Toliat MR - Search Results

1

Association of ALPL and ENPP1 gene polymorphisms with bone strength related skeletal traits in a Chuvashian population.

Ermakov S, Toliat MR, Cohen Z, Malkin I, Altmüller J, Livshits G, Nürnberg P. Ermakov S, et al. Among authors: toliat mr. Bone. 2010 May;46(5):1244-50. doi: 10.1016/j.bone.2009.11.018. Epub 2009 Nov 27. Bone. 2010. PMID: 19931660

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

Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification.

Rutsch F, Ruf N, Vaingankar S, Toliat MR, Suk A, Höhne W, Schauer G, Lehmann M, Roscioli T, Schnabel D, Epplen JT, Knisely A, Superti-Furga A, McGill J, Filippone M, Sinaiko AR, Vallance H, Hinrichs B, Smith W, Ferre M, Terkeltaub R, Nürnberg P. Rutsch F, et al. Among authors: toliat mr. Nat Genet. 2003 Aug;34(4):379-81. doi: 10.1038/ng1221. Nat Genet. 2003. PMID: 12881724

6

Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.

Izzi C, Barbon A, Toliat MR, Heils A, Becker C, Nürnberg P, Sander T, Barlati S. Izzi C, et al. Among authors: toliat mr. Am J Med Genet B Neuropsychiatr Genet. 2003 Nov 15;123B(1):59-63. doi: 10.1002/ajmg.b.20024. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 14582146

7

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

8

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

9

Association of ANKH gene polymorphisms with radiographic hand bone size and geometry in a Chuvasha population.

Malkin I, Dahm S, Suk A, Kobyliansky E, Toliat M, Ruf N, Livshits G, Nürnberg P. Malkin I, et al. Bone. 2005 Feb;36(2):365-73. doi: 10.1016/j.bone.2004.09.002. Bone. 2005. PMID: 15780964

10

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

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