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

Year Number of Results
2008 1
2009 1
2010 2
2011 1
2012 1
2013 1
2015 1
2016 1
2017 1
2018 1
2019 1
2020 1
2021 3
2024 0

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14 results

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Page 1
INFERNO: inferring the molecular mechanisms of noncoding genetic variants.
Amlie-Wolf A, Tang M, Mlynarski EE, Kuksa PP, Valladares O, Katanic Z, Tsuang D, Brown CD, Schellenberg GD, Wang LS. Amlie-Wolf A, et al. Among authors: mlynarski ee. Nucleic Acids Res. 2018 Sep 28;46(17):8740-8753. doi: 10.1093/nar/gky686. Nucleic Acids Res. 2018. PMID: 30113658 Free PMC article.
Centromere conversion and retention in somatic cell hybrids.
Brown JD, Carone DM, Flynn BL, Finn CE, Mlynarski EE, O'Neill RJ. Brown JD, et al. Among authors: mlynarski ee. Cytogenet Genome Res. 2011;134(3):182-90. doi: 10.1159/000328830. Epub 2011 Jun 29. Cytogenet Genome Res. 2011. PMID: 21709412
Divergent patterns of breakpoint reuse in Muroid rodents.
Mlynarski EE, Obergfell CJ, O'Neill MJ, O'Neill RJ. Mlynarski EE, et al. Mamm Genome. 2010 Feb;21(1-2):77-87. doi: 10.1007/s00335-009-9242-1. Epub 2009 Dec 22. Mamm Genome. 2010. PMID: 20033182
TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy.
Alquezar C, Schoch KM, Geier EG, Ramos EM, Scrivo A, Li KH, Argouarch AR, Mlynarski EE, Dombroski B, DeTure M, Dickson DW, Yokoyama JS, Cuervo AM, Burlingame AL, Schellenberg GD, Miller TM, Miller BL, Kao AW. Alquezar C, et al. Among authors: mlynarski ee. Sci Adv. 2021 Nov 5;7(45):eabg3897. doi: 10.1126/sciadv.abg3897. Epub 2021 Nov 5. Sci Adv. 2021. PMID: 34739309 Free PMC article.
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Philip N, Simon TJ, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Goldmuntz E, Bassett AS, Morrow BE, Emanuel BS; International Chromosome 22q11.2 Consortium. Mlynarski EE, et al. Hum Genet. 2016 Mar;135(3):273-85. doi: 10.1007/s00439-015-1623-9. Epub 2016 Jan 7. Hum Genet. 2016. PMID: 26742502 Free PMC article.
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Mlynarski EE, Sheridan MB, Xie M, Guo T, Racedo SE, McDonald-McGinn DM, Gai X, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Philip N, Simon TJ, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Shaikh TH, Bassett AS, Goldmuntz E, Morrow BE, Emanuel BS; International Chromosome 22q11.2 Consortium. Mlynarski EE, et al. Am J Hum Genet. 2015 May 7;96(5):753-64. doi: 10.1016/j.ajhg.2015.03.007. Epub 2015 Apr 16. Am J Hum Genet. 2015. PMID: 25892112 Free PMC article.
14 results