Steven E. Scherer

47.4k citations
74 papers · 34.5k · 8 hit papers · h-index 35

Impact in

  • Genetics top 0.1%
    • Genomics and Phylogenetic Studies
    • RNA and protein synthesis mechanisms
    • CRISPR and Genetic Engineering
    • RNA modifications and cancer
    • Genomics and Chromatin Dynamics
    • RNA Research and Splicing

Papers in

Steven E. Scherer

72 papers receiving 33.1k citations

Steven E. Scherer's Hit Papers

Butterfly genome reveals promiscuous exchange of mimicry adaptations among species 2012 · 938 citations
9380+8+17Years since publication5.0k10.0k15.0k

Peers

Steven E. Scherer
Comparison fields: 5 of 212
  • Genetics 9.0k
  • Molecular Biology 21.4k
  • Aging 440
  • Cancer Research 2.7k
  • Plant Science 6.7k
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Citations per field
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Citations per year

Countries citing papers authored by Steven E. Scherer

Since Specialization
Citations

This map shows the geographic impact of Steven E. Scherer'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. Scherer 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. Scherer more than expected).

Fields of papers citing papers by Steven E. Scherer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 74 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Initial sequencing and analysis of the human genome
Hit paper breakdown →
200117763
2
The Genome Sequence of Drosophila melanogaster
Hit paper breakdown →
20004745
3
Somatic mutations affect key pathways in lung adenocarcinoma
Hit paper breakdown →
20082237
4
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
Hit paper breakdown →
20041679
5
The genome of the model beetle and pest Tribolium castaneum
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20081188
6
Butterfly genome reveals promiscuous exchange of mimicry adaptations among species
Hit paper breakdown →
2012938
7
The DNA sequence of the human X chromosome
Hit paper breakdown →
2005857
8
Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease
Hit paper breakdown →
2009438
9 2011405
10 2015320
11 2002312
12 2010267
13 2017262
14 2014259
15 2006254
16 2007232
17 1987212
18 2014202
19 2013162
20 2015157

About Steven E. Scherer

Steven E. Scherer is a scholar working on Genetics, Pharmacology, Molecular Biology, Cardiology and Cardiovascular Medicine and Cancer Research, having authored 74 papers that have together received 34.5k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (11 papers), Pharmacogenetics and Drug Metabolism (10 papers), Genomics and Rare Diseases (9 papers), Chromosomal and Genetic Variations (8 papers), Epigenetics and DNA Methylation (7 papers), Bladder and Urothelial Cancer Treatments (6 papers), Cancer Genomics and Diagnostics (5 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Genetics (9.0k citations), Molecular Biology (21.4k citations), Aging (440 citations), Cancer Research (2.7k citations) and Plant Science (6.7k citations). Steven E. Scherer has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Richard A. Gibbs, C. Thomas Caskey, Gábor Veres, Dianna M. Milewicz, Yang Yu Zhao, Gregory M. Marcus, Gian Antonio Danieli, Jeffrey E. Saffitz, Andrea Pomrehn Myers and Han Liang. Their work appears in journals such as Nature, Laboratory Investigation, Science, Genetics in Medicine and The American Journal of Human Genetics.

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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