WP Robinson

495 citations
7 papers · 367 · h-index 7

Impact in

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

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic Syndromes and Imprinting 2
    • Prenatal Screening and Diagnostics 4

WP Robinson

7 papers receiving 328 citations

Peers

WP Robinson
Comparison fields: 5 of 57
  • Genetics 231
  • Pediatrics, Perinatology and Child Health 95
  • Aging 4
  • Molecular Biology 137
  • Immunology 40
Replace A. Caine with:
A. Caine United Kingdom
Neus Baena Spain
Uta‐Dorothee Immel Germany
Susan J. Hassed United States
Joo Wook Ahn United Kingdom
Michelle Merrill United States
Marcial Francis Galera Brazil
Christine Tyson Canada
Tabitha Jackson United Kingdom
Yoon Hee Jung United States
WP Robinson relative to A. Caine United Kingdom A. Caine's profile →
Citations per field
00.5×10×13×
A. Caine · 1×
Citations per year

Countries citing papers authored by WP Robinson

Since Specialization
Citations

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

Fields of papers citing papers by WP Robinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 12 scholars most cited alongside WP Robinson, 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 WP Robinson Line = papers co-authored together WP Robinson links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown

About WP Robinson

WP Robinson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Surgery and Political Science and International Relations, having authored 7 papers that have together received 367 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), Genetic Syndromes and Imprinting (2 papers), Congenital Anomalies and Fetal Surgery (1 paper), Gestational Trophoblastic Disease Studies (1 paper) and Canadian Policy and Governance (1 paper). The work is most often cited by research in Genetics (231 citations), Pediatrics, Perinatology and Child Health (95 citations), Aging (4 citations), Molecular Biology (137 citations) and Immunology (40 citations). WP Robinson has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Carolyn J. Brown, Louis Lefebvre, Hélène Bruyèrè, Rosemarie Rupps, Ruiwei Jiang, Laura Arbour, Deborah E. McFadden, Danielle K. Bourque, Sylvie Langlois and P. N. Howard‐Peebles. Their work appears in journals such as Clinical Genetics and International Migration Review.

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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