Has participated in:
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METTL3-dependent m6A modification of PSEN1 mRNA regulates craniofacial development through the Wnt/β-catenin signaling pathway
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Big data in der Diagnostik genetischer Schwerhörigkeit
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Molecular characterization of genes involved in hearing loss
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Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature