Steven E. Brenner

47.9k total citations · 4 hit papers
141 papers, 23.7k citations indexed

About

Steven E. Brenner is a scholar working on Molecular Biology, Genetics and Materials Chemistry. According to data from OpenAlex, Steven E. Brenner has authored 141 papers receiving a total of 23.7k indexed citations (citations by other indexed papers that have themselves been cited), including 105 papers in Molecular Biology, 30 papers in Genetics and 25 papers in Materials Chemistry. Recurrent topics in Steven E. Brenner's work include RNA and protein synthesis mechanisms (47 papers), Genomics and Phylogenetic Studies (31 papers) and Protein Structure and Dynamics (29 papers). Steven E. Brenner is often cited by papers focused on RNA and protein synthesis mechanisms (47 papers), Genomics and Phylogenetic Studies (31 papers) and Protein Structure and Dynamics (29 papers). Steven E. Brenner collaborates with scholars based in United States, United Kingdom and India. Steven E. Brenner's co-authors include John‐Marc Chandonia, Gavin E. Crooks, Gary C. Hon, Tim Hubbard, C. Chothia, Alexey G. Murzin, Richard E. Green, Benjamin P. Lewis, Liana F. Lareau and Naomi K. Fox and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Steven E. Brenner

140 papers receiving 23.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

WebLogo: A Sequence Logo Generator: Figure 1

2004 9.8k citations John‐Marc Chandonia, Steven E. Brenner et al. profile →
SCOP: A structural classification of proteins database for the investigation of sequences and structures

1995 5.1k citations Alexey G. Murzin, Steven E. Brenner et al. profile →
Evidence for the widespread coupling of alternative splicing and nonsense-mediated mRNA decay in humans

2002 813 citations Steven E. Brenner et al. profile →
SCOPe: Structural Classification of Proteins—extended, integrating SCOP and ASTRAL data and classification of new structures

2013 550 citations Naomi K. Fox, Steven E. Brenner et al. Nucleic Acids Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Steven E. Brenner United States	49	19.2k	3.4k	2.7k	2.6k	1.5k	141	23.7k
Burkhard Rost United States	79	24.1k 1.2×	4.9k 1.4×	3.0k 1.1×	1.7k 0.7×	1.1k 0.7×	280	28.9k
Stephen H. Bryant United States	55	14.1k 0.7×	2.9k 0.9×	1.6k 0.6×	2.4k 0.9×	1.2k 0.8×	156	21.5k
Geoffrey J. Barton United Kingdom	62	19.3k 1.0×	2.8k 0.8×	2.7k 1.0×	3.3k 1.3×	1.6k 1.1×	154	26.2k
A. Joachimiak United States	72	14.6k 0.8×	3.5k 1.0×	3.0k 1.1×	1.6k 0.6×	1.3k 0.8×	392	22.3k
Adam Godzik United States	77	20.9k 1.1×	3.3k 1.0×	2.2k 0.8×	2.3k 0.9×	2.8k 1.8×	293	28.2k
Andrew G. W. Leslie United Kingdom	57	23.9k 1.2×	5.7k 1.7×	2.2k 0.8×	1.2k 0.5×	1.5k 1.0×	97	30.8k
Lorenza Bordoli Switzerland	20	15.3k 0.8×	1.7k 0.5×	2.3k 0.9×	3.2k 1.2×	1.3k 0.8×	23	24.1k
Kevin Karplus United States	36	12.5k 0.6×	1.7k 0.5×	1.9k 0.7×	2.3k 0.9×	1.7k 1.1×	83	18.8k
William R. Pearson United States	44	16.4k 0.9×	1.2k 0.4×	3.0k 1.1×	3.2k 1.2×	2.0k 1.3×	100	22.6k
Gert Vriend Netherlands	63	15.3k 0.8×	3.7k 1.1×	1.8k 0.7×	1.1k 0.4×	617 0.4×	192	21.0k

Countries citing papers authored by Steven E. Brenner

Since Specialization

Citations

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

Fields of papers citing papers by Steven E. Brenner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven E. Brenner

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

All Works

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20 of 20 papers shown

Hu, Zhiqiang, et al.. (2024). Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictors. Human Genomics. 18(1). 90–90. 5 indexed citations

Catanzariti, Ann‐Maree, Julian R. Greenwood, Megan A. Outram, et al.. (2023). A rust‐fungus Nudix hydrolase effector decaps mRNAin vitro and interferes with plant immune pathways. New Phytologist. 239(1). 222–239. 14 indexed citations

Bromberg, Yana, Hannah Carter, & Steven E. Brenner. (2023). Session Introduction: Precision Medicine: Innovative methods for advanced understanding of molecular underpinnings of disease. PubMed. 29. 446–449.

