Matthew J. Simmonds

17.2k total citations
50 papers, 2.5k citations indexed

About

Matthew J. Simmonds is a scholar working on Immunology, Genetics and Genetics. According to data from OpenAlex, Matthew J. Simmonds has authored 50 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Immunology, 27 papers in Genetics and 10 papers in Genetics. Recurrent topics in Matthew J. Simmonds's work include Diabetes and associated disorders (26 papers), T-cell and B-cell Immunology (11 papers) and Phagocytosis and Immune Regulation (9 papers). Matthew J. Simmonds is often cited by papers focused on Diabetes and associated disorders (26 papers), T-cell and B-cell Immunology (11 papers) and Phagocytosis and Immune Regulation (9 papers). Matthew J. Simmonds collaborates with scholars based in United Kingdom, United States and Australia. Matthew J. Simmonds's co-authors include Stephen Gough, J. M. Heward, Jayne A. Franklyn, Paul Newby, Jackie Carr‐Smith, John A. Todd, Joanna M. M. Howson, J. A. Franklyn, Stephan Brand and Neil Walker and has published in prestigious journals such as Journal of Clinical Oncology, Blood and PLoS ONE.

In The Last Decade

Matthew J. Simmonds

45 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew J. Simmonds United Kingdom 25 1.0k 892 755 393 260 50 2.5k
Amanda K. Huber United States 26 641 0.6× 894 1.0× 651 0.9× 498 1.3× 139 0.5× 49 2.3k
J. M. Heward United Kingdom 27 1.5k 1.5× 1.0k 1.2× 994 1.3× 412 1.0× 179 0.7× 39 2.6k
Erlinda Concepcion United States 33 1.7k 1.7× 1.2k 1.3× 1.6k 2.1× 475 1.2× 214 0.8× 52 3.1k
Jason D. Cooper United Kingdom 11 1.6k 1.6× 932 1.0× 503 0.7× 543 1.4× 630 2.4× 13 2.6k
Yaron Tomer United States 21 910 0.9× 596 0.7× 887 1.2× 285 0.7× 104 0.4× 27 1.7k
Mauro Congia Italy 25 1.1k 1.0× 1.0k 1.2× 412 0.5× 447 1.1× 653 2.5× 50 2.7k
A. P. Weetman United Kingdom 31 626 0.6× 711 0.8× 1.3k 1.8× 442 1.1× 129 0.5× 77 2.5k
Yuji Hiromatsu Japan 30 488 0.5× 436 0.5× 1.1k 1.4× 462 1.2× 263 1.0× 101 2.5k
R. Finke Germany 21 647 0.6× 424 0.5× 828 1.1× 289 0.7× 251 1.0× 36 1.6k
Vito Lampasona Italy 34 2.0k 1.9× 512 0.6× 1.3k 1.8× 518 1.3× 1.7k 6.7× 100 3.5k

Countries citing papers authored by Matthew J. Simmonds

Since Specialization
Citations

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

Fields of papers citing papers by Matthew J. Simmonds

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew J. Simmonds. 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 Matthew J. Simmonds. The network helps show where Matthew J. Simmonds may publish in the future.

