John Dean

8.6k total citations
103 papers, 3.5k citations indexed

About

John Dean is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, John Dean has authored 103 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 34 papers in Molecular Biology and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in John Dean's work include Freshwater macroinvertebrate diversity and ecology (11 papers), Pharmacological Effects and Toxicity Studies (9 papers) and Genomics and Rare Diseases (8 papers). John Dean is often cited by papers focused on Freshwater macroinvertebrate diversity and ecology (11 papers), Pharmacological Effects and Toxicity Studies (9 papers) and Genomics and Rare Diseases (8 papers). John Dean collaborates with scholars based in United Kingdom, United States and Canada. John Dean's co-authors include D. J. Lloyd, Susan Moore, Peter D. Turnpenny, Z Miedzybrodzka, Lisa Strain, David T. Bonthron, Mark P.R. Hamilton, Barbara F. Crandall, Elina Ikonen and Deborah A. Driscoll and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Journal of Clinical Oncology.

In The Last Decade

John Dean

100 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John Dean United Kingdom 30 1.4k 1.3k 575 475 452 103 3.5k
Toshiyuki Yamamoto Japan 38 2.0k 1.5× 2.7k 2.1× 542 0.9× 405 0.9× 158 0.3× 392 6.5k
Kenjiro Kosaki Japan 35 1.8k 1.3× 2.7k 2.1× 591 1.0× 565 1.2× 164 0.4× 363 5.2k
Michael A. Morris Switzerland 37 1.7k 1.2× 2.1k 1.6× 427 0.7× 805 1.7× 108 0.2× 118 4.8k
Clinton T. Baldwin United States 42 1.4k 1.0× 2.5k 2.0× 713 1.2× 227 0.5× 218 0.5× 127 6.2k
Nicholas Lench United Kingdom 36 1.3k 1.0× 2.7k 2.2× 515 0.9× 471 1.0× 212 0.5× 107 5.5k
Jean‐François Deleuze France 35 749 0.5× 2.2k 1.7× 247 0.4× 318 0.7× 258 0.6× 192 5.7k
Josué Feingold France 34 791 0.6× 1.3k 1.0× 438 0.8× 213 0.4× 115 0.3× 89 3.8k
Giulio Genovese United States 33 1.8k 1.3× 2.6k 2.0× 242 0.4× 279 0.6× 176 0.4× 67 6.8k
Sally Ann Lynch Ireland 34 1.4k 1.0× 1.6k 1.3× 379 0.7× 125 0.3× 177 0.4× 146 3.7k
Joseph Glessner United States 39 3.4k 2.5× 2.2k 1.7× 426 0.7× 284 0.6× 163 0.4× 138 5.5k

Countries citing papers authored by John Dean

Since Specialization
Citations

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

Fields of papers citing papers by John Dean

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Dean

This figure shows the co-authorship network connecting the top 25 collaborators of John Dean. A scholar is included among the top collaborators of John Dean 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 John Dean. John Dean 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.
Kerr, Shona M., Lucija Klarić, Karen Johnston, et al.. (2025). Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results. The American Journal of Human Genetics. 112(4). 793–807.
2.
Wells, Alice, et al.. (2023). Taxonomic status and distribution of Australian caddisflies (Insecta: Trichoptera). Memoirs of Museum Victoria. 97–117. 2 indexed citations
3.
Kerr, Shona M., Lucija Klarić, Mihail Halachev, et al.. (2019). An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. Scientific Reports. 9(1). 10964–10964. 16 indexed citations
4.
Jackson, Adam, Rebecca Bromley, Pradeep Vasudevan, et al.. (2019). Exome sequencing in patients with antiepileptic drug exposure and complex phenotypes. Archives of Disease in Childhood. 105(4). 384–389. 2 indexed citations
5.
Yao, Baojin, Tommaso Pippucci, Joshua D. Smith, et al.. (2019). De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism. The American Journal of Human Genetics. 104(4). 777–777. 6 indexed citations
6.
Hamilton, Mark, Sarah A. Cumming, Helen Gregory, et al.. (2017). Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up study. PLoS ONE. 12(3). e0174166–e0174166. 29 indexed citations
7.
Dean, John, et al.. (2008). Phylogeny and distribution of the mayfly genus Austrophlebioides Campbell & Suter (Ephemeroptera : Leptophlebiidae). Invertebrate Systematics. 22(1). 29–36. 5 indexed citations
8.
Williams, Justin H. G., et al.. (2007). Characteristics of fetal anticonvulsant syndrome associated autistic disorder. Developmental Medicine & Child Neurology. 47(8). 551–555. 31 indexed citations
9.
Olsen, Rikke Katrine Jentoft, S. E. Olpin, Brage Storstein Andresen, et al.. (2007). ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. Brain. 130(8). 2045–2054. 215 indexed citations
10.
Dean, John, Victoria Louise Reid, Peter D. Turnpenny, et al.. (2007). Fetal anticonvulsant syndromes and polymorphisms in MTHFR, MTR, and MTRR. American Journal of Medical Genetics Part A. 143A(19). 2303–2311. 21 indexed citations
11.
Dean, John, Victoria Louise Reid, Susan Moore, et al.. (2007). A high frequency of the MTHFR 677C>T polymorphism in Scottish women with epilepsy: Possible role in pathogenesis. Seizure. 17(3). 269–275. 21 indexed citations
12.
Lloyd, D. J., et al.. (2005). Characteristics of fetal anticonvulsant syndrome associated autistic disorder. Developmental Medicine & Child Neurology. 47(8). 551–555. 335 indexed citations
13.
Baker, Andrew, Jane M. Hughes, John Dean, & Stuart E. Bunn. (2004). Mitochondrial DNA reveals phylogenetic structuring and cryptic diversity in Australian freshwater macroinvertebrate assemblages. Marine and Freshwater Research. 55(6). 629–640. 46 indexed citations
14.
Glover, Simon J., Anthony Quinn, Jane Hart, et al.. (2002). Ophthalmic findings in fetal anticonvulsant syndrome(s). Ophthalmology. 109(5). 942–947. 19 indexed citations
15.
Metcalfe, Kay, Leslie Smoot, Pascal McKeown, et al.. (2000). Elastin: mutational spectrum in supravalvular aortic stenosis. European Journal of Human Genetics. 8(12). 955–963. 110 indexed citations
16.
Yong, Dongeun, et al.. (1999). Chromosome 22q11 microdeletion and congenital heart disease - a survey in a paediatric population. European Journal of Pediatrics. 158(7). 566–570. 15 indexed citations
17.
Moore, Susan, Lisa Strain, Gary Cole, et al.. (1999). Fragile X syndrome with FMR1 and FMR2 deletion. Journal of Medical Genetics. 36(7). 565–566. 27 indexed citations
18.
Dean, John, et al.. (1999). Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene. Clinical Genetics. 56(3). 216–220. 52 indexed citations
19.
Turnpenny, Peter D., et al.. (1995). A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?. Clinical Dysmorphology. 4(4). 324–333. 5 indexed citations
20.
Miedzybrodzka, Zosia, Kevin F. Kelly, M. J. Davidson, et al.. (1992). Prenatal diagnosis for the cystic fibrosis mutation 1717‐1, G→A using arms. Prenatal Diagnosis. 12(10). 845–849. 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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