Daniel Fannar Gudbjartsson
Artificial Intelligence · 2000–2021
A researcher in the Science corpus: 42 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Artificial Intelligence — 19 citations into it
- Optimization & Training — 12 citations into it
- Computer Vision and Pattern Recognition — 11 citations into it
- Radiology, Nuclear Medicine and Imaging — 8 citations into it
Whom Daniel Fannar Gudbjartsson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Daniel Fannar Gudbjartsson overall
Papers from Daniel Fannar Gudbjartsson's perspective
Ordered by how strongly the researchers Daniel Fannar Gudbjartsson 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
- Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper
- Regression Shrinkage and Selection via the Lasso
- The PANTHER database of protein families, subfamilies, functions and pathways (Nucleic Acids Res.)
- Scikit-learn: Machine Learning in Python
- Fast and Accurate Deep Network Learning by Exponential Linear Units (ELUs)
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes (Nature Genetics)
- Gene Ontology: tool for the unification of biology
- Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. (Human Molecular Genetics)
Their papers
- 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
- 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
- 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
- Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes (2007) — 755 citations
- Sequence variants at the TERT- CLPTM1L locus associate with many cancer types (2009) — 638 citations
- The nature of nurture: Effects of parental genotypes (2017) — 849 citations
- Many sequence variants affecting diversity of adult human height (2008) — 709 citations
- A variant associated with nicotine dependence, lung cancer and peripheral arterial disease (2008) — 1,546 citations
- Large-scale integration of the plasma proteome with genetics and disease (2021) — 1,317 citations
- Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer (2007) — 786 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations