A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1
SNP Discovery and Haplotype Analysis in the Segmentally Duplicated DRD5 Coding Region
New Mutations of EXT1 and EXT2 Genes in German Patients with Multiple Osteochondromas
High-resolution Melting Facilitates Mutation Screening of PYGM in Patients with McArdle Disease
Revisiting MSUD in Portuguese Gypsies
Genetic Admixture in Brazilians Exposed to Infection with Leishmania chagasi
Inter- and Extra-Indian Admixture and Genetic Diversity in Reunion Island Revealed by Analysis of Mitochondrial DNA
Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys ) Variant
Using Case-parent Triads to Estimate Relative Risks Associated with a Candidate Haplotype
Evaluating the Ability of Tree-Based Methods and Logistic Regression for the Detection of SNP-SNP Interaction
The Cost Effectiveness of Duplicate Genotyping for Testing Genetic Association
CALHM1 Polymorphism is not Associated with Late-onset Alzheimer Disease
Spastic Paraplegia, Optic Atrophy, and Neuropathy