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Items: 22


Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes.

Gokoolparsadh A, Fang Z, Braidy N, Voineagu I.

Genom Data. 2016 Dec 23;11:113-115. doi: 10.1016/j.gdata.2016.12.005. eCollection 2017 Mar.


Transcriptional response to mitochondrial protease IMMP2L knockdown in human primary astrocytes.

Gokoolparsadh A, Fang Z, Braidy N, Lin P, Pardy CJ, Eapen V, Clarke R, Voineagu I.

Biochem Biophys Res Commun. 2017 Jan 22;482(4):1252-1258. doi: 10.1016/j.bbrc.2016.12.024. Epub 2016 Dec 5.


Chromosome conformation elucidates regulatory relationships in developing human brain.

Won H, de la Torre-Ubieta L, Stein JL, Parikshak NN, Huang J, Opland CK, Gandal MJ, Sutton GJ, Hormozdiari F, Lu D, Lee C, Eskin E, Voineagu I, Ernst J, Geschwind DH.

Nature. 2016 Oct 27;538(7626):523-527. doi: 10.1038/nature19847. Epub 2016 Oct 19.


Searching for convergent pathways in autism spectrum disorders: insights from human brain transcriptome studies.

Gokoolparsadh A, Sutton GJ, Charamko A, Green NF, Pardy CJ, Voineagu I.

Cell Mol Life Sci. 2016 Dec;73(23):4517-4530. Epub 2016 Jul 12. Review.


Transcriptome analysis of human brain tissue identifies reduced expression of complement complex C1Q Genes in Rett syndrome.

Lin P, Nicholls L, Assareh H, Fang Z, Amos TG, Edwards RJ, Assareh AA, Voineagu I.

BMC Genomics. 2016 Jun 6;17:427. doi: 10.1186/s12864-016-2746-7.


Coexpression networks identify brain region-specific enhancer RNAs in the human brain.

Yao P, Lin P, Gokoolparsadh A, Assareh A, Thang MW, Voineagu I.

Nat Neurosci. 2015 Aug;18(8):1168-74. doi: 10.1038/nn.4063. Epub 2015 Jul 13.


Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome.

Tian Y, Voineagu I, Paşca SP, Won H, Chandran V, Horvath S, Dolmetsch RE, Geschwind DH.

Genome Med. 2014 Oct 10;6(10):75. doi: 10.1186/s13073-014-0075-5. eCollection 2014.


Deep transcriptome profiling of mammalian stem cells supports a regulatory role for retrotransposons in pluripotency maintenance.

Fort A, Hashimoto K, Yamada D, Salimullah M, Keya CA, Saxena A, Bonetti A, Voineagu I, Bertin N, Kratz A, Noro Y, Wong CH, de Hoon M, Andersson R, Sandelin A, Suzuki H, Wei CL, Koseki H; FANTOM Consortium, Hasegawa Y, Forrest AR, Carninci P.

Nat Genet. 2014 Jun;46(6):558-66. doi: 10.1038/ng.2965. Epub 2014 Apr 28.


Autism susceptibility genes and the transcriptional landscape of the human brain.

Miyauchi S, Voineagu I.

Int Rev Neurobiol. 2013;113:303-18. doi: 10.1016/B978-0-12-418700-9.00010-1. Review.


Converging Pathways in Autism Spectrum Disorders: Interplay between Synaptic Dysfunction and Immune Responses.

Voineagu I, Eapen V.

Front Hum Neurosci. 2013 Nov 7;7:738. doi: 10.3389/fnhum.2013.00738. Review.


Current progress and challenges in the search for autism biomarkers.

Voineagu I, Yoo HJ.

Dis Markers. 2013;35(1):55-65. doi: 10.1155/2013/476276. Epub 2013 Jul 21. Review.


Role of DNA polymerases in repeat-mediated genome instability.

Shah KA, Shishkin AA, Voineagu I, Pavlov YI, Shcherbakova PV, Mirkin SM.

Cell Rep. 2012 Nov 29;2(5):1088-95. doi: 10.1016/j.celrep.2012.10.006. Epub 2012 Nov 8.


Autism: from genetics to biomarkers.

Voineagu I.

Dis Markers. 2012;33(5):223-4. doi: 10.3233/DMA-2012-0931. No abstract available.


Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Luo R, Sanders SJ, Tian Y, Voineagu I, Huang N, Chu SH, Klei L, Cai C, Ou J, Lowe JK, Hurles ME, Devlin B, State MW, Geschwind DH.

Am J Hum Genet. 2012 Jul 13;91(1):38-55. doi: 10.1016/j.ajhg.2012.05.011. Epub 2012 Jun 21.


Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.

Paşca SP, Portmann T, Voineagu I, Yazawa M, Shcheglovitov A, Paşca AM, Cord B, Palmer TD, Chikahisa S, Nishino S, Bernstein JA, Hallmayer J, Geschwind DH, Dolmetsch RE.

Nat Med. 2011 Nov 27;17(12):1657-62. doi: 10.1038/nm.2576.


Gene expression studies in autism: moving from the genome to the transcriptome and beyond.

Voineagu I.

Neurobiol Dis. 2012 Jan;45(1):69-75. doi: 10.1016/j.nbd.2011.07.017. Epub 2011 Jul 28. Review.


CCDC22: a novel candidate gene for syndromic X-linked intellectual disability.

Voineagu I, Huang L, Winden K, Lazaro M, Haan E, Nelson J, McGaughran J, Nguyen LS, Friend K, Hackett A, Field M, Gecz J, Geschwind D.

Mol Psychiatry. 2012 Jan;17(1):4-7. doi: 10.1038/mp.2011.95. Epub 2011 Aug 9. No abstract available.


Transcriptomic analysis of autistic brain reveals convergent molecular pathology.

Voineagu I, Wang X, Johnston P, Lowe JK, Tian Y, Horvath S, Mill J, Cantor RM, Blencowe BJ, Geschwind DH.

Nature. 2011 May 25;474(7351):380-4. doi: 10.1038/nature10110.


Large-scale expansions of Friedreich's ataxia GAA repeats in yeast.

Shishkin AA, Voineagu I, Matera R, Cherng N, Chernet BT, Krasilnikova MM, Narayanan V, Lobachev KS, Mirkin SM.

Mol Cell. 2009 Jul 10;35(1):82-92. doi: 10.1016/j.molcel.2009.06.017.


Checkpoint responses to unusual structures formed by DNA repeats.

Voineagu I, Freudenreich CH, Mirkin SM.

Mol Carcinog. 2009 Apr;48(4):309-18. doi: 10.1002/mc.20512. Review.


Replisome stalling and stabilization at CGG repeats, which are responsible for chromosomal fragility.

Voineagu I, Surka CF, Shishkin AA, Krasilnikova MM, Mirkin SM.

Nat Struct Mol Biol. 2009 Feb;16(2):226-8. doi: 10.1038/nsmb.1527. Epub 2009 Jan 11.


Replication stalling at unstable inverted repeats: interplay between DNA hairpins and fork stabilizing proteins.

Voineagu I, Narayanan V, Lobachev KS, Mirkin SM.

Proc Natl Acad Sci U S A. 2008 Jul 22;105(29):9936-41. doi: 10.1073/pnas.0804510105. Epub 2008 Jul 15.

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