Kit Doudney

1.2k total citations
25 papers, 762 citations indexed

About

Kit Doudney is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Kit Doudney has authored 25 papers receiving a total of 762 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Kit Doudney's work include Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Congenital heart defects research (4 papers). Kit Doudney is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Congenital heart defects research (4 papers). Kit Doudney collaborates with scholars based in United Kingdom, New Zealand and United States. Kit Doudney's co-authors include Philip Stanier, Gudrun E. Moore, Andrew J. Copp, Claire Braybrook, Alfreð Árnason, Ana Carolina B. Marçano, Nicholas D. E. Greene, Paul J. Goodfellow, Árni Björnsson and Michael A. Patton and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Kit Doudney

25 papers receiving 742 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kit Doudney United Kingdom 13 500 298 123 117 73 25 762
Monika Cohen Germany 11 551 1.1× 488 1.6× 113 0.9× 55 0.5× 49 0.7× 13 859
Miranda Splitt United Kingdom 15 598 1.2× 435 1.5× 65 0.5× 73 0.6× 173 2.4× 29 1.1k
J. Kunze Germany 14 328 0.7× 226 0.8× 61 0.5× 60 0.5× 56 0.8× 40 577
Pagon Ra United States 6 450 0.9× 260 0.9× 82 0.7× 44 0.4× 55 0.8× 291 791
Annalaura Torella Italy 18 697 1.4× 286 1.0× 103 0.8× 83 0.7× 60 0.8× 77 983
A Nivelon‐Chevallier France 9 339 0.7× 205 0.7× 96 0.8× 133 1.1× 85 1.2× 34 590
Elicia Estrella United States 15 678 1.4× 158 0.5× 88 0.7× 59 0.5× 83 1.1× 28 922
Sı̇bel Aylı̇n Uğur İşerı̇ Türkiye 13 283 0.6× 218 0.7× 103 0.8× 51 0.4× 40 0.5× 39 690
Carol A. Crowe United States 17 582 1.2× 318 1.1× 53 0.4× 100 0.9× 119 1.6× 28 904
Fabiola Quintero‐Rivera United States 16 634 1.3× 907 3.0× 123 1.0× 41 0.4× 99 1.4× 54 1.4k

Countries citing papers authored by Kit Doudney

Since Specialization
Citations

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

Fields of papers citing papers by Kit Doudney

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kit Doudney

This figure shows the co-authorship network connecting the top 25 collaborators of Kit Doudney. A scholar is included among the top collaborators of Kit Doudney 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 Kit Doudney. Kit Doudney 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.
Chan, Christina, Laura M. Belluscio, Kit Doudney, et al.. (2019). Comparing the variants of takotsubo syndrome: an observational study of the ECG and structural changes from a New Zealand tertiary hospital. BMJ Open. 9(5). e025253–e025253. 10 indexed citations
2.
Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 10(3-4). 282–282. 2 indexed citations
3.
Lacey, Cameron, Kit Doudney, Paul Bridgman, et al.. (2018). Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy. Scientific Reports. 8(1). 7548–7548. 7 indexed citations
4.
Chua, Eng Wee, Simone L. Cree, Murray L. Barclay, et al.. (2015). Exome sequencing and array-based comparative genomic hybridisation analysis of preferential 6-methylmercaptopurine producers. The Pharmacogenomics Journal. 15(5). 414–421. 2 indexed citations
5.
6.
Stevens, Aaron J., Simone L. Cree, Andrew Gibb, et al.. (2014). G-Quadruplex Structures and CpG Methylation Cause Drop-Out of the Maternal Allele in Polymerase Chain Reaction Amplification of the Imprinted MEST Gene Promoter. PLoS ONE. 9(12). e113955–e113955. 32 indexed citations
7.
Robinson, Alexis, Sarah Escuin, Kit Doudney, et al.. (2011). Mutations in the planar cell polarity genesCELSR1andSCRIBare associated with the severe neural tube defect craniorachischisis. Human Mutation. 33(2). 440–447. 146 indexed citations
8.
Doudney, Kit, et al.. (2009). Upstream genetic variant nearINSIG2, influences response to carnitine supplementation in bipolar patients with valproate-induced weight gain. Acta Neuropsychiatrica. 21(3). 133–140. 1 indexed citations
9.
Acevedo, Ana Carolina, et al.. (2009). Autosomal-dominant Ankyloglossia and Tooth Number Anomalies. Journal of Dental Research. 89(2). 128–132. 14 indexed citations
10.
Pauws, Erwin, Marius C. Jones, Manvendra K. Singh, et al.. (2007). TBX22 Missense Mutations Found in Patients with X-Linked Cleft Palate Affect DNA Binding, Sumoylation, and Transcriptional Repression. The American Journal of Human Genetics. 81(4). 700–712. 69 indexed citations
11.
Chitty, Lyn S., Katie A. Burren, Kit Doudney, et al.. (2006). Abnormal folate metabolism in foetuses affected by neural tube defects. Brain. 130(4). 1043–1049. 43 indexed citations
12.
Doudney, Kit & Philip Stanier. (2005). Epithelial cell polarity genes are required for neural tube closure. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 135C(1). 42–47. 36 indexed citations
13.
Murdoch, J., Kit Doudney, Dianne Gerrelli, et al.. (2003). Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia. Molecular and Cellular Neuroscience. 22(1). 62–74. 9 indexed citations
14.
Doudney, Kit, J. Murdoch, Claire Braybrook, et al.. (2002). Cloning and Characterization of Igsf9 in Mouse and Human: A New Member of the Immunoglobulin Superfamily Expressed in the Developing Nervous System. Genomics. 79(5). 663–670. 26 indexed citations
15.
Braybrook, Claire, Kit Doudney, Ana Carolina B. Marçano, et al.. (2001). The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia. Nature Genetics. 29(2). 179–183. 206 indexed citations
16.
Doudney, Kit, J. Murdoch, Caroline Paternotte, et al.. (2001). Comparative Physical and Transcript Maps of ∼1 Mb around loop-tail, a Gene for Severe Neural Tube Defects on Distal Mouse Chromosome 1 and Human Chromosome 1q22–q23. Genomics. 72(2). 180–192. 13 indexed citations
17.
Webb, Simon P., Kit Doudney, Mark A. Pook, S. Chamberlain, & Michael Hutchinson. (1999). A family with pseudodominant Friedreich's ataxia showing marked variation of phenotype between affected siblings. Journal of Neurology Neurosurgery & Psychiatry. 67(2). 217–219. 9 indexed citations
18.
Pook, Mark A., Jaime J. Carvajal, Kit Doudney, Renate Hillermann, & Susan Chamberlain. (1997). Exon–Intron Structure of a 2.7-kb Transcript of the STM7 Gene with Phosphatidylinositol-4-phosphate 5-Kinase Activity. Genomics. 42(1). 170–172. 2 indexed citations
19.
Carvajal, Jaime J., Mark A. Pook, Kit Doudney, et al.. (1996). The Friedreich's ataxia gene encodes a novel phosphatidylinositol–4–phosphate 5–kinase. Nature Genetics. 14(2). 157–162. 61 indexed citations
20.
Carvajal, Jaime J., Mark A. Pook, Kit Doudney, et al.. (1995). Friedreich's ataxia: a defect in signal transduction?. Human Molecular Genetics. 4(8). 1411–1419. 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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