D. A. Dyment

1.5k total citations
18 papers, 1.1k citations indexed

About

D. A. Dyment is a scholar working on Pathology and Forensic Medicine, Immunology and Molecular Biology. According to data from OpenAlex, D. A. Dyment has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pathology and Forensic Medicine, 10 papers in Immunology and 3 papers in Molecular Biology. Recurrent topics in D. A. Dyment's work include Multiple Sclerosis Research Studies (13 papers), Reproductive System and Pregnancy (4 papers) and Immunotherapy and Immune Responses (4 papers). D. A. Dyment is often cited by papers focused on Multiple Sclerosis Research Studies (13 papers), Reproductive System and Pregnancy (4 papers) and Immunotherapy and Immune Responses (4 papers). D. A. Dyment collaborates with scholars based in Canada, United Kingdom and United States. D. A. Dyment's co-authors include George C. Ebers, A. Dessa Sadovnick, Cristen J. Willer, Peter M. Rothwell, T. Jock Murray, Blanca Herrera, Matthew R. Lincoln, Sreeram V Ramagopalan, Melody Chao and J. L. Steckley and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

D. A. Dyment

18 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. A. Dyment Canada 14 768 541 172 170 103 18 1.1k
Sarah Orton United Kingdom 15 933 1.2× 515 1.0× 219 1.3× 289 1.7× 128 1.2× 27 1.4k
S. V. Ramagopalan United Kingdom 15 578 0.8× 331 0.6× 130 0.8× 164 1.0× 63 0.6× 19 803
KG Simon United States 6 746 1.0× 355 0.7× 104 0.6× 153 0.9× 71 0.7× 9 981
Maria Bäärnhielm Sweden 8 718 0.9× 321 0.6× 91 0.5× 100 0.6× 76 0.7× 9 940
Marja‐Liisa Sumelahti Finland 16 653 0.9× 179 0.3× 114 0.7× 145 0.9× 59 0.6× 45 911
Donald Brunet Canada 15 412 0.5× 267 0.5× 98 0.6× 178 1.0× 101 1.0× 25 932
P. O’Connor Canada 10 783 1.0× 233 0.4× 120 0.7× 152 0.9× 34 0.3× 16 1.0k
Cláudia Cristina Ferreira Vasconcelos Brazil 19 534 0.7× 283 0.5× 101 0.6× 128 0.8× 30 0.3× 62 966
P Cortinovis-Tourniaire France 5 909 1.2× 874 1.6× 104 0.6× 193 1.1× 85 0.8× 5 1.5k
Caterina Veroni Italy 17 391 0.5× 334 0.6× 193 1.1× 129 0.8× 41 0.4× 24 994

Countries citing papers authored by D. A. Dyment

Since Specialization
Citations

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

Fields of papers citing papers by D. A. Dyment

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. A. Dyment. 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 D. A. Dyment. The network helps show where D. A. Dyment may publish in the future.

Co-authorship network of co-authors of D. A. Dyment

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

All Works

18 of 18 papers shown
1.
Ebers, George C., S V Ramagopalan, D. A. Dyment, et al.. (2012). RARE VARIANTS IN THE CYP27B1 GENE ARE ASSOCIATED WITH MULTIPLE SCLEROSIS. Journal of Neurology Neurosurgery & Psychiatry. 83(Suppl 2). A35.1–A35. 2 indexed citations
2.
Jager, Philip L. De, et al.. (2011). HLA B*44: Protective effects in MS susceptibility and MRI outcome measures. Neurology. 77(6). 602–603. 6 indexed citations
3.
Chao, Melody, S. V. Ramagopalan, Blanca Herrera, et al.. (2011). MHC transmission. Neurology. 76(3). 242–246. 41 indexed citations
4.
Ramagopalan, S V, Jenny Link, Jake Byrnes, et al.. (2009). HLA-DRB1 and month of birth in multiple sclerosis. Neurology. 73(24). 2107–2111. 38 indexed citations
5.
Ward, Hamish E., Katie Morrison, S. V. Ramagopalan, et al.. (2009). Risk alleles for multiple sclerosis in multiplex families. Neurology. 72(23). 1984–1988. 50 indexed citations
6.
Ebers, George C., S V Ramagopalan, Narelle Maugeri, et al.. (2008). Expression of the multiple sclerosis associated MHC class II allele HLA-DRBI*1501 is regulated by vitamin D. Annals of Neurology. 64. 2 indexed citations
7.
Chao, Melody, Sreeram V Ramagopalan, Blanca Herrera, et al.. (2008). Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex. Human Molecular Genetics. 18(2). 261–266. 72 indexed citations
8.
Ramagopalan, S. V., Gabriele C. DeLuca, Katie Morrison, et al.. (2008). Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis. Journal of Neurology. 255(8). 1215–1219. 17 indexed citations
9.
Ramagopalan, Sreeram V, D. A. Dyment, Blanca Herrera, et al.. (2007). The Inheritance of Resistance Alleles in Multiple Sclerosis. PLoS Genetics. 3(9). e150–e150. 100 indexed citations
10.
Dyment, D. A., M. Zameel Cader, Blanca Herrera, et al.. (2007). A genome scan in a single pedigree with a high prevalence of multiple sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 79(2). 158–162. 12 indexed citations
11.
Chao, Melody, Martin Barnardo, Matthew R. Lincoln, et al.. (2007). Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium. Human Molecular Genetics. 16(16). 1951–1958. 35 indexed citations
12.
Cader, M. Zameel, J. L. Steckley, D. A. Dyment, R. S. McLachlan, & George C. Ebers. (2005). A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia. Neurology. 65(1). 156–158. 36 indexed citations
13.
Dyment, D. A.. (2004). An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. Human Molecular Genetics. 13(10). 1005–1015. 49 indexed citations
14.
Willer, Cristen J., D. A. Dyment, A. Dessa Sadovnick, et al.. (2004). Timing of birth and risk of multiple sclerosis: population based study. BMJ. 330(7483). 120–120. 332 indexed citations
15.
Steckley, J. L., D. A. Dyment, A. Dessa Sadovnick, et al.. (2000). Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients. Neurology. 54(3). 729–729. 80 indexed citations
16.
Ebers, George C. & D. A. Dyment. (1998). Genetics of Multiple Sclerosis. Seminars in Neurology. 18(3). 295–299. 54 indexed citations
17.
Dyment, D. A.. (1997). Genetics of multiple sclerosis [published erratum appears in Hum Mol Genet 1997 Nov;6(12):2189]. Human Molecular Genetics. 6(10). 1693–1698. 119 indexed citations
18.
Sadovnick, A. Dessa, D. A. Dyment, & George C. Ebers. (1997). Genetic Epidemiology of Multiple Sclerosis. Epidemiologic Reviews. 19(1). 99–106. 53 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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