Katrina Tatton‐Brown

4.7k total citations
32 papers, 1.0k citations indexed

About

Katrina Tatton‐Brown is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Katrina Tatton‐Brown has authored 32 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 20 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Katrina Tatton‐Brown's work include Genomics and Rare Diseases (11 papers), Genetic Syndromes and Imprinting (11 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Katrina Tatton‐Brown is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetic Syndromes and Imprinting (11 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Katrina Tatton‐Brown collaborates with scholars based in United Kingdom, United States and Australia. Katrina Tatton‐Brown's co-authors include Nazneen Rahman, Trevor Cole, I. Karen Temple, Jenny Douglas, Kim Coleman, Helen E. Hughes, Valérie Cormier‐Daire, Geneviève Baujat, Soma Das and Seval Türkmen and has published in prestigious journals such as Nature Genetics, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Katrina Tatton‐Brown

30 papers receiving 1000 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrina Tatton‐Brown United Kingdom 14 704 696 92 56 49 32 1.0k
Boris Keren France 21 649 0.9× 515 0.7× 154 1.7× 41 0.7× 105 2.1× 70 1.1k
Annalisa Vetro Italy 20 524 0.7× 552 0.8× 203 2.2× 28 0.5× 27 0.6× 51 1.0k
Rachel Schot Netherlands 16 355 0.5× 260 0.4× 100 1.1× 42 0.8× 57 1.2× 35 686
Dominique Martin‐Coignard France 14 522 0.7× 424 0.6× 78 0.8× 16 0.3× 36 0.7× 22 817
Elisabetta Lapi Italy 18 534 0.8× 477 0.7× 131 1.4× 66 1.2× 13 0.3× 48 957
Ruen Yao China 15 385 0.5× 334 0.5× 44 0.5× 55 1.0× 20 0.4× 64 657
Luitgard Graul‐Neumann Germany 19 539 0.8× 457 0.7× 57 0.6× 31 0.6× 17 0.3× 46 884
Soo‐Mi Park United Kingdom 15 464 0.7× 258 0.4× 46 0.5× 147 2.6× 31 0.6× 39 794
Maria Lisa Dentici Italy 19 704 1.0× 459 0.7× 75 0.8× 15 0.3× 26 0.5× 74 1.1k
Monika Cohen Germany 11 551 0.8× 488 0.7× 98 1.1× 12 0.2× 38 0.8× 13 859

Countries citing papers authored by Katrina Tatton‐Brown

Since Specialization
Citations

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

Fields of papers citing papers by Katrina Tatton‐Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katrina Tatton‐Brown. 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 Katrina Tatton‐Brown. The network helps show where Katrina Tatton‐Brown may publish in the future.

Co-authorship network of co-authors of Katrina Tatton‐Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Katrina Tatton‐Brown. A scholar is included among the top collaborators of Katrina Tatton‐Brown 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 Katrina Tatton‐Brown. Katrina Tatton‐Brown 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.
Miller, Edward J., et al.. (2025). Mainstreaming genomics in paediatrics. Archives of Disease in Childhood Education & Practice. 110(6). 279–282.
2.
Stödberg, Tommy, Malin Kvarnung, Katrina Tatton‐Brown, et al.. (2024). Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variant. Clinical Genetics. 106(4). 427–436. 1 indexed citations
3.
Nightingale, Karl P., et al.. (2024). Evaluation of the Master’s in Genomic Medicine framework: A national, multiprofessional program to educate health care professionals in NHS England. Genetics in Medicine. 27(1). 101277–101277. 2 indexed citations
4.
5.
Abraham, Jean, Katie Snape, Katrina Tatton‐Brown, et al.. (2023). Mainstreaming of genomics in oncology: a nationwide survey of the genomics training needs of UK oncologists. Clinical Medicine. 23(1). 9–15. 11 indexed citations
6.
Joekes, Katherine, et al.. (2023). Evaluation of two Massive Open Online Courses (MOOCs) in genomic variant interpretation for the NHS workforce. BMC Medical Education. 23(1). 540–540. 4 indexed citations
7.
Poole, Rebecca, Emilia K. Bijlsma, Gunnar Houge, et al.. (2023). The PHF21A neurodevelopmental disorder: an evaluation of clinical data from 13 patients. Clinical Dysmorphology. 32(2). 49–54. 2 indexed citations
8.
Josephs, Katherine, Alison Berner, Angela George, et al.. (2019). Genomics: the power, potential and pitfalls of the new technologies and how they are transforming healthcare. Clinical Medicine. 19(4). 269–272. 7 indexed citations
9.
Loveday, Chey, Anna Zachariou, Lucy‐Ann Behan, et al.. (2019). EED and EZH2 constitutive variants: A study to expand the Cohen‐Gibson syndrome phenotype and contrast it with Weaver syndrome. American Journal of Medical Genetics Part A. 179(4). 588–594. 23 indexed citations
10.
Tatton‐Brown, Katrina, Chey Loveday, Shawn Yost, et al.. (2017). Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability. The American Journal of Human Genetics. 100(5). 725–736. 128 indexed citations
11.
Loveday, Chey, Katrina Tatton‐Brown, Matthew Clarke, et al.. (2015). Mutations in the PP2A regulatory subunit B family genesPPP2R5B,PPP2R5CandPPP2R5Dcause human overgrowth. Human Molecular Genetics. 24(17). 4775–4779. 62 indexed citations
12.
Balasubramanian, Meena, Emma Shearing, Kath Smith, et al.. (2014). Pneumothorax from subpleural blebs—A new association of sotos syndrome?. American Journal of Medical Genetics Part A. 164(5). 1222–1226. 2 indexed citations
13.
Tatton‐Brown, Katrina & Rosanna Weksberg. (2013). Molecular Mechanisms of Childhood Overgrowth. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 163(2). 71–75. 29 indexed citations
14.
Tatton‐Brown, Katrina & Nazneen Rahman. (2013). The NSD1 and EZH2 Overgrowth Genes, Similarities and Differences. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 163(2). 86–91. 59 indexed citations
15.
Tatton‐Brown, Katrina, Daniela T. Pilz, Karen Helene Ørstavik, et al.. (2009). 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics Part A. 149A(2). 147–154. 55 indexed citations
16.
Douglas, Jenny, Deirdre Cilliers, Kim Coleman, et al.. (2007). Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. Nature Genetics. 39(8). 963–965. 70 indexed citations
17.
Tatton‐Brown, Katrina & Nazneen Rahman. (2006). Sotos syndrome. European Journal of Human Genetics. 15(3). 264–271. 101 indexed citations
18.
Tatton‐Brown, Katrina, Jenny Douglas, Kim Coleman, et al.. (2005). Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations. The American Journal of Human Genetics. 77(2). 193–204. 221 indexed citations
19.
Douglas, Jenny, Kim Coleman, Katrina Tatton‐Brown, et al.. (2004). Evaluation of NSD2 and NSD3 in overgrowth syndromes. European Journal of Human Genetics. 13(2). 150–153. 30 indexed citations
20.
Tatton‐Brown, Katrina & Nazneen Rahman. (2004). Clinical features of NSD1-positive Sotos syndrome. Clinical Dysmorphology. 13(4). 199–204. 75 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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