Christine J. Harrison

29.9k total citations · 5 hit papers
258 papers, 14.1k citations indexed

About

Christine J. Harrison is a scholar working on Public Health, Environmental and Occupational Health, Hematology and Molecular Biology. According to data from OpenAlex, Christine J. Harrison has authored 258 papers receiving a total of 14.1k indexed citations (citations by other indexed papers that have themselves been cited), including 160 papers in Public Health, Environmental and Occupational Health, 150 papers in Hematology and 81 papers in Molecular Biology. Recurrent topics in Christine J. Harrison's work include Acute Lymphoblastic Leukemia research (159 papers), Acute Myeloid Leukemia Research (100 papers) and Chronic Myeloid Leukemia Treatments (77 papers). Christine J. Harrison is often cited by papers focused on Acute Lymphoblastic Leukemia research (159 papers), Acute Myeloid Leukemia Research (100 papers) and Chronic Myeloid Leukemia Treatments (77 papers). Christine J. Harrison collaborates with scholars based in United Kingdom, United States and Netherlands. Christine J. Harrison's co-authors include Keith Wheatley, Anthony V. Moorman, David Grimwade, Alan K. Burnett, Helen M. Walker, Ian Hann, Anthony H. Goldstone, Richard Stevens, G Harrison and Anthony P. Goldstone and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Oncology.

In The Last Decade

Christine J. Harrison

254 papers receiving 13.8k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Importance of Diagnostic Cytogenetics on Outcome in AML: Analysis of 1,612 Patients Entered Into the MRC AML 10 Trial

1998 2.1k citations David Grimwade, Helen M. Walker et al. Blood profile →
Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials

2010 1.3k citations David Grimwade, Robert K. Hills et al. Blood profile →
Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

2006 502 citations Anthony V. Moorman, Christine J. Harrison et al. Blood profile →
Burkitt's lymphoma

2012 391 citations Christine J. Harrison, Simon Bailey et al. profile →
Acute lymphoblastic leukaemia

2024 52 citations Sai‐Juan Chen, Daniel Herranz et al. Nature Reviews Disease Primers profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christine J. Harrison United Kingdom	60	9.5k	7.3k	4.5k	2.5k	2.1k	258	14.1k
Elaine Coustan‐Smith United States	60	6.0k 0.6×	5.9k 0.8×	2.6k 0.6×	2.2k 0.9×	1.5k 0.7×	140	11.5k
Sheila Shurtleff United States	46	4.4k 0.5×	3.8k 0.5×	5.2k 1.2×	1.2k 0.5×	1.1k 0.5×	96	10.8k
Vincent H. J. van der Velden Netherlands	45	5.1k 0.5×	3.8k 0.5×	2.4k 0.5×	1.0k 0.4×	1.6k 0.8×	168	8.5k
Charlotte M. Niemeyer Germany	54	4.8k 0.5×	2.0k 0.3×	4.1k 0.9×	976 0.4×	1.8k 0.8×	260	10.3k
Dario Campana United States	85	9.1k 1.0×	8.7k 1.2×	5.2k 1.2×	3.6k 1.5×	2.5k 1.2×	287	22.5k
C. Ellen van der Schoot Netherlands	57	5.9k 0.6×	1.4k 0.2×	2.8k 0.6×	2.0k 0.8×	2.0k 0.9×	332	11.5k
Peter Bader Germany	50	5.3k 0.6×	2.2k 0.3×	1.4k 0.3×	1.1k 0.4×	1.3k 0.6×	270	8.9k
Partow Kebriaei United States	50	4.8k 0.5×	2.9k 0.4×	2.9k 0.6×	608 0.2×	1.8k 0.9×	396	11.8k
Brigitte Schlegelberger Germany	66	6.7k 0.7×	1.8k 0.3×	7.8k 1.7×	498 0.2×	3.7k 1.8×	395	16.3k
Susanne Schnittger Germany	71	13.1k 1.4×	3.8k 0.5×	7.7k 1.7×	262 0.1×	6.2k 3.0×	435	17.5k

Countries citing papers authored by Christine J. Harrison

Since Specialization

Citations

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

Fields of papers citing papers by Christine J. Harrison

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine J. Harrison. 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 Christine J. Harrison. The network helps show where Christine J. Harrison may publish in the future.

