Gieger C - Search Results

1

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, Baird PN, Vitart V, Paterson AD, Mitchell P, Saw SM, Fossarello M, Kazmierkiewicz K, Murgia F, Portas L, Schache M, Richardson A, Xie J, Wang JJ, Rochtchina E; DCCT/EDIC Research Group; Viswanathan AC, Hayward C, Wright AF, Polasek O, Campbell H, Rudan I, Oostra BA, Uitterlinden AG, Hofman A, Rivadeneira F, Amin N, Karssen LC, Vingerling JR, Hosseini SM, Döring A, Bettecken T, Vatavuk Z, Gieger C, Wichmann HE, Wilson JF, Fleck B, Foster PJ, Topouzis F, McGuffin P, Sim X, Inouye M, Holliday EG, Attia J, Scott RJ, Rotter JI, Meitinger T, Bailey-Wilson JE. Stambolian D, et al. Among authors: gieger c. Hum Mol Genet. 2013 Jul 1;22(13):2754-64. doi: 10.1093/hmg/ddt116. Epub 2013 Mar 7. Hum Mol Genet. 2013. PMID: 23474815 Free PMC article.

2

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.

Arking DE, Pfeufer A, Post W, Kao WH, Newton-Cheh C, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Gieger C, Guo CY, Larson MG, Wichmann HE, Marbán E, O'Donnell CJ, Hirschhorn JN, Kääb S, Spooner PM, Meitinger T, Chakravarti A. Arking DE, et al. Among authors: gieger c. Nat Genet. 2006 Jun;38(6):644-51. doi: 10.1038/ng1790. Epub 2006 Apr 30. Nat Genet. 2006. PMID: 16648850

3

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.

Akyol M, Jalilzadeh S, Sinner MF, Perz S, Beckmann BM, Gieger C, Illig T, Wichmann HE, Meitinger T, Kääb S, Pfeufer A. Akyol M, et al. Among authors: gieger c. Eur Heart J. 2007 Feb;28(3):305-9. doi: 10.1093/eurheartj/ehl460. Epub 2007 Jan 16. Eur Heart J. 2007. PMID: 17227789

4

Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations.

Fisher E, Nitz I, Gieger C, Grallert H, Gohlke H, Lindner I, Dahm S, Boeing H, Burwinkel B, Rathmann W, Wichmann HE, Schrezenmeir J, Illig T, Döring F. Fisher E, et al. Among authors: gieger c. Mol Nutr Food Res. 2007 Feb;51(2):178-84. doi: 10.1002/mnfr.200600163. Mol Nutr Food Res. 2007. PMID: 17262885

5

Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans.

Koch W, Hoppmann P, Michou E, Jung V, Pfeufer A, Mueller JC, Gieger C, Wichmann HE, Meitinger T, Schömig A, Kastrati A. Koch W, et al. Among authors: gieger c. Hum Mol Genet. 2007 Aug 1;16(15):1821-7. doi: 10.1093/hmg/ddm130. Epub 2007 May 21. Hum Mol Genet. 2007. PMID: 17517687

6

Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations.

Nitz I, Fisher E, Grallert H, Li Y, Gieger C, Rubin D, Boeing H, Spranger J, Lindner I, Schreiber S, Rathmann W, Gohlke H, Döring A, Wichmann HE, Schrezenmeir J, Döring F, Illig T. Nitz I, et al. Among authors: gieger c. J Clin Endocrinol Metab. 2007 Aug;92(8):3183-8. doi: 10.1210/jc.2006-2550. Epub 2007 Jun 12. J Clin Endocrinol Metab. 2007. PMID: 17566096

7

Genomewide association analysis of coronary artery disease.

Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, König IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H; WTCCC and the Cardiogenics Consortium. Samani NJ, et al. Among authors: gieger c. N Engl J Med. 2007 Aug 2;357(5):443-53. doi: 10.1056/NEJMoa072366. Epub 2007 Jul 18. N Engl J Med. 2007. PMID: 17634449 Free PMC article.

8

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Pütz B, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T. Winkelmann J, et al. Among authors: gieger c. Nat Genet. 2007 Aug;39(8):1000-6. doi: 10.1038/ng2099. Epub 2007 Jul 18. Nat Genet. 2007. PMID: 17637780

9

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants.

Luca D, Ringquist S, Klei L, Lee AB, Gieger C, Wichmann HE, Schreiber S, Krawczak M, Lu Y, Styche A, Devlin B, Roeder K, Trucco M. Luca D, et al. Among authors: gieger c. Am J Hum Genet. 2008 Feb;82(2):453-63. doi: 10.1016/j.ajhg.2007.11.003. Epub 2008 Jan 24. Am J Hum Genet. 2008. PMID: 18252225 Free PMC article.

10

A multimetric approach to analysis of genome-wide association by single markers and composite likelihood.

Gibson J, Tapper W, Cox D, Zhang W, Pfeufer A, Gieger C, Wichmann HE, Kääb S, Collins AR, Meitinger T, Morton N. Gibson J, et al. Among authors: gieger c. Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2592-7. doi: 10.1073/pnas.0711903105. Epub 2008 Feb 11. Proc Natl Acad Sci U S A. 2008. PMID: 18268331 Free PMC article.

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