B.E. Reus

1.1k citations
8 papers · 860 · 1 hit paper · h-index 7

Impact in

Papers in

    • Gene expression and cancer classification 2
    • Ion channel regulation and function 1
    • DNA Repair Mechanisms 1
    • RNA modifications and cancer 1
    • Genomic variations and chromosomal abnormalities 4
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1

B.E. Reus

8 papers receiving 830 citations

B.E. Reus's Hit Papers

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family 1998 · 729 citations
7290+9+18Years since publication200400600

Peers

B.E. Reus
Comparison fields: 5 of 67
  • Cellular and Molecular Neuroscience 459
  • Psychiatry and Mental health 245
  • Cardiology and Cardiovascular Medicine 295
  • Molecular Biology 695
  • Genetics 184
Replace Robyn Labrum with:
Robyn Labrum United Kingdom
Bryan Lynch Ireland
Antonio Falace Italy
Roland Spiegel Switzerland
Soledad Monges Argentina
Claude Mignard France
M L Savontaus Finland
Brigid M. Regan Australia
Amanda Lindy United States
Ann Löfgren Belgium
B.E. Reus relative to Robyn Labrum United Kingdom Robyn Labrum's profile →
Citations per field
00.5×2.6×
Robyn Labrum · 1×
Citations per year

Countries citing papers authored by B.E. Reus

Since Specialization
Citations

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

Fields of papers citing papers by B.E. Reus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

8 of 8 papers shown
#Work
1
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
Hit paper breakdown →
1998729
2 199759
3 199919
4 199616
5 199415
6
A radiation hybrid map of the BRCA1 region.
19949
7 19948
8 19915

About B.E. Reus

B.E. Reus is a scholar working on Molecular Biology, Genetics, Rheumatology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine, having authored 8 papers that have together received 860 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Bone and Dental Protein Studies (2 papers), Gene expression and cancer classification (2 papers), Cardiac electrophysiology and arrhythmias (1 paper), Ion channel regulation and function (1 paper), DNA Repair Mechanisms (1 paper), RNA modifications and cancer (1 paper) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (459 citations), Psychiatry and Mental health (245 citations), Cardiology and Cardiovascular Medicine (295 citations), Molecular Biology (695 citations) and Genetics (184 citations). B.E. Reus has collaborated with scholars based in United States, Sweden and Poland. Frequent co-authors include Robin J. Leach, Tracey Lewis, Mark Leppert, Carole Charlier, Nanda A. Singh, Stephen G. Ryan, Mary MacDougall, Gösta Holmgren, Paul H. Krebsbach and Kristina Forsman. Their work appears in journals such as Genomics, Journal of Dental Research, Nature Genetics, Nucleic Acids Research and Cytogenetic and Genome 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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