Andrew Farrell

2.9k total citations
14 papers, 436 citations indexed

About

Andrew Farrell is a scholar working on Genetics, Parasitology and Epidemiology. According to data from OpenAlex, Andrew Farrell has authored 14 papers receiving a total of 436 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 4 papers in Parasitology and 3 papers in Epidemiology. Recurrent topics in Andrew Farrell's work include Toxoplasma gondii Research Studies (4 papers), Genomics and Rare Diseases (3 papers) and Cancer Genomics and Diagnostics (3 papers). Andrew Farrell is often cited by papers focused on Toxoplasma gondii Research Studies (4 papers), Genomics and Rare Diseases (3 papers) and Cancer Genomics and Diagnostics (3 papers). Andrew Farrell collaborates with scholars based in United States, United Kingdom and Türkiye. Andrew Farrell's co-authors include Gábor Marth, Marc‐Jan Gubbels, D. C. E. Speller, David W. Warnock, Sivasakthivel Thirugnanam, David Ferguson, Alexander Lorestani, Jeffrey D. Dvorin, Manoj T. Duraisingh and Lynn B. Jorde and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and Cancer Research.

In The Last Decade

Andrew Farrell

14 papers receiving 418 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew Farrell United States 9 151 148 139 94 72 14 436
Shih‐Che Weng Taiwan 12 65 0.4× 95 0.6× 117 0.8× 26 0.3× 30 0.4× 21 394
Sarah Veloso Nogueira Brazil 11 73 0.5× 128 0.9× 129 0.9× 32 0.3× 35 0.5× 11 464
Binbin Ding China 10 49 0.3× 181 1.2× 303 2.2× 40 0.4× 44 0.6× 17 524
Seppo Saari Finland 11 70 0.5× 41 0.3× 64 0.5× 38 0.4× 65 0.9× 22 427
Rebeca Manning‐Cela Mexico 15 136 0.9× 285 1.9× 374 2.7× 33 0.4× 35 0.5× 44 667
Xibing Che United States 17 60 0.4× 113 0.8× 372 2.7× 61 0.6× 148 2.1× 24 665
Pauline Verlhac France 11 58 0.4× 131 0.9× 322 2.3× 29 0.3× 18 0.3× 19 460
Robert Faris United States 11 49 0.3× 200 1.4× 108 0.8× 26 0.3× 14 0.2× 28 458
L C Lim United States 14 329 2.2× 153 1.0× 72 0.5× 47 0.5× 19 0.3× 26 604
Emanuel Campoy Argentina 9 73 0.5× 162 1.1× 111 0.8× 20 0.2× 11 0.2× 14 345

Countries citing papers authored by Andrew Farrell

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Farrell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Farrell

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Farrell. A scholar is included among the top collaborators of Andrew Farrell 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 Andrew Farrell. Andrew Farrell 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.
2.
Wen, Ting, Andrew Farrell, Rong Mao, et al.. (2022). Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome. Molecular Case Studies. 8(7). a006242–a006242. 5 indexed citations
3.
Huang, Xiaomeng, 義行 高橋, Samuel W. Brady, et al.. (2021). Novel temporal and spatial patterns of metastatic colonization from breast cancer rapid-autopsy tumor biopsies. Genome Medicine. 13(1). 170–170. 8 indexed citations
4.
Farrell, Andrew, Julia Wynn, Barry Moore, et al.. (2020). Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias. SHILAP Revista de lepidopterología. 1(1). 100008–100008. 5 indexed citations
5.
Feusier, Julie, W. Scott Watkins, Jainy Thomas, et al.. (2019). Pedigree-based estimation of human mobile element retrotransposition rates. Genome Research. 29(10). 1567–1577. 67 indexed citations
6.
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
7.
Wooderchak‐Donahue, Whitney, Jamie McDonald, Andrew Farrell, et al.. (2018). Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia. Journal of Medical Genetics. 55(12). 824–830. 12 indexed citations
8.
高橋, 義行, Xiaomeng Huang, Dillon Lee, et al.. (2018). Abstract 3280: Utah somatic variant calling pipeline featuring multi-sample joint calling, variant-graph based accurate allele frequency estimation and subclone analysis. Cancer Research. 78(13_Supplement). 3280–3280. 1 indexed citations
9.
Cantarel, Brandi L., Yunping Lei, Daniel Weaver, et al.. (2015). Analysis of archived residual newborn screening blood spots after whole genome amplification. BMC Genomics. 16(1). 602–602. 4 indexed citations
10.
Brown, Kevin M., Elena S. Suvorova, Andrew Farrell, et al.. (2014). Forward Genetic Screening Identifies a Small Molecule That Blocks Toxoplasma gondii Growth by Inhibiting Both Host- and Parasite-Encoded Kinases. PLoS Pathogens. 10(6). e1004180–e1004180. 35 indexed citations
11.
Farrell, Andrew, Bradley I. Coleman, Kevin M. Brown, et al.. (2014). Whole genome profiling of spontaneous and chemically induced mutations in Toxoplasma gondii. BMC Genomics. 15(1). 354–354. 28 indexed citations
12.
Yang, Ninghan, Andrew Farrell, Wendy Niedelman, et al.. (2013). Genetic basis for phenotypic differences between different Toxoplasma gondii type I strains. BMC Genomics. 14(1). 467–467. 37 indexed citations
13.
Farrell, Andrew, Sivasakthivel Thirugnanam, Alexander Lorestani, et al.. (2012). A DOC2 Protein Identified by Mutational Profiling Is Essential for Apicomplexan Parasite Exocytosis. Science. 335(6065). 218–221. 103 indexed citations
14.
Warnock, David W., et al.. (1979). Resistogram Method for Differentiation of Strains of Candida albicans. Journal of Applied Bacteriology. 46(3). 571–578. 76 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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