Kári Stefánsson
Genetics · 2002–2022
A researcher in the Science corpus: 86 papers; trusts 5 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 1,115 citations into it; #4,156 of 6,854 by trust here, #13 by citations
- Artificial Intelligence — 27 citations into it
- Computer Vision and Pattern Recognition — 13 citations into it
- Optimization & Training — 12 citations into it
- Radiology, Nuclear Medicine and Imaging — 11 citations into it
Whom Kári Stefánsson trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- John Ashburner (in Computer Vision and Pattern Recognition)
- François Rousset (in Genetics)
- Laurent Excoffier (in Genetics)
- Sergey Ioffe (in Artificial Intelligence)
- Robert Tibshirani (in Optimization & Training)
Who trusts Kári Stefánsson
- J. K. Pritchard (in Genetics)
- Jonathan Marchini (in Genetics)
- Alkes L Price (in Genetics)
Papers from Kári Stefánsson's perspective
Ordered by how strongly the researchers Kári Stefánsson trusts endorse each paper. Same corpus, a different order for every researcher.
- Deep Residual Learning for Image Recognition (Computer Vision and Pattern Recognition)
- Gradient-based learning applied to document recognition
- Regression Shrinkage and Selection via the Lasso
- Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper
- Scikit-learn: Machine Learning in Python
- Fast and Accurate Deep Network Learning by Exponential Linear Units (ELUs)
- Addendum: Regularization and variable selection via the elastic net
- Deep Learning
- Ridge Regression: Biased Estimation for Nonorthogonal Problems
- Inferences from Spatial Population Genetics
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Genetics of gene expression and its effect on disease (2008) — 1,415 citations
- A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction (2007) — 898 citations
- A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline (2012) — 1,716 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes (2006) — 2,333 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia (2011) — 877 citations
- Large recurrent microdeletions associated with schizophrenia (2008) — 1,814 citations
- A common variant associated with prostate cancer in European and African populations (2006) — 733 citations
- Large-scale whole-genome sequencing of the Icelandic population (2015) — 776 citations
- A common inversion under selection in Europeans (2005) — 813 citations
- A high-resolution recombination map of the human genome (2002) — 1,832 citations
- A common variant on chromosome 9p21 affects the risk of myocardial infarction. (2007) — 961 citations
- Assessing population differentiation and isolation from single‐nucleotide polymorphism data (2002) — 244 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- A variant in CDKAL1 influences insulin response and risk of type 2 diabetes (2007) — 1,099 citations
- The gene encoding phosphodiesterase 4D confers risk of ischemic stroke (2003) — 611 citations
- Neuregulin 1 and susceptibility to schizophrenia. (2002) — 1,691 citations
- Identification of a large set of rare complete human knockouts (2015) — 219 citations