E. Parfitt

656 citations
14 papers · 387 · h-index 8

Impact in

  • Genetics top 10%
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic Syndromes and Imprinting
    • Schizophrenia research and treatment
    • Bipolar Disorder and Treatment

Papers in

    • Genetic Associations and Epidemiology 5
    • Genomics and Rare Diseases 2
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic and rare skin diseases. 2
    • BRCA gene mutations in cancer 2
    • 14-3-3 protein interactions 2

E. Parfitt

14 papers receiving 376 citations

Peers

E. Parfitt
Comparison fields: 5 of 52
  • Genetics 245
  • Psychiatry and Mental health 97
  • Biological Psychiatry 16
  • Cellular and Molecular Neuroscience 75
  • Pediatrics, Perinatology and Child Health 42
Replace Peter Propping with:
Peter Propping Germany
Claudia Hanses Germany
Sabine Purmann Germany
Hannu Juvonen Finland
Karl-Ludvig Reichelt Norway
Sonia De Zutter Belgium
Joel Wood United States
Michael J. Owen United Kingdom
S. G. Simpson United States
Jue Ji China
E. Parfitt relative to Peter Propping Germany Peter Propping's profile →
Citations per field
00.5×1.5×
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Citations per year

Countries citing papers authored by E. Parfitt

Since Specialization
Citations

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

Fields of papers citing papers by E. Parfitt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside E. Parfitt, 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 E. Parfitt Line = papers co-authored together E. Parfitt links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 1994146
2 199580
3 199341
4 199238
5 199425
6 199214
7 199914
8 199411
9 19964
10 19914
11
Linkage studies of schizophrenia with markers of chromosome-11q
19913
12 19923
13 19942
14
Susceptibility to schizophrenia and the dopamine d3 receptor gene
19932

About E. Parfitt

E. Parfitt is a scholar working on Genetics, Molecular Biology, Cell Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 14 papers that have together received 387 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and rare skin diseases. (2 papers), BRCA gene mutations in cancer (2 papers), 14-3-3 protein interactions (2 papers), Autism Spectrum Disorder Research (1 paper) and Folate and B Vitamins Research (1 paper). The work is most often cited by research in Genetics (245 citations), Psychiatry and Mental health (97 citations), Biological Psychiatry (16 citations), Cellular and Molecular Neuroscience (75 citations) and Pediatrics, Perinatology and Child Health (42 citations). E. Parfitt has collaborated with scholars based in United Kingdom, Japan and United States. Frequent co-authors include Peter McGuffin, Philip Asherson, R. Mant, M J Owen, Julie Williams, Michael Gill, John Powell, Mike Owen, Alison Clements and Jean Weissenbach. Their work appears in journals such as The British Journal of Psychiatry, Human Molecular Genetics, Human Genetics, Psychological Medicine and Nucleic Acids Research.

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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