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Stefansson, Kari

Faculty of Medicine, University of Iceland, Reykjavik, Iceland.

TitleYearPMID
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. 2010 20081858
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. 2010 20888040
Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium. 2010 20548021
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 2010 20418888
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 2010 21102462
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 2009 19836008
Common variants conferring risk of schizophrenia. 2009 19571808
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. 2009 19557161
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. 2009 19448622
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. 2009 19079260
Parental origin of sequence variants associated with complex diseases. 2009 20016592
The impact of divergence time on the nature of population structure: an example from Iceland. 2009 19503599
Association between microdeletion and microduplication at 16p11.2 and autism. 2008 18184952
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease. 2008 18385739
Detection of sharing by descent, long-range phasing and haplotype imputation. 2008 19165921
Genetics of gene expression and its effect on disease. 2008 18344981
Large recurrent microdeletions associated with schizophrenia. 2008 18668039
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. 2008 18372903
A common variant on chromosome 9p21 affects the risk of myocardial infarction. 2007 17478679
A common inversion under selection in Europeans. 2005 15654335
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