Co-authorship network of co-authors of Matthew J. Simmonds

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

All Works

20 of 20 papers shown
1.
2.
Rinaldi, Ciro R., et al.. (2023). Expression of CD47 and CALR in myeloproliferative neoplasms: Potential new therapeutical targets.. Journal of Clinical Oncology. 41(16_suppl). e19079–e19079.
3.
Hamilton, Alexander, Shruti Mittal, Martin Barnardo, et al.. (2015). Impact of HMOX1 Genetic Variation in Pancreas Transplant Recipients On Long-Term Graft Outcome. American Journal of Transplantation. 15. 1 indexed citations
4.
Chand, Sourabh, Colin D. Chue, Nicola C. Edwards, et al.. (2015). Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphism and Left Ventricular Function in Early Chronic Kidney Disease. PLoS ONE. 10(1). e0116160–e0116160. 9 indexed citations
5.
Simmonds, Matthew J., Fotini K. Kavvoura, Stephan Brand, et al.. (2013). Skewed X Chromosome Inactivation and Female Preponderance in Autoimmune Thyroid Disease: An Association Study and Meta-Analysis. The Journal of Clinical Endocrinology & Metabolism. 99(1). E127–E131. 58 indexed citations
6.
Simmonds, Matthew J.. (2013). GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis. Nature Reviews Endocrinology. 9(5). 277–287. 93 indexed citations
7.
Cooper, Jason D., Matthew J. Simmonds, Neil Walker, et al.. (2012). Seven newly identified loci for autoimmune thyroid disease. Human Molecular Genetics. 21(23). 5202–5208. 99 indexed citations
8.
Moore, Jason H., Amy Jayne McKnight, Bernd Döhler, et al.. (2012). Donor ABCB1 Variant Associates with Increased Risk for Kidney Allograft Failure. Journal of the American Society of Nephrology. 23(11). 1891–1899. 58 indexed citations
9.
Plagnol, Vincent, Joanna M. M. Howson, Deborah J. Smyth, et al.. (2011). Genome-Wide Association Analysis of Autoantibody Positivity in Type 1 Diabetes Cases. PLoS Genetics. 7(8). e1002216–e1002216. 186 indexed citations
10.
Simmonds, Matthew J., Stephan Brand, Jeffrey C. Barrett, et al.. (2010). Association of Fc receptor‐like 5 (FCRL5) with Graves’ disease is secondary to the effect of FCRL3. Clinical Endocrinology. 73(5). 654–660. 23 indexed citations
11.
Hargreaves, Chantal E., Paul Newby, Stephan Brand, et al.. (2010). Association of FcGRIIa with Graves’ disease: a potential role for dysregulated autoantibody clearance in disease onset/progression. Clinical Endocrinology. 73(1). 119–125. 10 indexed citations
12.
Płoski, Rafał, Stephan Brand, Beata Jurecka‐Lubieniecka, et al.. (2010). Thyroid Stimulating Hormone Receptor (TSHR) Intron 1 Variants Are Major Risk Factors for Graves' Disease in Three European Caucasian Cohorts. PLoS ONE. 5(11). e15512–e15512. 35 indexed citations
13.
Heward, J. M., Paul Newby, Jackie Carr‐Smith, et al.. (2008). Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves’ disease. Genes and Immunity. 9(4). 358–363. 81 indexed citations
14.
Wood, Alice M., Matthew J. Simmonds, D Bayley, et al.. (2008). The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency. Respiratory Research. 9(1). 52–52. 37 indexed citations
15.
Syed, Mohamed Ahmed, Matthew J. Simmonds, Stephan Brand, et al.. (2007). Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves’ ophthalmopathy. Clinical Endocrinology. 67(5). 663–667. 13 indexed citations
16.
Simmonds, Matthew J. & Stephen Gough. (2007). The HLA Region and Autoimmune Disease: Associations and Mechanisms of Action. Current Genomics. 8(7). 453–465. 332 indexed citations
17.
Simmonds, Matthew J., J. M. Heward, Jeffrey C. Barrett, J. A. Franklyn, & Stephen Gough. (2006). Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves’ disease appears to be secondary to DRB1 exon 2 position β74. Clinical Endocrinology. 65(4). 429–432. 22 indexed citations
18.
Simmonds, Matthew J., Joanna M. M. Howson, J. M. Heward, et al.. (2004). Regression Mapping of Association between the Human Leukocyte Antigen Region and Graves Disease. The American Journal of Human Genetics. 76(1). 157–163. 116 indexed citations
19.
Simmonds, Matthew J., J. M. Heward, Joanna M. M. Howson, et al.. (2004). A systematic approach to the assessment of known TNF-α polymorphisms in Graves' disease. Genes and Immunity. 5(4). 267–273. 37 indexed citations
20.
Represa, Alfonso, Takuya Shimazaki, Matthew J. Simmonds, & Samuel Weiss. (2001). EGF‐responsive neural stem cells are a transient population in the developing mouse spinal cord. European Journal of Neuroscience. 14(3). 452–462. 28 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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