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Omony, Jimmy; Thölken, Clemens; Salimi, Azam; Laubhahn, Kristina; Illi, Sabina; Weckmann, Markus; Grychtol, Ruth; Rabe, Klaus Friedrich; Thiele, Dominik; Foth, Svenja; Weber, Stefanie; Brinkmann, Folke; Kopp, Matthias Volkmar; Hansen, Gesine; Renz, Harald; von Mutius, Erika; Schaub, Bianca; Skevaki, Chrysanthi (2024). Urinary eosinophil-derived neurotoxin is associated with reduced lung function in pediatric asthma. Pediatric allergy and immunology, 35(6) Wiley-Blackwell 10.1111/pai.14172
Jakwerth, Constanze A; Weckmann, Markus; Illi, Sabina; Charles, Helen; Zissler, Ulrich M; Oelsner, Madlen; Guerth, Ferdinand; Omony, Jimmy; Nemani, Sai Sneha Priya; Grychtol, Ruth; Dittrich, Anna-Maria; Skevaki, Chrysanthi; Foth, Svenja; Weber, Stefanie; Alejandre Alcazar, Miguel A; van Koningsbruggen-Rietschel, Silke; Brock, Robert; Blau, Samira; Hansen, Gesine; Bahmer, Thomas; ... (2024). 17q21 Variants Disturb Mucosal Host Defense in Childhood Asthma. American journal of respiratory and critical care medicine, 209(8), pp. 947-959. American Lung Association 10.1164/rccm.202305-0934OC
Grychtol, Ruth; Riemann, Lennart; Gaedcke, Svenja; Liu, Bin; DeLuca, David; Förster, Reinhold; Maison, Nicole; Thiele, Dominik; Jakobs, Nikolas; Bahmer, Thomas; Meyer, Meike; Foth, Svenja; Weber, Stefanie; Rietschel, Ernst; Rabe, Klaus F; Kopp, Matthias V; von Mutius, Erika; Dittrich, Anna-Maria; Hansen, Gesine (2023). Validation of the Asthma Severity Scoring System (ASSESS) in the ALLIANCE cohort. The Journal of allergy and clinical immunology, 151(6), 1525-1535.e4. Elsevier 10.1016/j.jaci.2023.01.027
Brockschmidt, Antje; Chung, Boidinh; Weber, Stefanie; Fischer, Dagmar-Christiane; Kolatsi-Joannou, Maria; Christ, Laura; Heimbach, André; Shtiza, Diamant; Klaus, Günter; Simonetti, Giacomo D; Konrad, Martin; Winyard, Paul; Haffner, Dieter; Schaefer, Franz; Weber, Ruthild G (2012). CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrology, dialysis, transplantation, 27(6), pp. 2355-64. Oxford: Oxford University Press 10.1093/ndt/gfr649
Konrad, Martin; Hou, Jianghui; Weber, Stefanie; Dötsch, Jörg; Kari, Jameela A; Seeman, Tomas; Kuwertz-Bröking, Eberhard; Peco-Antic, Amira; Tasic, Velibor; Dittrich, Katalin; Alshaya, Hammad O; von Vigier, Rodo O; Gallati, Sabina; Goodenough, Daniel A; Schaller, André (2008). CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Journal of the American Society of Nephrology, 19(1), pp. 171-81. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1681/ASN.2007060709
Konrad, Martin; Schaller, André; Seelow, Dominik; Pandey, Amit Vikram; Waldegger, Siegfried; Lesslauer, Annegret; Vitzthum, Helga; Suzuki, Yoshiro; Luk, John M; Becker, Christian; Schlingmann, Karl P; Schmid, Marcel; Rodriguez-Soriano, Juan; Ariceta, Gema; Cano, Francisco; Enriquez, Ricardo; Juppner, Harald; Bakkaloglu, Sevcan A; Hediger, Matthias A; Gallati, Sabina; ... (2006). Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. American journal of human genetics, 79(5), pp. 949-57. New York, N.Y.: Cell Press 10.1086/508617
