Derek Gordon

6.2k total citations
129 papers, 3.5k citations indexed

About

Derek Gordon is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Derek Gordon has authored 129 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Genetics, 46 papers in Molecular Biology and 15 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Derek Gordon's work include Genetic Associations and Epidemiology (48 papers), Genetic Mapping and Diversity in Plants and Animals (27 papers) and Gene expression and cancer classification (17 papers). Derek Gordon is often cited by papers focused on Genetic Associations and Epidemiology (48 papers), Genetic Mapping and Diversity in Plants and Animals (27 papers) and Gene expression and cancer classification (17 papers). Derek Gordon collaborates with scholars based in United States, United Kingdom and Israel. Derek Gordon's co-authors include Jürg Ott, Stephen J. Finch, Chad Haynes, Michael Nothnagel, Mark A. Levenstien, Angela M. Christiano, Simon Heath, A. Bowcock, Carol A. Wise and Sun Jung Kang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Derek Gordon

127 papers receiving 3.4k citations

Author Peers

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

Author Last Decade Papers Cites
Derek Gordon 1.5k 1.3k 401 340 262 129 3.5k
Nobutake Matsuo 1.2k 0.8× 1.5k 1.2× 221 0.6× 205 0.6× 204 0.8× 107 3.2k
Philippe Touraine 1.6k 1.1× 2.4k 1.9× 534 1.3× 342 1.0× 228 0.9× 195 6.1k
Kenjiro Kosaki 1.8k 1.2× 2.7k 2.1× 623 1.6× 335 1.0× 193 0.7× 363 5.2k
Jianfeng Xu 1.3k 0.9× 1.5k 1.2× 281 0.7× 420 1.2× 287 1.1× 159 4.4k
Siu Yuen Chan 712 0.5× 1.4k 1.1× 292 0.7× 402 1.2× 226 0.9× 99 3.5k
Tomonobu Hasegawa 2.1k 1.4× 3.2k 2.5× 756 1.9× 319 0.9× 130 0.5× 360 6.1k
Peter Farndon 969 0.6× 1.4k 1.1× 272 0.7× 249 0.7× 281 1.1× 63 3.0k
Toshiro Nagai 1.8k 1.2× 2.0k 1.5× 327 0.8× 250 0.7× 109 0.4× 138 3.5k
Erik A. Sistermans 2.7k 1.8× 2.9k 2.2× 322 0.8× 395 1.2× 224 0.9× 123 5.6k
Dani Bercovich 696 0.5× 1.2k 0.9× 284 0.7× 230 0.7× 505 1.9× 74 2.9k

Countries citing papers authored by Derek Gordon

Since Specialization
Citations

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

Fields of papers citing papers by Derek Gordon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Derek Gordon