Sharo, Andrew G., Zhiqiang Hu, Shamil Sunyaev, & Steven E. Brenner. (2022). StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants. The American Journal of Human Genetics. 109(2). 195–209. 37 indexed citations

Shieh, Joseph T.C., K. Wong, Michal Levy‐Sakin, et al.. (2021). Application of full-genome analysis to diagnose rare monogenic disorders. npj Genomic Medicine. 6(1). 77–77. 29 indexed citations

Kuzuoğlu‐Öztürk, Duygu, Zhiqiang Hu, Emily N. Devericks, et al.. (2021). Revealing molecular pathways for cancer cell fitness through a genetic screen of the cancer translatome. Cell Reports. 35(13). 109321–109321. 11 indexed citations

Chandonia, John‐Marc, et al.. (2021). SCOPe: improvements to the structural classification of proteins – extended database to facilitate variant interpretation and machine learning. Nucleic Acids Research. 50(D1). D553–D559. 86 indexed citations

Andreoletti, Gaia, Lipika R. Pal, John Moult, & Steven E. Brenner. (2019). Reports from the fifth edition of CAGI: The Critical Assessment of Genome Interpretation. Human Mutation. 40(9). 1197–1201. 37 indexed citations

Hu, Zhiqiang, Changhua Yu, Gaia Andreoletti, et al.. (2019). VIPdb, a genetic Variant Impact Predictor Database. Human Mutation. 40(9). 1202–1214. 20 indexed citations

10.

Chan, Alice, Divya Punwani, Theresa A. Kadlecek, et al.. (2016). A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70. The Journal of Experimental Medicine. 213(2). 155–165. 54 indexed citations

11.

Punwani, Divya, Yong Zhang, Jason Yu, et al.. (2016). Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. New England Journal of Medicine. 375(22). 2165–2176. 77 indexed citations

12.

Caswell‐Jin, Jennifer L., Roman Camarda, Alicia Y. Zhou, et al.. (2015). Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors. Human Molecular Genetics. 24(25). 7421–7431. 16 indexed citations

13.

Patel, Jay, Jennifer M. Puck, Kunal Kundu, et al.. (2015). Nijmegen Breakage Syndrome Detected By Newborn Screening for T Cell Receptor Excision Circles (TRECs). Journal of Allergy and Clinical Immunology. 135(2). AB14–AB14. 6 indexed citations

14.

Hansen, Kasper D., Steven E. Brenner, & Sandrine Dudoit. (2010). Biases in Illumina transcriptome sequencing caused by random hexamer priming. Nucleic Acids Research. 38(12). e131–e131. 480 indexed citations

15.

Brenner, Steven E.. (2000). The ASTRAL compendium for protein structure and sequence analysis. Nucleic Acids Research. 28(1). 254–256. 406 indexed citations

16.

Brenner, Steven E., Derren Barken, & Michael Levitt. (1999). The PRESAGE database for structural genomics. Nucleic Acids Research. 27(1). 251–253. 41 indexed citations

17.

Brenner, Steven E., C. Chothia, & Tim Hubbard. (1997). Population statistics of protein structures. Current Opinion in Structural Biology. 7(3). 5 indexed citations

18.

Murzin, Alexey G., Steven E. Brenner, Tim Hubbard, & C. Chothia. (1996). Understanding protein structure. Methods in enzymology on CD-ROM/Methods in enzymology. 266. 3 indexed citations

19.

Brenner, Steven E. & Tim Hubbard. (1995). Proceedings Of The Third International Conference On Intelligent Systems For Molecular Biology. National Conference on Artificial Intelligence. 64 indexed citations

20.

Brandt, Lawrence J., et al.. (1976). Extrahepatic biliary tract obstruction secondary to a hepatoma-containing blood clot in the common bile duct. Digestive Diseases and Sciences. 21(10). 905–909. 19 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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