David Coote

947 total citations
5 papers, 30 citations indexed

About

David Coote is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, David Coote has authored 5 papers receiving a total of 30 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in David Coote's work include Muscle Physiology and Disorders (3 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). David Coote is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). David Coote collaborates with scholars based in Australia, Spain and France. David Coote's co-authors include Nigel G. Laing, Gianina Ravenscroft, Hayley Goullée, Mark R. Davis, Macarena Cabrera‐Serrano, Kristen L. Nowak, Zornitza Stark, Erik Andersen, Merrilee Needham and Ryosuke Ishimura and has published in prestigious journals such as Journal of Medical Genetics, European Journal of Human Genetics and Acta Neuropathologica Communications.

In The Last Decade

David Coote

5 papers receiving 30 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Coote Australia	3	25	14	9	4	4	5	30
Ikhlas Ben Ayed Tunisia	4	22 0.9×	13 0.9×	5 0.6×	2 0.5×	4 1.0×	12	40
Anoud Albader Saudi Arabia	3	19 0.8×	9 0.6×	11 1.2×	5 1.3×	2 0.5×	4	29
Thais S. Rizzi Netherlands	3	12 0.5×	6 0.4×	7 0.8×	2 0.5×	2 0.5×	5	59
Dace Ruklisa United Kingdom	4	25 1.0×	11 0.8×	5 0.6×	7 1.8×	12 3.0×	7	49
Lauren E. Schwartz United States	4	34 1.4×	13 0.9×	11 1.2×		4 1.0×	5	47
Aaina Kochhar United States	4	17 0.7×	13 0.9×	6 0.7×		5 1.3×	5	28
Pierre Sinajon Canada	3	29 1.2×	26 1.9×	8 0.9×		2 0.5×	3	71
Clarissa Rocca United Kingdom	4	15 0.6×	9 0.6×	6 0.7×	2 0.5×	2 0.5×	8	36
Melanie Patterson United States	4	46 1.8×	19 1.4×	16 1.8×	1 0.3×	4 1.0×	6	61
Sarah Jones United States	4	21 0.8×	5 0.4×	6 0.7×	3 0.8×	5 1.3×	12	54

Countries citing papers authored by David Coote

Since Specialization

Citations

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

Fields of papers citing papers by David Coote

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Coote

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

All Works

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5 of 5 papers shown

1.

Cabrera‐Serrano, Macarena, David Coote, Dimitar N. Azmanov, et al.. (2020). A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy. Journal of Medical Genetics. 57(12). 835–842. 19 indexed citations

2.

Clayton, Joshua S., Elyshia McNamara, Hayley Goullée, et al.. (2020). Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy. Acta Neuropathologica Communications. 8(1). 142–142. 4 indexed citations

3.

Coote, David, Mark R. Davis, Macarena Cabrera‐Serrano, et al.. (2018). CUGC for Duchenne muscular dystrophy (DMD). European Journal of Human Genetics. 26(5). 749–757. 2 indexed citations

4.

Coote, David, Mark R. Davis, Macarena Cabrera‐Serrano, et al.. (2018). Clinical Utility Gene Card for: Becker muscular dystrophy. European Journal of Human Genetics. 26(7). 1065–1071. 2 indexed citations

5.

Coote, David, Mark R. Davis, Macarena Cabrera‐Serrano, et al.. (2018). Clinical Utility Gene Card for: autosomal dominant myotonia congenita (Thomsen Disease). European Journal of Human Genetics. 26(7). 1072–1077. 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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