Steven C. Munger

2.6k total citations
25 papers, 1.5k citations indexed

About

Steven C. Munger is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Steven C. Munger has authored 25 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 20 papers in Genetics and 2 papers in Surgery. Recurrent topics in Steven C. Munger's work include Genetic Mapping and Diversity in Plants and Animals (12 papers), Epigenetics and DNA Methylation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Steven C. Munger is often cited by papers focused on Genetic Mapping and Diversity in Plants and Animals (12 papers), Epigenetics and DNA Methylation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Steven C. Munger collaborates with scholars based in United States, United Kingdom and France. Steven C. Munger's co-authors include Gary A. Churchill, Karen L. Svenson, Daniel M. Gatti, Blanche Capel, Anirudh Natarajan, Narayanan Raghupathy, Kwangbom Choi, Steven P. Gygi, Tony DeFalco and Jonah Cool and has published in prestigious journals such as Nature, Genes & Development and The EMBO Journal.

In The Last Decade

Steven C. Munger

24 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven C. Munger United States 16 986 742 180 134 111 25 1.5k
Hidesato Ogawa Japan 18 2.1k 2.1× 765 1.0× 123 0.7× 88 0.7× 85 0.8× 38 2.7k
D. Alan Underhill Canada 23 1.6k 1.6× 387 0.5× 101 0.6× 63 0.5× 52 0.5× 49 2.1k
Rika Suzuki Japan 18 1.6k 1.6× 696 0.9× 199 1.1× 300 2.2× 59 0.5× 57 2.3k
Haifeng Wan China 18 1.2k 1.2× 337 0.5× 233 1.3× 367 2.7× 98 0.9× 32 1.6k
Yuichi Ozaki Japan 23 594 0.6× 571 0.8× 274 1.5× 61 0.5× 55 0.5× 54 1.6k
Hirokazu Fujimoto Japan 22 1.2k 1.2× 607 0.8× 347 1.9× 278 2.1× 61 0.5× 45 1.6k
Eva Brundell Sweden 14 1.2k 1.2× 351 0.5× 244 1.4× 268 2.0× 29 0.3× 15 1.5k
Meredith Calvert United States 16 590 0.6× 203 0.3× 113 0.6× 187 1.4× 35 0.3× 29 1.0k
Rebecca Rimini Italy 12 694 0.7× 263 0.4× 83 0.5× 37 0.3× 67 0.6× 13 1.1k
Motohito Goto Japan 17 587 0.6× 196 0.3× 113 0.6× 118 0.9× 87 0.8× 42 1.1k

Countries citing papers authored by Steven C. Munger

Since Specialization
Citations

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

Fields of papers citing papers by Steven C. Munger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven C. Munger

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

All Works

20 of 20 papers shown
1.
2.
Munger, Steven C., et al.. (2024). An in vitro neurogenetics platform for precision disease modeling in the mouse. Science Advances. 10(14). eadj9305–eadj9305. 2 indexed citations
3.
Zhang, Tian, Gregory R. Keele, Matthew Vincent, et al.. (2023). Multi-omics analysis identifies drivers of protein phosphorylation. Genome biology. 24(1). 52–52. 9 indexed citations
4.
Zhang, Tian, Gregory R. Keele, Daniel A. Skelly, et al.. (2023). Genetic dissection of the pluripotent proteome through multi-omics data integration. Cell Genomics. 3(4). 100283–100283. 8 indexed citations
5.
Skelly, Daniel A., Anne Czechanski, Steven C. Munger, et al.. (2023). Imputation of 3D genome structure by genetic–epigenetic interaction modeling in mice. eLife. 12. 1 indexed citations
6.
Chick, Joel M., Gregory R. Keele, Steven C. Munger, et al.. (2022). Genome-wide transcript and protein analysis highlights the role of protein homeostasis in the aging mouse heart. Genome Research. 32(5). 838–852. 17 indexed citations
7.
Keele, Gregory R., Tian Zhang, Matthew Vincent, et al.. (2021). Regulation of protein abundance in genetically diverse mouse populations. Cell Genomics. 1(1). 100003–100003. 24 indexed citations
8.
Katz, David C., J. David Aponte, Wei Liu, et al.. (2020). Facial shape and allometry quantitative trait locus intervals in the Diversity Outbred mouse are enriched for known skeletal and facial development genes. PLoS ONE. 15(6). e0233377–e0233377. 13 indexed citations
9.
Ortmann, Daniel, Stephanie Brown, Anne Czechanski, et al.. (2020). Naive Pluripotent Stem Cells Exhibit Phenotypic Variability that Is Driven by Genetic Variation. Cell stem cell. 27(3). 470–481.e6. 31 indexed citations
10.
Liang, Zhengzheng, Irène Cimino, Binnaz Yalcin, et al.. (2020). Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. PLoS Genetics. 16(9). e1008916–e1008916. 17 indexed citations
11.
Raghupathy, Narayanan, Kwangbom Choi, Matthew Vincent, et al.. (2018). Hierarchical analysis of RNA-seq reads improves the accuracy of allele-specific expression. Bioinformatics. 34(13). 2177–2184. 53 indexed citations
12.
Tyler, Anna L., Bo Ji, Daniel M. Gatti, et al.. (2017). Epistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice. Genetics. 206(2). 621–639. 36 indexed citations
13.
Chick, Joel M., Steven C. Munger, Petr Šimeček, et al.. (2016). Defining the consequences of genetic variation on a proteome-wide scale. Nature. 534(7608). 500–505. 244 indexed citations
14.
Munger, Steven C., Narayanan Raghupathy, Kwangbom Choi, et al.. (2014). RNA-Seq Alignment to Individualized Genomes Improves Transcript Abundance Estimates in Multiparent Populations. Genetics. 198(1). 59–73. 53 indexed citations
15.
French, John E., Daniel M. Gatti, Daniel L. Morgan, et al.. (2014). Diversity Outbred Mice Identify Population-Based Exposure Thresholds and Genetic Factors that Influence Benzene-Induced Genotoxicity. Environmental Health Perspectives. 123(3). 237–245. 92 indexed citations
16.
Munger, Steven C., Anirudh Natarajan, Loren L. Looger, Uwe Ohler, & Blanche Capel. (2013). Fine Time Course Expression Analysis Identifies Cascades of Activation and Repression and Maps a Putative Regulator of Mammalian Sex Determination. PLoS Genetics. 9(7). e1003630–e1003630. 73 indexed citations
17.
Natarajan, Anirudh, Jonah Cool, Tony DeFalco, et al.. (2012). Temporal Transcriptional Profiling of Somatic and Germ Cells Reveals Biased Lineage Priming of Sexual Fate in the Fetal Mouse Gonad. PLoS Genetics. 8(3). e1002575–e1002575. 225 indexed citations
18.
Churchill, Gary A., Daniel M. Gatti, Steven C. Munger, & Karen L. Svenson. (2012). The diversity outbred mouse population. Mammalian Genome. 23(9-10). 713–718. 315 indexed citations
19.
Cook, Matthew S., Steven C. Munger, Joseph H. Nadeau, & Blanche Capel. (2010). Regulation of male germ cell cycle arrest and differentiation by DND1 is modulated by genetic background. Development. 138(1). 23–32. 83 indexed citations
20.
Munger, Steven C., et al.. (2009). Elucidation of the transcription network governing mammalian sex determination by exploiting strain-specific susceptibility to sex reversal. Genes & Development. 23(21). 2521–2536. 59 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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