Kāri Stefánsson - Concepedia

Author

Kāri Stefánsson

Also Known As

Adam S. Butterworth, Alessandro Serretti, Alessio Squassina, Alexander Hatoum, Ali Amin Al Olama, Alisa K. Manning, Andres J Lopez-Contreras, Andres Metspalu, Andrew J. Lotery, Andrew M. McIntosh

1.1K

Publications

205.6K

Citations

217

H-Index

421

Concepts

All Affiliations

deCODE Genetics (Iceland)University of Iceland National University Hospital of Iceland Reykjavík University Harvard University

About

Kāri Stefánsson is an author at deCODE Genetics (Iceland) specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	129	259	75.8K
2	Engineering	9	9	3.2K
3	Health Sciences	8	8	3.8K
4	Education	3	3	1.2K
5	Language Studies	2	2	490

Kāri Stefánsson

489

Publications

110.5K

Citations

168

H-Index

Page 1

	Year	Citations
Variant of <i>TREM2</i> Associated with the Risk of Alzheimer's Disease Thorlákur Jónsson, Hreinn Stefánsson, Stacy Steinberg, New England Journal of Medicine	2012	2.5K
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes Struan F.A. Grant, Inga Reynisdóttir, Rafn Benediktsson, Nature Genetics Metabolic SyndromeGenetic DeterminantDiabetes EpidemiologyGeneticsDiabetes	2006	2.3K
Rate of de novo mutations and the importance of father’s age to disease risk Augustine Kong, Michael L. Frigge, Gísli Másson, Nature Genetic TestingGenetic DisorderGeneticsGenetic EpidemiologyMedical Genetics	2012	2.2K
Hundreds of variants clustered in genomic loci and biological pathways affect human height Hana Lango Allen, Karol Estrada, Guillaume Lettre, Nature Genome-wide Association StudyGenetic AnalysisAllelic VariantQuantitative GeneticsGenotype-phenotype Association	2010	2K
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps Anubha Mahajan, Daniel Taliun, Matthias Thurner, Nature Genetics Genome-wide Association StudyAllelic VariantGenetic DeterminantSingle-variant ResolutionVariant Interpretation	2018	1.9K
A high-resolution recombination map of the human genome Augustine Kong, Daníel F. Guðbjartsson, Jesús Sainz, Nature Genetics GeneticsGenome StructureGenomicsHuman GenomeRecombination Dynamic	2002	1.7K
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline Thorlákur Jónsson, Jasvinder K. Atwal, Stacy Steinberg, Nature Neurodegenerative DiseasesAlzheimer's DiseaseAgingApp ProtectsGenetics	2012	1.7K
Neuregulin 1 and Susceptibility to Schizophrenia Hreinn Stefánsson, Hannes Pétursson, Engilbert Sigurðsson, The American Journal of Human Genetics PsychiatryPsychotic DisorderPsychiatric GeneticsNeuregulin 1Schizophrenia	2002	1.7K
Large-scale association analysis identifies new risk loci for coronary artery disease Panos Deloukas, Stavroula Kanoni, Christina Willenborg, Nature Genetics Genome-wide Association StudyLarge-scale Association AnalysisEpidemiologyCardiovascular EpidemiologyCardiovascular Disease	2012	1.7K
A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction Anna Helgadóttir, Andrei Manolescu, Sólveig Grétarsdóttir, Science GeneticsGenetic EpidemiologyHuman PolymorphismPathologyMolecular Genetics	2007	1.6K

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