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1. A deep catalogue of protein-coding variation in 983,578 individuals

2. Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank

3. “PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black Patients”

4. Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study

5. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

6. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

7. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

8. Biallelic BRCA Loss and Homologous Recombination Deficiency in Nonbreast/Ovarian Tumors in Germline BRCA1/2 Carriers

9. Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

10. Multi-ethnic heterozygote frequencies of cancer susceptibility genes to inform counseling of reproductive risk

11. PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients

12. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions

13. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

14. Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle‐aged and older adults: A population‐based cohort study

15. Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study

16. Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank

17. Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study

18. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581]

19. Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study

20. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

21. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

22. MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

23. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

24. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

25. Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

26. Thrombotic risk determined by rare and common SERPINA1variants in a population‐based cohort study

27. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581]

28. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

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