Rachel Stapleton

498 total citations
11 papers, 136 citations indexed

About

Rachel Stapleton is a scholar working on Genetics, Hematology and Physiology. According to data from OpenAlex, Rachel Stapleton has authored 11 papers receiving a total of 136 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Hematology and 3 papers in Physiology. Recurrent topics in Rachel Stapleton's work include Blood groups and transfusion (4 papers), Erythrocyte Function and Pathophysiology (3 papers) and Genomics and Rare Diseases (2 papers). Rachel Stapleton is often cited by papers focused on Blood groups and transfusion (4 papers), Erythrocyte Function and Pathophysiology (3 papers) and Genomics and Rare Diseases (2 papers). Rachel Stapleton collaborates with scholars based in Nigeria, Australia and New Zealand. Rachel Stapleton's co-authors include C. C. Bowley, Belinda Chong, Dean Phelan, D. Voak, Sebastian Lunke, Zornitza Stark, Susan M. White, Matthew Regan, Justine E. Marum and Ian Woodcock and has published in prestigious journals such as Human Genetics, Vox Sanguinis and Seminars in Pediatric Neurology.

In The Last Decade

Rachel Stapleton

10 papers receiving 126 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rachel Stapleton Nigeria	5	57	38	26	20	19	11	136
Juliet Yuen United States	5	52 0.9×	31 0.8×	13 0.5×	15 0.8×	9 0.5×	9	137
C. R. Greenberg Canada	8	88 1.5×	72 1.9×	13 0.5×	9 0.5×	51 2.7×	13	218
Aisha Al Shamsi United Arab Emirates	6	35 0.6×	67 1.8×	10 0.4×	20 1.0×	18 0.9×	13	129
Dennis W. Bartholomew United States	8	48 0.8×	121 3.2×	8 0.3×	12 0.6×	52 2.7×	17	192
Petter Cappelen Endresen Norway	7	14 0.2×	78 2.1×	19 0.7×	11 0.6×	7 0.4×	11	159
S Jansen South Africa	6	65 1.1×	159 4.2×	11 0.4×	10 0.5×	4 0.2×	14	216
Katalin Szakszon Hungary	10	103 1.8×	178 4.7×	7 0.3×	26 1.3×	27 1.4×	29	276
U Theile Germany	9	147 2.6×	144 3.8×	9 0.3×	9 0.5×	4 0.2×	23	242
Gordon J. Hildick-Smith United States	7	15 0.3×	121 3.2×	33 1.3×	49 2.5×	22 1.2×	9	204
Elena Nicchia Italy	6	17 0.3×	96 2.5×	32 1.2×	15 0.8×	8 0.4×	6	136

Countries citing papers authored by Rachel Stapleton

Since Specialization

Citations

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

Fields of papers citing papers by Rachel Stapleton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Stapleton

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

All Works

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11 of 11 papers shown

Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Rachel Stapleton, et al.. (2021). A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum. Human Genetics. 140(6). 933–944. 16 indexed citations

Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations

Stapleton, Rachel, Tim Morgan, Ian Hayes, et al.. (2018). A pilot study of exome sequencing in a diverse New Zealand cohort with undiagnosed disorders and cancer. Journal of the Royal Society of New Zealand. 48(4). 262–279. 3 indexed citations

Woodcock, Ian, Manoj P. Menezes, Lee Coleman, et al.. (2017). Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome. Seminars in Pediatric Neurology. 26. 2–9. 25 indexed citations

Stapleton, Rachel. (1970). Pepsin ‘A’ Substance ‐ Further Uses. Vox Sanguinis. 18(3). 287–288. 2 indexed citations

Voak, D., et al.. (1970). The Incidence of H Deficient A₂ and A₂B Bloods and Family Studies on the AH/ABH Status of an A_int, and Some New Variant Blood Types (A_{int H↓}^A₁, A_2↑Hw^A₁, A._2↑B_H^A₁B and A_2↓B_H^A₂B. Vox Sanguinis. 19(1). 73–84. 20 indexed citations

Voak, D., Rachel Stapleton, & C. C. Bowley. (1968). A(2h)^A1 New Variant of A(h), in two Group A Membersof an English Family. Vox Sanguinis. 14(1). 18–30. 1 indexed citations

Stapleton, Rachel, et al.. (1968). A_2h^A1 a New Variant of A_h, in two Group A Members of an English Family.. Vox Sanguinis. 14(1). 18–30. 18 indexed citations

Dunsford, I. & Rachel Stapleton. (1959). Bloods from Recently Delivered Women which Were Found Lacking the Expected Anti‐A or Anti‐B Antibodies. Vox Sanguinis. 4(5). 409–412. 1 indexed citations

10.

Dunsford, I. & Rachel Stapleton. (1959). In vitro Absorption of the Rhesus Antibody Anti‐D by Rhesus Negative Red Cells. Vox Sanguinis. 4(5). 406–408. 3 indexed citations

11.

Stapleton, Rachel, et al.. (1951). Blood Grouping on Blotting-paper. BMJ. 1(4703). 416–416. 3 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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