Cognitive phenotypes in Alzheimer's disease and genetic risk

Julie S. Snowden; Cheryl L. Stopford; Camille L. Julien; Jennifer C. Thompson; Yvonne Davidson; Linda Gibbons; Antonia Pritchard; Corinne L. Lendon; Anna M. Richardson; Anoop Varma; David Neary; David M. A. Mann

doi:10.1016/S0010-9452(08)70683-X

Cognitive phenotypes in Alzheimer's disease and genetic risk

Julie S. Snowden
, Cheryl L. Stopford
, Camille L. Julien
, Jennifer C. Thompson
, Yvonne Davidson
, Linda Gibbons
, Antonia Pritchard
, Corinne L. Lendon
, Anna M. Richardson
, Anoop Varma
, David Neary
, David M. A. Mann

Division of Biomedical Sciences

科研成果: Article › 同行评审

223 引用（Scopus）

源语言	English
页（从-至）	835-845
页数	11
期刊	Cortex
卷	43
期	7
DOI	https://doi.org/10.1016/S0010-9452(08)70683-X
出版状态	Published - 10月 2007

访问文件

10.1016/S0010-9452(08)70683-X许可: CC BY-NC-ND

引用此

@article{4b05a6281d5642ebbd52f9d7b0740fa6,

title = "Cognitive phenotypes in Alzheimer's disease and genetic risk",

keywords = "Alzheimer's disease, APOE epsilon 4, cognitive impairment, genetic risk",

author = "Snowden, \{Julie S.\} and Stopford, \{Cheryl L.\} and Julien, \{Camille L.\} and Thompson, \{Jennifer C.\} and Yvonne Davidson and Linda Gibbons and Antonia Pritchard and Lendon, \{Corinne L.\} and Richardson, \{Anna M.\} and Anoop Varma and David Neary and Mann, \{David M. A.\}",

note = "Copyright {\textcopyright} 2007 Elsevier",

year = "2007",

month = oct,

doi = "10.1016/S0010-9452(08)70683-X",

language = "English",

volume = "43",

pages = "835--845",

journal = "Cortex",

issn = "0010-9452",

publisher = "Masson SpA",

number = "7",

}

TY - JOUR

T1 - Cognitive phenotypes in Alzheimer's disease and genetic risk

AU - Snowden, Julie S.

AU - Stopford, Cheryl L.

AU - Julien, Camille L.

AU - Thompson, Jennifer C.

AU - Davidson, Yvonne

AU - Gibbons, Linda

AU - Pritchard, Antonia

AU - Lendon, Corinne L.

AU - Richardson, Anna M.

AU - Varma, Anoop

AU - Neary, David

AU - Mann, David M. A.

PY - 2007/10

Y1 - 2007/10

KW - Alzheimer's disease

KW - APOE epsilon 4

KW - cognitive impairment

KW - genetic risk

U2 - 10.1016/S0010-9452(08)70683-X

DO - 10.1016/S0010-9452(08)70683-X

M3 - Article

SN - 0010-9452

VL - 43

SP - 835

EP - 845

JO - Cortex

JF - Cortex

IS - 7

ER -