D A Couzin

561 citations
24 papers · 418 · h-index 12

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Prenatal Screening and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 10
    • Genetics and Neurodevelopmental Disorders 2
    • Congenital heart defects research 3
    • DNA Repair Mechanisms 2
    • Hedgehog Signaling Pathway Studies 2

D A Couzin

23 papers receiving 342 citations

Peers

D A Couzin
Comparison fields: 5 of 54
  • Genetics 241
  • Pediatrics, Perinatology and Child Health 125
  • Plant Science 118
  • Reproductive Medicine 19
  • Aging 4
Replace E. J. Maher with:
E. J. Maher United Kingdom
Gordon S. Stephen United Kingdom
Ko–ichiro Yoshiura Japan
M. Crocker United Kingdom
Frank S. Grass United States
N. Morichon-Delvallez France
Morag N. Collinson United Kingdom
Sue Ann Berend United States
Sandra Peacock United States
H. F. de France Netherlands
D A Couzin relative to E. J. Maher United Kingdom E. J. Maher's profile →
Citations per field
00.5×1.5×
E. J. Maher · 1×
Citations per year

Countries citing papers authored by D A Couzin

Since Specialization
Citations

This map shows the geographic impact of D A Couzin'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 Couzin 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 Couzin more than expected).

Fields of papers citing papers by D A Couzin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 24 scholars most cited alongside D A Couzin, 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 D A Couzin Line = papers co-authored together D A Couzin links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 198567
2 198947
3 198746
4 198640
5 197426
6 199925
7 197922
8 199119
9 198319
10 199916
11 198414
12 198313
13 198111
14 198611
15 19789
16 19897
17 19986
18 19796
19 19735
20 19863

About D A Couzin

D A Couzin is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 24 papers that have together received 418 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (8 papers), Chromosomal and Genetic Variations (4 papers), Congenital heart defects research (3 papers), DNA Repair Mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Carcinogens and Genotoxicity Assessment (2 papers). The work is most often cited by research in Genetics (241 citations), Pediatrics, Perinatology and Child Health (125 citations), Plant Science (118 citations), Reproductive Medicine (19 citations) and Aging (4 citations). D A Couzin has collaborated with scholars based in United Kingdom, Sri Lanka and Germany. Frequent co-authors include J L Watt, Gordon S. Stephen, D. P. Fox, D.G. Papworth, Alan Johnston, John Dean, Ken Ward, Elizabeth Gray, A W Johnston and M.J.W. Faed. Their work appears in journals such as Journal of Medical Genetics, Prenatal Diagnosis, Chromosoma, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis and Genetic Epidemiology.

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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