Eleanor Howard

2.3k total citations · 1 hit paper
3 papers, 862 citations indexed

About

Eleanor Howard is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Eleanor Howard has authored 3 papers receiving a total of 862 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 1 paper in Surgery and 1 paper in Genetics. Recurrent topics in Eleanor Howard's work include RNA modifications and cancer (1 paper), Genetic factors in colorectal cancer (1 paper) and DNA Repair Mechanisms (1 paper). Eleanor Howard is often cited by papers focused on RNA modifications and cancer (1 paper), Genetic factors in colorectal cancer (1 paper) and DNA Repair Mechanisms (1 paper). Eleanor Howard collaborates with scholars based in United Kingdom, Germany and Saudi Arabia. Eleanor Howard's co-authors include Alison J. Coffey, Clare L. Scott, Iwanka Kozarewa, Daniel J. Turner, Jay Shendure, Lira Mamanova, Akash Kumar, Emily H. Turner, Carol Scott and Claire E. L. Smith and has published in prestigious journals such as SHILAP Revista de lepidopterología, Nature Methods and American Journal of Medical Genetics Part A.

In The Last Decade

Eleanor Howard

3 papers receiving 845 citations

Hit Papers

Target-enrichment strategies for next-generation sequencing 2010 2026 2015 2020 2010 250 500 750

Peers

Eleanor Howard
Alison J. Coffey United Kingdom
John P. Didion United States
Joshua Paul United States
Lira Mamanova United Kingdom
Jarret Glasscock United States
Lynne Nazareth United States
Nam Nguyen United States
Alison J. Coffey United Kingdom
Eleanor Howard
Citations per year, relative to Eleanor Howard Eleanor Howard (= 1×) peers Alison J. Coffey

Countries citing papers authored by Eleanor Howard

Since Specialization
Citations

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

Fields of papers citing papers by Eleanor Howard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eleanor Howard

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

All Works

3 of 3 papers shown
1.
Raffan, Eleanor, Liam A. Hurst, Saeed Al Turki, et al.. (2011). Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. SHILAP Revista de lepidopterología. 2. 8–8. 9 indexed citations
2.
Mamanova, Lira, Alison J. Coffey, Clare L. Scott, et al.. (2010). Target-enrichment strategies for next-generation sequencing. Nature Methods. 7(2). 111–118. 841 indexed citations breakdown →
3.
Wieczorek, Dagmar, Charles Shaw‐Smith, Jürgen Kohlhase, et al.. (2007). Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup‐shaped ears, congenital heart defect, and mental retardation—New MCA/MR syndrome in two affected sibs and a mildly affected mother?. American Journal of Medical Genetics Part A. 143A(11). 1135–1142. 12 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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