PD Dr. Francesca Pasutto

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Medizinische Fakultät
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Analysis of genetically determined gene expression suggest role of inflammatory processes in etiology of exfoliation syndrome (2020) Hirbo J, Pasutto F, Sealock J, Evans P, Pawar P, Tao R, Straub P, et al. Conference contribution Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variants (2020) Souzeau E, Siggs OM, Pasutto F, Knight LSW, Perez-Jurado LA, Mcgregor L, Le Blanc S, et al. Journal article Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression (2020) Craig JE, Han X, Qassim A, Hassall M, Bailey JNC, Kinzy TG, Khawaja AP, et al. Journal article Advanced in early- and adult-onset glaucoma genetics (2019) Pasutto F Conference contribution Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma (2019) Siggs OM, Souzeau E, Pasutto F, Dubowsky A, Smith JEH, Taranath D, Pater J, et al. Journal article IMPACT OF SINGLE NUCLEOTIDE POLYMORPHISMS RS1870377 A > T AND RS2305948 C > T ON ENDOTHELIAL CELL ACTIVATION UNDER NON-UNIFORM SHEAR STRESS (2017) Urschel K, Schacher N, Pasutto F, Achenbach S, Raaz-Schrauder D, Schrauder MG, Stumpfe F, Dietel B Conference contribution Angiopoietin-1 is required for Schlemm's canal development in mice and humans (2017) Thomson BR, Souma T, Tompson SW, Onay T, Kizhatil K, Siggs OM, Feng L, et al. Journal article
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