Published in Genet Epidemiol on November 01, 2002
Control of confounding of genetic associations in stratified populations. Am J Hum Genet (2003) 7.99
Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium. Am J Epidemiol (2010) 2.86
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology (2008) 2.16
A powerful strategy to account for multiple testing in the context of haplotype analysis. Am J Hum Genet (2004) 2.07
Little loss of information due to unknown phase for fine-scale linkage-disequilibrium mapping with single-nucleotide-polymorphism genotype data. Am J Hum Genet (2004) 2.06
A comprehensive literature review of haplotyping software and methods for use with unrelated individuals. Hum Genomics (2005) 1.84
Haplotype and missing data inference in nuclear families. Genome Res (2004) 1.69
Power comparisons between similarity-based multilocus association methods, logistic regression, and score tests for haplotypes. Genet Epidemiol (2009) 1.68
IL4R alpha mutations are associated with asthma exacerbations and mast cell/IgE expression. Am J Respir Crit Care Med (2006) 1.57
Entropy-based SNP selection for genetic association studies. Hum Genet (2003) 1.36
The impact of using related individuals for haplotype reconstruction in population studies. Genetics (2005) 1.31
Integration of association statistics over genomic regions using Bayesian adaptive regression splines. Hum Genomics (2003) 1.28
Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. Haematologica (2010) 1.20
IL1 gene cluster polymorphisms and its haplotypes may predict the risk to develop invasive pulmonary aspergillosis and modulate C-reactive protein level. J Clin Immunol (2008) 1.06
Secreted modular calcium-binding protein 2 haplotypes are associated with pulmonary function. Am J Respir Crit Care Med (2007) 1.01
Genetic variation in sodium-dependent vitamin C transporters SLC23A1 and SLC23A2 and risk of advanced colorectal adenoma. Nutr Cancer (2008) 0.96
A survey of current software for haplotype phase inference. Hum Genomics (2004) 0.94
Efficacy assessment of SNP sets for genome-wide disease association studies. Nucleic Acids Res (2007) 0.90
Evidence from mouse and man for a role of neuregulin 3 in nicotine dependence. Mol Psychiatry (2013) 0.87
The value of molecular haplotypes in a family-based linkage study. Am J Hum Genet (2006) 0.86
Haplotype analysis of the beta2 adrenergic receptor gene and risk of myocardial infarction in humans. Genetics (2004) 0.85
A new method for haplotype inference including full-sib information. Genetics (2007) 0.78
A novel tool for individual haplotype inference using mixed data. J Biomed Sci (2009) 0.75