C. Roselli
Genetics · 2017–2018
A researcher in the Science corpus: 4 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 85 citations into it
Whom C. Roselli trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from C. Roselli's perspective
Ordered by how strongly the researchers C. Roselli trusts endorse each paper. Same corpus, a different order for every researcher.
- Next-generation genotype imputation service and methods (Nature Genetics)
- GENCODE: The reference human genome annotation for The ENCODE Project (Genome Research)
- The Ensembl Variant Effect Predictor
- HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants (Nucleic Acids Res.)
- Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
- Human demographic history impacts genetic risk prediction across diverse populations
- Second-generation PLINK: rising to the challenge of larger and richer datasets (GigaScience)
- Exact and Asymptotic Weighted Logrank Tests for Interval Censored Data: The interval R package (Journal of Statistical Software)
- METAL: fast and efficient meta-analysis of genomewide association scans (Bioinform.)
- Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting
Their papers
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease (2017) — 34 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations (2018) — 2,683 citations
- Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation (2018) — 699 citations