Mark Effingham

10.9k citations
11 papers · 6.1k · 2 hit papers · h-index 8

Impact in

  • Genetics top 1%
    • Genetic Associations and Epidemiology
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetic and phenotypic traits in livestock
    • Genomics and Rare Diseases

Papers in

    • Genetic Associations and Epidemiology 6
    • Genomics and Rare Diseases 3
    • Diabetes and associated disorders 1
    • Cancer Genomics and Diagnostics 4
    • Cancer-related molecular mechanisms research 1

Mark Effingham

10 papers receiving 6.0k citations

Mark Effingham's Hit Papers

Prospective study design and data analysis in UK Biobank 2024 · 121 citations
1210+2+5Years since publication10002.0k3.0k4.0k5.0k

Peers

Mark Effingham
Comparison fields: 5 of 149
  • Genetics 2.3k
  • Biological Psychiatry 61
  • Aging 41
  • Health Informatics 33
  • Molecular Biology 1.3k
Replace Allan Motyer with:
Allan Motyer Australia
Lloyd T. Elliott Canada
Clare Bycroft United Kingdom
Samantha Welsh United Kingdom
Kevin Sharp United States
Saiju Pyarajan United States
Carolina Roselli United States
Rachel L. Kember United States
Seung Hoan Choi United States
Tero Hiekkalinna Finland
Mark Effingham relative to Allan Motyer Australia Allan Motyer's profile →
Citations per field
00.5×1.5×
Allan Motyer · 1×
Citations per year

Countries citing papers authored by Mark Effingham

Since Specialization
Citations

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

Fields of papers citing papers by Mark Effingham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1
The UK Biobank resource with deep phenotyping and genomic data
Hit paper breakdown →
20185681
2
Prospective study design and data analysis in UK Biobank
Hit paper breakdown →
2024121
3 202293
4 201987
5 202528
6 202427
7 202316
8 202315
9 20231
10 20231
11 20250

About Mark Effingham

Mark Effingham is a scholar working on Genetics, Cancer Research, Statistics and Probability, Molecular Biology and Infectious Diseases, having authored 11 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (6 papers), Cancer Genomics and Diagnostics (4 papers), Genomics and Rare Diseases (3 papers), COVID-19 Clinical Research Studies (1 paper), Biomedical Text Mining and Ontologies (1 paper), Cancer-related molecular mechanisms research (1 paper), Advanced Causal Inference Techniques (1 paper) and Diabetes and associated disorders (1 paper). The work is most often cited by research in Genetics (2.3k citations), Biological Psychiatry (61 citations), Aging (41 citations), Health Informatics (33 citations) and Molecular Biology (1.3k citations). Mark Effingham has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Naomi Allen, Clare Bycroft, Allan Motyer, Damjan Vukcevic, Lloyd T. Elliott, Kevin Sharp, Olivier Delaneau, Gavin Band, Gil McVean and Jonathan Marchini. Their work appears in journals such as Nature, Journal of Epidemiology & Community Health, British Journal of Pharmacology, Science Translational Medicine and Nature Reviews 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.

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