Publikationen

Filterkriterien: Autor gleich Franke, Andre  [Alle Filter deaktivieren]
2019
Liwinski T, Zenouzi R, John C, et al. "Alterations of the bile microbiome in primary sclerosing cholangitis." Gut. 2019.
Rühlemann M, Liwinski T, Heinsen F-A, et al. "Consistent alterations in faecal microbiomes of patients with primary sclerosing cholangitis independent of associated colitis." Aliment. Pharmacol. Ther.. 2019;50(5):580-589.
Degenhardt F, Wendorff M, Wittig M, et al. "Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles." Hum. Mol. Genet.. 2019;28(12):2078-2092.
Chen Z, Chen JA, Shatunov A, et al. "Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy." Mov. Disord.. 2019;34(7):1049-1059.
Rühlemann MChristoph, Solovjeva MEmmy Leni, Zenouzi R, et al. "Gut mycobiome of primary sclerosing cholangitis patients is characterised by an increase of and species." Gut. 2019.
Pryor R, Norvaisas P, Marinos G, et al. "Host-Microbe-Drug-Nutrient Screen Identifies Bacterial Effectors of Metformin Therapy." Cell. 2019;178(6):1299-1312.e29.
Munz M, Richter GM, Loos BG, et al. "Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci." Eur. J. Hum. Genet.. 2019;27(1):102-113.
Hopfner F, Müller SH, Steppat D, et al. "No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors." Transl Neurodegener. 2019;8:11.
Jennings A, Koch M, Jensen MK, et al. "The role of the gut microbiome in the association between habitual anthocyanin intake and visceral abdominal fat in population-level analysis." Am. J. Clin. Nutr.. 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.
Bustos BI, Pérez-Palma E, Buch S, et al. "Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry." Sci Rep. 2019;9(1):772.
2017
Neidhardt G, Hauke J, Ramser J, et al. "Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer." JAMA Oncol. 2017;3(9):1245-1248.
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.
Rühlemann MChristoph, Heinsen F-A, Zenouzi R, Lieb W, Franke A, Schramm C. "Faecal microbiota profiles as diagnostic biomarkers in primary sclerosing cholangitis." Gut. 2017;66(4):753-754.
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.
Luedde M, Winkler T, Heinsen F-A, et al. "Heart failure is associated with depletion of core intestinal microbiota." ESC Heart Fail. 2017;4(3):282-290.
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.
Bauer CR, Knecht C, Fretter C, et al. "Interdisciplinary approach towards a systems medicine toolbox using the example of inflammatory diseases." Brief. Bioinformatics. 2017;18(3):479-487.
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.
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
Ellinghaus D, Jostins L, Spain SL, et al. "Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci." Nat. Genet.. 2016;48(5):510-8.
Heinsen F-A, Fangmann D, Müller N, et al. "Beneficial Effects of a Dietary Weight Loss Intervention on Human Gut Microbiome Diversity and Metabolism Are Not Sustained during Weight Maintenance." Obes Facts. 2016;9(6):379-391.
Stitziel NO, Stirrups KE, Masca NGD, et al. "Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease." N. Engl. J. Med.. 2016;374(12):1134-44.
Pattaro C, Teumer A, Gorski M, et al. "Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function." Nat Commun. 2016;7:10023.
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.
van Rheenen W, Shatunov A, Dekker AM, et al. "Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis." Nat. Genet.. 2016;48(9):1043-8.
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.
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.
Flachsbart F, Ellinghaus D, Gentschew L, et al. "Immunochip analysis identifies association of the RAD50/IL13 region with human longevity." Aging Cell. 2016;15(3):585-8.