Joannah Score

3.2k total citations · 1 hit paper
23 papers, 2.1k citations indexed

About

Joannah Score is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Joannah Score has authored 23 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 16 papers in Hematology and 12 papers in Molecular Biology. Recurrent topics in Joannah Score's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (12 papers), Acute Myeloid Leukemia Research (10 papers) and Chronic Myeloid Leukemia Treatments (8 papers). Joannah Score is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (12 papers), Acute Myeloid Leukemia Research (10 papers) and Chronic Myeloid Leukemia Treatments (8 papers). Joannah Score collaborates with scholars based in United Kingdom, Germany and Greece. Joannah Score's co-authors include Nicholas C.P. Cross, Claire Hidalgo-Curtis, Thomas Ernst, Amy V. Jones, Katerina Zoi, Andreas Reiter, Andrew Chase, Francis Grand, David Oscier and Andrew Duncombe and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Joannah Score

22 papers receiving 2.1k citations

Hit Papers

align trajectories

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.

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

2010 807 citations Thomas Ernst, Andrew Chase et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joannah Score United Kingdom	14	1.3k	1.1k	830	278	239	23	2.1k
Francis Grand United Kingdom	20	1.3k 1.0×	1.3k 1.2×	1.1k 1.3×	555 2.0×	122 0.5×	36	2.3k
Véronique Gelsi‐Boyer France	19	1.2k 0.9×	1.6k 1.5×	964 1.2×	105 0.4×	146 0.6×	28	2.1k
Claire Hidalgo-Curtis United Kingdom	11	1.1k 0.9×	989 0.9×	763 0.9×	206 0.7×	79 0.3×	16	1.6k
Roberta La Starza Italy	24	796 0.6×	976 0.9×	370 0.4×	239 0.9×	183 0.8×	91	1.8k
Guntram Büsche Germany	21	636 0.5×	801 0.7×	733 0.9×	258 0.9×	82 0.3×	63	1.5k
Carin Lassen Sweden	21	642 0.5×	570 0.5×	297 0.4×	196 0.7×	122 0.5×	35	1.3k
N Philippe France	13	545 0.4×	1.1k 1.0×	626 0.8×	231 0.8×	70 0.3×	33	1.5k
Anne Murati France	18	640 0.5×	866 0.8×	598 0.7×	120 0.4×	80 0.3×	28	1.2k
Nadine Carbuccia France	19	749 0.6×	841 0.8×	581 0.7×	99 0.4×	73 0.3×	35	1.5k
George F. Barker United States	6	713 0.6×	924 0.9×	470 0.6×	376 1.4×	79 0.3×	7	1.6k

Countries citing papers authored by Joannah Score

Since Specialization

Citations

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

Fields of papers citing papers by Joannah Score

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joannah Score

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Tapper, William, Joannah Score, Andrew Chase, et al.. (2025). Genome-wide analysis defines genetic determinants of MPN subtypes and identifies a sex-specific association at CDH22 / CD40. Blood. 146(26). 3228–3233.

Abecasis, Manuel, Nicholas C.P. Cross, Kathleen M. Sakamoto, et al.. (2020). Is cancer latency an outdated concept? Lessons from chronic myeloid leukemia. Leukemia. 34(9). 2279–2284. 13 indexed citations

Chase, Andrew, Joannah Score, Feng Lin, et al.. (2020). Mutational mechanisms of EZH2 inactivation in myeloid neoplasms. Leukemia. 34(12). 3206–3214. 9 indexed citations

Chase, Andrew, Andrea Pellagatti, Shalini Singh, et al.. (2018). PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia. Leukemia. 33(5). 1184–1194. 6 indexed citations

Tapper, William, Nicola Foulds, Nicholas C.P. Cross, et al.. (2014). Megalencephaly Syndromes: Exome Pipeline Strategies for Detecting Low-Level Mosaic Mutations. PLoS ONE. 9(1). e86940–e86940. 16 indexed citations

