B.E. Reus

1.1k citations
8 papers · 886 · 1 hit paper · h-index 6

Impact in

Papers in

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

B.E. Reus

7 papers receiving 839 citations

B.E. Reus's Hit Papers

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family 1998 · 766 citations
7660+9+18Years since publication250500750

Peers

B.E. Reus
Comparison fields: 5 of 64
  • Cellular and Molecular Neuroscience 440
  • Psychiatry and Mental health 227
  • Cardiology and Cardiovascular Medicine 292
  • Molecular Biology 656
  • Rheumatology 93
Replace R.A. Ophoff with:
R.A. Ophoff Netherlands
Bryan Lynch Ireland
Claude Mignard France
Brigid M. Regan Australia
Torsten Kraya Germany
Marie‐Christine Arné‐Bes France
Maéva Langouët United States
Aldrín E. Molero United States
G. Sabbadini Italy
Hartwig Heyck Germany
B.E. Reus relative to R.A. Ophoff Netherlands R.A. Ophoff's profile →
Citations per field
00.5×5×10×13.3×
R.A. Ophoff · 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 →
1998766
2 199761
3 199921
4 199415
5
A radiation hybrid map of the BRCA1 region.
199410
6 19948
7 19915
8 20080

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 886 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Gene expression and cancer classification (2 papers), Bone and Dental Protein Studies (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Cardiac electrophysiology and arrhythmias (1 paper), Ubiquitin and proteasome pathways (1 paper), DNA Repair Mechanisms (1 paper) and Ion channel regulation and function (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (440 citations), Psychiatry and Mental health (227 citations), Cardiology and Cardiovascular Medicine (292 citations), Molecular Biology (656 citations) and Rheumatology (93 citations). B.E. Reus has collaborated with scholars based in United States, Poland and Sweden. Frequent co-authors include Robin J. Leach, Tracey Lewis, Stephen G. Ryan, Nanda A. Singh, Carole Charlier, Mark Leppert, Mary MacDougall, Darrin Simmons, Kristina Forsman and Gösta Holmgren. Their work appears in journals such as Genomics, Journal of Dental Research, Nucleic Acids Research, Nature Genetics and PubMed.

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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