Mathew Barber

3.1k citations
8 papers · 940 · 1 hit paper · h-index 6

Impact in

Papers in

    • Genetic Associations and Epidemiology 7
    • Genetic Mapping and Diversity in Plants and Animals 3
    • Genetic and phenotypic traits in livestock 2
    • Forensic and Genetic Research 1
    • Genetics and Neurodevelopmental Disorders 1
    • Pancreatic function and diabetes 1
    • Cholesterol and Lipid Metabolism 1
    • Pancreatitis Pathology and Treatment 1

Mathew Barber

8 papers receiving 927 citations

Mathew Barber's Hit Papers

Computationally efficient whole-genome regression for quantitative and binary traits 2021 · 512 citations
5120+1+3Years since publication100200300400500

Peers

Mathew Barber
Comparison fields: 5 of 112
  • Genetics 510
  • Endocrinology, Diabetes and Metabolism 100
  • Nephrology 40
  • Pharmacology 42
  • Surgery 182
Replace Bong-Jo Kim with:
Bong-Jo Kim South Korea
Lisa A. Bastarache United States
Xueling Sim Singapore
Benjamin B. Sun United Kingdom
Philippe Couvert France
Karen Tan Singapore
Judong Shen United States
Sharon L.R. Kardia United States
Toomas Haller Estonia
Judy Z. Louie United States
Mathew Barber relative to Bong-Jo Kim South Korea Bong-Jo Kim's profile →
Citations per field
00.5×3.8×
Bong-Jo Kim · 1×
Citations per year

Countries citing papers authored by Mathew Barber

Since Specialization
Citations

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

Fields of papers citing papers by Mathew Barber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

8 of 8 papers shown
#Work
1
Computationally efficient whole-genome regression for quantitative and binary traits
Hit paper breakdown →
2021512
2 2010180
3 2008129
4 201761
5 200634
6 200419
7 20054
8 20051

About Mathew Barber

Mathew Barber is a scholar working on Genetics, Surgery, Nephrology, Pathology and Forensic Medicine and Endocrine and Autonomic Systems, having authored 8 papers that have together received 940 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (7 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers), Genetic and phenotypic traits in livestock (2 papers), Forensic and Genetic Research (1 paper), Pancreatic function and diabetes (1 paper), Cholesterol and Lipid Metabolism (1 paper), Pancreatitis Pathology and Treatment (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (510 citations), Endocrinology, Diabetes and Metabolism (100 citations), Nephrology (40 citations), Pharmacology (42 citations) and Surgery (182 citations). Mathew Barber has collaborated with scholars based in United Kingdom and United States. Frequent co-authors include Andrey Ziyatdinov, Manuel A. R. Ferreira, Christian Benner, Evan K. Maxwell, Joshua Backman, Jonathan Marchini, Joelle Mbatchou, Aris Baras, Lukas Habegger and Anthony Marcketta. Their work appears in journals such as Genetic Epidemiology, BMC Genetics, The American Journal of Human Genetics, Nature Genetics and PLoS ONE.

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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