| The contribution of de novo coding mutations to autism spectrum disorder I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ... Nature 515 (7526), 216-221, 2014 | 2677 | 2014 |
| De novo gene disruptions in children on the autistic spectrum I Iossifov, M Ronemus, D Levy, Z Wang, I Hakker, J Rosenbaum, ... Neuron 74 (2), 285-299, 2012 | 1689 | 2012 |
| Rare de novo and transmitted copy-number variation in autistic spectrum disorders D Levy, M Ronemus, B Yamrom, Y Lee, A Leotta, J Kendall, S Marks, ... Neuron 70 (5), 886-897, 2011 | 896 | 2011 |
| Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses SR Gilman, I Iossifov, D Levy, M Ronemus, M Wigler, D Vitkup Neuron 70 (5), 898-907, 2011 | 839 | 2011 |
| De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ... Science 350 (6265), 1262-1266, 2015 | 804 | 2015 |
| Demethylation-induced developmental pleiotropy in Arabidopsis MJ Ronemus, M Galbiati, C Ticknor, J Chen, SL Dellaporta Science 273 (5275), 654-657, 1996 | 569 | 1996 |
| The role of de novo mutations in the genetics of autism spectrum disorders M Ronemus, I Iossifov, D Levy, M Wigler Nature Reviews Genetics 15 (2), 133-141, 2014 | 466 | 2014 |
| Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data JT Glessner, AG Bick, K Ito, JG Homsy, L Rodriguez-Murillo, M Fromer, ... Circulation research 115 (10), 884-896, 2014 | 280 | 2014 |
| MicroRNA-targeted and small interfering RNA–mediated mRNA degradation is regulated by Argonaute, Dicer, and RNA-dependent RNA polymerase in Arabidopsis M Ronemus, MW Vaughn, RA Martienssen The Plant Cell 18 (7), 1559-1574, 2006 | 202 | 2006 |
| Reducing INDEL calling errors in whole genome and exome sequencing data H Fang, Y Wu, G Narzisi, JA ORawe, LTJ Barrón, J Rosenbaum, ... Genome medicine 6, 1-17, 2014 | 201 | 2014 |
| Low load for disruptive mutations in autism genes and their biased transmission I Iossifov, D Levy, J Allen, K Ye, M Ronemus, Y Lee, B Yamrom, M Wigler Proceedings of the National Academy of Sciences 112 (41), E5600-E5607, 2015 | 168 | 2015 |
| 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 … D Warburton, M Ronemus, J Kline, V Jobanputra, I Williams, ... Human genetics 133, 11-27, 2014 | 140 | 2014 |
| Indel variant analysis of short-read sequencing data with Scalpel H Fang, EA Bergmann, K Arora, V Vacic, MC Zody, I Iossifov, JA O'rawe, ... Nature protocols 11 (12), 2529-2548, 2016 | 120 | 2016 |
| What can stutterers learn from the neurodiversity movement? CD Constantino Seminars in Speech and Language 39 (04), 382-396, 2018 | 68 | 2018 |
| Transposons, tandem repeats, and the silencing of imprinted genes R Martienssen, Z Lippman, B May, M Ronemus, M Vaughn Cold Spring Harbor symposia on quantitative biology 69, 371-380, 2004 | 33 | 2004 |
| Rare de novo germline copy-number variation in testicular cancer ZK Stadler, D Esposito, S Shah, J Vijai, B Yamrom, D Levy, Y Lee, ... The American Journal of Human Genetics 91 (2), 379-383, 2012 | 31 | 2012 |
| Methylation mystery M Ronemus, R Martienssen Nature 433 (7025), 472-473, 2005 | 31 | 2005 |
| Rates of contributory de novo mutation in high and low-risk autism families S Yoon, A Munoz, B Yamrom, Y Lee, P Andrews, S Marks, Z Wang, ... Communications biology 4 (1), 1026, 2021 | 30 | 2021 |
| SMASH, a fragmentation and sequencing method for genomic copy number analysis Z Wang, P Andrews, J Kendall, B Ma, I Hakker, L Rodgers, M Ronemus, ... Genome research 26 (6), 844-851, 2016 | 22 | 2016 |
| Reducing system noise in copy number data using principal components of self-self hybridizations Y Lee, M Ronemus, J Kendall, B Lakshmi, A Leotta, D Levy, D Esposito, ... Proceedings of the National Academy of Sciences 109 (3), E103-E110, 2012 | 17 | 2012 |
