JM Heward

671 citations
13 papers · 533 · h-index 9

Impact in

Papers in

JM Heward

13 papers receiving 525 citations

Peers

JM Heward
Comparison fields: 5 of 57
  • Genetics 153
  • Pathology and Forensic Medicine 146
  • Immunology 118
  • Hematology 44
  • Molecular Biology 248
Replace Anatoliy Koval with:
Anatoliy Koval United States
Elisabeth Oelmann Germany
M Fukumoto Japan
Valentina Pettirossi Italy
Peter Kjellén Sweden
Toshiko Yamochi Japan
Hilda Martinez-Diaz United States
Carol Sawyer United Kingdom
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Citations per field
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Citations per year

Countries citing papers authored by JM Heward

Since Specialization
Citations

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

Fields of papers citing papers by JM Heward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside JM Heward, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with JM Heward Line = papers co-authored together JM Heward links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 1986185
2 199686
3 199479
4 199943
5
Concurrent activation of MYC and BCL2 in B cell non-Hodgkin lymphoma cell lines by translocation of both oncogenes to the same immunoglobulin heavy chain locus.
199633
6 199432
7 199330
8 199322
9
A new human T-cell lymphoma cell line (Karpas 384) of the T-cell receptor gamma/delta lineage with translocation t(7:14) (p13;q11.2).
199314
10 19944
11 19943
12
Association of the FCRL3 gene with Graves disease in the UK Caucasian population
20061
13 19931

About JM Heward

JM Heward is a scholar working on Genetics, Pathology and Forensic Medicine, Molecular Biology, Immunology and Public Health, Environmental and Occupational Health, having authored 13 papers that have together received 533 indexed citations. Recurring topics across this work include Chronic Lymphocytic Leukemia Research (7 papers), Lymphoma Diagnosis and Treatment (6 papers), Acute Lymphoblastic Leukemia research (3 papers), Chronic Myeloid Leukemia Treatments (2 papers), Diabetes and associated disorders (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Acute Myeloid Leukemia Research (1 paper) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Genetics (153 citations), Pathology and Forensic Medicine (146 citations), Immunology (118 citations), Hematology (44 citations) and Molecular Biology (248 citations). JM Heward has collaborated with scholars based in United Kingdom and Netherlands. Frequent co-authors include Martin J.S. Dyer, J. Paul Luzio, Michael D. Baron, Maria A. Soos, Jaime Bellatin, Kenneth Siddle, E. S. Lennox, D Jadayel, Daniel Catovsky and E Nacheva. Their work appears in journals such as Blood, Biochemical Journal, Annals of the Rheumatic Diseases and PubMed.

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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