Brian Coppin

1.1k citations
7 papers · 680 · 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
    • Protein Tyrosine Phosphatases 1

Brian Coppin

7 papers receiving 628 citations

Brian Coppin's Hit Papers

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function 1997 · 522 citations
5220+9+19Years since publication100200300400500

Peers

Brian Coppin
Comparison fields: 5 of 78
  • Genetics 484
  • Cognitive Neuroscience 160
  • Gender Studies 53
  • Developmental Neuroscience 21
  • Molecular Biology 314
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
Susan Howell United States
Laura B. K. Herzing 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 18 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 680 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chromosomal and Genetic Variations (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Sexual Differentiation and Disorders (2 papers), Peptidase Inhibition and Analysis (1 paper), Ubiquitin and proteasome pathways (1 paper), Animal Genetics and Reproduction (1 paper) and Protein Tyrosine Phosphatases (1 paper). The work is most often cited by research in Genetics (484 citations), Cognitive Neuroscience (160 citations), Gender Studies (53 citations), Developmental Neuroscience (21 citations) and Molecular Biology (314 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 Rowena S. James. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Human Genetics, Nature and Annals of Human Genetics.

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