Winden KD - Search Results

1

Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling.

Rosen EY, Wexler EM, Versano R, Coppola G, Gao F, Winden KD, Oldham MC, Martens LH, Zhou P, Farese RV Jr, Geschwind DH. Rosen EY, et al. Among authors: winden kd. Neuron. 2011 Sep 22;71(6):1030-42. doi: 10.1016/j.neuron.2011.07.021. Epub 2011 Sep 21. Neuron. 2011. PMID: 21943601 Free PMC article.

2

The organization of the transcriptional network in specific neuronal classes.

Winden KD, Oldham MC, Mirnics K, Ebert PJ, Swan CH, Levitt P, Rubenstein JL, Horvath S, Geschwind DH. Winden KD, et al. Mol Syst Biol. 2009;5:291. doi: 10.1038/msb.2009.46. Epub 2009 Jul 28. Mol Syst Biol. 2009. PMID: 19638972 Free PMC article.

3

Human-specific transcriptional regulation of CNS development genes by FOXP2.

Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, Peng S, Preuss TM, Wohlschlegel JA, Geschwind DH. Konopka G, et al. Nature. 2009 Nov 12;462(7270):213-7. doi: 10.1038/nature08549. Nature. 2009. PMID: 19907493 Free PMC article.

4

A systems level, functional genomics analysis of chronic epilepsy.

Winden KD, Karsten SL, Bragin A, Kudo LC, Gehman L, Ruidera J, Geschwind DH, Engel J Jr. Winden KD, et al. PLoS One. 2011;6(6):e20763. doi: 10.1371/journal.pone.0020763. Epub 2011 Jun 14. PLoS One. 2011. PMID: 21695113 Free PMC article.

5

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.

Peñagarikano O, Abrahams BS, Herman EI, Winden KD, Gdalyahu A, Dong H, Sonnenblick LI, Gruver R, Almajano J, Bragin A, Golshani P, Trachtenberg JT, Peles E, Geschwind DH. Peñagarikano O, et al. Among authors: winden kd. Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040. Cell. 2011. PMID: 21962519 Free PMC article.

6

Human-specific transcriptional networks in the brain.

Konopka G, Friedrich T, Davis-Turak J, Winden K, Oldham MC, Gao F, Chen L, Wang GZ, Luo R, Preuss TM, Geschwind DH. Konopka G, et al. Neuron. 2012 Aug 23;75(4):601-17. doi: 10.1016/j.neuron.2012.05.034. Neuron. 2012. PMID: 22920253 Free PMC article.

7

Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex.

Ercan E, Han JM, Di Nardo A, Winden K, Han MJ, Hoyo L, Saffari A, Leask A, Geschwind DH, Sahin M. Ercan E, et al. J Exp Med. 2017 Mar 6;214(3):681-697. doi: 10.1084/jem.20160446. Epub 2017 Feb 9. J Exp Med. 2017. PMID: 28183733 Free PMC article.

8

Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy.

Winden KD, Bragin A, Engel J, Geschwind DH. Winden KD, et al. Neurobiol Dis. 2015 Jun;78:35-44. doi: 10.1016/j.nbd.2015.02.011. Epub 2015 Mar 25. Neurobiol Dis. 2015. PMID: 25818007 Free PMC article.

9

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. Voineagu I, et al. Mol Psychiatry. 2012 Jan;17(1):4-7. doi: 10.1038/mp.2011.95. Epub 2011 Aug 9. Mol Psychiatry. 2012. PMID: 21826058 Free PMC article. No abstract available.

10

Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophy.

Wertz MH, Winden K, Neveu P, Ng SY, Ercan E, Sahin M. Wertz MH, et al. Hum Mol Genet. 2016 Jun 1;25(11):2168-2181. doi: 10.1093/hmg/ddw084. Epub 2016 Mar 22. Hum Mol Genet. 2016. PMID: 27005422 Free PMC article.

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