Earl Hubbell
Nature Genetics · 2002–2020
A researcher in the Science corpus: 6 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Whom Earl Hubbell trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Earl Hubbell overall
Papers from Earl Hubbell's perspective
Ordered by how strongly the researchers Earl Hubbell trusts endorse each paper. Same corpus, a different order for every researcher.
- Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection. (Proceedings of the National Academy of Sciences of the United States of America)
- Individual Comparisons by Ranking Methods
- Robust estimators for expression analysis (Bioinform.)
- Importance of replication in microarray gene expression studies: statistical methods and evidence from repetitive cDNA hybridizations. (Proceedings of the National Academy of Sciences of the United States of America)
- Statistical Analysis With Missing Data
- Analysis of high density expression microarrays with signed-rank call algorithms (Bioinform.)
- Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
- Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
- Diet and the evolution of human amylase gene copy number variation (Nature Genetics)
- Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn’s disease (Nature Genetics)
Their papers
- Robust estimators for expression analysis (2002) — 660 citations
- Analysis of high density expression microarrays with signed-rank call algorithms (2002) — 475 citations
- High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants (2019) — 647 citations
- Sensitive and specific multi-cancer detection and localization using methylation signatures in cell-free DNA (2020) — 1,145 citations
- Integrated detection and population-genetic analysis of SNPs and copy number variation (2008) — 996 citations
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs (2008) — 833 citations