Co-authorship network of co-authors of Christine J. Harrison

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

All Works

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20 of 20 papers shown

Berri, Stefano, John F. Peden, Claire Fielding, et al.. (2025). A dedicated caller for DUX4 rearrangements from whole-genome sequencing data. BMC Medical Genomics. 18(1). 24–24. 1 indexed citations

Chen, Sai‐Juan, Daniel Herranz, Cristina Mecucci, et al.. (2024). Acute lymphoblastic leukaemia. Nature Reviews Disease Primers. 10(1). 41–41. 52 indexed citations breakdown →

Gao, Qingsong & Christine J. Harrison. (2024). B-ALL with intrachromosomal amplification of chromosome 21 in a carrier of the Robertsonian translocation rob(14;21)c. Blood. 143(25). 2672–2672.

Sinclair, Paul, Prahlad V. Raninga, Sarra Ryan, et al.. (2023). Disruption to the FOXO-PRDM1 axis resulting from deletions of chromosome 6 in acute lymphoblastic leukaemia. Leukemia. 37(3). 636–649. 4 indexed citations

Crossland, Rachel E., Sarah Wilkinson, Amir Enshaei, et al.. (2021). Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma. Leukemia. 36(3). 781–789. 23 indexed citations

Bruford, Elspeth A., Cristina R. Antonescu, Andrew J. Carroll, et al.. (2021). HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia. 35(11). 3040–3043. 47 indexed citations

O’Connor, David, Amir Enshaei, Jack Bartram, et al.. (2017). Genotype-Specific Minimal Residual Disease Interpretation Improves Stratification in Pediatric Acute Lymphoblastic Leukemia. Journal of Clinical Oncology. 36(1). 34–43. 99 indexed citations

Harrison, Christine J., et al.. (2017). Unlocking the potential of anti-CD33 therapy in adult and childhood acute myeloid leukemia. Experimental Hematology. 54. 40–50. 27 indexed citations

Schwab, Claire, Sarra Ryan, Lucy Chilton, et al.. (2016). EBF1-PDGFRB fusion in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL): genetic profile and clinical implications. Blood. 127(18). 2214–2218. 80 indexed citations

10.

Russell, Lisa J., Amir Enshaei, Lisa Jones, et al.. (2014). IGH @ Translocations Are Prevalent in Teenagers and Young Adults With Acute Lymphoblastic Leukemia and Are Associated With a Poor Outcome. Journal of Clinical Oncology. 32(14). 1453–1462. 57 indexed citations

11.

Irving, Julie, Elizabeth Matheson, Lynne Minto, et al.. (2014). Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition. Blood. 124(23). 3420–3430. 163 indexed citations

12.

Veer, Arian van der, Esmé Waanders, Rob Pieters, et al.. (2013). Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL. Blood. 122(15). 2622–2629. 187 indexed citations

13.

Grimwade, David, Robert K. Hills, Anthony V. Moorman, et al.. (2010). Refinement of cytogenetic classification in acute myeloid leukaemia: Determination of prognostic significance of rarer recurring chromosomal abnormalities amongst 5,876 younger adult patients treated in the UK Medical Research Council trials. British Journal of Haematology. 149. 17–17. 29 indexed citations

14.

Grimwade, David, Robert K. Hills, Anthony V. Moorman, et al.. (2009). REFINEMENT OF CYTOGENETIC CLASSIFICATION IN AML: DETERMINATION OF PROGNOSTIC SIGNIFICANCE OF RARE RECURRING CHROMOSOMAL ABNORMALITIES AMONGST 5635 YOUNGER ADULTS TREATED IN THE UK MRC TRIALS. Haematologica. 94. 217–217. 5 indexed citations

15.

Sulong, Sarina, Anthony V. Moorman, Julie Irving, et al.. (2008). A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups. Blood. 113(1). 100–107. 134 indexed citations

16.

Case, Marian, Elizabeth Matheson, Lynne Minto, et al.. (2008). Mutation of Genes Affecting the RAS Pathway Is Common in Childhood Acute Lymphoblastic Leukemia. Cancer Research. 68(16). 6803–6809. 90 indexed citations

17.

Jalali, G R, Qi An, Zoë J. Konn, et al.. (2007). Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia. Leukemia. 22(1). 114–123. 13 indexed citations

18.

Sinclair, Paul, et al.. (2004). A Fluorescence in Situ Hybridization Map of 6q Deletions in Acute Lymphocytic Leukemia. Cancer Research. 64(12). 4089–4098. 39 indexed citations

19.

Harrison, Christine J., Anthony V. Moorman, Robert K. Hills, et al.. (2003). Cytogenetics of childhood AML from UK medical research council treatment trials, AML10 & 12.. Blood. 102(11). 333–333. 3 indexed citations

20.

Harrison, Christine J., et al.. (1983). The fragile X: a scanning electron microscope study.. Journal of Medical Genetics. 20(4). 280–285. 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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