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6. Molecular diagnoses and candidate gene identification in the congenital heart disease cohorts of the 100,000 genomes project

8. The genomic natural history of the aurochs

26. De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome

31. Donor genetic burden for cerebrovascular risk and kidney transplant outcome

33. A bispecific CD40 agonistic antibody allowing for antibody-peptide conjugate formation to enable cancer-specific peptide delivery, resulting in improved T Cell proliferation and anti-tumor immunity in mice

34. Inhibition of GPX4 enhances CDK4/6 inhibitor and endocrine therapy activity in breast cancer

42. Rare variants analyses suggest novel cleft genes in the African population

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