Hreinn Stefansson
Artificial Intelligence · 2002–2022
A researcher in the Science corpus: 38 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Artificial Intelligence — 15 citations into it
- Computer Vision and Pattern Recognition — 14 citations into it
- Radiology, Nuclear Medicine and Imaging — 12 citations into it
- Optimization & Training — 11 citations into it
Whom Hreinn Stefansson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Hreinn Stefansson overall
Papers from Hreinn Stefansson's perspective
Ordered by how strongly the researchers Hreinn Stefansson trusts endorse each paper. Same corpus, a different order for every researcher.
- Deep Residual Learning for Image Recognition (Computer Vision and Pattern Recognition)
- Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper
- Gradient-based learning applied to document recognition
- Regression Shrinkage and Selection via the Lasso
- Scikit-learn: Machine Learning in Python
- Human-mouse alignments with BLASTZ. (Genome Research)
- MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment (Briefings Bioinform.)
- Detection of large-scale variation in the human genome (Nature Genetics)
- Fast and Accurate Deep Network Learning by Exponential Linear Units (ELUs)
- Gene Ontology: tool for the unification of biology
Their papers
- Genetics of gene expression and its effect on disease (2008) — 1,415 citations
- A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline (2012) — 1,716 citations
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes (2006) — 2,333 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 inversion under selection in Europeans (2005) — 813 citations
- Neuregulin 1 and susceptibility to schizophrenia. (2002) — 1,691 citations
- Identification of a large set of rare complete human knockouts (2015) — 219 citations
- Seven New Loci Associated with Age-Related Macular Degeneration (2013) — 796 citations
- Many sequence variants affecting diversity of adult human height (2008) — 709 citations
- CNVs conferring risk of autism or schizophrenia affect cognition in controls (2013) — 669 citations
- A variant associated with nicotine dependence, lung cancer and peripheral arterial disease (2008) — 1,546 citations
- A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
- Large-scale integration of the plasma proteome with genetics and disease (2021) — 1,317 citations
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) — 2,006 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) — 813 citations
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) — 1,654 citations
- Brain age prediction using deep learning uncovers associated sequence variants (2019) — 361 citations