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You searched for: Author/Creator Jansen, Iris E.

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2. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. (18th October 2016)

3. BDNF‐Met polymorphism on top of amyloid pathology predisposes for faster cognitive decline in cognitively normal elderly: The SCIENCe Project: Genetics/genetic factors of Alzheimer's disease. (7th December 2020)

4. Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer's disease. (1st February 2022)

5. Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer's disease. (December 2021)

6. Functional interpretation of genetic risk loci for dementia using a protein quantitative trait loci (pQTLs) approach in cerebrospinal fluid: Genetics: Molecular genetics of AD and ADRD. (7th December 2020)

7. Immune response and endocytosis pathways are associated with the resilience against Alzheimer's disease: Genetics: Molecular genetics of AD and ADRD. (7th December 2020)

8. Novel genetic effects on amyloid and tau protein levels in cerebrospinal fluid: Towards a better knowledge of the genetics of Alzheimer's disease, the European Alzheimer Disease Biobank (EADB) Consortium. (7th December 2020)

9. O5‐04‐01: A RARE GENETIC VARIANT IN THE PLCG2 GENE IS ASSOCIATED WITH A REDUCED RISK OF ALL MAJOR TYPES OF DEMENTIA AND AN INCREASED RISK TO REACH AN EXTREMELY OLD AGE. (1st July 2006)

10. P2‐134: THE ADDED VALUE OF EXTREME PHENOTYPES IN ALZHEIMER'S DISEASE CASE‐CONTROL STUDIES. (1st July 2006)