Publikationen

Filterkriterien: Schlüsselwort gleich Polymorphism, Single Nucleotide  [Alle Filter deaktivieren]
2019
Thingholm L, Rühlemann M, Wang J, et al. "Sucrase-isomaltase 15Phe IBS risk variant in relation to dietary carbohydrates and faecal microbiota composition." Gut. 2019;68(1):177-178.
2018
Alberts R, de Vries EMG, Goode EC, et al. "Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis." Gut. 2018;67(8):1517-1524.
Mueller SH, Färber A, Prüss H, et al. "Genetic predisposition in anti-LGI1 and anti-NMDA receptor encephalitis." Ann. Neurol.. 2018;83(4):863-869.
Munz M, Richter GM, Loos BG, et al. "Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus." Sci Rep. 2018;8(1):13678.
Jüptner M, Flachsbart F, Caliebe A, et al. "Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosus." Lupus. 2018;27(4):600-609.
2017
Westerlind H, Mellander M-R, Bresso F, et al. "Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis." Gut. 2017;66(3):421-428.
Dand N, Mucha S, Tsoi LC, et al. "Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling." Hum. Mol. Genet.. 2017;26(21):4301-4313.
Ji S-G, Juran BD, Mucha S, et al. "Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease." Nat. Genet.. 2017;49(2):269-273.
Munz M, Chen H, Jockel-Schneider Y, et al. "A haplotype block downstream of plasminogen is associated with chronic and aggressive periodontitis." J. Clin. Periodontol.. 2017;44(10):962-970.
Flachsbart F, Dose J, Gentschew L, et al. "Identification and characterization of two functional variants in the human longevity gene FOXO3." Nat Commun. 2017;8(1):2063.
Rühle F, Witten A, Barysenka A, et al. "Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism." Blood. 2017;129(6):783-790.
Jansen H, Willenborg C, Lieb W, et al. "Rheumatoid Arthritis and Coronary Artery Disease: Genetic Analyses Do Not Support a Causal Relation." J. Rheumatol.. 2017;44(1):4-10.
Webb TR, Erdmann J, Stirrups KE, et al. "Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease." J. Am. Coll. Cardiol.. 2017;69(7):823-836.
2016
Köpp J, Fleßa S, Lieb W, et al. "Association of PNPLA3 rs738409 and TM6SF2 rs58542926 with health services utilization in a population-based study." BMC Health Serv Res. 2016;16:41.
Joshi AD, Andersson C, Buch S, et al. "Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies." Gastroenterology. 2016;151(2):351-363.e28.
Taudien S, Lausser L, Giamarellos-Bourboulis EJ, et al. "Genetic Factors of the Disease Course After Sepsis: Rare Deleterious Variants Are Predictive." EBioMedicine. 2016;12:227-238.
Wang J, Thingholm LB, Skiecevičienė J, et al. "Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota." Nat. Genet.. 2016;48(11):1396-1406.
Müller SH, Girard SL, Hopfner F, et al. "Genome-wide association study in essential tremor identifies three new loci." Brain. 2016;139(Pt 12):3163-3169.
Degenhardt F, Niklowitz P, Szymczak S, et al. "Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases." Hum Mol Genet. 2016;25(13):2881-2891.
2015
Buch S, Stickel F, Trépo E, et al. "A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis." Nat Genet. 2015;47(12):1443-8.
Marenholz I, Esparza-Gordillo J, Rüschendorf F, et al. "Meta-analysis identifies seven susceptibility loci involved in the atopic march." Nat Commun. 2015;6:8804.
Paternoster L, Standl M, Waage J, et al. "Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis." Nat. Genet.. 2015;47(12):1449-1456.
Dankowski T, Buck D, Andlauer TFM, et al. "Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array." Genet Epidemiol. 2015;39(8):601-8.
Kato N, Loh M, Takeuchi F, et al. "Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation." Nat Genet. 2015;47(11):1282-1293.