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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1999 2
2004 1
2005 1
2006 1
2011 3
2012 3
2013 1
2014 5
2015 2
2016 2
2018 1
2020 1
2021 1
2023 1
2024 0

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24 results

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Page 1
The contribution of de novo coding mutations to autism spectrum disorder.
Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei L, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang Z, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma B, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M. Iossifov I, et al. Among authors: ronemus m. Nature. 2014 Nov 13;515(7526):216-21. doi: 10.1038/nature13908. Epub 2014 Oct 29. Nature. 2014. PMID: 25363768 Free PMC article.
De novo gene disruptions in children on the autistic spectrum.
Iossifov I, Ronemus M, Levy D, Wang Z, Hakker I, Rosenbaum J, Yamrom B, Lee YH, Narzisi G, Leotta A, Kendall J, Grabowska E, Ma B, Marks S, Rodgers L, Stepansky A, Troge J, Andrews P, Bekritsky M, Pradhan K, Ghiban E, Kramer M, Parla J, Demeter R, Fulton LL, Fulton RS, Magrini VJ, Ye K, Darnell JC, Darnell RB, Mardis ER, Wilson RK, Schatz MC, McCombie WR, Wigler M. Iossifov I, et al. Among authors: ronemus m. Neuron. 2012 Apr 26;74(2):285-99. doi: 10.1016/j.neuron.2012.04.009. Neuron. 2012. PMID: 22542183 Free PMC article.
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA Jr, Kim R, Bilguvar K, López-Giráldez F, Tikhonova I, Mane S, Romano-Adesman A, Qi H, Vardarajan B, Ma L, Daly M, Roberts AE, Russell MW, Mital S, Newburger JW, Gaynor JW, Breitbart RE, Iossifov I, Ronemus M, Sanders SJ, Kaltman JR, Seidman JG, Brueckner M, Gelb BD, Goldmuntz E, Lifton RP, Seidman CE, Chung WK. Homsy J, et al. Among authors: ronemus m. Science. 2015 Dec 4;350(6265):1262-6. doi: 10.1126/science.aac9396. Science. 2015. PMID: 26785492 Free PMC article.
Partial bisulfite conversion for unique template sequencing.
Kumar V, Rosenbaum J, Wang Z, Forcier T, Ronemus M, Wigler M, Levy D. Kumar V, et al. Among authors: ronemus m. Nucleic Acids Res. 2018 Jan 25;46(2):e10. doi: 10.1093/nar/gkx1054. Nucleic Acids Res. 2018. PMID: 29161423 Free PMC article.
Transposons, tandem repeats, and the silencing of imprinted genes.
Martienssen R, Lippman Z, May B, Ronemus M, Vaughn M. Martienssen R, et al. Among authors: ronemus m. Cold Spring Harb Symp Quant Biol. 2004;69:371-9. doi: 10.1101/sqb.2004.69.371. Cold Spring Harb Symp Quant Biol. 2004. PMID: 16117670 Review. No abstract available.
Sharing parental genomes by siblings concordant or discordant for autism.
Wroten M, Yoon S, Andrews P, Yamrom B, Ronemus M, Buja A, Krieger AM, Levy D, Ye K, Wigler M, Iossifov I. Wroten M, et al. Among authors: ronemus m. Cell Genom. 2023 May 8;3(6):100319. doi: 10.1016/j.xgen.2023.100319. eCollection 2023 Jun 14. Cell Genom. 2023. PMID: 37388917 Free PMC article.
RNA interference: methylation mystery.
Ronemus M, Martienssen R. Ronemus M, et al. Nature. 2005 Feb 3;433(7025):472-3. doi: 10.1038/433472a. Nature. 2005. PMID: 15690027 No abstract available.
Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies.
Jobanputra V, Andrews P, Felice V, Abhyankar A, Kozon L, Robinson D, London F, Hakker I, Wrzeszczynski K, Ronemus M. Jobanputra V, et al. Among authors: ronemus m. J Mol Diagn. 2020 Dec;22(12):1476-1481. doi: 10.1016/j.jmoldx.2020.09.009. Epub 2020 Oct 23. J Mol Diagn. 2020. PMID: 33132082 Free PMC article.
24 results