Publikationen

Filterkriterien: Schlüsselwort gleich Polymorphism, Single Nucleotide  [Alle Filter deaktivieren]
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.