A. E. Watmore

1.8k total citations · 1 hit paper
23 papers, 1.2k citations indexed

About

A. E. Watmore is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, A. E. Watmore has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Hematology, 14 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in A. E. Watmore's work include Acute Myeloid Leukemia Research (16 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers) and Chronic Lymphocytic Leukemia Research (6 papers). A. E. Watmore is often cited by papers focused on Acute Myeloid Leukemia Research (16 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers) and Chronic Lymphocytic Leukemia Research (6 papers). A. E. Watmore collaborates with scholars based in United Kingdom, India and United States. A. E. Watmore's co-authors include A. M. Potter, Curt I. Civin, Frederick G. Behm, R. Becher, J. Michael Andresen, Julian Borrow, Felix Mitelman, Stefano Volinia, Vincent P. Stanton and David E. Housman and has published in prestigious journals such as Nature Genetics, British Journal of Cancer and British Journal of Haematology.

In The Last Decade

A. E. Watmore

23 papers receiving 1.2k 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.

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

1996 603 citations Julian Borrow, Vincent P. Stanton 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
A. E. Watmore United Kingdom	14	701	638	359	135	125	23	1.2k
Paul Sinclair United Kingdom	16	306 0.4×	474 0.7×	285 0.8×	137 1.0×	153 1.2×	24	827
Traudl Henn Austria	14	426 0.6×	492 0.8×	303 0.8×	66 0.5×	117 0.9×	21	1.0k
Jastinder Sohal United Kingdom	11	408 0.6×	452 0.7×	200 0.6×	70 0.5×	173 1.4×	19	772
Marie‐Josée Le Bris France	18	420 0.6×	551 0.9×	235 0.7×	220 1.6×	63 0.5×	55	986
Françoise Brizard France	14	278 0.4×	343 0.5×	252 0.7×	77 0.6×	87 0.7×	33	680
KS Chang United States	8	811 1.2×	899 1.4×	167 0.5×	69 0.5×	57 0.5×	13	1.2k
CM Rubin United States	15	432 0.6×	847 1.3×	228 0.6×	121 0.9×	42 0.3×	20	1.0k
ID Dube Canada	13	347 0.5×	434 0.7×	225 0.6×	157 1.2×	41 0.3×	25	845
OA Haas Austria	15	407 0.6×	656 1.0×	221 0.6×	66 0.5×	57 0.5×	18	904
Odile Maarek France	13	352 0.5×	645 1.0×	411 1.1×	75 0.6×	231 1.8×	24	1.0k

Countries citing papers authored by A. E. Watmore

Since Specialization

Citations

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

Fields of papers citing papers by A. E. Watmore

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. E. Watmore. 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 A. E. Watmore. The network helps show where A. E. Watmore may publish in the future.

Co-authorship network of co-authors of A. E. Watmore

This figure shows the co-authorship network connecting the top 25 collaborators of A. E. Watmore. A scholar is included among the top collaborators of A. E. Watmore 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 A. E. Watmore. A. E. Watmore 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

Dingli, David, Francis Grand, Jack L. Spurbeck, et al.. (2005). Der(6)t(1;6)(q21–23;p21.3): a specific cytogenetic abnormality in myelofibrosis with myeloid metaplasia. British Journal of Haematology. 130(2). 229–232. 24 indexed citations

Reilly, John T., et al.. (2001). Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14. British Journal of Haematology. 113(2). 365–368. 16 indexed citations

Tan, Soo‐Yong, Susan A. Burchill, Samantha Brownhill, et al.. (2001). Small Round Cell Tumor with Biphenotypic Differentiation and Variant of t(21;22)(q22;q12). Pediatric and Developmental Pathology. 4(4). 391–396. 8 indexed citations

Cuthbert, Gavin, Karen Thompson, A. E. Watmore, et al.. (2000). MLL amplification in acute leukaemia: a United Kingdom Cancer Cytogenetics Group (UKCCG) study. Leukemia. 14(11). 1885–1891. 38 indexed citations