Schwaab, Juliana, Claudia Haferlach, Georgia Metzgeroth, et al.. (2014). Limited duration of complete remission on ruxolitinib in myeloid neoplasms with PCM1-JAK2 and BCR-JAK2 fusion genes. Annals of Hematology. 94(2). 233–238. 51 indexed citations

Forsberg, Lars A., Chiara Rasi, Hanna Davies, et al.. (2014). Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer. Nature Genetics. 46(6). 624–628. 287 indexed citations

Mead, Adam J., Onima Chowdhury, C. Pecquet, et al.. (2013). Impact of isolated germline JAK2V617I mutation on human hematopoiesis. Blood. 121(20). 4156–4165. 35 indexed citations

Score, Joannah & Nicholas C.P. Cross. (2012). Acquired Uniparental Disomy in Myeloproliferative Neoplasms. Hematology/Oncology Clinics of North America. 26(5). 981–991. 10 indexed citations

10.

Cazzaniga, Giovanni, Frederik W. van Delft, Luca Lo Nigro, et al.. (2011). Developmental origins and impact of BCR-ABL1 fusion and IKZF1 deletions in monozygotic twins with Ph+ acute lymphoblastic leukemia. Blood. 118(20). 5559–5564. 67 indexed citations

11.

Ernst, Thomas, Joannah Score, Michael W. Deininger, et al.. (2011). Identification of FOXP1 and SNX2 as novel ABL1 fusion partners in acute lymphoblastic leukaemia. British Journal of Haematology. 153(1). 43–46. 29 indexed citations

12.

Score, Joannah, Claire Hidalgo-Curtis, Amy V. Jones, et al.. (2011). Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms. Blood. 119(5). 1208–1213. 125 indexed citations

13.

Guglielmelli, Paola, Flavia Biamonte, Joannah Score, et al.. (2011). EZH2 mutational status predicts poor survival in myelofibrosis. Blood. 118(19). 5227–5234. 199 indexed citations

14.

Cross, Nicholas C.P., Joannah Score, Claire Hidalgo-Curtis, et al.. (2011). Inactivation of Polycomb Repressive Complex 2 Components in Myeloproliferative and Myelodysplastic/Myeloproliferative Neoplasms. Blood. 118(21). 617–617. 4 indexed citations

15.

Walz, Christoph, Philipp Erben, Michael Ritter, et al.. (2011). Response of ETV6-FLT3–positive myeloid/lymphoid neoplasm with eosinophilia to inhibitors of FMS-like tyrosine kinase 3. Blood. 118(8). 2239–2242. 67 indexed citations

16.

Soverini, Simona, Angela Poerio, Alberto Ferrarini, et al.. (2010). Whole-Transcriptome Sequencing In Chronic Myeloid Leukemia Reveals Novel Gene Mutations That May Be Associated with Disease Pathogenesis and Progression. Blood. 116(21). 885–885. 3 indexed citations

17.

Ernst, Thomas, Andrew Chase, Joannah Score, et al.. (2010). Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nature Genetics. 42(8). 722–726. 807 indexed citations breakdown →

18.

Isoda, Takeshi, Anthony M. Ford, Daisuke Tomizawa, et al.. (2009). Immunologically silent cancer clone transmission from mother to offspring. Proceedings of the National Academy of Sciences. 106(42). 17882–17885. 44 indexed citations

19.

Grand, Francis, Claire Hidalgo-Curtis, Thomas Ernst, et al.. (2009). Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms. Blood. 113(24). 6182–6192. 273 indexed citations

20.

Sobrinho‐Simões, Manuel, Joannah Score, Nicholas C.P. Cross, Jane F. Apperley, & Junia V. Melo. (2007). How Cured Are CML Patients in Complete Molecular Remission (CMR) after Stem Cell Transplantation or Imatinib?.. Blood. 110(11). 1009–1009. 1 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.

Explore authors with similar magnitude of impact