Andrew E. Timms

5.7k total citations
62 papers, 1.9k citations indexed

About

Andrew E. Timms is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Andrew E. Timms has authored 62 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 20 papers in Genetics and 14 papers in Rheumatology. Recurrent topics in Andrew E. Timms's work include Spondyloarthritis Studies and Treatments (12 papers), Rheumatoid Arthritis Research and Therapies (8 papers) and CRISPR and Genetic Engineering (6 papers). Andrew E. Timms is often cited by papers focused on Spondyloarthritis Studies and Treatments (12 papers), Rheumatoid Arthritis Research and Therapies (8 papers) and CRISPR and Genetic Engineering (6 papers). Andrew E. Timms collaborates with scholars based in United States, United Kingdom and Australia. Andrew E. Timms's co-authors include Matthew A. Brown, B P Wordsworth, Andrei Călin, David R. Beier, L Bradbury, Sinéad Brophy, Steven H. Laval, Anthony Barnett, Michael Dunn and Amanda Wilson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Immunology.

In The Last Decade

Andrew E. Timms

59 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew E. Timms United States	25	723	591	501	386	214	62	1.9k
Bruno Leheup France	29	1.1k 1.5×	758 1.3×	171 0.3×	238 0.6×	239 1.1×	97	2.2k
Markus Bergmann Germany	27	988 1.4×	192 0.3×	472 0.9×	476 1.2×	221 1.0×	88	3.8k
Mohammed Al‐Owain Saudi Arabia	25	1.1k 1.5×	595 1.0×	350 0.7×	356 0.9×	68 0.3×	87	2.0k
Koichi Miyake Japan	26	1.2k 1.7×	379 0.6×	117 0.2×	144 0.4×	182 0.9×	73	2.1k
Nessa Hawkins United States	16	971 1.3×	343 0.6×	307 0.6×	710 1.8×	140 0.7×	22	2.4k
Edward C. Hsiao United States	29	1.7k 2.4×	363 0.6×	1.1k 2.2×	442 1.1×	417 1.9×	100	3.8k
Phillip J. Dexheimer United States	19	664 0.9×	326 0.6×	214 0.4×	321 0.8×	483 2.3×	36	1.5k
Tetsuya Niihori Japan	27	1.8k 2.6×	495 0.8×	604 1.2×	659 1.7×	189 0.9×	78	2.9k
Douglas J. Wilkin United States	22	1.4k 1.9×	1.1k 1.9×	311 0.6×	109 0.3×	260 1.2×	29	2.7k
Minna Pöyhönen Finland	31	865 1.2×	260 0.4×	783 1.6×	249 0.6×	206 1.0×	76	3.7k

Countries citing papers authored by Andrew E. Timms

Since Specialization

Citations

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

Fields of papers citing papers by Andrew E. Timms

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew E. Timms

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

All Works

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20 of 20 papers shown

Timms, Andrew E., et al.. (2023). Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes. International Journal of Molecular Sciences. 24(6). 5353–5353. 1 indexed citations

VandenBosch, Leah S., et al.. (2022). Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis -Regulatory Elements. Translational Vision Science & Technology. 11(4). 16–16. 5 indexed citations

Ha, Seungshin, Scott Houghtaling, Andrew E. Timms, et al.. (2022). The arginine methyltransferaseCarm1is necessary for heart development. G3 Genes Genomes Genetics. 12(8). 4 indexed citations

Timms, Andrew E., Xiao Fan, Kimberly Foss, et al.. (2022). Clinical, neuroimaging and molecular characteristics of PPP2R5D-related neurodevelopmental disorders: an expanded series with functional characterisation and genotype–phenotype analysis. Journal of Medical Genetics. 60(5). 511–522. 15 indexed citations

