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3. The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants

5. PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry

8. Epigenetic Regulation of F2RL3 Associates with Myocardial Infarction and Platelet Function

10. Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

12. Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

13. Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

14. The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants

15. A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk

16. Outcome monitoring and risk stratification after cardiac procedure in neonates, infants, children and young adults born with congenital heart disease: protocol for a multicentre prospective cohort study (Children OMACp)

19. PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry

20. Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

21. A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss

22. A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

23. Mutations in the U4 snRNA gene RNU4-2cause one of the most prevalent monogenic neurodevelopmental disorders

24. Corrigendum to ‘The Hemophilia Joint Health Score version 2.1 Validation in Adult Patients Study: A multicenter international study’ [Research and Practice in Thrombosis and Haemostasis, 6/2, (2022) e12690]

25. Corrigendum to Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH [J Thromb Haemost. 2022 Jul;20(7):1735-1743]

27. Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia

32. Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH

34. The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2

35. Advances in understanding the pathogenesis of hereditary macrothrombocytopenia

38. Rare missense variants in Tropomyosin‐4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects, and excessive bleeding

40. Whole-genome sequencing of patients with rare diseases in a national health system

41. Pseudohomozygous dysfibrinogenemia

46. Recombinant ADAMTS13 reduces abnormally up-regulated von Willebrand factor in plasma from patients with severe COVID-19

47. The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology

48. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

49. Whole-genome sequencing of patients with rare diseases in a national health system

50. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

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