Georgina Hall

4.4k total citations
83 papers, 2.0k citations indexed

About

Georgina Hall is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Georgina Hall has authored 83 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 22 papers in Genetics and 19 papers in Hematology. Recurrent topics in Georgina Hall's work include Retinal Development and Disorders (14 papers), Lymphoma Diagnosis and Treatment (14 papers) and Genomics and Rare Diseases (11 papers). Georgina Hall is often cited by papers focused on Retinal Development and Disorders (14 papers), Lymphoma Diagnosis and Treatment (14 papers) and Genomics and Rare Diseases (11 papers). Georgina Hall collaborates with scholars based in United Kingdom, France and United States. Georgina Hall's co-authors include Graeme C. Black, Simon Ramsden, M. C. Berenbaum, A D Hoyes, James O’Sullivan, Sanjeev S. Bhaskar, Ananth Shankar, Jamie M. Ellingford, Panagiotis I. Sergouniotis and Andrew R. Webster and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Georgina Hall

83 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Georgina Hall United Kingdom 25 774 468 424 344 339 83 2.0k
Ryu Watanabe Japan 28 522 0.7× 113 0.2× 289 0.7× 123 0.4× 175 0.5× 125 2.7k
Jianrong Wu United States 38 1.5k 1.9× 229 0.5× 389 0.9× 184 0.5× 491 1.4× 158 4.5k
Kathy L. Moser United States 25 844 1.1× 844 1.8× 109 0.3× 127 0.4× 353 1.0× 49 4.2k
Stephen Yip Canada 30 1.0k 1.3× 178 0.4× 567 1.3× 52 0.2× 261 0.8× 150 2.8k
Alexia Savignoni France 30 607 0.8× 315 0.7× 155 0.4× 28 0.1× 397 1.2× 108 2.4k
Jorge R. Quesada United States 25 613 0.8× 139 0.3× 814 1.9× 374 1.1× 652 1.9× 67 3.3k
Heikki Helin Finland 32 985 1.3× 343 0.7× 235 0.6× 135 0.4× 348 1.0× 117 3.9k
Eoin McKinney United Kingdom 24 615 0.8× 562 1.2× 121 0.3× 65 0.2× 104 0.3× 40 2.6k
Attilio Guarini Italy 25 558 0.7× 49 0.1× 433 1.0× 533 1.5× 458 1.4× 112 2.1k
Thomas Hielscher Germany 39 3.3k 4.3× 252 0.5× 1.5k 3.6× 1.3k 3.9× 412 1.2× 181 5.9k

