Kári Stefánsson
Kári Stefánsson 1949-
Kári Stefánsson íslenskur taugalæknir og forstjóri Íslenskrar erfðagreiningar
Stefansson, Kari
VIAF ID: 54119801 ( Personal )
Permalink: http://viaf.org/viaf/54119801
Preferred Forms
- 100 0 _ ‡a Kari Stefansson
- 100 0 _ ‡a Kari Stefansson
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- 100 0 _ ‡a Kári Stefánsson ‡c íslenskur taugalæknir og forstjóri Íslenskrar erfðagreiningar
- 100 1 _ ‡a Stefansson, Kari
4xx's: Alternate Name Forms (11)
Works
Title | Sources |
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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans | |
Advances in cellular neurobiology. | |
Áhyggjulaust er lífið leiðinlegt : viðtal. | |
Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland | |
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | |
Association of vitamin D binding protein variants with chronic mucus hypersecretion in Iceland | |
Athugasemd við (lög um) söfnun og verndun persónuupplýsinga. | |
An atlas of genetic determinants of forearm fracture | |
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD | |
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma | |
Cracking the code of life | |
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality | |
Distinct clinical differences between HLA-Cw*0602 positive and negative psoriasis patients – : an analysis of 1019 HLA-C- and HLA-B-typed patients | |
A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries | |
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis a genome-wide study. | |
Effects of a 5-Lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction : a randomized trial | |
Ekki skynsamlegt að sníða þekkingarsköpun stakk : viðtal. | |
Familial aggregation of atrial fibrillation in Iceland | |
A few members of the family of nervous system glycoproteins that contain the HNK-1 epitope : a study in disease and development | |
Fjaran : (eða krossfiskar og hrúðurkarlar án krossfiska) | |
Genes for schizophrenia can be detected : data from Iceland implicates neuregulin 1 | |
Genetic insights into resting heart rate and its role in cardiovascular disease | |
Genetics of common disease, 2004: | |
A genome-wide association search for type 2 diabetes genes in African Americans. | |
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm | |
Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis | |
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture | |
A genome-wide scan for preeclampsia in the Netherlands | |
A genome-wide study of allelic imbalance in human testicular germ cell tumors using mocrosatellite markers | |
Global Biobank Meta-analysis Initiative Powering genetic discovery across human disease. | |
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification | |
Horizon | |
Hver erum við? | |
An Icelandic example of the impact of population structure on association studies | |
The Icelandic healthcare database and informed consent | |
Identification of a novel neurerulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk halotype | |
Impact of genetics on low bone mass in adults | |
The inheritance of hip osteoarthritis in Iceland | |
Meta-analysis identifies 13 new loci association with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution | |
MtDNA variation in unuit populations of Greenland and Canada : migration history and population structure | |
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction | |
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset | |
The nature of nurture : effects of parental genotypes | |
Nauðsynlegt að laga ýmislegt í frumvarpinu um gagnagrunninn : segir Kári Stefánsson forstjóri Íslenskrar erfðagreiningar. | |
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration) | |
Parental influence on human germline de novo mutations in 1,548 trios from Iceland | |
A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas | |
The population genomic legacy of the second plague pandemic | |
Psoriasis patients who are homozygous for the HLA-Cw*0602 allele have a 2.5-fold increased risk of developing psoriasis compared with Cw6 heterozygotes | |
Reconstructing an African haploid genome from the 18th century | |
Response to Comments on "An Association Between the Kinship and Fertility of Human Couples" | |
Rival genetic tests leave buyers confused | |
The Role of Adiposity in Cardiometabolic Traits a Mendelian Randomization Analysis. | |
A saturated map of common genetic variants associated with human height | |
Several common variants modulate heart rate, PR interval and QRS duration | |
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability | |
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits | |
A statistical approach to identify ancient template DNA | |
Stóráfangi ef lyfið fer á markað : Kári Stefánsson, forstjóri Íslenskrar erfðagreiningar, ræðir tilraunalyfið DG031 | |
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies | |
Trú, kirkja og samfélag : séð með augum tveggja íslenskra athafnamanna | |
Who are we? | |
Wild is the wind : [interview] |