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1. Lack of functional TCR-epitope interaction is associated with herpes zoster through reduced downstream T cell activation

2. Unraveling the Immune Signature of Herpes Zoster: Insights Into the Pathophysiology and Human Leukocyte Antigen Risk Profile.

3. Clinical variability and onset age modifiers in an extended Belgian GRN founder family

4. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

5. Unraveling the immune signature of herpes zoster: Insights into pathophysiology and the HLA risk profile

6. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

7. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

9. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

10. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

11. Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort

13. Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

16. ABCA7 PTC mutation carriers present with Alzheimer’s disease pathology and cerebral amyloid angiopathy

17. Highly Frequent MAPT p.R406W Carriers with a Nonconforming FTD Phenotype in the Belgian Flemish Population (1127)

18. In a Large Belgian AD Cohort Loss of ABCA7 Mutations Are Associated with Alzheimer’s Disease and Cerebral Amyloid Angiopathy. (1779)

22. Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family

24. Mutations Other Than Null Mutations Producing a Pathogenic Loss of Progranulin in Frontotemporal Dementia

25. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

28. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

31. Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk

32. Clinical variability and onset age modifiers in an extended Belgian GRN founder family.

33. Clinical variability and onset age modifiers in an extended Belgian GRN founder family

34. Clinical Evidence of Disease Anticipation in Families Segregating aC9orf72Repeat Expansion

35. Krimpcafé

38. The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

39. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

40. Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort

41. Clinical Evidence for Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion (S21.006)

42. Clinical Features of TBK1 Carriers and Comparison with C9orf72, GRN and Nonmutation Carriers in a Belgian Patient Cohort (S21.007)

43. Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

44. Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort

45. Clinical features ofTBK1carriers compared withC9orf72,GRNand non-mutation carriers in a Belgian cohort

46. Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort

47. Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study

48. P4-194: The identification of high-penetrant loss-of-function mutations in abca7 in Alzheimer's disease

49. DT-02-01: Loss-of-function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort

50. Clinical evidence for genetic anticipation in C9orf72 pedigrees

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