Alexandra Evans

1.1k total citations
4 papers, 21 citations indexed

About

Alexandra Evans is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Alexandra Evans has authored 4 papers receiving a total of 21 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Pulmonary and Respiratory Medicine and 1 paper in Molecular Biology. Recurrent topics in Alexandra Evans's work include Ethics in Clinical Research (1 paper), Genomics and Rare Diseases (1 paper) and Neonatal Respiratory Health Research (1 paper). Alexandra Evans is often cited by papers focused on Ethics in Clinical Research (1 paper), Genomics and Rare Diseases (1 paper) and Neonatal Respiratory Health Research (1 paper). Alexandra Evans collaborates with scholars based in United Kingdom. Alexandra Evans's co-authors include Jérémy Hall, George Kirov, Samuel J. R. A. Chawner, Michael O’Donovan, Anita Thapar, Neena Modi, F. Lucy Raymond, Michael J. Owen, Nigel Williams and David Skuse and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and BMJ Open.

In The Last Decade

Alexandra Evans

4 papers receiving 21 citations

Peers

Alexandra Evans

MB

GENET

EPIDE

PPCH

PRM

Urszula Szymańska Poland

Diana A. Hobbs United States

A.G. Egorova Russia

David Skuse India

Олег Геннадьевич Мотовилин Russia

Jazib Hussain Denmark

Fuling Ji China

Cristina Dragomir Romania

Lindsay Lambie South Africa

Jennifer Cameron United States

Urszula Szymańska Poland

Alexandra Evans

5 ×0.8

MB

4 ×0.7

GENET

8 ×1.6

EPIDE

0 ×0.0

PPCH

5 ×1.3

PRM

Citations per year, relative to Alexandra Evans Alexandra Evans (= 1×) peers Urszula Szymańska

Countries citing papers authored by Alexandra Evans

Since Specialization

Citations

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

Fields of papers citing papers by Alexandra Evans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandra Evans

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

All Works

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4 of 4 papers shown

1.

Chawner, Samuel J. R. A., Alexandra Evans, Jeanne Wolstencroft, et al.. (2023). Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry. 13(1). 7–7. 8 indexed citations

2.

Chawner, Samuel J. R. A., Amy L. Paine, Matt J. Dunn, et al.. (2023). Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. SHILAP Revista de lepidopterología. 3(2). e12162–e12162. 5 indexed citations

3.

Warne, Naomi, Rhys Bevan Jones, Rachel Brown, et al.. (2022). Collecting genetic samples and linked mental health data from adolescents in schools: protocol coproduction and a mixed-methods pilot of feasibility and acceptability. BMJ Open. 12(2). e049283–e049283. 3 indexed citations

4.

Wong, Hilary, Alexandra Evans, George Kirov, et al.. (2020). Contribution of de novo and inherited rare CNVs to very preterm birth. Journal of Medical Genetics. 57(8). 552–557. 5 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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