Riolobos, Laura, Ekram Gad, Piper M. Treuting, et al.. (2019). The Effect of Mouse Strain, Sex, and Carcinogen Dose on Toxicity and the Development of Lung Dysplasia and Squamous Cell Carcinomas in Mice. Cancer Prevention Research. 12(8). 507–516. 9 indexed citations

Clarke, Christine M., Jennifer A. Gustafson, Matthew D. Smyth, et al.. (2017). Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. American Journal of Medical Genetics Part A. 176(2). 290–300. 33 indexed citations

Timms, Andrew E. & Marshall S. Horwitz. (2010). KLHDC8Bin Hodgkin lymphoma and possibly twinning. Communicative & Integrative Biology. 3(2). 154–158. 3 indexed citations

Carter, Kim W., Anna Pluzhnikov, Andrew E. Timms, et al.. (2007). Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis. Lara D. Veeken. 46(5). 763–771. 50 indexed citations

Pointon, J J, Andrew E. Timms, L Bradbury, Matthew A. Brown, & P Wordsworth. (2006). Analysis of positional candidate genes in ankylosing spondylitis: A possible role for ENPP1. Lara D. Veeken. 45. 1 indexed citations

10.

Pluzhnikov, Anna, Andrew E. Timms, Corinne Miceli‐Richard, et al.. (2005). Meta-analysis in ankylosing spondylitis (AS) - Genomewide linkage map including 589 affected sibling pairs. Queensland's institutional digital repository (The University of Queensland). 52(5). 368–369.

11.

Timms, Andrew E., et al.. (2005). Fine-mapping of the IL-1 gene cluster pinpoints genetic associations with ankylosing spondylitis.. Queensland's institutional digital repository (The University of Queensland). 52(9). 2 indexed citations

12.

Timms, Andrew E., Alison M. Crane, Heather J. Cordell, et al.. (2004). The Interleukin 1 Gene Cluster Contains a Major Susceptibility Locus for Ankylosing Spondylitis. The American Journal of Human Genetics. 75(4). 587–595. 98 indexed citations

13.

Timms, Andrew E., et al.. (2003). Genetic testing for haemochromatosis in patients with chondrocalcinosis (vol 61, pg 745, 2002). Annals of the Rheumatic Diseases. 62. 192–192. 1 indexed citations

14.

Timms, Andrew E., et al.. (2003). Investigation of the role of ANKH in ankylosing spondylitis. Queensland's institutional digital repository (The University of Queensland). 3 indexed citations

15.

Brown, Matthew A., Andrew E. Timms, Youming Zhang, & R.G.G. Russell. (2003). Genetics of chondrocalcinosis and related disorders. Annals of the Rheumatic Diseases. 62. 26–26. 1 indexed citations

16.

Timms, Andrew E., et al.. (2003). Investigation of the role of ANKHin ankylosing spondylitis. Arthritis & Rheumatism. 1 indexed citations

17.

Williams, Charlene J., Yun Zhang, Andrew E. Timms, et al.. (2002). Autosomal Dominant Familial Calcium Pyrophosphate Dihydrate Deposition Disease Is Caused by Mutation in the Transmembrane Protein ANKH. The American Journal of Human Genetics. 71(4). 985–991. 85 indexed citations

18.

Brophy, Sinéad, L Bradbury, Andrew E. Timms, et al.. (2001). Towards defining the genetic determinants of disease severity in ankylosing spondylitis.. Queensland's institutional digital repository (The University of Queensland). 44(9). 5 indexed citations

19.

Edwards, Steven W., Andrew E. Timms, L Bradbury, B P Wordsworth, & Matthew A. Brown. (2001). Interleukin-1 and susceptibility to ankylosing spondylitis. Lara D. Veeken. 40. 17–17. 2 indexed citations

20.

Brown, Matthew A., S.H. Laval, Andrew E. Timms, et al.. (2000). Confirmation of non-MHC genetic loci by whole genome linkage studies in ankylosing spondylitis.. Queensland's institutional digital repository (The University of Queensland). 43(9). 1 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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