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1. A defective flexible loop contributes to the processing and gating defects of the predominant cystic fibrosis‐causing mutation. Issue 4 (22nd January 2019)

5. Assigning pathogenicity for TAB2 variants using a novel scalable functional assay and expanding TAB2 disease spectrum. Issue 6 (14th October 2022)

6. CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis. Issue 1 (13th November 2016)

8. Cobalt–platinum intermetallic composite loaded on pyridinic N-enriched carbon for acidic hydrogen evolution catalysis with ultralow overpotential. (9th March 2023)