On the asymptotic equivalence of allelic and trend statistic under Hardy-Weinberg equilibrium
Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot-Marie-Tooth Subtype CMT2B1 in Families from North Western Africa
Genetic Epidemiology of Subclinical Cardiovascular Disease in the Diabetes Heart Study
Quantification of the Genetic Component of Basal C-Reactive Protein Expression in SLE Nuclear Families
A Genome-wide Scan in an Amish Pedigree with Parkinsonism
Cognitive Functioning and Survival in the Elderly
Identification of Association of Common AGGF1 Variants with Susceptibility for Klippel-Trenaunay Syndrome Using the Structure Association Program
Correlation Analyses Reveal a Substantial Influence of Allelic Gaps on the Investigation of Genetic Diversity of Modern Human Populations with Microsatellites
Four SNPS on Chromosome 9p21 Confer Risk to Premature, Familial CAD and MI in an American Caucasian Population (GeneQuest)
A Bayesian Spatial Multimarker Genetic Random-Effect Model for Fine-Scale Mapping
Identifying Modifier Loci in Existing Genome Scan Data
Exact Trait-Model-Free Tests for Linkage Detection in Pedigrees
HMBS Mutations in Chinese Patients with Acute Intermittent Porphyria
Genome-wide Linkage and Genome-wide Association – Can they be Reconciled?
Detection, Imputation and Association Analysis of Small Deletions and Null-alleles on Oligonucleotide Arrays
Analysis of population structure and genetic matching in European samples using genome-wide marker sets
A score statistic for genetic association given linkage
G.H.Hardy and Hardy–Weinberg equilibrium (1908)
The Statistical Equivalent Of The Binary TDT For Quantitative Traits
Association Analysis of SNP Data Imputed with the EM-Algorithm
Searching for genotype-phenotype structure
False negative replication of disease associations can be caused by differences in marker allele frequencies between study populations
A Polygenic Model for Integration of Linkage and Pathway Information
Haplotypes, Siblings and Continuous Phenotypes
Meta-analysis of gene/disease association studies
Unbiased estimation of effect sizes from genome-wide association scans with replication
A simple method for co-segregation analysis to evaluate the pathogenicity of DNA variants of unknown significance in BRCA1 and BRCA2
HD_IBD – a new method for tracing allelic inheritance in deep complex pedigrees
Multi-locus epistasis leads to hybrid inferiority in domestic fowl
A Critical Review of Genomic Control Methods
A Test for Gene Conversion and Results in the Human Growth Hormone (GH1) Gene Promoter
Gene-environment interactions involved in type 2 diabetes
SNPs to pathways – making biological sense of GWA results
A simulation study using a hierarchical stochastic search approach
Haplotype reconstruction algorithm SHARE using genotype sharing combined with Mantel Statistics Using Haplotype Sharing
Score test for age at onset linkage analysis of selected nuclear families
Prediction models for SNP data
Extended meta-analysis of genome-wide linkage studies in schizophrenia
In silico genome-wide association mapping of complex traits
Effects of the underlying model in multiple imputation
Analysing Complex Canine Pedigrees
Comparison of the power of different methods for the analysis of haplotype-environment interactions when haplotype phase is ambiguous
QTLMAP, a software for QTL detection in outbred populations
Meta-analysis of linkage studies in celiac disease
Markov model developed to calculate the prevalence of quantitative factors
Genome-wide prediction of functional gene-gene interactions in case-control association studies
Contribution of Gender-Specific Genetic Factors to Osteoporosis Risk