C. Carlson
Nature Genetics · 2004–2019
A researcher in the Science corpus: 9 papers; trusts 0 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Whom C. Carlson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Matthew Stephens
- B. Ewing
- Philip Green
- Kui Zhang
- Stacey Gabriel
- J. K. Pritchard
- David Botstein
- David Reich
- N. J. Smith
Who trusts C. Carlson overall
- Reedik Mägi
- Jonathan Marchini
- David J. Balding
- Sharon R. Browning
- Frank Steemers
- J. Rutkoski
- Peter Donnelly
- Brian L. Browning
- P. Phillips
- Joseph K. Pickrell
Papers from C. Carlson's perspective
Ordered by how strongly the researchers C. Carlson trusts endorse each paper. Same corpus, a different order for every researcher.
- Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)
- Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 (Science)
- Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease (Nature Genetics)
- Base-calling of automated sequencer traces using phred. II. Error probabilities.
- On the allelic spectrum of human disease. (Trends in Genetics)
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms (Nature)
- Haplotype tagging for the identification of common disease genes (Nature Genetics)
Their papers
- Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (2004) — 1,649 citations
- Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease (2011) — 1,887 citations
- Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) — 2,422 citations
- Genetic analyses of diverse populations improves discovery for complex traits (2019) — 901 citations
- Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk (2013) — 177 citations
- Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study (2013) — 238 citations
- Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study (2012) — 287 citations
- Comprehensive assessment of T-cell receptor beta-chain diversity in alphabeta T cells. (2009) — 1,065 citations
- Mapping complex disease loci in whole-genome association studies (2004) — 662 citations