Lon R. Cardon

Genetics · 2000–2015

A researcher in the Science corpus: 26 papers; trusts 6 researchers and is trusted by 50 researchers here, as inferred from the citation graph.

Subfields

Genetics — 301 citations into it; #217 of 6,854 by trust here, #31 by citations
Molecular Biology — 173 citations into it; #1,569 of 17,773 by trust here, #807 by citations

Whom Lon R. Cardon trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

Who trusts Lon R. Cardon overall

Papers from Lon R. Cardon's perspective

Ordered by how strongly the researchers Lon R. Cardon trusts endorse each paper. Same corpus, a different order for every researcher.

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
Genome-wide association studies for common diseases and complex traits (Nature reviews genetics)
A method for quantifying differentiation between populations at multi-allelic loci and its implications for investigating identity and paternity (Genetica)
Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration (Science)
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Haploview: analysis and visualization of LD and haplotype maps (Bioinform.)
Complement Factor H Polymorphism in Age-Related Macular Degeneration (Science)
A genome-wide association study of global gene expression (Nature Genetics)

Their papers

A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
Thousands of chemical starting points for antimalarial lead identification (2010) — 1,007 citations
Genome-wide association studies for complex traits: consensus, uncertainty and challenges (2008) — 3,055 citations
Genome-wide strategies for detecting multiple loci that influence complex diseases (2005) — 978 citations
Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (2002) — 3,521 citations
Multiple type 2 diabetes susceptibility genes following genome-wide association scan in UK samples (2007) — 2,209 citations
A general test of association for quantitative traits in nuclear families. (2000) — 1,192 citations
Replicating genotype–phenotype associations (2007) — 1,394 citations
The support of human genetic evidence for approved drug indications (2015) — 1,489 citations
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. (2004) — 771 citations
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (2012) — 717 citations
Basic statistical analysis in genetic case-control studies (2011) — 537 citations
An 18-kDa Translocator Protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28 (2011) — 774 citations
Data quality control in genetic case-control association studies (2010) — 1,348 citations
Finding the missing heritability of complex diseases (2009) — 8,360 citations
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits (2009) — 1,015 citations
Finding the missing heritability of complex (2009) — 88 citations
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (2008) — 2,710 citations
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (2007) — 704 citations
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity (2007) — 4,583 citations