Brian J. Beres

438 total citations
9 papers, 359 citations indexed

About

Brian J. Beres is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Brian J. Beres has authored 9 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Genetics. Recurrent topics in Brian J. Beres's work include Muscle Physiology and Disorders (3 papers), Virus-based gene therapy research (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Brian J. Beres is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Virus-based gene therapy research (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Brian J. Beres collaborates with scholars based in United States and Canada. Brian J. Beres's co-authors include Jeanne Wilson‐Rawls, Joshua Johnson, Alan Rawls, David H. Holman, Gregory A. Helm, Gerald R. Hankins, Debra D. Pittman, Randall J. Dumont, Tsutomu Sasaki and Douglas M. Anderson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Development and Molecular Therapy.

In The Last Decade

Brian J. Beres

9 papers receiving 353 citations

Peers

Brian J. Beres

MB

GENET

BE

SURGE

PHEOH

Miki Maehara Japan

Aya Uchida Japan

Mohammad Mousaei Ghasroldasht United States

Jung Im Yun South Korea

Geun‐Ho Maeng South Korea

Jennifer Kajahn Germany

Katarzyna Stefańska Poland

Yoko Tokuyama Japan

Aby J. Mathew United States

Jerry KY Chan Singapore

Miki Maehara Japan

Brian J. Beres

168 ×0.8

MB

89 ×1.0

GENET

37 ×0.6

BE

158 ×2.5

SURGE

82 ×1.3

PHEOH

Citations per year, relative to Brian J. Beres Brian J. Beres (= 1×) peers Miki Maehara

Countries citing papers authored by Brian J. Beres

Since Specialization

Citations

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

Fields of papers citing papers by Brian J. Beres

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian J. Beres. 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 Brian J. Beres. The network helps show where Brian J. Beres may publish in the future.

Co-authorship network of co-authors of Brian J. Beres

This figure shows the co-authorship network connecting the top 25 collaborators of Brian J. Beres. A scholar is included among the top collaborators of Brian J. Beres 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 Brian J. Beres. Brian J. Beres is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

George, Rajani M., Stefano Biressi, Brian J. Beres, et al.. (2013). Numb-deficient satellite cells have regeneration and proliferation defects. Proceedings of the National Academy of Sciences. 110(46). 18549–18554. 37 indexed citations

2.

Beres, Brian J., Rajani M. George, C. Michael Barton, et al.. (2011). Numb regulates Notch1, but not Notch3, during myogenesis. Mechanisms of Development. 128(5-6). 247–257. 33 indexed citations

3.

Anderson, Douglas M., Brian J. Beres, Jeanne Wilson‐Rawls, & Alan Rawls. (2009). The homeobox gene Mohawk represses transcription by recruiting the sin3A/HDAC co‐repressor complex. Developmental Dynamics. 238(3). 572–580. 32 indexed citations

4.

Beres, Brian J., et al.. (2008). A deficiency of lunatic fringe is associated with cystic dilation of the rete testis. Reproduction. 137(1). 79–93. 25 indexed citations

5.

Johnson, Joshua, et al.. (2006). A loss of lunatic fringe is associated with female infertility. Development. 133(4). 579–580. 2 indexed citations

6.

Li, Jin Zhong, David H. Holman, Hongwei Li, et al.. (2005). Long‐term tracing of adenoviral expression in rat and rabbit using luciferase imaging. The Journal of Gene Medicine. 7(6). 792–802. 11 indexed citations

7.

Johnson, Joshua, et al.. (2005). Lunatic fringe null female mice are infertile due to defects in meiotic maturation. Development. 132(4). 817–828. 89 indexed citations

8.

Sasaki, Tsutomu, David H. Holman, Brian J. Beres, et al.. (2003). Osteogenic potential of five different recombinant human bone morphogenetic protein adenoviral vectors in the rat. Gene Therapy. 10(20). 1735–1743. 114 indexed citations

9.

Li, Jin Zhong, Hongwei Li, David H. Holman, et al.. (2003). Rat strain differences in the ectopic osteogenic potential of recombinant human BMP adenoviruses. Molecular Therapy. 8(5). 822–829. 16 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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