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
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Kari Stefansson
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100 3 _ ‡a Kari Stefansson
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Kari Stefansson
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100 4 _ ‡a Kári ‡1 Stefánsson ‡d 1949-
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100 0 _ ‡a Kári Stefánsson
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Kári Stefánsson
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íslenskur taugalæknir og forstjóri Íslenskrar erfðagreiningar
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Stefansson, Kari
4xx's: Alternate Name Forms (11)
Works
| Title | Sources |
|---|---|
| 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans |
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| Advances in cellular neurobiology. |
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| Áhyggjulaust er lífið leiðinlegt : viðtal. |
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| Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland |
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| Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index |
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| Association of vitamin D binding protein variants with chronic mucus hypersecretion in Iceland |
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| Athugasemd við (lög um) söfnun og verndun persónuupplýsinga. |
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| CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD |
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| Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma |
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| Cracking the code of life |
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| Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
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| Distinct clinical differences between HLA-Cw*0602 positive and negative psoriasis patients – : an analysis of 1019 HLA-C- and HLA-B-typed patients |
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| A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries |
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| Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis a genome-wide study. |
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| Effects of a 5-Lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction : a randomized trial |
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| Ekki skynsamlegt að sníða þekkingarsköpun stakk : viðtal. |
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| Familial aggregation of atrial fibrillation in Iceland |
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| A few members of the family of nervous system glycoproteins that contain the HNK-1 epitope : a study in disease and development |
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| Fjaran : (eða krossfiskar og hrúðurkarlar án krossfiska) |
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| Genes for schizophrenia can be detected : data from Iceland implicates neuregulin 1 |
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| Genetic insights into resting heart rate and its role in cardiovascular disease |
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| Genetics of common disease, 2004: |
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| A genome-wide association search for type 2 diabetes genes in African Americans. |
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| Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm |
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| Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture |
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| A genome-wide scan for preeclampsia in the Netherlands |
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| A genome-wide study of allelic imbalance in human testicular germ cell tumors using mocrosatellite markers |
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| Horizon |
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| Hver erum við? |
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| An Icelandic example of the impact of population structure on association studies |
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| The Icelandic healthcare database and informed consent |
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| Identification of a novel neurerulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk halotype |
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| Impact of genetics on low bone mass in adults |
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| The inheritance of hip osteoarthritis in Iceland |
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| Meta-analysis identifies 13 new loci association with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution |
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| MtDNA variation in unuit populations of Greenland and Canada : migration history and population structure |
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| Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction |
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| Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset |
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| The nature of nurture : effects of parental genotypes |
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| Nauðsynlegt að laga ýmislegt í frumvarpinu um gagnagrunninn : segir Kári Stefánsson forstjóri Íslenskrar erfðagreiningar. |
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| A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration) |
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| Parental influence on human germline de novo mutations in 1,548 trios from Iceland |
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| A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas |
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| The population genomic legacy of the second plague pandemic |
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| 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 |
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| Reconstructing an African haploid genome from the 18th century |
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| Response to Comments on "An Association Between the Kinship and Fertility of Human Couples" |
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| Rival genetic tests leave buyers confused |
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| The Role of Adiposity in Cardiometabolic Traits a Mendelian Randomization Analysis. |
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| A saturated map of common genetic variants associated with human height |
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| Several common variants modulate heart rate, PR interval and QRS duration |
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| Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability |
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| Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits |
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| A statistical approach to identify ancient template DNA |
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| Stóráfangi ef lyfið fer á markað : Kári Stefánsson, forstjóri Íslenskrar erfðagreiningar, ræðir tilraunalyfið DG031 |
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| Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies |
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| Trú, kirkja og samfélag : séð með augum tveggja íslenskra athafnamanna |
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| Who are we? |
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| Wild is the wind : [interview] |
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