Klassen T - Search Results

1

Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.

Klassen T, Davis C, Goldman A, Burgess D, Chen T, Wheeler D, McPherson J, Bourquin T, Lewis L, Villasana D, Morgan M, Muzny D, Gibbs R, Noebels J. Klassen T, et al. Cell. 2011 Jun 24;145(7):1036-48. doi: 10.1016/j.cell.2011.05.025. Cell. 2011. PMID: 21703448 Free PMC article.

2

Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy.

Chen TT, Klassen TL, Goldman AM, Marini C, Guerrini R, Noebels JL. Chen TT, et al. Among authors: klassen tl. Neurology. 2013 Mar 19;80(12):1078-85. doi: 10.1212/WNL.0b013e31828868e7. Epub 2013 Feb 13. Neurology. 2013. PMID: 23408874 Free PMC article.

3

Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy.

Glasscock E, Yoo JW, Chen TT, Klassen TL, Noebels JL. Glasscock E, et al. Among authors: klassen tl. J Neurosci. 2010 Apr 14;30(15):5167-75. doi: 10.1523/JNEUROSCI.5591-09.2010. J Neurosci. 2010. PMID: 20392939 Free PMC article.

4

Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population.

Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, Macdonald RL. Hernandez CC, et al. PLoS One. 2016 Sep 13;11(9):e0162883. doi: 10.1371/journal.pone.0162883. eCollection 2016. PLoS One. 2016. PMID: 27622563 Free PMC article.

5

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.

Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL. Goldman AM, et al. Among authors: klassen tl. Sci Transl Med. 2009 Oct 14;1(2):2ra6. doi: 10.1126/scitranslmed.3000289. Sci Transl Med. 2009. PMID: 20368164 Free PMC article.

6

Selective Loss of Presynaptic Potassium Channel Clusters at the Cerebellar Basket Cell Terminal Pinceau in Adam11 Mutants Reveals Their Role in Ephaptic Control of Purkinje Cell Firing.

Kole MJ, Qian J, Waase MP, Klassen TL, Chen TT, Augustine GJ, Noebels JL. Kole MJ, et al. Among authors: klassen tl. J Neurosci. 2015 Aug 12;35(32):11433-44. doi: 10.1523/JNEUROSCI.1346-15.2015. J Neurosci. 2015. PMID: 26269648 Free PMC article.

7

Comparative analytical utility of DNA derived from alternative human specimens for molecular autopsy and diagnostics.

Klassen TL, von Rüden EL, Drabek J, Noebels JL, Goldman AM. Klassen TL, et al. J Mol Diagn. 2012 Sep;14(5):451-7. doi: 10.1016/j.jmoldx.2012.04.005. Epub 2012 Jul 13. J Mol Diagn. 2012. PMID: 22796560 Free PMC article.

8

Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots.

Klassen TL, Drabek J, Tomson T, Sveinsson O, von Döbeln U, Noebels JL, Goldman AM. Klassen TL, et al. J Mol Diagn. 2013 May;15(3):283-90. doi: 10.1016/j.jmoldx.2013.01.003. Epub 2013 Mar 19. J Mol Diagn. 2013. PMID: 23518217 Free PMC article.

9

High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.

Klassen TL, Bomben VC, Patel A, Drabek J, Chen TT, Gu W, Zhang F, Chapman K, Lupski JR, Noebels JL, Goldman AM. Klassen TL, et al. Epilepsia. 2014 Feb;55(2):e6-12. doi: 10.1111/epi.12489. Epub 2013 Dec 24. Epilepsia. 2014. PMID: 24372310 Free PMC article.

10

Correction: Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population.

Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, Macdonald RL. Hernandez CC, et al. PLoS One. 2016 Nov 21;11(11):e0167264. doi: 10.1371/journal.pone.0167264. eCollection 2016. PLoS One. 2016. PMID: 27870904 Free PMC article.

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