Publications 2007
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Selected publications which refer to KORA and KORA-gen
- Sedlmeier EM, Grallert H, Huth C, Lowel H, Herder C, Strassburger K, Giani G, Wichmann HE, Hauner H, Illig T, Rathmann W
Gene variants of monocyte chemoattractant protein 1 and components of metabolic syndrome in KORA S4, Augsburg
Eur J Endocrinol. 2007 Mar;156(3):377-85 - Akyol M, Jalilzadeh S, Sinner MF, Perz S, Beckmann BM, Gieger C, Illig T, Wichmann HE, Meitinger T, Kaab S, Pfeufer A
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
Eur Heart J. 2007 Feb;28(3):305-9. Epub 2007 Jan 16 - 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, Doring F
Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations
Mol Nutr Food Res. 2007 Feb;51(2):178-84 - Marzi C, Huth C, Kolz M, Grallert H, Meisinger C, Wichmann HE, Rathmann W, Herder C, Illig T
Variants of the transcription factor 7-like 2 gene (TCF7L2) are strongly associated with type 2 diabetes but not with the metabolic syndrome in the MONICA/KORA surveys
Horm Metab Res. 2007 Jan;39(1):46-52 - Huth C, Siegert N, Meisinger C, Konig J, Kaab S, Wichmann HE, Doering A, KORA study group
Individuals with very low alcohol consumption: a heterogeneous group
J Stud Alcohol Drugs. 2007 Jan;68(1):6-10 - Vollmert C, Hahn S, Lamina C, Huth C, Kolz M, Schopfer-Wendels A, Mann K, Bongardt F, Mueller JC, Kronenberg F, Wichmann HE, Herder C, Holle R, Lowel H, Illig T, Janssen OE, KORA study group
Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians
Am J Physiol Endocrinol Metab. 2007 Mar;292(3):E836-44. Epub 2006 Nov 14 - Kolleritz B, Fliser D, Heid IM, Ritz E, Kronenberg F
Sex-specific association of adiponectin as a predictor of progression of chronic kidney disease: The Mild to Moderate Kidney Disease (MMKD) Study
Kidney Int. 2007 Jun;71(12):1279-86 - Kabesch M, Depner M, Dahmen I, Weiland SK, Vogelberg C, Niggemann B, Lau S, Illig T, Klopp N, Wahn U, Reinhardt D, von Mutius E, Nickel R
Polymorphisms in eosinophil pathway genes, asthma and atopy
Allergy. 2007 Apr;62(4):423-8 - Schirmbeck F, Georgi A, Strohmaier J, Schmael C, Knorr C, Jamra RA, Schumacher J, Becker T, Klopp N, Illig T, Wulf M, Schwarz M, Maier W, Propping P, Cichon S, Nothen MM, Schulze TG, Rietschel M
No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample
Psychiatr Genet. 2007 Apr;17(2):127 - Strohmaier J, Georgi A, Schirmbeck F, Schmael C, Jamra RA, Schumacher J, Becker T, Hofels S, Klopp N, Illig T, Propping P, Cichon S, Nothen MM, Rietschel M, Schulze TG
No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample
Psychiatr Genet. 2007 Apr;17(2):125 - Sedlacek K, Neureuther K, Mueller JC, Stark K, Fischer M, Baessler A, Reinhard W, Broeckel U, Lieb W, Erdmann J, Schunkert H, Riegger G, Illig T, Meitinger T, Hengstenberg C
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations
J Mol Med. 2007 Sep;85(9):997-1004 - Depner M, Kormann MS, Klopp N, Illig T, Vogelberg C, Weiland SK, von Mutius E, Combadiere C, Kabesch M
CX3CR1 Polymorphisms Are Associated with Atopy but Not Asthma in German Children
Int Arch Allergy Immunol. 2007 May 15;144(1):91-94 - Nitz I, Fisher E, Grallert H, Yun Li, Gieger C, Rubin D, Boeing H, Spranger J, Lindner I, Schreiber S, Rathmann W, Gohlke H, Doering A, Wichmann HE, Schrezenmeir J, Doering F, Illig T
Association of Prostaglandin E Synthase 2 (PTGES2) Arg298His Polymorphism with Type 2 Diabetes in two German Study Populations
J Clin Endocrinol Metab. 2007 Aug;92(8):3183-8 - 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, Mueller-Myhsok B, Meitinger T
