Daniel Ward

1.0k total citations
14 papers, 564 citations indexed

About

Daniel Ward is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Daniel Ward has authored 14 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Genetics. Recurrent topics in Daniel Ward's work include Acute Myeloid Leukemia Research (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers). Daniel Ward is often cited by papers focused on Acute Myeloid Leukemia Research (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers). Daniel Ward collaborates with scholars based in United Kingdom, Germany and Greece. Daniel Ward's co-authors include Sarah Ennis, Anna Murray, Nicholas C.P. Cross, Andrew Chase, Amy V. Jones, C. Mattocks, Joannah Score, Katerina Zoi, Konstanze Döhner and Reuben J. Pengelly and has published in prestigious journals such as Blood, Scientific Reports and Molecular Ecology.

In The Last Decade

Daniel Ward

14 papers receiving 549 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Ward United Kingdom 10 279 227 108 100 97 14 564
Dennis Burian United States 12 109 0.4× 412 1.8× 164 1.5× 72 0.7× 108 1.1× 24 871
Violaine Bourdon France 12 309 1.1× 607 2.7× 267 2.5× 102 1.0× 44 0.5× 27 955
James Tepperberg United States 15 532 1.9× 362 1.6× 86 0.8× 67 0.7× 14 0.1× 28 889
Frank X. Donovan United States 15 194 0.7× 621 2.7× 55 0.5× 40 0.4× 47 0.5× 26 784
Wendy Horsfall Canada 9 109 0.4× 175 0.8× 106 1.0× 41 0.4× 83 0.9× 13 408
Anne W. Higgins United States 11 360 1.3× 529 2.3× 101 0.9× 70 0.7× 32 0.3× 17 885
Azzedine Aboura France 17 525 1.9× 311 1.4× 55 0.5× 53 0.5× 25 0.3× 40 767
Irene Homminga Netherlands 14 77 0.3× 412 1.8× 200 1.9× 39 0.4× 115 1.2× 21 828
A. Dutra United States 8 315 1.1× 416 1.8× 100 0.9× 45 0.5× 58 0.6× 10 599
Merete Bugge Denmark 10 584 2.1× 935 4.1× 31 0.3× 34 0.3× 57 0.6× 15 1.2k

Countries citing papers authored by Daniel Ward

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Ward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Ward

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

All Works

14 of 14 papers shown
1.
Ward, Daniel, et al.. (2021). On the use of genome‐wide data to model and date the time of anthropogenic hybridisation: An example from the Scottish wildcat. Molecular Ecology. 30(15). 3688–3702. 16 indexed citations
2.
Pengelly, Reuben J., Daniel Ward, David Hunt, C. Mattocks, & Sarah Ennis. (2020). Comparison of Mendeliome exome capture kits for use in clinical diagnostics. Scientific Reports. 10(1). 3235–3235. 9 indexed citations
3.
Cree, Angela J., Daniel Ward, Helen Griffiths, et al.. (2019). Comprehensive sequencing of the myocilin gene in a selected cohort of severe primary open-angle glaucoma patients. Scientific Reports. 9(1). 3100–3100. 7 indexed citations
4.
Gibson, Jane Whitney, Reuben J. Pengelly, Diana Baralle, et al.. (2017). Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B). Scientific Reports. 7(1). 4415–4415. 46 indexed citations
5.
Rae, William, Daniel Ward, C. Mattocks, et al.. (2017). Clinical efficacy of a next‐generation sequencing gene panel for primary immunodeficiency diagnostics. Clinical Genetics. 93(3). 647–655. 45 indexed citations
6.
Rae, William, Daniel Ward, C. Mattocks, et al.. (2017). Autoimmunity/inflammation in a monogenic primary immunodeficiency cohort. Clinical & Translational Immunology. 6(9). e155–e155. 15 indexed citations
7.
Jones, Amy V., Daniel Ward, Matthew Lyon, et al.. (2014). Evaluation of methods to detect CALR mutations in myeloproliferative neoplasms. Leukemia Research. 39(1). 82–87. 46 indexed citations
8.
Score, Joannah, Claire Hidalgo-Curtis, Amy V. Jones, et al.. (2011). Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms. Blood. 119(5). 1208–1213. 125 indexed citations
9.
Cross, Nicholas C.P., Joannah Score, Claire Hidalgo-Curtis, et al.. (2011). Inactivation of Polycomb Repressive Complex 2 Components in Myeloproliferative and Myelodysplastic/Myeloproliferative Neoplasms. Blood. 118(21). 617–617. 4 indexed citations
10.
Mattocks, C., Daniel Ward, Tom Janssens, et al.. (2010). Interlaboratory Diagnostic Validation of Conformation-Sensitive Capillary Electrophoresis for Mutation Scanning. Clinical Chemistry. 56(4). 593–602. 10 indexed citations
11.
Ennis, Sarah, Daniel Ward, & Anna Murray. (2005). Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers. European Journal of Human Genetics. 14(2). 253–255. 130 indexed citations
12.
Zeggini, Eleftheria, Anne Barton, Stephen Eyre, et al.. (2005). Characterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definition. BMC Genetics. 6(1). 21–21. 9 indexed citations
13.
Barton, Anne, Francine Jury, Stephen Eyre, et al.. (2004). Haplotype analysis in simplex families and novel analytic approaches in a case–control cohort reveal no evidence of association of the CTLA‐4 gene with rheumatoid arthritis. Arthritis & Rheumatism. 50(3). 748–752. 44 indexed citations
14.
Tenesa, Albert, Sara Knott, Daniel Ward, et al.. (2003). Estimation of linkage disequilibrium in a sample of the United Kingdom dairy cattle population using unphased genotypes1. Journal of Animal Science. 81(3). 617–623. 58 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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