Watmore, A. E., et al.. (2000). Acute Monocytic Leukemia with a Novel 10;11 Rearrangement Resolved by Fluorescence In Situ Hybridization. Cancer Genetics and Cytogenetics. 118(1). 20–23. 4 indexed citations

Rowe, David W., Simon Cotterill, F. M. Ross, et al.. (2000). Cytogenetically cryptic AML1-ETO and CBFbeta-MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia. British Journal of Haematology. 111(4). 1051–1056. 47 indexed citations

Carapeti, Melina, Ricardo C.T. Aguiar, A. E. Watmore, John M. Goldman, & Nicholas C.P. Cross. (1999). Consistent Fusion of MOZ and TIF2 in AML with inv(8)(p11q13). Cancer Genetics and Cytogenetics. 113(1). 70–72. 46 indexed citations

Chase, Andrew, Kim Orchard, A. E. Watmore, et al.. (1998). Two cases of inv(8)(p11q13) in AML with erythrophagocytosis: a new cytogenetic variant. British Journal of Haematology. 100(3). 561–563. 29 indexed citations

Sinclair, Elizabeth, A. M. Potter, A. E. Watmore, M Fitchett, & Fiona M. Ross. (1998). Trisomy 15 Associated with Loss of the Y Chromosome in Bone Marrow. Cancer Genetics and Cytogenetics. 105(1). 20–23. 23 indexed citations

10.

Richards, Michael J., et al.. (1998). Trisomy 21 associated transient neonatal myeloproliferation in the absence of Down’s syndrome. Archives of Disease in Childhood Fetal & Neonatal. 79(3). F215–F217. 26 indexed citations

11.

Reilly, John T., John A. Snowden, Ruth Spearing, et al.. (1997). Cytogenetic abnormalities and their prognostic significance in idiopathic myelofibrosis: a study of 106 cases. British Journal of Haematology. 98(1). 96–102. 139 indexed citations

12.

Borrow, Julian, Vincent P. Stanton, J. Michael Andresen, et al.. (1996). The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein. Nature Genetics. 14(1). 33–41. 603 indexed citations breakdown →

13.

Murphy, Philip, et al.. (1995). Acute lymphoblastic transformation of essential thrombocythaemia. British Journal of Haematology. 89(4). 921–922. 6 indexed citations

14.

Reilly, John T., Gill Wilson, David Barnett, A. E. Watmore, & A. M. Potter. (1994). Karyotypic and ras gene mutational analysis in idiopathic myelofibrosis. British Journal of Haematology. 88(3). 575–581. 39 indexed citations

15.

Watmore, A. E., et al.. (1991). Chromosomes in childhood acute lymphoblastic leukaemia: karyotypic patterns in disease subtypes.. Journal of Clinical Pathology. 44(1). 48–51. 11 indexed citations

16.

Yaseen, Nahi Y., A. E. Watmore, A. M. Potter, et al.. (1990). Chromosome studies in eleven colorectal tumors. Cancer Genetics and Cytogenetics. 44(1). 83–97. 25 indexed citations

17.

Griffiths, Helen R., et al.. (1989). Mithramycin therapy for resistant hypercalcaemia in transformed chronic granulocytic leukaemia. Clinical & Laboratory Haematology. 11(2). 156–159. 3 indexed citations

18.

Potter, A. M., et al.. (1988). Methotrexate and bone marrow metaphases. Cancer Genetics and Cytogenetics. 33(2). 213–224. 6 indexed citations

19.

Watmore, A. E., et al.. (1985). Nonendemic Burkitt's lymphoma with complex chromosome abnormalities involving chromosomes 2 and 8. Cancer Genetics and Cytogenetics. 16(4). 283–288. 3 indexed citations

20.

Lilleyman, J S, A. M. Potter, A. E. Watmore, et al.. (1978). Myeloid Karyotype and the Malignant Phase of Chronic Granulocytic Leukaemia. British Journal of Haematology. 39(3). 317–323. 26 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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