Thomas D. Dyer

13.1k total citations
186 papers, 6.7k citations indexed

About

Thomas D. Dyer is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Thomas D. Dyer has authored 186 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Genetics, 62 papers in Molecular Biology and 26 papers in Epidemiology. Recurrent topics in Thomas D. Dyer's work include Genetic Associations and Epidemiology (68 papers), Genetic Mapping and Diversity in Plants and Animals (36 papers) and Genetic and phenotypic traits in livestock (32 papers). Thomas D. Dyer is often cited by papers focused on Genetic Associations and Epidemiology (68 papers), Genetic Mapping and Diversity in Plants and Animals (36 papers) and Genetic and phenotypic traits in livestock (32 papers). Thomas D. Dyer collaborates with scholars based in United States, Australia and United Kingdom. Thomas D. Dyer's co-authors include John Blangero, Laura Almasy, Joanne E. Curran, Michael C. Mahaney, Ravindranath Duggirala, Harald H.H. Göring, Michael P. Stern, Anthony G. Comuzzie, Jean W. MacCluer and Jack W. Kent and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Thomas D. Dyer

185 papers receiving 6.6k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Thomas D. Dyer	2.4k	2.3k	863	802	691	186	6.7k
Ian N.M. Day	2.4k 1.0×	2.9k 1.3×	631 0.7×	764 1.0×	790 1.1×	162	7.5k
Joanne E. Curran	1.5k 0.6×	2.3k 1.0×	878 1.0×	809 1.0×	501 0.7×	197	5.8k
Michael C. Mahaney	1.8k 0.8×	2.4k 1.0×	1.0k 1.2×	1.3k 1.6×	961 1.4×	176	6.8k
David Meyre	1.8k 0.7×	1.5k 0.7×	577 0.7×	1.0k 1.3×	557 0.8×	116	5.3k
Caroline Hayward	2.3k 1.0×	2.7k 1.2×	457 0.5×	754 0.9×	327 0.5×	220	8.1k
Bertram Müller‐Myhsok	1.7k 0.7×	2.0k 0.9×	880 1.0×	729 0.9×	471 0.7×	197	8.7k
Inês Barroso	2.4k 1.0×	3.5k 1.5×	798 0.9×	1.6k 2.0×	878 1.3×	96	6.7k
Cecilia M. Lindgren	3.1k 1.3×	3.9k 1.7×	741 0.9×	1.5k 1.8×	844 1.2×	159	8.9k
Mara Helena Hutz	2.2k 0.9×	1.3k 0.6×	515 0.6×	498 0.6×	502 0.7×	273	7.4k
Andrew D. Johnson	1.9k 0.8×	2.8k 1.2×	411 0.5×	645 0.8×	430 0.6×	127	6.6k

Countries citing papers authored by Thomas D. Dyer

Since Specialization

Citations

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

Fields of papers citing papers by Thomas D. Dyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas D. Dyer

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas D. Dyer. A scholar is included among the top collaborators of Thomas D. Dyer 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 Thomas D. Dyer. Thomas D. Dyer 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

Knowles, Emma, Samuel R. Mathias, Josephine Mollon, et al.. (2018). A QTL on chromosome 3q23 influences processing speed in humans. Genes Brain & Behavior. 18(4). e12530–e12530. 1 indexed citations

Ramstetter, Monica D., Sushila Shenoy, Thomas D. Dyer, et al.. (2018). Inferring Identical-by-Descent Sharing of Sample Ancestors Promotes High-Resolution Relative Detection. The American Journal of Human Genetics. 103(1). 30–44. 23 indexed citations

Ramstetter, Monica D., Thomas D. Dyer, Donna M. Lehman, et al.. (2017). Benchmarking Relatedness Inference Methods with Genome-Wide Data from Thousands of Relatives. Genetics. 207(1). 75–82. 56 indexed citations

Kulkarni, Hemant, Manju Mamtani, Juan M. Peralta, et al.. (2016). Lack of Association betweenSLC30A8Variants and Type 2 Diabetes in Mexican American Families. Journal of Diabetes Research. 2016. 1–9. 5 indexed citations