This figure shows the co-authorship network connecting the top 25 collaborators of Derek Gordon. A scholar is included among the top collaborators of Derek Gordon 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 Derek Gordon. Derek Gordon 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.
Nasello, Cara, Junbing Wu, Joshua K. Thackray, et al.. (2024). Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Proceedings of the National Academy of Sciences. 121(19). e2307156121–e2307156121. 8 indexed citations
2.
Bosque‐Plata, Laura del, Mutaz Amin, Ricardo González‐Ramírez, et al.. (2023). LD block disorder-specific pleiotropic roles of novel CRHR1 in type 2 diabetes and depression disorder comorbidity. European Archives of Psychiatry and Clinical Neuroscience. 275(4). 1025–1035. 2 indexed citations
3.
Sharma, Swarkar, Xiaochong Gao, Douglas Londoño, et al.. (2011). Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. Human Molecular Genetics. 20(7). 1456–1466. 134 indexed citations
4.
5.
Petukhova, Lynn, Amalia Martı́nez-Mir, Lawrence Shapiro, et al.. (2008). Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation. Genomics. 92(5). 273–278. 23 indexed citations
6.
Gordon, Derek & Marcella Devoto. (2008). Introduction. Human Heredity. 66(2). 65–66. 2 indexed citations
7.
Gao, Xiaochong, Derek Gordon, Dongping Zhang, et al.. (2007). CHD7 Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Scoliosis. The American Journal of Human Genetics. 80(5). 957–965. 108 indexed citations
8.
Yang, Yang, Jung Yeon Lee, Wenyang Mao, et al.. (2007). Mixture modeling of microarray gene expression data. BMC Proceedings. 1(S1). S50–S50. 2 indexed citations
9.
Gordon, Derek, Chad Haynes, Yaning Yang, Patricia L. Kramer, & Stephen J. Finch. (2007). Linear trend tests for case–control genetic association that incorporate random phenotype and genotype misclassification error. Genetic Epidemiology. 31(8). 853–870. 25 indexed citations
10.
Tintle, Nathan, Kwangmi Ahn, Nancy R. Mendell, Derek Gordon, & Stephen J. Finch. (2005). Characteristics of replicated single-nucleotide polymorphism genotypes from COGA: Affymetrix and Center for Inherited Disease Research. BMC Genetics. 6(S1). S154–S154. 17 indexed citations
11.
Frishberg, Yaacov, Orit Topaz, Richard N. Bergman, et al.. (2004). Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders. Journal of Molecular Medicine. 83(1). 33–38. 84 indexed citations
12.
Martı́nez-Mir, Amalia, Abraham Zlotogorski, Jürg Ott, Derek Gordon, & Angela M. Christiano. (2003). Genetic Linkage Studies in Alopecia Areata. Journal of Investigative Dermatology Symposium Proceedings. 8(2). 199–203. 22 indexed citations
13.
Martı́nez-Mir, Amalia, Benjamin Gläser, Gary S. Chuang, et al.. (2003). Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata. Journal of Investigative Dermatology. 121(4). 741–744. 44 indexed citations
14.
Martı́nez-Mir, Amalia, Abraham Zlotogorski, Douglas Londoño, et al.. (2003). Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24. Journal of Medical Genetics. 40(12). 872–878. 18 indexed citations
15.
Martı́nez-Mir, Amalia, Derek Gordon, Liran Horev, et al.. (2002). Multiple Cutaneous and Uterine Leiomyomas: Refinement of the Genetic Locus for Multiple Cutaneous and Uterine Leiomyomas on Chromosome 1q42.3–43. Journal of Investigative Dermatology. 118(5). 876–880. 17 indexed citations
16.
Finch, Stephen J., et al.. (2001). A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model‐free multipoint linkage methods. Genetic Epidemiology. 21(4). 315–325. 8 indexed citations
17.
Gordon, Derek. (1999). Quaternionic discrete series. Representation Theory of the American Mathematical Society. 3(2). 32–57.
18.
Gordon, Derek, et al.. (1999). True Pedigree Errors More Frequent Than Apparent Errors for Single Nucleotide Polymorphisms. Human Heredity. 49(2). 65–70. 68 indexed citations
19.
Gordon, Derek, C. G. Semple, & Ken Paterson. (1991). Do Different Frequencies of Self‐monitoring of Blood Glucose Influence Control in Type 1 Diabetic Patients?. Diabetic Medicine. 8(7). 679–682. 16 indexed citations
20.
Thomson, John A., et al.. (1985). Treatment of presumed prolactinoma by transsphenoidal operation: early and late results.. BMJ. 291(6508). 1550–1553. 29 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Nobutake Matsuo Breakdown of academic impact, for papers by Philippe Touraine Breakdown of academic impact, for papers by Kenjiro Kosaki Breakdown of academic impact, for papers by Jianfeng Xu Breakdown of academic impact, for papers by Siu Yuen Chan Breakdown of academic impact, for papers by Tomonobu Hasegawa Breakdown of academic impact, for papers by Peter Farndon Breakdown of academic impact, for papers by Toshiro Nagai Breakdown of academic impact, for papers by Erik A. Sistermans Breakdown of academic impact, for papers by Dani Bercovich
Rankless by CCL
2026