Genome-wide association study in restless legs syndrome identifies common variants in three genomic regions
Nat Genet. 2007 Aug;39(8):1000-6 - Jaremko M, Justenhoven C, Schroth W, Abraham BK, Fritz P, Vollmert C, Illig T, Simon W, Schwab M, Brauch H
Polymorphism of the DNA repair enzyme XRCC1 is associated with treatment prediction in anthracycline and yclophosphamide/methotrexate/5-fluorouracil-based chemotherapy of patients with primary invasive breast cancer
Pharmacogenet Genomics. 2007 Jul;17(7):529-38 - Novak N, Yu CF, Bussmann C, Maintz L, Peng WM, Hart J, Hagemann T, Diaz-Lacava A, Baurecht HJ, Klopp N, Wagenpfeil S, Behrendt H, Bieber T, Ring J, Illig T, Weidinger S
Putative association of a TLR9 promoter polymorphism with atopic eczema
Allergy. 2007 Jul;62(7):766-72 - Moffatt MF, Kabesch M, Liang L, Dixon AL, Strachan D, Heath S, Depner M, von Berg A, Bufe A, Rietschel E, Heinzmann A, Simma B, Frischer T, Willis-Owen SA, Wong KC, Illig T, Vogelberg C, Weiland SK, von Mutius E, Abecasis GR, Farrall M, Gut IG, Lathrop GM, Cookson WO
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
Nature, 2007 Jul 26;448(7152):470-3 - Justenhoven C, Hamann U, Schubert F, Zapatka M, Pierl CB, Rabstein S, Selinski S, Mueller T, Ickstadt K, Gilbert M, Ko YD, Baisch C, Pesch B, Harth V, Bolt HM, Vollmert C, Illig T, Eils R, Dippon J, Brauch H
Breast cancer: a candidate gene approach across the estrogen metabolic pathway
Breast Cancer Res Treat. 2008 Mar; 108(1):137-49. Epub 2007 Jun 23 - Kramer U, Illig T, Grune T, Krutmann J, Esser C
Strong associations of psoriasis with antigen processing LMP and transport genes TAP differ by gender and phenotype
Genes Immun. 2007 Sep;8(6):513-7 - Schoenborn V, Gohlke H, Heid IM, Illig T, Utermann G, Kronenberg F
Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: to separate the wheat from the chaff
Hum Mutat 2007, in press - Holzapfel C, Klopp N, Grallert H, Huth C, Gieger C, Meisinger C, Strassburger K, Giani G, Wichmann HE, Laumen H, Hauner H, Herder C, Rathmann W, Illig T
Genetic variants in the leukemia-associated Rho guanine nucleotide exchange factor (ARHGEF12) gene are not associated with T2DM and related parameters in Caucasians (KORA study)
Eur J Endocrinol. 2007 Sep;157(3):R1-R5 - Pauli S, Soker T, Klopp N, Illig T, Engel W, Graw J
Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene
Mol Vis. 2007 Jun 19;13:962-7 - Grallert H, Sedlmeier EM, Huth C, Kolz M, Heid IM, Meisinger C, Herder C, Strassburger K, Giani G, Kronenberg F, Wichmann HE, Adamski J, Paulweber B, Illig T, Rathmamn W
APOA5 variants: Role in the metabolic syndrome? Results from KORA S4 and SAPHIR, two population based studies
J Lipid Res. 2007 Dec; 48(12):2614-21. Epub 2007 Sep 3 - Georgi A, Jamra RA, Klein K, Villela AW, Schumacher J, Becker T, Paul T, Schmael C, Hofels S, Klopp N, Illig T, Propping P, Cichon S, Nothen MM, Schulze TG, Rietschel M
Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample
Psychiatr Genet. 2007 Oct;17(5):308-310 - Herder C, Klopp N, Baumert J, Mueller M, Khuseyinova N, Meisinger C, Martin S, Illig T, Koenig W, Thorand B
Effect of macrophage migration inhibitory factor (MIF) gene variants and MIF serum concentrations on the risk of type 2 diabetes: results from the MONICA/KORA Augsburg Case-Cohort Study, 1984-2002
Diabetologia. 2007 Aug 22 - Kolz M, Koenig W , Mueller M, Andreani M, Greven S, Illig T, Khuseyinova N, Panagiotakos D, Pershagen G, Salomaa V, Sunyer J, Peters A
