Prof. Dr. André Wiesmann da Silva Reis

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Lehrstuhl für Humangenetik

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Publications

(219)

Biallelic SEMA3A defects cause a novel type of syndromic short stature (2013) Hofmann K, Zweier M, Sticht H, Zweier C, Wittmann W, Hoyer J, Uebe S, et al. Journal article Patients with unstable angina pectoris show an increased frequency of the Fc gamma RIIa R131 allele (2012) Raaz-Schrauder D, Ekici AB, Munoz LE, Klinghammer L, Voll RE, Leusen JH, Van De Winkel JG, et al. Journal article Variants in ASB10 are associated with open-angle glaucoma (2012) Pasutto F, Keller KE, Weisschuh N, Sticht H, Samples JR, Yang YF, Zenkel M, et al. Journal article Common genetic determinants of intraocular pressure and primary open-angle glaucoma (2012) Van Koolwijk LME, Ramdas WD, Ikram MK, Jansonius NM, Pasutto F, Hysi PG, Macgregor S, et al. Journal article Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome (2011) Krumbiegel M, Pasutto F, Schlötzer-Schrehardt U, Uebe S, Zenkel M, Mardin CY, Weisschuh N, et al. Journal article Evidence for RPGRIP1 gene as risk factor for primary open angle glaucoma (2011) Fernández Martinez L, Letteboer S, Mardin CY, Weisschuh N, Gramer E, Weber BHF, Rautenstrauß B, et al. Journal article Common genetic variants associated with open-angle glaucoma (2011) Ramdas WD, Van Koolwijk LME, Lemij HG, Pasutto F, Cree AJ, Thorleifsson G, Janssen SF, et al. Journal article FcγRIIa genotype is associated with acute coronary syndromes as first manifestation of coronary artery disease (2009) Raaz D, Herrmann M, Ekici AB, Klinghammer L, Lausen B, Voll RE, Leusen JH, et al. Journal article Functional characterization of a novel CFTR mutation P67S identified in a patient with atypical cystic fibrosis (2007) Kraus C, Reis A, Naehrlich L, Dötsch J, Korbmacher C, Rauh R Journal article

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