Countries citing papers authored by Georgina Hall

Since Specialization
Citations

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

Fields of papers citing papers by Georgina Hall

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georgina Hall

This figure shows the co-authorship network connecting the top 25 collaborators of Georgina Hall. A scholar is included among the top collaborators of Georgina Hall 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 Georgina Hall. Georgina Hall 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.
Jalil, Assad, Mariantonia Ferrara, Neil R. A. Parry, et al.. (2025). Real-world outcomes of Voretigene Neparvovec: a single-centre consecutive case series. Eye. 39(7). 1356–1363. 1 indexed citations
2.
Oldenburg, Johannes, Susan Halimeh, Georgina Hall, et al.. (2023). Design of a Real-World Observational Study in Previously Untreated and Minimally Treated Hemophilia A Patients: Protect-NOW. SHILAP Revista de lepidopterología. 7(2). e110–e116. 1 indexed citations
3.
Taylor, Rachel L., Simon G. Williams, Jane Ashworth, et al.. (2022). Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia. Orphanet Journal of Rare Diseases. 17(1). 110–110. 5 indexed citations
4.
Hart, Daniel P., Jayanthi Alamelu, Neha Bhatnagar, et al.. (2021). Immune tolerance induction in severe haemophilia A: A UKHCDO inhibitor and paediatric working party consensus update. Haemophilia. 27(6). 932–937. 17 indexed citations
5.
Campbell, Patrick, Jamie M. Ellingford, Neil R. A. Parry, et al.. (2019). Clinical and genetic variability in children with partial albinism. Scientific Reports. 9(1). 16576–16576. 30 indexed citations
6.
Payne, Katherine, Martin Eden, Marion McAllister, et al.. (2017). Exploring the feasibility of delivering standardized genomic care using ophthalmology as an example. Genetics in Medicine. 19(9). 1032–1039. 14 indexed citations
7.
Eden, Martin, Katherine Payne, Stuart Wright, et al.. (2016). Identifying variation in models of care for the genomic-based diagnosis of inherited retinal dystrophies in the United Kingdom. Eye. 30(7). 966–971. 3 indexed citations
8.
Lennon, Rachel, et al.. (2015). Pinpointing clinical diagnosis through whole exome sequencing to direct patient care.. The Lancet. 1 indexed citations
9.
Ellingford, Jamie M., Panagiotis I. Sergouniotis, Rachel Lennon, et al.. (2015). Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome. The Lancet. 385(9980). 1916–1916. 21 indexed citations
10.
Ramsden, Simon, Anna O’Grady, Tracy Fletcher, et al.. (2013). A clinical molecular genetic service for United Kingdom families with choroideraemia. European Journal of Medical Genetics. 56(8). 432–438. 16 indexed citations
11.
Combs, Ryan, Georgina Hall, Katherine Payne, et al.. (2013). Understanding the expectations of patients with inherited retinal dystrophies. British Journal of Ophthalmology. 97(8). 1057–1061. 23 indexed citations
12.
Combs, Ryan, Marion McAllister, Katherine Payne, et al.. (2013). Understanding the impact of genetic testing for inherited retinal dystrophy. European Journal of Human Genetics. 21(11). 1209–1213. 27 indexed citations
13.
Shankar, Ananth, Georgina Hall, Dirk Hasenclever, et al.. (2011). Treatment outcome after low intensity chemotherapy [CVP] in children and adolescents with early stage nodular lymphocyte predominant Hodgkin’s lymphoma – An Anglo-French collaborative report. European Journal of Cancer. 48(11). 1700–1706. 45 indexed citations
14.
Hall, Georgina, CR Pinkerton, Gary Nicolin, et al.. (2007). Outcome of children with nodular lymphocyte predominant Hodgkin lymphoma – a Children's Cancer and Leukaemia Group report. British Journal of Haematology. 138(6). 761–768. 31 indexed citations
15.
Hall, Georgina. (2006). Shwachman-Diamond syndrome: UK perspective. Archives of Disease in Childhood. 91(6). 521–524. 26 indexed citations
16.
Hall, Georgina, et al.. (2004). Resolution of Orbitocerebral Aspergillosis During Combination Treatment With Voriconazole and Amphotericin Plus Adjunctive Cytokine Therapy. Journal of Pediatric Hematology/Oncology. 26(5). 304–307. 11 indexed citations
17.
Hall, Georgina. (2001). Childhood myeloid leukaemias. Best Practice & Research Clinical Haematology. 14(3). 573–591. 18 indexed citations
18.
Ho, P. Joy, Georgina Hall, Lei Luo, D. J. Weatherall, & Swee Lay Thein. (1998). Phenotypic Prediction in β‐Thalassemia. Annals of the New York Academy of Sciences. 850(1). 436–441. 6 indexed citations
19.
Hall, Georgina, RA Barnetson, & SL Thein. (1992). Beta thalassaemia in the indigenous British population. British Journal of Haematology. 82(3). 584–588. 21 indexed citations
20.
Hall, Georgina, I M Franklin, Thanyachai Sura, & Swee Lay Thein. (1991). A NOVEL MUTATION (NONSENSE β 127) IN EXON 3 OF THE β GLOBIN GENE PRODUCES A VARIABLE THALASSAEMIC PHENOTYPE. British Journal of Haematology. 79(2). 342–344. 20 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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