Michael Neat

1.7k total citations
38 papers, 1.1k citations indexed

About

Michael Neat is a scholar working on Hematology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Michael Neat has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Hematology, 14 papers in Pathology and Forensic Medicine and 12 papers in Oncology. Recurrent topics in Michael Neat's work include Acute Myeloid Leukemia Research (15 papers), Lymphoma Diagnosis and Treatment (11 papers) and Chronic Lymphocytic Leukemia Research (9 papers). Michael Neat is often cited by papers focused on Acute Myeloid Leukemia Research (15 papers), Lymphoma Diagnosis and Treatment (11 papers) and Chronic Lymphocytic Leukemia Research (9 papers). Michael Neat collaborates with scholars based in United Kingdom, Ireland and United States. Michael Neat's co-authors include Tim Lister, A. Z. S. Rohatiner, John Amess, Nicola Foot, Debra M. Lillington, Ivana N. Micallef, Janet Matthews, Natalie J. Foot, Jude Fitzgibbon and T. Andrew Lister and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Michael Neat

37 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael Neat United Kingdom	18	557	493	298	259	188	38	1.1k
Blanca Sánchez‐González Spain	20	598 1.1×	721 1.5×	381 1.3×	304 1.2×	101 0.5×	70	1.5k
Barbara Crescenzi Italy	18	476 0.9×	344 0.7×	161 0.5×	207 0.8×	162 0.9×	55	1.0k
Anna Aventı́n Spain	20	495 0.9×	372 0.8×	232 0.8×	152 0.6×	185 1.0×	58	938
Barbara Gamberi Italy	18	597 1.1×	444 0.9×	283 0.9×	440 1.7×	107 0.6×	70	1.1k
James Dalton United States	8	497 0.9×	550 1.1×	228 0.8×	210 0.8×	646 3.4×	14	1.3k
Mitchell A. Bitter United States	14	556 1.0×	301 0.6×	398 1.3×	260 1.0×	186 1.0×	23	1.1k
Zhenya Tang United States	20	456 0.8×	375 0.8×	280 0.9×	335 1.3×	108 0.6×	111	1.2k
MA Bitter United States	11	661 1.2×	301 0.6×	269 0.9×	292 1.1×	163 0.9×	18	1.1k
Maya Thangavelu United States	17	494 0.9×	318 0.6×	287 1.0×	187 0.7×	207 1.1×	36	1.2k
Pascale Lepelley France	21	742 1.3×	376 0.8×	105 0.4×	366 1.4×	132 0.7×	51	1.2k

Countries citing papers authored by Michael Neat

Since Specialization

Citations

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

Fields of papers citing papers by Michael Neat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Neat

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

Torricelli, Federica, Alka Saxena, Rosamond Nuamah, et al.. (2020). Genomic analysis in short- and long-term patients with malignant pleura mesothelioma treated with palliative chemotherapy. European Journal of Cancer. 132. 104–111. 5 indexed citations

Ortíz-Zapater, Elena, Richard Lee, William J. Owen, et al.. (2017). MET-EGFR dimerization in lung adenocarcinoma is dependent on EGFR mtations and altered by MET kinase inhibition. PLoS ONE. 12(1). e0170798–e0170798. 22 indexed citations

Abdul‐Wahab, Alya, Alistair Robson, Stephen Morris, et al.. (2014). Chromosomal anomalies in primary cutaneous follicle center cell lymphoma do not portend a poor prognosis. Journal of the American Academy of Dermatology. 70(6). 1010–1020. 23 indexed citations

Foot, Nicola, et al.. (2011). Fluorescence in situ hybridisation analysis of formalin-fixed paraffin-embedded tissue sections in the diagnostic work-up of non-Burkitt high grade B-cell non-Hodgkin's lymphoma: a single centre's experience. Journal of Clinical Pathology. 64(9). 802–808. 29 indexed citations

Dadzie, O.E., Michael Neat, Andrew Emley, Jag Bhawan, & Meera Mahalingam. (2010). Molecular Diagnostics—An Emerging Frontier in Dermatopathology. American Journal of Dermatopathology. 33(1). 1–16. 8 indexed citations

