Shin Lin
Genetics · with Cutler · 2006–2008
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 20 citations into it
Whom Shin Lin trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Shin Lin's perspective
Ordered by how strongly the researchers Shin Lin 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)
- Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
- Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (American Journal of Human Genetics)
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
- 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)
Their papers
- A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. (2008) — 608 citations
- A comparison of phasing algorithms for trios and unrelated individuals. (2006) — 345 citations