John Dean

8.1k citations
136 papers · 5.9k · 1 hit paper · h-index 39

Impact in

  • Genetics top 1%
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Connective tissue disorders research
    • Genomic variations and chromosomal abnormalities
    • Metabolism and Genetic Disorders

Papers in

    • Genomic variations and chromosomal abnormalities 15
    • Genomics and Rare Diseases 15
    • Genetics and Neurodevelopmental Disorders 15
    • Connective tissue disorders research 8
    • Pharmacological Effects and Toxicity Studies 10
    • Prenatal Screening and Diagnostics 7

John Dean

133 papers receiving 5.6k citations

John Dean's Hit Papers

Evidence for 28 genetic disorders discovered by combining healthcare and research data 2020 · 402 citations
4020+2+4Years since publication100200300400

Peers

John Dean
Comparison fields: 5 of 159
  • Genetics 2.2k
  • Clinical Biochemistry 312
  • Molecular Biology 2.4k
  • Pediatrics, Perinatology and Child Health 578
  • Immunology 601
Replace Eamonn G. Sheridan with:
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John Dean relative to Eamonn G. Sheridan United Kingdom Eamonn G. Sheridan's profile →
Citations per field
00.5×1.6×
Eamonn G. Sheridan · 1×
Citations per year

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-authors

The 25 scholars most cited alongside John Dean, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with John Dean Line = papers co-authored together John Dean links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 136 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Hit paper breakdown →
2020402
2 2007373
3 2007339
4 2007258
5 2005253
6 2007212
7 2002195
8 2011194
9 2013177
10 1995169
11 2018146
12 1998132
13 2000132
14 2017111
15 201999
16 199295
17 201891
18 199490
19 199582
20 199581

About John Dean

John Dean is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Rheumatology and Cellular and Molecular Neuroscience, having authored 136 papers that have together received 5.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Genomics and Rare Diseases (15 papers), Genetics and Neurodevelopmental Disorders (15 papers), Freshwater macroinvertebrate diversity and ecology (11 papers), Pharmacological Effects and Toxicity Studies (10 papers), Connective tissue disorders research (8 papers), Invertebrate Taxonomy and Ecology (7 papers) and Prenatal Screening and Diagnostics (7 papers). The work is most often cited by research in Genetics (2.2k citations), Clinical Biochemistry (312 citations), Molecular Biology (2.4k citations), Pediatrics, Perinatology and Child Health (578 citations) and Immunology (601 citations). John Dean has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Susan Moore, Peter D. Turnpenny, Lisa Strain, Mark P.R. Hamilton, David T. Bonthron, Z Miedzybrodzka, N E Haites, Laurel L. Estabrooks, William Newman and Barbara F. Crandall. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Heart, Clinical Genetics and Genetics in Medicine.

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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