Ryan, Jacqueline, Fiona Quinn, Ludmila Boublíková, et al.. (2008). Minimal residual disease detection in childhood acute lymphoblastic leukaemia patients at multiple time‐points reveals high levels of concordance between molecular and immunophenotypic approaches. British Journal of Haematology. 144(1). 107–115. 42 indexed citations

Lo, Ken C., Jane Chalker, Sabine Strehl, et al.. (2008). Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome. British Journal of Haematology. 142(6). 934–945. 7 indexed citations

Smith, Matthew, Lan‐Lan Smith, Nigel J. Bainton, et al.. (2005). Development of a human acute myeloid leukaemia screening panel and consequent identification of novel gene mutation in FLT3 and CCND3. British Journal of Haematology. 128(3). 318–323. 28 indexed citations

Smith, Matthew, Michael Neat, Amanda Dixon‐McIver, et al.. (2003). Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2. Genes Chromosomes and Cancer. 37(1). 72–78. 89 indexed citations

10.

Davies, Jeff, et al.. (2003). Autoimmune cytopenias in the 22q11.2 deletion syndrome. Clinical & Laboratory Haematology. 25(3). 195–197. 35 indexed citations

11.

Neat, Michael, Nicola Foot, Loretta M. Byrne, et al.. (2002). Comparative genomic hybridization and multiplex-fluorescence in situ hybridization: an appraisal in elderly patients with acute myelogenous leukemia. The Hematology Journal. 3(6). 290–298. 5 indexed citations

12.

Neat, Michael, Nicola Foot, Lindsey K. Goff, et al.. (2001). Localisation of a novel region of recurrent amplification in follicular lymphoma to an ∼6.8 Mb region of 13q32‐33. Genes Chromosomes and Cancer. 32(3). 236–243. 35 indexed citations

13.

Chaplin, Tracy, Ananth Shankar, Michael Neat, et al.. (2001). Identification and molecular characterisation of a CALM-AF10 fusion in acute megakaryoblastic leukaemia. Leukemia. 15(6). 910–914. 10 indexed citations

14.

Grimwade, David, Antonio Biondi, Julien Mozziconacci, et al.. (2000). Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party. Groupe Francais de Cytogenetique Hematologique, Groupe de Francais d'Hematologie Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concerted Action "Molecular Cytogenetic Diagnosis in Haematological Malignancies". SPIRE - Sciences Po Institutional REpository. 30 indexed citations

15.

Fitzgibbon, Jude, Michael Neat, Natalie J. Foot, et al.. (2000). Assignment<footref rid="foot01"><sup>1</sup></footref> of brain acid-soluble protein 1 (BASP1) to human chromosome 5p15.1→p14, differential expression in human cancer cell lines as a result of alterations in gene dosage. Cytogenetic and Genome Research. 89(3-4). 147–149. 6 indexed citations

16.

Lillington, Debra M., R J Jaju, Ananth Shankar, et al.. (2000). Cytogenetic and molecular evidence of marrow involvement in extramedullary acute myeloid leukaemia. British Journal of Haematology. 110(3). 547–551. 15 indexed citations

17.

Fitzgibbon, Jude, et al.. (2000). Assignment<footref rid="foot01"><sup>1</sup></footref> of B-cell lymphoma 6, member B (zinc finger protein) gene (BCL6B) to human chromosome 17p13.1 by in situ hybridization. Cytogenetic and Genome Research. 89(3-4). 218–219. 5 indexed citations

18.

Grimwade, David, Andrea Biondi, Julien Mozziconacci, et al.. (2000). Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17):. Radboud Repository (Radboud University). 224 indexed citations

19.

Goff, Louise M., Michael Neat, Charles Crawley, et al.. (2000). The use of real-time quantitative polymerase chain reaction and comparative genomic hybridization to identify amplification of the REL gene in follicular lymphoma. British Journal of Haematology. 111(2). 618–625. 61 indexed citations

20.

Jaju, R J, Michael Neat, Jochen Harbott, et al.. (1998). A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood AML.. Blood. 92. 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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