Eimear E. Kenny
Genetics · 2012–2022
A researcher in the Science corpus: 9 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 204 citations into it
- Molecular Biology — 137 citations into it
- Statistics and Probability — 8 citations into it
Whom Eimear E. Kenny trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Eimear E. Kenny's perspective
Ordered by how strongly the researchers Eimear E. Kenny trusts endorse each paper. Same corpus, a different order for every researcher.
- Conditional Random Fields: Probabilistic Models for Segmenting and Labeling Sequence Data
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. (American Journal of Human Genetics)
- Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
- Analysis of protein-coding genetic variation in 60,706 humans
- A Draft Sequence of the Neandertal Genome (Science)
- The UK Biobank resource with deep phenotyping and genomic data
- On Discriminative vs. Generative Classifiers: A comparison of logistic regression and naive Bayes
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- A general framework for estimating the relative pathogenicity of human genetic variants
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- The Human Pangenome Project: a global resource to map genomic diversity (2022) — 392 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Genetic analyses of diverse populations improves discovery for complex traits (2019) — 901 citations
- Human demographic history impacts genetic risk prediction across diverse populations (2016) — 1,291 citations
- RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (2013) — 854 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations