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1. Genetic variants for head size share genes and pathways with cancer

2. Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

3. Genomic Studies Across the Lifespan Point to Early Mechanisms Determining Subcortical Volumes

4. Circulating Metabolome and White Matter Hyperintensities in Women and Men

5. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

6. Associations Between Brainstem Volume and Alzheimer's Disease Pathology in Middle-Aged Individuals of the Framingham Heart Study.

7. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

8. Cerebral small vessel disease genomics and its implications across the lifespan.

9. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

10. Stroke genetics informs drug discovery and risk prediction across ancestries

11. Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

12. Genetic architecture of subcortical brain structures in 38,851 individuals

13. Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

14. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

15. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

16. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.

17. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

19. Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities

20. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

21. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

22. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

23. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

24. Mendelian Randomization Applied to Neurology

26. Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries

27. SNX19 in human autopsy brains and cerebral organoids

28. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

29. Complexities of cerebral small vessel disease, blood pressure, and dementia relationship: new insights from genetics

30. Genetic variants for head size share genes and pathways with cancer

31. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

33. Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study

34. Cerebrovascular disease and dementia: exploring causal pathways

35. Genetic insights of all‐cause and vascular dementia through genome‐wide association studies

38. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

39. Circulating Metabolome and White Matter Hyperintensities in Females and Males

40. Migraine, Stroke, and Cervical Arterial Dissection

41. Stroke genetics informs drug discovery and risk prediction across ancestries

42. A meta-analysis of genome-wide association studies identifies new genetic loci associated with all-cause and vascular dementia

43. Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function

44. Abstract 9674: Stroke, Migraine, and Cervical Arterial Dissection: Shared Genetics Reveals Concordant and Opposing Risk Mechanisms

45. GENOME-WIDE ASSOCIATIONS OF AORTIC DISTENSIBILITY SUGGEST CAUSAL RELATIONSHIPS WITH AORTIC ANEURYSMS AND BRAIN WHITE MATTER HYPERINTENSITIES

46. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

47. Stroke-associated intergenic variants modulate a human FOXF2 transcriptional enhancer.

48. Cerebral small vessel disease genomics and its implications across the lifespan

49. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

50. Cerebral small vessel disease genomics and its implications across the lifespan

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