Becker T - Search Results

1

Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males.

El-Maarri O, Becker T, Junen J, Manzoor SS, Diaz-Lacava A, Schwaab R, Wienker T, Oldenburg J. El-Maarri O, et al. Among authors: becker t. Hum Genet. 2007 Dec;122(5):505-14. doi: 10.1007/s00439-007-0430-3. Epub 2007 Sep 13. Hum Genet. 2007. PMID: 17851693

2

A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation.

El-Maarri O, Kareta MS, Mikeska T, Becker T, Diaz-Lacava A, Junen J, Nüsgen N, Behne F, Wienker T, Waha A, Oldenburg J, Chédin F. El-Maarri O, et al. Among authors: becker t. Hum Mol Genet. 2009 May 15;18(10):1755-68. doi: 10.1093/hmg/ddp088. Epub 2009 Feb 26. Hum Mol Genet. 2009. PMID: 19246518 Free article.

3

Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci.

Singer H, Walier M, Nüsgen N, Meesters C, Schreiner F, Woelfle J, Fimmers R, Wienker T, Kalscheuer VM, Becker T, Schwaab R, Oldenburg J, El-Maarri O. Singer H, et al. Among authors: becker t. Hum Mol Genet. 2012 Jan 1;21(1):219-35. doi: 10.1093/hmg/ddr456. Epub 2011 Oct 4. Hum Mol Genet. 2012. PMID: 21972244 Free PMC article.

4

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

Schumacher J, Otte AC, Becker T, Sun Y, Wienker TF, Wirth B, Franke P, Abou Jamra R, Propping P, Deckert J, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: becker t. Hum Genet. 2003 Dec;114(1):115-7. doi: 10.1007/s00439-003-1022-5. Epub 2003 Sep 25. Hum Genet. 2003. PMID: 14513359

5

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.

Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nothen MM. Hillmer AM, et al. Among authors: becker t. Am J Hum Genet. 2005 Jul;77(1):140-8. doi: 10.1086/431425. Epub 2005 May 18. Am J Hum Genet. 2005. PMID: 15902657 Free PMC article.

6

Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13.

Becker T, Jansen S, Tamm S, Wienker TF, Tümmler B, Stanke F. Becker T, et al. Eur J Hum Genet. 2007 Jul;15(7):774-8. doi: 10.1038/sj.ejhg.5201825. Epub 2007 Apr 4. Eur J Hum Genet. 2007. PMID: 17406643

7

Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.

Stanke F, Becker T, Hedtfeld S, Tamm S, Wienker TF, Tümmler B. Stanke F, et al. Among authors: becker t. Hum Genet. 2010 Apr;127(4):383-94. doi: 10.1007/s00439-009-0779-6. Epub 2010 Jan 3. Hum Genet. 2010. PMID: 20047061

8

The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis.

Stanke F, Becker T, Cuppens H, Kumar V, Cassiman JJ, Jansen S, Radojkovic D, Siebert B, Yarden J, Ussery DW, Wienker TF, Tümmler B. Stanke F, et al. Among authors: becker t. Hum Genet. 2006 Apr;119(3):331-43. doi: 10.1007/s00439-006-0140-2. Epub 2006 Feb 4. Hum Genet. 2006. PMID: 16463024

9

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: becker t. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994

10

Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.

Steffens M, Becker T, Sander T, Fimmers R, Herold C, Holler DA, Leu C, Herms S, Cichon S, Bohn B, Gerstner T, Griebel M, Nöthen MM, Wienker TF, Baur MP. Steffens M, et al. Among authors: becker t. Hum Hered. 2010;69(4):268-84. doi: 10.1159/000295896. Epub 2010 Mar 31. Hum Hered. 2010. PMID: 20357478

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