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 Netherlands. Michael Ronemus's co-authors include Ivan Iossifov, Michael Wigler, Dan Levy, Dennis Vitkup, Massimo Galbiati, Jychian Chen, Stephen L. Dellaporta, Christine Ticknor, Boris Yamrom and Matthew Vaughn 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

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.

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

2011 484 citations Dan Levy, Michael Ronemus et al. Neuron profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Exploring genome-transcriptome correlations in cancer 2025 ·Biochemical Society Transactions ·Michael Ronemus, Daniel W. Bradford, Zvi Laster, (unknown)	0
2	Sharing parental genomes by siblings concordant or discordant for autism 2023 ·Cell Genomics ·(unknown), Seungtai Yoon, Peter Andrews, Boris Yamrom, Michael Ronemus, Andreas Buja, Abba Μ. Krieger, Dan Levy, Kenny Ye, Michael Wigler, Ivan Iossifov	3
3	Rates of contributory de novo mutation in high and low-risk autism families 2021 ·Communications Biology ·Seungtai Yoon, Adriana Muñoz, Boris Yamrom, Yoon-ha Lee, Peter Andrews, Steven C. Marks, Zihua Wang, Catherine Reeves, Lara Winterkorn, Abba Μ. Krieger, Andreas Buja, Kith Pradhan, Michael Ronemus, Kristin K. Baldwin, Dan Levy, Michael Wigler, Ivan Iossifov	19
4	Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies 2020 ·Journal of Molecular Diagnostics ·Vaidehi Jobanputra, Peter Andrews, Vanessa Felice, Avinash Abhyankar, (unknown), (unknown), (unknown), Inessa Hakker, Kazimierz O. Wrzeszczyński, Michael Ronemus	1
5	Partial bisulfite conversion for unique template sequencing 2017 ·Nucleic Acids Research ·Vijay Kumar, Julie Rosenbaum, Zihua Wang, (unknown), Michael Ronemus, Michael Wigler, Dan Levy	5
6	Indel variant analysis of short-read sequencing data with Scalpel 2016 ·Nature Protocols ·Han Fang, Ewa A. Bergmann, Kanika Arora, Vladimir Vacic, Michael C. Zody, Ivan Iossifov, Jason O'Rawe, Yiyang Wu, (unknown), Julie Rosenbaum, Michael Ronemus, Yoon-ha Lee, Zihua Wang, Esra Dikoglu, Vaidehi Jobanputra, Gholson J. Lyon, Michael Wigler, Michael C. Schatz, Giuseppe Narzisi	77
7	SMASH, a fragmentation and sequencing method for genomic copy number analysis 2016 ·Genome Research ·Zihua Wang, Peter M. Andrews, Jude Kendall, Beicong Ma, Inessa Hakker, Linda Rodgers, Michael Ronemus, Michael Wigler, Dan Levy	15
8	Low load for disruptive mutations in autism genes and their biased transmission 2015 ·Proceedings of the National Academy of Sciences ·Ivan Iossifov, Dan Levy, (unknown), Kenny Ye, Michael Ronemus, Yoonha Lee, Boris Yamrom, Michael Wigler	102
9	Reducing INDEL calling errors in whole genome and exome sequencing data 2014 ·Genome Medicine ·Han Fang, Yiyang Wu, Giuseppe Narzisi, Jason O'Rawe, (unknown), Julie Rosenbaum, Michael Ronemus, Ivan Iossifov, Michael C. Schatz, Gholson J. Lyon	112
10	The role of de novo mutations in the genetics of autism spectrum disorders 2014 ·Nature Reviews Genetics ·Michael Ronemus, Ivan Iossifov, Dan Levy, Michael Wigler	250
11	The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease 2013 ·Human Genetics ·Dorothy Warburton, Michael Ronemus, Jennie Kline, Vaidehi Jobanputra, Ismee Williams, Kwame Anyane‐Yeboa, Wendy K. Chung, Lan Yu, Nancy Wong, Danielle Awad, Chih‐Yu Yu, Anthony Leotta, Jude Kendall, Boris Yamrom, Yoon-ha Lee, Michael Wigler, Dan Levy	80
12	Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders breakdown → 2011 ·Neuron ·Dan Levy, Michael Ronemus, Boris Yamrom, Yoonha Lee, Anthony Leotta, Jude Kendall, Steven C. Marks, B. Lakshmi, Deepa Pai, Kenny Ye, Andreas Buja, Abba Μ. Krieger, Seungtai Yoon, Jennifer Troge, Linda Rodgers, Ivan Iossifov, Michael Wigler	484
13	Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses 2011 ·Neuron ·(unknown), Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup	489
14	Reducing system noise in copy number data using principal components of self-self hybridizations 2011 ·Proceedings of the National Academy of Sciences ·Yoon-ha Lee, Michael Ronemus, Jude Kendall, B. Lakshmi, Anthony Leotta, Dan Levy, Diane Esposito, Vladimir Grubor, Kenny Ye, Michael Wigler, Boris Yamrom	7
15	RareDeNovoandTransmittedCopy-NumberVariation in Autistic Spectrum Disorders 2011 ·Dan Levy, Michael Ronemus, Boris Yamrom, Yoon-ha Lee, Anthony Leotta, Jude Kendall, Steven C. Marks, Andreas Buja, Ivan Iossifov, Michael Wigler	1
16	MicroRNA-Targeted and Small Interfering RNA–Mediated mRNA Degradation Is Regulated by Argonaute, Dicer, and RNA-Dependent RNA Polymerase in Arabidopsis 2006 ·The Plant Cell ·Michael Ronemus, Matthew Vaughn, Robert A. Martienssen	124
17	Transposons, Tandem Repeats, and the Silencing of Imprinted Genes 2004 ·Cold Spring Harbor Symposia on Quantitative Biology ·Robert A. Martienssen, Zachary B. Lippman, Bruce May, Michael Ronemus, Matthew Vaughn	25
18	A new match-maker 2000 ·Nature Medicine ·Michael Ronemus	1
19	Shuffling viral tropism 2000 ·Nature Biotechnology ·Michael Ronemus	0
20	Demethylation-Induced Developmental Pleiotropy in *Arabidopsis* 1996 ·Science ·Michael Ronemus, Massimo Galbiati, Christine Ticknor, Jychian Chen, Stephen L. Dellaporta	381

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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