Marcus Coyle

1.3k total citations
2 papers, 4 citations indexed

About

Marcus Coyle is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Hematology. According to data from OpenAlex, Marcus Coyle has authored 2 papers receiving a total of 4 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Genetics, 1 paper in Pediatrics, Perinatology and Child Health and 1 paper in Hematology. Recurrent topics in Marcus Coyle's work include Genomic variations and chromosomal abnormalities (2 papers), Acute Myeloid Leukemia Research (1 paper) and Chromosomal and Genetic Variations (1 paper). Marcus Coyle is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Acute Myeloid Leukemia Research (1 paper) and Chromosomal and Genetic Variations (1 paper). Marcus Coyle collaborates with scholars based in United Kingdom and United States. Marcus Coyle's co-authors include John D. West, Katrine West, Peter Ellis, Patricia Hixson, Ankita Patel, Chung-Che Chang, Sau Wai Cheung and Weimin Bi and has published in prestigious journals such as Blood and Molecular Reproduction and Development.

In The Last Decade

Marcus Coyle

2 papers receiving 4 citations

Peers

Marcus Coyle

PS

GENET

MB

PPCH

Kristine Bonnevie Norway

Tatiana Rodríguez Czechia

A. D. Hall

Alfred Charles True

A. de Bary Burkina Faso

Dave Saunders United Kingdom

William C. Davis United States

Robert Henry Aders Plimmer

Helmholtz Zentrum München Netherlands

A. Skovsted United Kingdom

Kristine Bonnevie Norway

Marcus Coyle

2 ×0.5

PS

4 ×1.3

GENET

1 ×1.0

MB

0 ×0.0

PPCH

Citations per year, relative to Marcus Coyle Marcus Coyle (= 1×) peers Kristine Bonnevie

Countries citing papers authored by Marcus Coyle

Since Specialization

Citations

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

Fields of papers citing papers by Marcus Coyle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcus Coyle

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

All Works

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2 of 2 papers shown

1.

Patel, Ankita, Patricia Hixson, Weimin Bi, et al.. (2011). Is It Time for Arraycgh to Be the First Line Test for Detection of Chromosome Abnormalities in Hematological Disorders-Example Multiple Myeloma. Blood. 118(21). 2543–2543. 1 indexed citations

2.

Ellis, Peter, et al.. (1990). Relevance to prenatal diagnosis of the identification of a human Y/autosome translocation by Y‐chromosome‐specific in situ hybridisation. Molecular Reproduction and Development. 25(1). 37–41. 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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