Hannah Titheradge

1.1k total citations
19 papers, 433 citations indexed

About

Hannah Titheradge is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Hannah Titheradge has authored 19 papers receiving a total of 433 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Immunology. Recurrent topics in Hannah Titheradge's work include Genetic Syndromes and Imprinting (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Inflammasome and immune disorders (2 papers). Hannah Titheradge is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Inflammasome and immune disorders (2 papers). Hannah Titheradge collaborates with scholars based in United Kingdom, United States and Canada. Hannah Titheradge's co-authors include Rune Busk Damgaard, David Komander, Andrew N. J. McKenzie, Neil V. Morgan, Eamonn R. Maher, P.R. Elliott, Paola Marco‐Casanova, Jennifer A. Walker, Duncan McHale and Susan Davies and has published in prestigious journals such as Cell, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Hannah Titheradge

17 papers receiving 425 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hannah Titheradge United Kingdom 9 297 158 91 80 61 19 433
L. Alexander Liggett United States 7 193 0.6× 110 0.7× 57 0.6× 92 1.1× 32 0.5× 7 446
Sonja Smith United States 10 206 0.7× 117 0.7× 73 0.8× 25 0.3× 39 0.6× 19 399
Shiyue Mei China 11 235 0.8× 106 0.7× 124 1.4× 80 1.0× 35 0.6× 40 385
Peter D. Pioli United States 10 188 0.6× 234 1.5× 43 0.5× 39 0.5× 65 1.1× 22 466
Hemanth Tummala United Kingdom 14 406 1.4× 76 0.5× 50 0.5× 135 1.7× 73 1.2× 35 621
Christoph Herbel Germany 8 202 0.7× 134 0.8× 62 0.7× 81 1.0× 155 2.5× 14 380
Nicole Yeager United States 8 251 0.8× 118 0.7× 47 0.5× 153 1.9× 118 1.9× 11 541
Laìa Masvidal Sweden 11 340 1.1× 152 1.0× 56 0.6× 23 0.3× 89 1.5× 17 552
Luca Mariani Italy 9 298 1.0× 237 1.5× 82 0.9× 57 0.7× 100 1.6× 21 634
Iris A. Schulkens Netherlands 10 314 1.1× 192 1.2× 60 0.7× 41 0.5× 85 1.4× 16 465

Countries citing papers authored by Hannah Titheradge

Since Specialization
Citations

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

Fields of papers citing papers by Hannah Titheradge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hannah Titheradge

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

All Works

19 of 19 papers shown
1.
Morgan, Tim, Grégory Gimenez, Zandra A. Jenkins, et al.. (2024). Pathogenic FLNA variants affecting the hinge region of filamin A are associated with male survival. American Journal of Medical Genetics Part A. 194(10). e63779–e63779.
2.
Lewis, Helen, et al.. (2023). BG10 A case of pachydermoperiostosis (primary hypertrophic osteoarthropathy). British Journal of Dermatology. 188(Supplement_4).
3.
Low, Karen, Ramya Nair, Francis H. Sansbury, et al.. (2023). Expanding the phenotypic spectrum of Chromosome 16p13.11 microduplication: A multicentric analysis of 206 patients. European Journal of Medical Genetics. 66(4). 104714–104714. 2 indexed citations
4.
Omoyinmi, Ebun, Charalampia Papadopoulou, Eslam Al‐Abadi, et al.. (2023). Genetic testing of Behçet’s disease using next-generation sequencing to identify monogenic mimics and HLA-B*51. Lara D. Veeken. 63(12). 3457–3470. 4 indexed citations
5.
McDermott, Helen, et al.. (2023). Paediatric survivors beyond infancy with Stüve-Wiedemann syndrome – A case series from the West Midlands, UK. European Journal of Medical Genetics. 66(8). 104788–104788. 1 indexed citations
6.
7.
Morgan, Neil V., Bryndís Yngvadóttir, Mary O’Driscoll, et al.. (2021). Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL. Brain Communications. 3(1). fcab002–fcab002. 11 indexed citations
8.
Damgaard, Rune Busk, Helen E. Jolin, Michael Allison, et al.. (2020). OTULIN protects the liver against cell death, inflammation, fibrosis, and cancer. Cell Death and Differentiation. 27(5). 1457–1474. 59 indexed citations
9.
Titheradge, Hannah, Nicola Cooper, Frances Elmslie, et al.. (2020). Expanding the genotype–phenotype correlation ofde novoheterozygous missense variants inYWHAGas a cause of developmental and epileptic encephalopathy. American Journal of Medical Genetics Part A. 182(4). 713–720. 14 indexed citations
10.
Nixon, Kevin C., Justine Rousseau, Sophie Ehresmann, et al.. (2019). A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies. The American Journal of Human Genetics. 104(4). 596–610. 27 indexed citations
11.
Titheradge, Hannah, Nicola Cooper, Frances Elmslie, et al.. (2019). De novo, heterozygous missense variants in YWHAG as a novel cause of developmental and epileptic encephalopathy. White Rose Research Online (University of Leeds, The University of Sheffield, University of York). 1 indexed citations
12.
Pagnamenta, Alistair T., Yoshiko Murakami, Consuelo Anzilotti, et al.. (2018). A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephaly. Human Mutation. 39(6). 822–826. 17 indexed citations
13.
Webb, Emma, Meena Balasubramanian, Nadja Fratzl‐Zelman, et al.. (2017). Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect. The Journal of Clinical Endocrinology & Metabolism. 102(6). 2019–2028. 28 indexed citations
14.
Damgaard, Rune Busk, Jennifer A. Walker, Paola Marco‐Casanova, et al.. (2016). The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity. Cell. 166(5). 1215–1230.e20. 231 indexed citations
15.
Foster, Alison, Hannah Titheradge, & Jenny Morton. (2015). Genetics of learning disability. Paediatrics and Child Health. 25(10). 450–457. 3 indexed citations
16.
Titheradge, Hannah, Chirag Patel, & Nicola Ragge. (2014). Branchio–oculo–facial syndrome. Clinical Dysmorphology. 24(1). 13–16. 5 indexed citations
17.
Titheradge, Hannah, Fiona S. Togneri, Dominic McMullan, et al.. (2014). Axenfeld‐Rieger syndrome: Further clinical and array delineation of four unrelated patients with a 4q25 microdeletion. American Journal of Medical Genetics Part A. 164(7). 1695–1701. 12 indexed citations
18.
Jewell, Rosalyn, Jeannette Kraft, Paul Chumas, et al.. (2013). Craniosynostosis. Clinical Dysmorphology. 23(1). 12–15. 7 indexed citations
19.
Titheradge, Hannah, et al.. (2011). Methaemoglobinaemia with G6PD deficiency: rare cause of persistently low saturations in neonates. Acta Paediatrica. 100(7). e47–8. 8 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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