{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T20:45:07Z","timestamp":1791405907462,"version":"4.3.3"},"reference-count":23,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2006,6,2]],"date-time":"2006-06-02T00:00:00Z","timestamp":1149206400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt B"],"published-print":{"date-parts":[[2006,7,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A recent study demonstrated a significant genetic association between the ATP\u2010binding cassette transporter A2 (ABCA2) and the risk for Alzheimer's disease (AD) in a large Caucasian sample. The rare <jats:italic>T<\/jats:italic> allele of the synonymous exonic single nucleotide polymorphism (SNP) rs908832 was overrepresented in early\u2010onset AD patients as compared to cognitively healthy controls. Here we confirm the association of rs908832 with AD in a Western European population (n\u2009=\u2009291, <jats:italic>P<\/jats:italic>\u2009=\u20090.008). In a second sample from Southern Europe, rs908832 was not associated with AD. Interestingly, rs908832 was not polymorphic in a Japanese sample. Furthermore, rs908832 was not associated with either serum cholesterol levels or with the risk for coronary artery disease, but seemed to be related to cholesterol levels in the cerebrospinal fluid. These data suggest that ABCA2 may exert population\u2010dependent effects on the genetic risk for sporadic AD and support a role of ABC lipid transporters in the pathogenesis of this disease. \u00a9 2006 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.b.30345","type":"journal-article","created":{"date-parts":[[2006,6,2]],"date-time":"2006-06-02T15:34:28Z","timestamp":1149262468000},"page":"534-536","source":"Crossref","is-referenced-by-count":42,"title":["Ethnicity\u2010dependent genetic association of <i>ABCA2<\/i> with sporadic Alzheimer's disease"],"prefix":"10.1002","volume":"141B","author":[{"given":"M. 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