Toliat MR - Search Results

1

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.

Rakovic A, Stiller B, Djarmati A, Flaquer A, Freudenberg J, Toliat MR, Linnebank M, Kostic V, Lohmann K, Paus S, Nürnberg P, Kubisch C, Klein C, Wüllner U, Ramirez A. Rakovic A, et al. Among authors: toliat mr. Mov Disord. 2009 Feb 15;24(3):429-33. doi: 10.1002/mds.22399. Mov Disord. 2009. PMID: 19097176 Free article.

2

Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsy.

Sander T, Toliat MR, Heils A, Becker C, Nürnberg P. Sander T, et al. Among authors: toliat mr. Epilepsy Res. 2002 Apr;49(2):173-7. doi: 10.1016/s0920-1211(02)00025-6. Epilepsy Res. 2002. PMID: 12049805

3

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.

Sander T, Toliat MR, Heils A, Leschik G, Becker C, Rüschendorf F, Rohde K, Mundlos S, Nürnberg P. Sander T, et al. Among authors: toliat mr. Epilepsy Res. 2002 Oct;51(3):249-55. doi: 10.1016/s0920-1211(02)00152-3. Epilepsy Res. 2002. PMID: 12399075

4

Evaluation of a potential epigenetic biomarker by quantitative methyl-single nucleotide polymorphism analysis.

Uhlmann K, Brinckmann A, Toliat MR, Ritter H, Nürnberg P. Uhlmann K, et al. Among authors: toliat mr. Electrophoresis. 2002 Dec;23(24):4072-9. doi: 10.1002/elps.200290023. Electrophoresis. 2002. PMID: 12481262

5

Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol.

Knoblauch H, Bauerfeind A, Toliat MR, Becker C, Luganskaja T, Günther UP, Rohde K, Schuster H, Junghans C, Luft FC, Nürnberg P, Reich JG. Knoblauch H, et al. Among authors: toliat mr. Hum Mol Genet. 2004 May 15;13(10):993-1004. doi: 10.1093/hmg/ddh119. Epub 2004 Mar 25. Hum Mol Genet. 2004. PMID: 15044381

6

Association of the serum and glucocorticoid regulated kinase (sgk1) gene with QT interval.

Busjahn A, Seebohm G, Maier G, Toliat MR, Nürnberg P, Aydin A, Luft FC, Lang F. Busjahn A, et al. Among authors: toliat mr. Cell Physiol Biochem. 2004;14(3):135-42. doi: 10.1159/000078105. Cell Physiol Biochem. 2004. PMID: 15107590

7

Application of genomewide SNP arrays for detection of simulated susceptibility loci.

Kulle B, Schirmer M, Toliat MR, Suk A, Becker C, Tzvetkov MV, Brockmöller J, Bickeböller H, Hasenfuss G, Nürnberg P, Wojnowski L. Kulle B, et al. Among authors: toliat mr. Hum Mutat. 2005 Jun;25(6):557-65. doi: 10.1002/humu.20174. Hum Mutat. 2005. PMID: 15880731

8

Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha population.

Suk EK, Malkin I, Dahm S, Kalichman L, Ruf N, Kobyliansky E, Toliat M, Rutsch F, Nürnberg P, Livshits G. Suk EK, et al. Arthritis Res Ther. 2005;7(5):R1082-90. doi: 10.1186/ar1786. Epub 2005 Jul 13. Arthritis Res Ther. 2005. PMID: 16207325 Free PMC article.

9

New universal primers facilitate Pyrosequencing.

Aydin A, Toliat MR, Bähring S, Becker C, Nürnberg P. Aydin A, et al. Among authors: toliat mr. Electrophoresis. 2006 Feb;27(2):394-7. doi: 10.1002/elps.200500467. Electrophoresis. 2006. PMID: 16331584

10

Genetic signature consistent with selection against the CYP3A4*1B allele in non-African populations.

Schirmer M, Toliat MR, Haberl M, Suk A, Kamdem LK, Klein K, Brockmöller J, Nürnberg P, Zanger UM, Wojnowski L. Schirmer M, et al. Among authors: toliat mr. Pharmacogenet Genomics. 2006 Jan;16(1):59-71. doi: 10.1097/01.fpc.0000182779.03180.ba. Pharmacogenet Genomics. 2006. PMID: 16344723

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