Michael Ronemus

8.7k total citations · 1 hit paper
21 papers, 2.2k citations indexed

About

Michael Ronemus is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Michael Ronemus has authored 21 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Michael Ronemus's work include Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (5 papers) and Chromosomal and Genetic Variations (5 papers). Michael Ronemus is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (5 papers) and Chromosomal and Genetic Variations (5 papers). Michael Ronemus collaborates with scholars based in United States, Mexico and Canada. Michael Ronemus's co-authors include Ivan Iossifov, Michael Wigler, Dan Levy, Dennis Vitkup, Christine Ticknor, Massimo Galbiati, Stephen L. Dellaporta, Jychian Chen, Boris Yamrom and Robert A. Martienssen and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Michael Ronemus

18 papers receiving 2.1k citations

Hit Papers

Rare De Novo and Transmit... 2011 2026 2016 2021 2011 100 200 300 400

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Michael Ronemus 1.1k 1.1k 836 512 137 21 2.2k
Mona D. Shahbazian 1.5k 1.3× 2.3k 2.1× 877 1.0× 228 0.4× 180 1.3× 12 3.1k
Bai-Lin Wu 1.4k 1.2× 1.0k 0.9× 646 0.8× 154 0.3× 67 0.5× 43 2.2k
Svetlana G. Vorsanova 2.1k 1.8× 1.5k 1.3× 315 0.4× 572 1.1× 162 1.2× 175 3.1k
Alan Packer 975 0.9× 1.4k 1.3× 592 0.7× 103 0.2× 97 0.7× 25 2.4k
Cindy Skinner 1.6k 1.4× 1.4k 1.3× 907 1.1× 101 0.2× 257 1.9× 64 2.5k
Melissa B. Ramocki 1.2k 1.1× 1.1k 1.0× 497 0.6× 157 0.3× 222 1.6× 29 1.9k
Seungtai Yoon 1.0k 0.9× 821 0.7× 433 0.5× 133 0.3× 67 0.5× 16 1.5k
Irina Voineagu 1.3k 1.2× 2.3k 2.1× 994 1.2× 158 0.3× 440 3.2× 34 3.3k
Sylvain Briault 1.6k 1.4× 1.8k 1.6× 610 0.7× 140 0.3× 426 3.1× 64 3.1k
Rui Luo 748 0.7× 1.1k 1.0× 493 0.6× 80 0.2× 128 0.9× 15 1.8k

Countries citing papers authored by Michael Ronemus

Since Specialization
Citations

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

Fields of papers citing papers by Michael Ronemus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael Ronemus. 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 Michael Ronemus. The network helps show where Michael Ronemus may publish in the future.

Co-authorship network of co-authors of Michael Ronemus

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Ronemus. A scholar is included among the top collaborators of Michael Ronemus 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 Michael Ronemus. Michael Ronemus 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.
Ronemus, Michael, et al.. (2025). Exploring genome-transcriptome correlations in cancer. Biochemical Society Transactions. 53(1). 113–120.
2.
Yoon, Seungtai, Peter Andrews, Boris Yamrom, et al.. (2023). Sharing parental genomes by siblings concordant or discordant for autism. Cell Genomics. 3(6). 100319–100319. 3 indexed citations
3.
Yoon, Seungtai, Adriana Muñoz, Boris Yamrom, et al.. (2021). Rates of contributory de novo mutation in high and low-risk autism families. Communications Biology. 4(1). 1026–1026. 19 indexed citations
4.
Jobanputra, Vaidehi, Peter Andrews, Vanessa Felice, et al.. (2020). Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies. Journal of Molecular Diagnostics. 22(12). 1476–1481. 1 indexed citations
5.
Kumar, Vijay, Julie Rosenbaum, Zihua Wang, et al.. (2017). Partial bisulfite conversion for unique template sequencing. Nucleic Acids Research. 46(2). e10–e10. 5 indexed citations
6.
Wang, Zihua, Peter M. Andrews, Jude Kendall, et al.. (2016). SMASH, a fragmentation and sequencing method for genomic copy number analysis. Genome Research. 26(6). 844–851. 15 indexed citations
7.
Fang, Han, Ewa A. Bergmann, Kanika Arora, et al.. (2016). Indel variant analysis of short-read sequencing data with Scalpel. Nature Protocols. 11(12). 2529–2548. 77 indexed citations
8.
Iossifov, Ivan, Dan Levy, Kenny Ye, et al.. (2015). Low load for disruptive mutations in autism genes and their biased transmission. Proceedings of the National Academy of Sciences. 112(41). E5600–7. 102 indexed citations
9.
Fang, Han, Yiyang Wu, Giuseppe Narzisi, et al.. (2014). Reducing INDEL calling errors in whole genome and exome sequencing data. Genome Medicine. 6(10). 89–89. 112 indexed citations
10.
Ronemus, Michael, Ivan Iossifov, Dan Levy, & Michael Wigler. (2014). The role of de novo mutations in the genetics of autism spectrum disorders. Nature Reviews Genetics. 15(2). 133–141. 250 indexed citations
11.
12.
Levy, Dan, Michael Ronemus, Boris Yamrom, et al.. (2011). Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders. Neuron. 70(5). 886–897. 484 indexed citations breakdown →
14.
Lee, Yoon-ha, Michael Ronemus, Jude Kendall, et al.. (2011). Reducing system noise in copy number data using principal components of self-self hybridizations. Proceedings of the National Academy of Sciences. 109(3). E103–10. 7 indexed citations
15.
Levy, Dan, Michael Ronemus, Boris Yamrom, et al.. (2011). RareDeNovoandTransmittedCopy-NumberVariation in Autistic Spectrum Disorders. 1 indexed citations
16.
Ronemus, Michael, Matthew Vaughn, & Robert A. Martienssen. (2006). MicroRNA-Targeted and Small Interfering RNA–Mediated mRNA Degradation Is Regulated by Argonaute, Dicer, and RNA-Dependent RNA Polymerase in Arabidopsis. The Plant Cell. 18(7). 1559–1574. 124 indexed citations
17.
Martienssen, Robert A., Zachary B. Lippman, Bruce May, Michael Ronemus, & Matthew Vaughn. (2004). Transposons, Tandem Repeats, and the Silencing of Imprinted Genes. Cold Spring Harbor Symposia on Quantitative Biology. 69(0). 371–380. 25 indexed citations
18.
Ronemus, Michael. (2000). Shuffling viral tropism. Nature Biotechnology. 18(9). 913–913.
19.
Ronemus, Michael. (2000). A new match-maker. Nature Medicine. 6(1). 19–19. 1 indexed citations
20.
Ronemus, Michael, Massimo Galbiati, Christine Ticknor, Jychian Chen, & Stephen L. Dellaporta. (1996). Demethylation-Induced Developmental Pleiotropy in Arabidopsis . Science. 273(5275). 654–657. 381 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026