# Genetic Studies of Alzheimer's Disease in Jewish and Arab Populations

> **NIH NIH U01** · BOSTON UNIVERSITY MEDICAL CAMPUS · 2024 · $3,067,892

## Abstract

Most discoveries of the genetic basis of Alzheimer disease (AD) were made in Caucasians of European ancestry
(EAs) and required samples between 10,000 and 150,000 subjects to detect them. We and others have
demonstrated that discovery of AD risk variants can be accomplished in more genetically homogeneous cohorts
comprising several thousand or fewer subjects. Studies of non-EA populations also afford the opportunity to
discover variants that are relatively rare or absent in EAs and that display a smaller effect size in EAs due to
modification by other genes and environmental factors. We will focus on Jews and Arabs currently living in Israel
who are descended from the Middle East and North Africa (MENA). Although MENA Jews assimilated to some
extent with their non-Jewish neighbors, they have maintained a distinctive genetic profile that reflects some
admixture with non-Jews, ancient Jewish background, and a unique component reflecting genetic drift and new
mutations during the last two millennia. Our previous studies of Arabs living in the Israeli village called Wadi Ara
revealed a genome-wide significant association for AD with ACE, were central to the establishment of SORL1
as an AD gene, and contributed to a trans-ethnic GWAS leading to the discovery of several novel AD genes. In
this project, we will leverage the genetic architecture of MENA Jews and Israeli-Arabs, as well as their distinctive
environmental exposures and lifestyles, to promote discovery of AD-related genes and variants. Specifically, we
will recruit 3,000 MENA Jews at three sites in Israel, as well as 1,000 Israeli-Arabs located in multiple villages
(equal numbers of AD cases and controls in the total sample). We will obtain from each participant a blood
specimen for DNA and biomarker studies, and phenotypic data including clinical, cognitive test, medical history
and lifestyle information, as well as brain MRI data for a portion of the sample. DNA specimens will be whole
genome sequenced (WGS). WGS data will be processed using pipelines established by the Alzheimer Disease
Sequencing Project (ADSP). We will conduct a GWAS for AD using admixture mapping and methods for single
variant and gene-based tests. Top-findings will be replicated in Ashkenazi Jewish and non-Jewish datasets
assembled by the Alzheimer Disease Genetics Consortium and ADSP using trans-ethnic analysis and
approaches that focus on variants affecting protein structure, transcription, and gene expression. We will also
conduct GWAS for age at onset and AD biomarkers using single outcome and pleiotropy models. Next, we will
identify gene targets of the top-ranked SNPs by performing expression quantitative trait locus analysis using
locally derived and publicly available data containing genotype and gene expression data in brain and other
tissues, and establish functional connections among the top-ranked SNPs and genes using pathway, co-
expression network, and Mendelian randomization analysis. Finally, we will e...

## Key facts

- **NIH application ID:** 10914777
- **Project number:** 5U01AG081230-02
- **Recipient organization:** BOSTON UNIVERSITY MEDICAL CAMPUS
- **Principal Investigator:** Lindsay A. Farrer
- **Activity code:** U01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $3,067,892
- **Award type:** 5
- **Project period:** 2023-09-01 → 2028-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10914777

## Citation

> US National Institutes of Health, RePORTER application 10914777, Genetic Studies of Alzheimer's Disease in Jewish and Arab Populations (5U01AG081230-02). Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/grant/nih/10914777. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
