David J. Cutler
Genetics · 2003–2019
A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 116 citations into it; #4,646 of 6,854 by trust here, #382 by citations
Whom David J. Cutler trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts David J. Cutler overall
Papers from David J. Cutler's perspective
Ordered by how strongly the researchers David J. Cutler trusts endorse each paper. Same corpus, a different order for every researcher.
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper
- A comparison of bayesian methods for haplotype reconstruction from population genotype data. (American Journal of Human Genetics)
- Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
- Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. (Genetics)
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
- Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
- Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease (Nature Genetics)
- Detecting recent positive selection in the human genome from haplotype structure (Nature)
- Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (American Journal of Human Genetics)
Their papers
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Comparative analyses of multi-species sequences from targeted genomic regions (2003) — 664 citations
- Genomic alterations in cultured human embryonic stem cells (2005) — 648 citations
- A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. (2008) — 608 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
- Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples (2016) — 373 citations
- A comparison of phasing algorithms for trios and unrelated individuals. (2006) — 345 citations
- A note on exact tests of Hardy-Weinberg equilibrium. (2005) — 1,541 citations