Sinéad Walsh

1.4k total citations
15 papers, 928 citations indexed

About

Sinéad Walsh is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Sinéad Walsh has authored 15 papers receiving a total of 928 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Sinéad Walsh's work include Genomics, phytochemicals, and oxidative stress (4 papers), Glutathione Transferases and Polymorphisms (4 papers) and Craniofacial Disorders and Treatments (3 papers). Sinéad Walsh is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (4 papers), Glutathione Transferases and Polymorphisms (4 papers) and Craniofacial Disorders and Treatments (3 papers). Sinéad Walsh collaborates with scholars based in United Kingdom, Ireland and Spain. Sinéad Walsh's co-authors include Andrew O.M. Wilkie, Steven A. Wall, Martin S. Williamson, Terence Lewis, Michael Kristensen, G. D. Moores, A. L. Devonshire, Stephen R.F. Twigg, Navaratnam Elanko and Jane A. Hurst and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Biochemical Journal.

In The Last Decade

Sinéad Walsh

15 papers receiving 899 citations

Peers

Sinéad Walsh
Sinéad Walsh
Citations per year, relative to Sinéad Walsh Sinéad Walsh (= 1×) peers Deborah C. I. Goberdhan

Countries citing papers authored by Sinéad Walsh

Since Specialization
Citations

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

Fields of papers citing papers by Sinéad Walsh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sinéad Walsh

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

All Works

15 of 15 papers shown
1.
Walsh, Sinéad, et al.. (2013). Facilitating relational framing in children and individuals with developmental delay using the relational completion procedure. Journal of the Experimental Analysis of Behavior. 101(1). 51–60. 9 indexed citations
2.
Robertson, Stephen P., Sinéad Walsh, Michael Oldridge, et al.. (2001). Linkage of Otopalatodigital Syndrome Type 2 (OPD2) to Distal Xq28: Evidence for Allelism with OPD1. The American Journal of Human Genetics. 69(1). 223–227. 18 indexed citations
3.
Walsh, Sinéad, G. D. Moores, Michael Kristensen, et al.. (2001). Identification and characterization of mutations in housefly (Musca domestica) acetylcholinesterase involved in insecticide resistance. Biochemical Journal. 359(1). 175–175. 109 indexed citations
4.
Walsh, Sinéad, G. D. Moores, Michael Kristensen, et al.. (2001). Identification and characterization of mutations in housefly (Musca domestica) acetylcholinesterase involved in insecticide resistance. Biochemical Journal. 359(1). 175–181. 195 indexed citations
5.
Wilkie, Andrew O.M., Zequn Tang, Navaratnam Elanko, et al.. (2000). Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nature Genetics. 24(4). 387–390. 216 indexed citations
6.
Glaser, Rivka L., Wen G. Jiang, Simeon A. Boyadjiev, et al.. (2000). Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome. The American Journal of Human Genetics. 66(3). 768–777. 125 indexed citations
7.
Johnson, David, Sharon W. Horsley, Dominique M. Moloney, et al.. (1998). A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1. The American Journal of Human Genetics. 63(5). 1282–1293. 143 indexed citations
8.
Vega, M. Cristina, Sinéad Walsh, Timothy J. Mantle, & Miquel Coll. (1998). The Three-dimensional Structure of Cys-47-modified Mouse Liver Glutathione S-Transferase P1-1. Journal of Biological Chemistry. 273(5). 2844–2850. 37 indexed citations
9.
Parraga, A., I. Garcia-Saez, Sinéad Walsh, Timothy J. Mantle, & Miquel Coll. (1998). The three-dimensional structure of a class-Pi glutathione S-transferase complexed with glutathione: the active-site hydration provides insights into the reaction mechanism. Biochemical Journal. 333(3). 811–816. 19 indexed citations
10.
Hall, Frances, Matthew A. Brown, Daniel E. Weeks, et al.. (1997). A linkage study across the T cell receptor A and T cell receptor B loci in families with rheumatoid arthritis. Arthritis & Rheumatism. 40(10). 1798–1802. 9 indexed citations
11.
Orozco, Modesto, A. Parraga, I. Garcia-Saez, et al.. (1997). On the reaction mechanism of class Pi glutathione S-transferase. Proteins Structure Function and Bioinformatics. 28(4). 530–542. 10 indexed citations
12.
Wordsworth, P, et al.. (1996). Genetic linkage mapping of susceptibility loci in rheumatoid arthritis.. Oxford University Research Archive (ORA) (University of Oxford). 39. 789–789. 2 indexed citations
13.
Walsh, Sinéad, et al.. (1996). Linkage study across the TCRA and TCRB loci in multiplex families with rheumatoid arthritis.. Oxford University Research Archive (ORA) (University of Oxford). 39. 201–201. 1 indexed citations
14.
Loughlin, John, et al.. (1995). Linkage of the gene that encodes the α1 chain of type V collagen (COL5A1) to type II Ehlers-Danlos syndrome (EDS II). Human Molecular Genetics. 4(9). 1649–1651. 33 indexed citations
15.
Walsh, Sinéad & Timothy J. Mantle. (1995). Modification of Mouse Liver Glutathione S-Transferase Pi by Iodoacetic acid. Biochemical Society Transactions. 23(3). 485S–485S. 2 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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