Has participated in:
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Molekulargenetische Veränderungen bei Patienten mit Erkrankungen der primären Hämostase
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High-throughput microfluidic blood testing to phenotype genetically linked platelet disorders: an aid to diagnosis
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Hermansky-Pudlak Syndrome: identification of novel variants in the genes HPS3, HPS5, and DTNBP1 (HPS-7)