DNA variants, plasma levels and variability of C-reactive protein in myocardial infarction survivors: Results from the AIRGENE study
European Heart Journal. 2007 in press - Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, Konig 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
Genomewide association analysis of coronary artery disease
N Engl J Med. 2007 Aug 2;357(5):443-53 - Koch W, Hoppmann P, Michou E, Jung V, Pfeufer A, Mueller JC, Gieger C, Wichmann HE, Meitinger T, Schomig A, Kastrati A
Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans
Hum Mol Genet. 2007 Aug 1;16(15):1821-7 - Wichmann HE, Gieger C
Biobanks
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2007 Feb;50(2):192-9 - Herbert A, Gerry NP, McQueen MB, Heid IM, Pfeufer A, Illig T, Wichmann HE, Meitinger T, Hunter D, Hu FB, Colditz G, Hinney A, Hebebrand J, Koberwitz K, Zhu X, Cooper R, Ardlie K, Lyon H, Hirschhorn J, Laird N, Lenburg ME, Lange C, Christman MF
Response to Comments on A Common Genetic Variant Is Associated with Adult and Childhood Obesity
Science 2007. 315, 187e - Lyon HN, Emilsson V, Hinney A, Heid IM, Lasky-Su J, Zhu X, Thorleifsson G, Gunnarsdottir S, Walters GB, Thorsteinsdottir U, Kong A, Gulcher J, Nguyen T, Scherag A, Pfeufer A, Meitinger T, Broenner G, Rief W, Soto-Quiros ME, Avila L, Klanderman B, Raby BA, Silverman EK, Weiss S, Laird N, Ding X, Groop L, Tuomi T, Isomaa B, Bengtsson K, Butler JL, Cooper RS, Fox CS, O´Donnell CJ, Vollmert C, Celedón JC, Wichmann HE, Hebebrand J, Stefansson K, Lange C, Hirschhorn JN
The Association of a SNP Upstream of INSIG2 with Body Mass Index is Peproduced in Several but Not All Cohorts
PLOS Genet 2007, 3(4): e61 - Hoffmann K, Mattheisen M, Dahm S, Nurnberg P, Roe C, Johnson J, Cox NJ, Wichmann HE, Wienker TF, Schulze J, Schwarz PE, Lindner TH
A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2
Diabetologia. 2007 Jul;50(7):1418-22 - Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C
Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease
Hum Mol Genet. 2007 Apr 15;16(8):887-99 - Thorand B, Baumert J, Herder C, Meisinger C, Koenig W
Soluble thrombomodulin as a predictor of type 2 diabetes: results from the MONICA/KORA Augsburg case-cohort study, 1984-1998
Diabetologia. 2007 Mar;50(3):545-8 - Thorand B, Baumert J, Kolb H, Meisinger C, Chambless L, Koenig W, Herder C
Sex differences in the prediction of type 2 diabetes by inflammatory markers: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002
Diabetes Care. 2007 Apr;30(4):854-60 - Justenhoven C, Pierl CB, Haas S, Fischer HP, Baisch C, Hamann U, Harth V, Pesch B, Bruening T, Vollmert C, Illig T, Dippon J, Ko YD, Brauch H
The CYP1B1_1358_GG genotype is associated with estrogen receptor-negative breast cancer
Breast Cancer Res Treat, Stand 10/2007: Online first - Freilinger T, Bevan S, Ripke S, Gschwendtner A, Lichtner P, Mueller-Myhsok B, Wichmann HE, Markus HS, Meitinger T, Dichgans M
Genetic Variation in the Lymphotoxin-Alpha Pathway and the Risk of Ischaemic Stroke in European Populations
Stroke, Stand 12/2007: Online first - Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wuellner U, Illig T, Sharma M, Gasser T
The transcription factor PITX3 is associated with sporadic Parkinson`s disease
Neurobiology Aging, Stand 10/2007: Epub ahead of print - Novak N, Baurecht H, Schaefer T, Rodriguez E, Wagenpfeil S, Klopp N, Heinrich J, Behrendt H, Ring J, Wichmann HE, Illig T, Weidinger S
Loss-of-Function Mutations in the Filaggrin Gene and Allergic Contact Sensitization to Nickel
J Invest Dermatology, Stand 12/2007: online first erschienen
