Vacant niches and the possible operation of natural laws in ecosystems.

A response to Rhode: natural laws, vacant niches and superorganisms. Riv Biol (2008) 1.07

On the possible operation of natural laws in ecosystems. Riv Biol (2008) 2.50

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus. Nat Genet (2007) 4.76

Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol. Hum Mol Genet (2004) 2.45

A common variant on chromosome 11q13 is associated with atopic dermatitis. Nat Genet (2009) 1.91

A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis. Nat Genet (2006) 1.90

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease. Nat Genet (2008) 1.38

Distinct methylation profiles of glioma subtypes. Int J Cancer (2003) 1.38

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis. PLoS Biol (2007) 1.21

An interaction between filaggrin mutations and early food sensitization improves the prediction of childhood asthma. J Allergy Clin Immunol (2009) 1.19

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy. Epilepsy Res (2002) 1.17

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study. Hum Mol Genet (2002) 1.03

Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population. Hum Mol Genet (2002) 1.02

Quantitative trait locus analysis reveals two intragenic sites that influence O6-alkylguanine-DNA alkyltransferase activity in peripheral blood mononuclear cells. Carcinogenesis (2005) 0.97

The effect of single-nucleotide polymorphism marker selection on patterns of haplotype blocks and haplotype frequency estimates. Am J Hum Genet (2005) 0.92

Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p. Hum Mol Genet (2003) 0.91

Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression. PLoS One (2013) 0.87

Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips. J Mol Med (Berl) (2005) 0.80

Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis. BMC Med Genet (2012) 0.80

Lack of association of the G protein-coupled receptor for asthma susceptibility gene with atopic dermatitis. J Allergy Clin Immunol (2005) 0.76

Simulation of Rapoport's rule for latitudinal species spread. Theory Biosci (2006) 0.76

Natural laws, vacant niches and superorganisms. A response to Woodley. Riv Biol (2009) 0.75