Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

Nature Genetics

Volumn 47, Issue 5, 2015, Pages 445-447

  Steinberg, Stacy ^a   Stefansson, Hreinn ^a   Jonsson, Thorlakur ^a   Johannsdottir, Hrefna ^a   Ingason, Andres ^a   Helgason, Hannes ^a   Sulem, Patrick ^a   Magnusson, Olafur Th ^a   Gudjonsson, Sigurjon A ^a   Unnsteinsdottir, Unnur ^a   Kong, Augustine ^a   Helisalmi, Seppo ^b,c   Soininen, Hilkka ^b,c   Lah, James J ^d   Aarsland, Dag ^e,f,g   Fladby, Tormod ^g,h   Ulstein, Ingun D ^g,i   Djurovic, Srdjan ^i,j   Sando, Sigrid B ^k,l   White, Linda R ^k,l   Knudsen, Gun Peggy ^m   Westlye, Lars T ^g,i   Selbæk, Geir ⁿ   Giegling, Ina ^o   Hampel, Harald ^p   Hiltunen, Mikko ^b,c   Levey, Allan I ^d   Andreassen, Ole A ^g,i   Rujescu, Dan ^o   Jonsson, Palmi V ^q,r   Bjornsson, Sigurbjorn ^r   Snaedal, Jon ^r   Stefansson, Kari ^a,q   more..

^a DECODE GENETICS   (Iceland)

^b UNIVERSITY OF EASTERN FINLAND   (Finland)

^c KUOPIO UNIVERSITY HOSPITAL   (Finland)

^d EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e KAROLINSKA INSTITUTE   (Sweden)

^f STAVANGER UNIVERSITY HOSPITAL   (Norway)

^g UNIVERSITY OF OSLO   (Norway)

^h AKERSHUS UNIVERSITY HOSPITAL   (Norway)

ⁱ OSLO UNIVERSITY HOSPITAL   (Norway)

^j UNIVERSITY OF BERGEN   (Norway)

^k NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^l TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

^m NORWEGIAN INSTITUTE OF PUBLIC HEALTH   (Norway)

ⁿ VESTFOLD HOSPITAL TRUST   (Norway)

^o MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^p SORBONNE UNIVERSITÉ   (France)

^q UNIVERSITY OF ICELAND   (Iceland)

^r LANDSPITALI UNIVERSITY HOSPITAL   (Iceland)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A7; UNCLASSIFIED DRUG; ABCA7 PROTEIN, HUMAN;

ALZHEIMER DISEASE; ARTICLE; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; ICELANDER; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RISK; UNITED STATES; CASE CONTROL STUDY; DNA SEQUENCE; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; META ANALYSIS; MUTATION;

ALZHEIMER DISEASE; ATP-BINDING CASSETTE TRANSPORTERS; CASE-CONTROL STUDIES; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MUTATION; RISK; SEQUENCE ANALYSIS, DNA;

EID: 84929432198     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.3246     Document Type: Article

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