliki Malliri and has published in prestigious journals such as Annals of Oncology, Journal of Autism and Developmental Disorders and Developmental Medicine & Child Neurology.

In The Last Decade

Emma Burkitt‐Wright

17 papers receiving 382 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emma Burkitt‐Wright United Kingdom	10	196	127	85	40	39	18	386
Gabrielle R. Wilson Australia	13	178 0.9×	90 0.7×	59 0.7×	11 0.3×	14 0.4×	18	469
Kit San Yeung Hong Kong	13	252 1.3×	245 1.9×	20 0.2×	12 0.3×	35 0.9×	29	529
Anne‐Sophie Lia France	13	298 1.5×	77 0.6×	85 1.0×	45 1.1×	7 0.2×	40	577
Olga Dratviman‐Storobinsky Israel	15	214 1.1×	82 0.6×	32 0.4×	40 1.0×	31 0.8×	31	509
Dominique J. Verlaan Canada	12	224 1.1×	122 1.0×	327 3.8×	12 0.3×	35 0.9×	13	655
Cristina Domínguez‐González Spain	13	277 1.4×	88 0.7×	101 1.2×	20 0.5×	10 0.3×	80	503
Linda Manwaring United States	8	136 0.7×	175 1.4×	33 0.4×	12 0.3×	13 0.3×	15	374
Sietske H. Kevelam Netherlands	10	283 1.4×	83 0.7×	100 1.2×	6 0.1×	14 0.4×	11	473
Hyon J. Kim South Korea	14	191 1.0×	292 2.3×	39 0.5×	8 0.2×	12 0.3×	28	532
Renske Oegema Netherlands	13	245 1.3×	217 1.7×	37 0.4×	12 0.3×	12 0.3×	21	534

Countries citing papers authored by Emma Burkitt‐Wright

Since Specialization

Citations

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

Fields of papers citing papers by Emma Burkitt‐Wright

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emma Burkitt‐Wright. 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 Emma Burkitt‐Wright. The network helps show where Emma Burkitt‐Wright may publish in the future.

Co-authorship network of co-authors of Emma Burkitt‐Wright

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

All Works

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18 of 18 papers shown

Evans, D. Gareth, et al.. (2024). Six at Sixty. Malignant peripheral nerve sheath tumours in NF1: 20-year review of a highly cited paper. Journal of Medical Genetics. 61(12). 1132–1134. 1 indexed citations

Geoffray, Marie‐Maude, Bruno Falissard, Jonathan Green, et al.. (2021). Autism Spectrum Disorder Symptom Profile Across the RASopathies. Frontiers in Psychiatry. 11. 585700–585700. 17 indexed citations

Pobric, Gorana, Jason R. Taylor, Louise Robinson, et al.. (2021). Cognitive and Electrophysiological Correlates of Working Memory Impairments in Neurofibromatosis Type 1. Journal of Autism and Developmental Disorders. 52(4). 1478–1494. 21 indexed citations

García‐Miñáur, Sixto, Emma Burkitt‐Wright, Alain Verloès, et al.. (2021). European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe. European Journal of Medical Genetics. 65(1). 104371–104371. 5 indexed citations

Édouard, Thomas, Martin Zenker, Ingegerd Östman‐Smith, et al.. (2021). Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey. European Journal of Medical Genetics. 65(1). 104404–104404. 8 indexed citations

Wolf, Cordula M., Martin Zenker, Emma Burkitt‐Wright, et al.. (2021). Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists. European Journal of Medical Genetics. 65(1). 104372–104372. 11 indexed citations

Murphy, Christopher, Grace Vassallo, Emma Burkitt‐Wright, et al.. (2020). A retrospective regional study of aqueduct stenosis and fourth ventricle outflow obstruction in the paediatric complex neurofibromatosis type 1 population; Aetiology, clinical presentation and management. Clinical Neurology and Neurosurgery. 193. 105791–105791. 2 indexed citations

Burkitt‐Wright, Emma, et al.. (2020). Germline and sporadic cancers driven by the RAS pathway: parallels and contrasts. Annals of Oncology. 31(7). 873–883. 34 indexed citations

George, K. Joshi, Emma Burkitt‐Wright, Federico Roncaroli, et al.. (2019). Neurosurgical contribution within a complex NF1 supraregional service. Clinical Neurology and Neurosurgery. 180. 18–24. 2 indexed citations

10.

Walkden, Andrew, Emma Burkitt‐Wright, & Leon Au. (2019). <p>Brittle cornea syndrome: current perspectives [Response to Letter]</p>. Clinical ophthalmology. Volume 13. 1895–1896.

11.

McDonald, Bryan, Manuela Pigors, David P. Kelsell, et al.. (2018). Noonan syndrome with multiple lentigines and associated craniosynostosis. Clinical and Experimental Dermatology. 43(3). 357–359. 8 indexed citations

12.

Garg, Shruti, Amy Burns, Emma Burkitt‐Wright, et al.. (2017). Autism spectrum disorder and other neurobehavioural comorbidities in rare disorders of the Ras/MAPK pathway. Developmental Medicine & Child Neurology. 59(5). 544–549. 45 indexed citations

13.

Burkitt‐Wright, Emma, et al.. (2017). A heterozygous microdeletion of 20p12.2–3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency. American Journal of Medical Genetics Part A. 173(8). 2261–2267. 6 indexed citations

14.

Evans, D. Gareth, Naomi L. Bowers, Emma Burkitt‐Wright, et al.. (2016). Comprehensive RNA Analysis of the NF1 Gene in Classically Affected NF1 Affected Individuals Meeting NIH Criteria has High Sensitivity and Mutation Negative Testing is Reassuring in Isolated Cases With Pigmentary Features Only. EBioMedicine. 7. 212–220. 50 indexed citations

15.

Rauen, Katherine A., Susan Huson, Emma Burkitt‐Wright, et al.. (2014). Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues. American Journal of Medical Genetics Part A. 167(1). 1–10. 36 indexed citations

16.

Rohrbach, Marianne, Helen Spencer, Louise F. Porter, et al.. (2013). ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. Molecular Genetics and Metabolism. 109(3). 289–295. 58 indexed citations

17.

Burkitt‐Wright, Emma, Lisa Bradley, Vivienne McConnell, et al.. (2012). Neonatal lethal Costello syndrome and unusual dinucleotide deletion/insertion mutations in HRAS predicting p.Gly12Val. American Journal of Medical Genetics Part A. 158A(5). 1102–1110. 18 indexed citations

18.

Clayton‐Smith, Jill, Sarah Walters, Emma Hobson, et al.. (2008). Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance. European Journal of Human Genetics. 17(4). 434–443. 64 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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