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1. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

2. Expansion of phenotype and genotypic data in CRB2-related syndrome

3. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

11. Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

15. The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing

18. De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

21. De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

29. Genetic Risk, Vascular Function, and Subjective Cognitive Complaints Predict Objective Cognitive Function in Healthy Older Adults: Results From the Brain in Motion Study

30. De novo variants in MPP5 cause global developmental delay and behavioral changes

37. The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy

40. Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)

45. An Algorithm Measuring Donor Cell-Free DNA in Plasma of Cellular and Solid Organ Transplant Recipients That Does Not Require Donor or Recipient Genotyping

47. Cardiometabolic risk factors predict cerebrovascular health in older adults: results from theBrain in Motionstudy

50. RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans

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