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Variant ofTREM2Associated with the Risk of Alzheimer's Disease
Author(s) -
Thorlákur Jónsson,
Hreinn Stefánsson,
Stacy Steinberg,
Ingileif Jónsdóttir,
Pálmi V. Jónsson,
Jón Snædal,
Sigurbjörn Björnsson,
Johanna Huttenlocher,
Allan I. Levey,
James J. Lah,
Dan Rujescu,
Harald Hampel,
Ina Giegling,
Ole A. Andreassen,
Knut Engedal,
Ingun Ulstein,
Srdjan Djurovic,
Carla A. IbrahimVerbaas,
Albert Hofman,
M. Arfan Ikram,
Cornelia M. van Duijn,
Unnur Þorsteinsdóttir,
Augustine Kong,
Kári Stéfansson
Publication year - 2012
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1211103
Subject(s) - trem2 , odds ratio , alzheimer's disease , medicine , disease , allele , case control study , missense mutation , apolipoprotein e , population , confidence interval , genetics , mutation , biology , gene , receptor , myeloid cells , environmental health
Sequence variants, including the ε4 allele of apolipoprotein E, have been associated with the risk of the common late-onset form of Alzheimer's disease. Few rare variants affecting the risk of late-onset Alzheimer's disease have been found.

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