F. Boardman-Pretty

687 citations
11 papers · 514 · 1 hit paper · h-index 7

Impact in

  • Genetics top 10%
    • Genomics and Rare Diseases
    • Craniofacial Disorders and Treatments
    • BRCA gene mutations in cancer
    • Vascular Anomalies and Treatments
    • Genetic Associations and Epidemiology

Papers in

    • Genomics and Rare Diseases 3
    • Vascular Anomalies and Treatments 2
    • Genetic and Kidney Cyst Diseases 1
    • Parathyroid Disorders and Treatments 1

F. Boardman-Pretty

10 papers receiving 507 citations

F. Boardman-Pretty's Hit Papers

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS 2018 · 339 citations
3390+2+5Years since publication100200300

Peers

F. Boardman-Pretty
Comparison fields: 5 of 60
  • Genetics 268
  • Genetics 41
  • Health Informatics 11
  • Cancer Research 28
  • Molecular Biology 89
Replace C. E. H. Craig with:
C. E. H. Craig United Kingdom
Omar Serang United States
Justin H. Gundelach United States
Derick C. Hoskinson United States
Anthony Attwood United Kingdom
Stéphane Liva France
Richard Lao United States
Javier Núñez-Fontarnau Finland
Nathan Denton United Kingdom
Jennyfer M. Garcí­a-Cárdenas Ecuador
F. Boardman-Pretty relative to C. E. H. Craig United Kingdom C. E. H. Craig's profile →
Citations per field
00.5×2×4×5.9×
C. E. H. Craig · 1×
Citations per year

Countries citing papers authored by F. Boardman-Pretty

Since Specialization
Citations

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

Fields of papers citing papers by F. Boardman-Pretty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. Boardman-Pretty. 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 F. Boardman-Pretty. The network helps show where F. Boardman-Pretty may publish in the future.

Co-authors

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

All Works

11 of 11 papers shown
#Work
1
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
Hit paper breakdown →
2018339
2 202146
3 202040
4 202227
5 202125
6 201513
7 202212
8 20235
9 20244
10 20243
11 20240

About F. Boardman-Pretty

F. Boardman-Pretty is a scholar working on Genetics, Genetics, Nephrology, General Health Professions and Cardiology and Cardiovascular Medicine, having authored 11 papers that have together received 514 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Vascular Anomalies and Treatments (2 papers), Cardiovascular Health and Disease Prevention (1 paper), Health Services Management and Policy (1 paper), Genetic and Kidney Cyst Diseases (1 paper), Machine Learning in Healthcare (1 paper), Parathyroid Disorders and Treatments (1 paper) and Neuroendocrine Tumor Research Advances (1 paper). The work is most often cited by research in Genetics (268 citations), Genetics (41 citations), Health Informatics (11 citations), Cancer Research (28 citations) and Molecular Biology (89 citations). F. Boardman-Pretty has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Geraldine Anne Thomas, Lasse Folkersen, Giuseppe Danilo Norata, M. Zulf Mughal, John Eric Deanfield, Mika Kivimaki B, Nichola Cooper, Olle Melander, Jutta Palmen and Karl Gertow. Their work appears in journals such as Genetics in Medicine, BMJ, The Journal of Clinical Endocrinology & Metabolism, Circulation Cardiovascular Genetics and British Journal of Cancer.

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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