Brian Coppin

1.1k citations
7 papers · 681 · 1 hit paper · h-index 6

Impact in

  • Genetics top 5%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Autism Spectrum Disorder Research

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
    • Genetics and Neurodevelopmental Disorders 2
    • Animal Genetics and Reproduction 1
    • Sexual Differentiation and Disorders 2
    • Ubiquitin and proteasome pathways 1

Brian Coppin

7 papers receiving 630 citations

Brian Coppin's Hit Papers

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function 1997 · 523 citations
5230+9+19Years since publication100200300400500

Peers

Brian Coppin
Comparison fields: 5 of 75
  • Genetics 464
  • Cognitive Neuroscience 146
  • Gender Studies 47
  • Molecular Biology 286
  • Developmental Neuroscience 15
Replace R S James with:
R S James United Kingdom
David S. Hong United States
James A. Salbenblatt United States
Mary Puck United States
Sheila Youings United Kingdom
Laura B. K. Herzing United States
Judith Brooks United States
Mary G. Linden United States
S G Ratcliffe United Kingdom
Tuck C. Ngun United States
Brian Coppin relative to R S James United Kingdom R S James's profile →
Citations per field
00.5×1.5×
R S James · 1×
Citations per year

Countries citing papers authored by Brian Coppin

Since Specialization
Citations

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

Fields of papers citing papers by Brian Coppin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 19 scholars most cited alongside Brian Coppin, 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 Brian Coppin Line = papers co-authored together Brian Coppin links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown

About Brian Coppin

Brian Coppin is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Cognitive Neuroscience, having authored 7 papers that have together received 681 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (2 papers), Sexual Differentiation and Disorders (2 papers), Chromosomal and Genetic Variations (2 papers), Ubiquitin and proteasome pathways (1 paper), Autism Spectrum Disorder Research (1 paper), Galectins and Cancer Biology (1 paper) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Genetics (464 citations), Cognitive Neuroscience (146 citations), Gender Studies (47 citations), Molecular Biology (286 citations) and Developmental Neuroscience (15 citations). Brian Coppin has collaborated with scholars based in United Kingdom and Greece. Frequent co-authors include P. A. Jacobs, R S James, Pamela Dalton, Dorothy Bishop, Rhona McGurk, Cathy Creswell, David Skuse, I. Karen Temple, Andrew J. Sharp and Paola Dalton. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Annals of Human Genetics, Human Genetics and Nature.

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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