E Belcher

2.8k total citations
9 papers, 65 citations indexed

About

E Belcher is a scholar working on Physiology, Hematology and Genetics. According to data from OpenAlex, E Belcher has authored 9 papers receiving a total of 65 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Physiology, 3 papers in Hematology and 3 papers in Genetics. Recurrent topics in E Belcher's work include Erythrocyte Function and Pathophysiology (4 papers), Genomics and Rare Diseases (3 papers) and Blood groups and transfusion (3 papers). E Belcher is often cited by papers focused on Erythrocyte Function and Pathophysiology (4 papers), Genomics and Rare Diseases (3 papers) and Blood groups and transfusion (3 papers). E Belcher collaborates with scholars based in Canada and United States. E Belcher's co-authors include Gail Coghlan, Sylvia Philipps, M. Lewis, Hiroko Kaita, P.J. McAlpine, R. A. Woods, L.E. Seargeant, Jane Evans, B.N. Chodirker and Cheryl R. Greenberg and has published in prestigious journals such as Genomics, Cancers and Transfusion.

In The Last Decade

E Belcher

8 papers receiving 64 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E Belcher Canada	5	22	21	18	16	14	9	65
Sakshi Gera United States	7	37 1.7×	10 0.5×	14 0.8×	31 1.9×	14 1.0×	12	114
Beata Samelko United States	6	33 1.5×	5 0.2×	10 0.6×	7 0.4×	12 0.9×	6	104
Beata Gyorgy France	4	26 1.2×	28 1.3×	8 0.4×	15 0.9×	29 2.1×	6	91
Charles E. Bills United States	2	15 0.7×	4 0.2×	24 1.3×	12 0.8×	19 1.4×	4	91
Ranadheer R. Dande United States	4	19 0.9×	5 0.2×	7 0.4×	7 0.4×	6 0.4×	5	88
Purdey J. Campbell Australia	4	25 1.1×	13 0.6×	8 0.4×	31 1.9×	43 3.1×	10	120
Mona Al-Maarri Germany	3	34 1.5×	6 0.3×	29 1.6×	13 0.8×	7 0.5×	3	113
Myriam Boyer-Clavel France	4	38 1.7×	9 0.4×	27 1.5×	5 0.3×	4 0.3×	5	95
Anne Thorwarth Germany	4	35 1.6×	11 0.5×	4 0.2×	14 0.9×	16 1.1×	15	70
Amy Hietala United States	4	113 5.1×	26 1.2×	18 1.0×	37 2.3×	15 1.1×	7	137

Countries citing papers authored by E Belcher

Since Specialization

Citations

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

Fields of papers citing papers by E Belcher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E Belcher

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

All Works

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9 of 9 papers shown

1.

Zhang, Shulin, Nan Lin, E Belcher, et al.. (2024). Feasibility and Clinical Utility of Reporting Hereditary Cancer Predisposition Pathogenic Variants Identified in Research Germline Sequencing: A Prospective Interventional Study. JCO Precision Oncology. 8(8). e2300266–e2300266. 1 indexed citations

2.

Zhang, Shulin, Nan Lin, James W. Keck, et al.. (2022). Real-World Evaluation of a Population Germline Genetic Screening Initiative for Family Medicine Patients. Journal of Personalized Medicine. 12(8). 1297–1297. 3 indexed citations

3.

Kolesar, Jill, E Belcher, Donna K. Arnett, et al.. (2022). Preliminary Research on a COVID-19 Test Strategy to Guide Quarantine Interval in University Students. COVID. 2(3). 254–260.

4.

Lin, Nan, Shulin Zhang, Catherine R. Sears, et al.. (2021). Real-World Evaluation of Universal Germline Screening for Cancer Treatment-Relevant Pharmacogenes. Cancers. 13(18). 4524–4524. 5 indexed citations

5.

Coghlan, Gail, Hiroko Kaita, E Belcher, Sylvia Philipps, & Marion Lewis. (1989). Evidence for Genetic Linkage between the KEL and YT Blood Group Loci. Vox Sanguinis. 57(1). 88–89. 5 indexed citations

6.

Lewis, M., Hiroko Kaita, Sylvia Philipps, et al.. (1988). The Swann Phenotype 700:4,‐41; Genetic Studies. Vox Sanguinis. 54(3). 184–187. 4 indexed citations

7.

Zelinski, Teresa, Hiroko Kaita, M. Lewis, et al.. (1988). The Colton blood group locus. Transfusion. 28(5). 435–438. 7 indexed citations

8.

Lewis, M., Hiroko Kaita, Gail Coghlan, et al.. (1988). The chromosome 19 linkage group LDLR, C3, LW, APOC2, LU, SE in man. Annals of Human Genetics. 52(2). 137–144. 18 indexed citations

9.

Chodirker, B.N., Jane Evans, M. Lewis, et al.. (1987). Infantile hypophosphatasia—Linkage with the RH locus. Genomics. 1(3). 280–282. 22 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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