B.E. Reus

1.1k total citations · 1 hit paper
8 papers, 860 citations indexed

About

B.E. Reus is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, B.E. Reus has authored 8 papers receiving a total of 860 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Rheumatology. Recurrent topics in B.E. Reus's work include Genomic variations and chromosomal abnormalities (4 papers), Bone and Dental Protein Studies (2 papers) and Gene expression and cancer classification (2 papers). B.E. Reus is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Bone and Dental Protein Studies (2 papers) and Gene expression and cancer classification (2 papers). B.E. Reus collaborates with scholars based in United States, Sweden and Poland. B.E. Reus's co-authors include Robin J. Leach, Tracey Lewis, Stephen G. Ryan, Carole Charlier, Mark Leppert, Nanda A. Singh, Mary MacDougall, Paul H. Krebsbach, Kristina Forsman and Darrin Simmons and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Dental Research.

In The Last Decade

B.E. Reus

8 papers receiving 830 citations

Hit Papers

A pore mutation in a novel KQT-like potassium channel gen... 1998 2026 2007 2016 1998 200 400 600

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
B.E. Reus United States 7 695 459 295 245 184 8 860
Robyn Labrum United Kingdom 14 488 0.7× 400 0.9× 145 0.5× 93 0.4× 84 0.5× 21 772
M L Savontaus Finland 15 1.2k 1.7× 218 0.5× 41 0.1× 32 0.1× 158 0.9× 18 1.4k
Bryan Lynch Ireland 13 378 0.5× 141 0.3× 79 0.3× 170 0.7× 217 1.2× 32 659
Soledad Monges Argentina 12 360 0.5× 110 0.2× 135 0.5× 35 0.1× 52 0.3× 28 509
Antonio Falace Italy 12 383 0.6× 131 0.3× 28 0.1× 75 0.3× 204 1.1× 21 640
Ann Löfgren Belgium 13 722 1.0× 502 1.1× 25 0.1× 227 0.9× 189 1.0× 16 1.1k
Brigid M. Regan Australia 10 245 0.4× 127 0.3× 75 0.3× 314 1.3× 336 1.8× 10 643
Roland Spiegel Switzerland 12 654 0.9× 595 1.3× 92 0.3× 15 0.1× 140 0.8× 28 950
Claude Mignard France 5 690 1.0× 688 1.5× 43 0.1× 51 0.2× 49 0.3× 7 865
A.-E. Lehesjoki Finland 12 241 0.3× 128 0.3× 22 0.1× 133 0.5× 310 1.7× 16 610

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-authorship network of co-authors of B.E. Reus

This figure shows the co-authorship network connecting the top 25 collaborators of B.E. Reus. A scholar is included among the top collaborators of B.E. Reus based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with B.E. Reus. B.E. Reus is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
1.
MacDougall, Mary, Tingting Gu, B.E. Reus, et al.. (1999). Genetic Linkage of the Dentinogenesis Imperfecta Type III Locus to Chromosome 4q. Journal of Dental Research. 78(6). 1277–1282. 19 indexed citations
2.
Charlier, Carole, Nanda A. Singh, Stephen G. Ryan, et al.. (1998). A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nature Genetics. 18(1). 53–55. 729 indexed citations breakdown →
3.
MacDougall, Mary, Barbara R. DuPont, Darrin Simmons, et al.. (1997). Ameloblastin Gene (AMBN) Maps within the Critical Region for Autosomal Dominant Amelogenesis Imperfecta at Chromosome 4q21. Genomics. 41(1). 115–118. 59 indexed citations
4.
Naylor, Susan L., Shanna L. Moore, Dawn Garcia, et al.. (1996). Mapping 638 STSs to regions of human chromosome 3. Cytogenetic and Genome Research. 72(1). 90–94. 16 indexed citations
5.
Leach, Robin J., et al.. (1994). Confirmation of the Assignment of the Human Tartrate-Resistant Acid Phosphatase Gene (ACP5) to Chromosome 19. Genomics. 19(1). 180–181. 8 indexed citations
6.
Leach, Robin J., B.E. Reus, Shirley J. Hayes, et al.. (1994). Regional Localization of 188 Sequence Tagged Sites on a Somatic Cell Hybrid Mapping Panel for Human Chromosome 3. Genomics. 24(3). 549–556. 15 indexed citations
7.
O’Connell, P., Hans Albertsen, Nori Matsunami, et al.. (1994). A radiation hybrid map of the BRCA1 region.. PubMed. 54(3). 526–34. 9 indexed citations
8.
Johnson, T.L., et al.. (1991). Detection of a length polymorphism for human GIP gene by polymerase chain reaction. Nucleic Acids Research. 19(15). 4312–4312. 5 indexed citations

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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