TY  - GEN
AU  - Steinthorsdottir,Valgerdur
AU  - Thorleifsson,Gudmar
AU  - Sulem,Patrick
AU  - Helgason,Hannes
AU  - Grarup,Niels
AU  - Sigurdsson,Asgeir
AU  - Helgadottir,Hafdis T
AU  - Johannsdottir,Hrefna
AU  - Magnusson,Olafur T
AU  - Gudjonsson,Sigurjon A
AU  - Justesen,Johanne M
AU  - Harder,Marie N
AU  - Jørgensen,Marit E
AU  - Christensen,Cramer
AU  - Brandslund,Ivan
AU  - Sandbæk,Annelli
AU  - Lauritzen,Torsten
AU  - Vestergaard,Henrik
AU  - Linneberg,Allan
AU  - Jørgensen,Torben
AU  - Hansen,Torben
AU  - Daneshpour,Maryam S
AU  - Fallah,Mohammad-Sadegh
AU  - Hreidarsson,Astradur B
AU  - Sigurdsson,Gunnar
AU  - Azizi,Fereidoun
AU  - Benediktsson,Rafn
AU  - Masson,Gisli
AU  - Helgason,Agnar
AU  - Kong,Augustine
AU  - Gudbjartsson,Daniel F
AU  - Pedersen,Oluf
AU  - Thorsteinsdottir,Unnur
AU  - Stefansson,Kari
TI  - Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
SN  - 1546-1718
PY  - 2014///0423
KW  - Amidine-Lyases
KW  - genetics
KW  - Body Height
KW  - Body Weight
KW  - Case-Control Studies
KW  - Cyclin D2
KW  - Denmark
KW  - Diabetes Mellitus, Type 2
KW  - Female
KW  - Gene Frequency
KW  - Genetic Predisposition to Disease
KW  - Genetic Variation
KW  - Genome-Wide Association Study
KW  - Homeodomain Proteins
KW  - Humans
KW  - Iceland
KW  - Iran
KW  - Male
KW  - Mixed Function Oxygenases
KW  - Polymorphism, Single Nucleotide
KW  - Risk Factors
KW  - Trans-Activators
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ng.2882
ER  -