Alistair Ward

62.3k total citations
7 papers, 313 citations indexed

About

Alistair Ward is a scholar working on Molecular Biology, Genetics and Artificial Intelligence. According to data from OpenAlex, Alistair Ward has authored 7 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Artificial Intelligence. Recurrent topics in Alistair Ward's work include Genomics and Rare Diseases (6 papers), Genomics and Phylogenetic Studies (4 papers) and Biomedical Text Mining and Ontologies (3 papers). Alistair Ward is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomics and Phylogenetic Studies (4 papers) and Biomedical Text Mining and Ontologies (3 papers). Alistair Ward collaborates with scholars based in United States. Alistair Ward's co-authors include Gábor Marth, Chip Stewart, Michael P. Strömberg, Erik Garrison, Jerilyn A. Walker, Miriam K. Konkel, Mark A. Batzer, Jiantao Wu, Chase Miller and Russell J. Butterfield and has published in prestigious journals such as PLoS ONE, Scientific Reports and BMC Genomics.

In The Last Decade

Alistair Ward

7 papers receiving 307 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alistair Ward United States	5	168	121	89	28	25	7	313
Christine Lambert United States	8	241 1.4×	171 1.4×	87 1.0×	55 2.0×	24 1.0×	11	411
Eric T. Dawson United States	6	228 1.4×	160 1.3×	105 1.2×	15 0.5×	39 1.6×	10	370
Oscar Westesson United States	8	181 1.1×	113 0.9×	52 0.6×	20 0.7×	17 0.7×	15	296
Wesley Brashear United States	12	169 1.0×	198 1.6×	64 0.7×	19 0.7×	46 1.8×	28	406
Chandana Tennakoon United Kingdom	11	334 2.0×	81 0.7×	86 1.0×	41 1.5×	25 1.0×	27	486
Junhao Su Hong Kong	6	140 0.8×	58 0.5×	35 0.4×	24 0.9×	15 0.6×	16	216
Alexander Payne United Kingdom	6	351 2.1×	74 0.6×	70 0.8×	54 1.9×	67 2.7×	8	453
Sarah Behrens Germany	11	205 1.2×	65 0.5×	62 0.7×	15 0.5×	30 1.2×	17	359
Harish Swaminathan United States	11	273 1.6×	154 1.3×	41 0.5×	19 0.7×	51 2.0×	15	419
Shining Ma United States	9	173 1.0×	89 0.7×	25 0.3×	22 0.8×	9 0.4×	21	253

Countries citing papers authored by Alistair Ward

Since Specialization

Citations

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

Fields of papers citing papers by Alistair Ward

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alistair Ward

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

All Works

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7 of 7 papers shown

1.

Ward, Alistair, Matt Velinder, Barry Moore, et al.. (2022). Clin.iobio: A Collaborative Diagnostic Workflow to Enable Team-Based Precision Genomics. Journal of Personalized Medicine. 12(1). 73–73. 2 indexed citations

2.

Velinder, Matt, Alistair Ward, 義行高橋, et al.. (2021). Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization. Scientific Reports. 11(1). 20307–20307. 11 indexed citations

3.

Velinder, Matt, et al.. (2019). Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists. BMC Medical Genomics. 12(1). 190–190. 4 indexed citations

4.

Ostrander, Betsy, Russell J. Butterfield, Brent S. Pedersen, et al.. (2018). Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy. npj Genomic Medicine. 3(1). 22–22. 54 indexed citations

5.

Ward, Alistair, Mary Anne Karren, Chase Miller, et al.. (2017). Rapid clinical diagnostic variant investigation of genomic patient sequencing data with iobio web tools. Journal of Clinical and Translational Science. 1(6). 381–386. 4 indexed citations

6.

Wu, Jiantao, Alistair Ward, Jerilyn A. Walker, et al.. (2014). Tangram: a comprehensive toolbox for mobile element insertion detection. BMC Genomics. 15(1). 795–795. 44 indexed citations

7.

Strömberg, Michael P., et al.. (2014). MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping. PLoS ONE. 9(3). e90581–e90581. 194 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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