Emma Hobson

4.5k total citations
24 papers, 405 citations indexed

About

Emma Hobson is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Emma Hobson has authored 24 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Emma Hobson's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Emma Hobson is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Emma Hobson collaborates with scholars based in United Kingdom, United States and Italy. Emma Hobson's co-authors include Pradeep Vasudevan, Mohnish Suri, Sally Ann Lynch, Katrina Prescott, Emma Burkitt‐Wright, Sahar Mansour, Sarah Walters, Orsetta Zuffardi, Stanislas Lyonnet and Annick Toutain and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Emma Hobson

22 papers receiving 390 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma Hobson United Kingdom 9 256 213 42 40 40 24 405
Vanesa López‐González Spain 15 311 1.2× 264 1.2× 85 2.0× 32 0.8× 46 1.1× 24 532
Diana Alcantara United Kingdom 9 192 0.8× 274 1.3× 21 0.5× 44 1.1× 29 0.7× 11 426
A Baxová Czechia 10 246 1.0× 243 1.1× 33 0.8× 39 1.0× 23 0.6× 40 416
Pietro Sirleto Italy 12 137 0.5× 221 1.0× 13 0.3× 30 0.8× 33 0.8× 25 399
Karen J. Harrison Canada 10 252 1.0× 248 1.2× 17 0.4× 43 1.1× 88 2.2× 17 461
Sonia Nizard France 10 227 0.9× 131 0.6× 36 0.9× 28 0.7× 87 2.2× 12 357
Natalie C. Butterfield Australia 12 162 0.6× 332 1.6× 55 1.3× 33 0.8× 14 0.3× 16 482
Geneviève Pierquin Belgium 10 173 0.7× 188 0.9× 14 0.3× 31 0.8× 59 1.5× 24 318
Glen R. Monroe Netherlands 12 313 1.2× 216 1.0× 11 0.3× 23 0.6× 44 1.1× 20 524
Yukiko Kuroda Japan 11 178 0.7× 127 0.6× 17 0.4× 27 0.7× 31 0.8× 40 271

Countries citing papers authored by Emma Hobson

Since Specialization
Citations

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

Fields of papers citing papers by Emma Hobson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Hobson

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Hobson. A scholar is included among the top collaborators of Emma Hobson 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 Hobson. Emma Hobson 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.
Albaba, Shadi, Glenda Sobey, Jessica Bowen, et al.. (2025). Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome. European Journal of Human Genetics. 33(10). 1309–1315.
2.
Ochoa, Eguzkine, Ilona Zvetkova, Nozomi Takahashi, et al.. (2025). Germline variants in UHRF1 are associated with multilocus imprinting disturbance in humans and mice. Proceedings of the National Academy of Sciences. 122(34). e2505884122–e2505884122.
3.
Harris, Erica, Vincent Roy, Martin Montagne, et al.. (2023). A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes. The American Journal of Human Genetics. 111(1). 119–132. 4 indexed citations
4.
Wood, K, Jamie M. Ellingford, Huw B. Thomas, et al.. (2021). Expanding the genotypic spectrum of TXNL4A variants in Burn‐McKeown syndrome. Clinical Genetics. 101(2). 255–259. 4 indexed citations
5.
Murch, Oliver, Kay Metcalfe, Emma Hobson, et al.. (2021). Further delineation of the clinical spectrum of White–Sutton syndrome: 12 new individuals and a review of the literature. European Journal of Human Genetics. 30(1). 95–100. 6 indexed citations
6.
Sárközy, Anna, Rahul Phadke, Anne‐Marie Childs, et al.. (2020). Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy. Neuromuscular Disorders. 31(4). 359–366. 3 indexed citations
7.
Best, Sunayna, James A. Poulter, Verity Hartill, et al.. (2020). Novel loss-of-function mutation in HERC2 is associated with severe developmental delay and paediatric lethality. Journal of Medical Genetics. 58(5). 334–341. 13 indexed citations
8.
Balasubramanian, Meena, Emma Hobson, Mars Skae, Janine McCaughey, & David Stephens. (2019). Developing pathways to clarify pathogenicity of unclassified variants in Osteogenesis Imperfecta genetic analysis. Molecular Genetics & Genomic Medicine. 7(12). e912–e912. 1 indexed citations
9.
Novelli, Antonio, M. Cristina Digilio, David Bourn, et al.. (2018). Duplications of GPC3 and GPC4 genes in symptomatic female carriers of Simpson-Golabi-Behmel syndrome type 1. European Journal of Medical Genetics. 62(4). 243–247. 16 indexed citations
10.
King, Daniel A., Alejandro Sifrim, Tomas Fitzgerald, et al.. (2017). Detection of structural mosaicism from targeted and whole-genome sequencing data. Genome Research. 27(10). 1704–1714. 38 indexed citations
11.
Bermúdez, C., María Molina, Arwin Thomasson, et al.. (2017). Lung Transplant Experience with Public Health Services Increased Risk Donors: Recipient Outcomes and Incidence of Transmission and Conversion. The Journal of Heart and Lung Transplantation. 36(4). S52–S52. 1 indexed citations
12.
Jewell, Rosalyn, et al.. (2017). 3q27.3 Microdeletion syndrome: further delineation of the second region of overlap and atopic dermatitis as a phenotypic feature. Clinical Dysmorphology. 26(3). 154–156. 2 indexed citations
13.
Pollitt, Rebecca C., Vrinda Saraff, Ann Dalton, et al.. (2016). Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations. American Journal of Medical Genetics Part A. 170(12). 3150–3156. 27 indexed citations
14.
Hartill, Verity, et al.. (2013). Mowat–Wilson syndrome associated with craniosynostosis. Clinical Dysmorphology. 23(1). 16–19. 7 indexed citations
15.
Jewell, Rosalyn, Jeannette Kraft, Paul Chumas, et al.. (2013). Craniosynostosis. Clinical Dysmorphology. 23(1). 12–15. 7 indexed citations
16.
Searle, Claire, et al.. (2013). A Large Intragenic Deletion in the ACADM Gene Can Cause MCAD Deficiency but is not Detected on Routine Sequencing. JIMD Reports. 11. 13–16. 2 indexed citations
17.
Ogi, Tomoo, Sarah Walker, Tom Stiff, et al.. (2012). Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome. PLoS Genetics. 8(11). e1002945–e1002945. 79 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
19.
Barber, John, Viv Maloney, Shuwen Huang, et al.. (2007). 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH. European Journal of Human Genetics. 16(1). 18–27. 67 indexed citations
20.
Hobson, Emma, et al.. (2007). Nasopharyngeal teratoma associated with a complex congenital cardiac anomaly. Clinical Dysmorphology. 16(2). 113–114. 2 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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