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You searched for: Author/Creator Rolati, Sophie

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1. [P2–114]: PATIENT‐DERIVED IPSC MODEL OF AN ABCA7 FRAMESHIFT DELETION ASSOCIATED WITH ALZHEIMER's DISEASE IN AFRICAN AMERICANS. (1st July 2017)

2. ABCA7 frameshift deletion associated with Alzheimer disease in African Americans. (June 2016)

3. Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets. Issue 10 (3rd January 2022)

4. O1‐03‐02: ABCA7 Frameshift Deletion Associated with Alzheimer's Disease in African Americans. (1st July 2016)

5. O1‐03‐03: Identification of Novel Candidate Genes for Early‐Onset Alzheimer's Disease Through Integrated Whole‐Exome Sequencing and Exome Chip Array Association Analysis. (1st July 2016)

6. O1‐09‐02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer's Disease Genes. (1st July 2016)

7. O2‐01‐05: MULTI‐ETHNIC ALZHEIMER'S DISEASE RELATED CHANGES OF RNA EDITING AFFECT IMMUNE REGULATION, ENDOCYTOSIS, AND AMYLOID PRECURSOR PROTEIN CATABOLISM. (1st July 2006)

8. O3‐06‐06: IDENTIFYING A PROTECTIVE VARIANT THAT LOWERS THE RISK FOR DEVELOPING AD IN APOE‐E4 CARRIERS. (1st July 2006)

9. O3‐13‐02: Whole‐exome sequencing in early‐onset Alzheimer disease cases identifies novel candidate genes. (1st July 2015)

10. O3–01–04: The identification of rare variants in late‐onset Alzheimer's disease using extended families. (1st July 2013)