Hodgson, Karen, Laura Almasy, Emma Knowles, et al.. (2016). The genetic basis of the comorbidity between cannabis use and major depression. Addiction. 112(1). 113–123. 28 indexed citations

Steele, John & Thomas D. Dyer. (2014). Use of KWLs in the Online Classroom as It Correlates to Increased Participation.. 3. 8–14. 7 indexed citations

Mamtani, Manju, Hemant Kulkarni, Thomas D. Dyer, et al.. (2014). Increased waist circumference is independently associated with hypothyroidism in Mexican Americans: replicative evidence from two large, population-based studies. BMC Endocrine Disorders. 14(1). 46–46. 10 indexed citations

Curran, Joanne E., Dean McKay, Anderson M. Winkler, et al.. (2013). Identification of Pleiotropic Genetic Effects on Obesity and Brain Anatomy. Human Heredity. 75(2-4). 136–143. 20 indexed citations

Knowles, Emma, Melanie A. Carless, Marcio Almeida, et al.. (2013). Genome‐wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(1). 84–95. 30 indexed citations

10.

Zhang, Yi, Jack W. Kent, Michael Olivier, et al.. (2013). A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation. BMC Medical Genomics. 6(1). 14–14. 22 indexed citations

11.

Curran, Joanne E., Thomas D. Dyer, Jack W. Kent, et al.. (2013). Variation in osteoarthritis biomarker serum comp levels in Mexican Americans is associated with SNPs in a region of chromosome 22q encompassing MICAL3, BCL2L13, and BID. Osteoarthritis and Cartilage. 21. S172–S172. 3 indexed citations

12.

Glahn, David C., Joanne E. Curran, Anderson M. Winkler, et al.. (2011). High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes. Biological Psychiatry. 71(1). 6–14. 125 indexed citations

13.

Cummings, Nik, Joanne E. Curran, Kiymet Bozaoglu, et al.. (2011). Genetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass. International Journal of Obesity. 36(2). 201–206. 18 indexed citations

14.

Towne, Bradford, John Blangero, Stefan A. Czerwinski, et al.. (2008). Presentation, Heritability, and Genome-Wide Linkage Analysis of the Midchildhood Growth Spurt in Healthy Children from the Fels Longitudinal Study. Human Biology. 80(6). 623–636. 2 indexed citations

15.

Farook, Vidya S., Gerald D. Dodd, Sobha Puppala, et al.. (2008). Autosomal Genome-Wide Linkage Analysis to Identify Loci for Gallbladder Wall Thickness in Mexican Americans. Human Biology. 80(1). 11–28.

16.

Coletta, Dawn K., Jennifer L. Schneider, Thomas D. Dyer, et al.. (2008). Genome-Wide Linkage Scan for Genes Influencing Plasma Triglyceride Levels in the Veterans Administration Genetic Epidemiology Study. Diabetes. 58(1). 279–284. 17 indexed citations

17.

Cai, Guowen, Juan Carlos López-Alvarenga, Jack W. Kent, et al.. (2007). A Chromosome 11q Quantitative-Trait Locus Influences Change of Blood-Pressure Measurements over Time in Mexican Americans of the San Antonio Family Heart Study. The American Journal of Human Genetics. 81(4). 744–755. 20 indexed citations

18.

Stern, Michael P., et al.. (2006). Heritability and linkage analysis of hand, foot, and eye preference in Mexican Americans. Laterality Asymmetries of Body Brain and Cognition. 11(6). 508–524. 44 indexed citations

19.

Duggirala, Ravindranath, John Blangero, Laura Almasy, et al.. (2000). A Major Susceptibility Locus Influencing Plasma Triglyceride Concentrations Is Located on Chromosome 15q in Mexican Americans. The American Journal of Human Genetics. 66(4). 1237–1245. 94 indexed citations

20.

Duggirala, Ravindranath, John Blangero, Laura Almasy, et al.. (1999). Linkage of Type 2 Diabetes Mellitus and of Age at Onset to a Genetic Location on Chromosome 10q in Mexican Americans. The American Journal of Human Genetics. 64(4). 1127–1140. 252 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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