Allelic Association and Recombination Hotspots in the Mucin Gene (MUC) Complex on Chromosome 11p15.5
Mapping of a Gene for Alopecia with Mental Retardation Syndrome (APMR3) on Chromosome 18q11.2-q12.2
Three Common Intronic Variants in the Maternal and Fetal Thiamine Pyrophosphokinase Gene (TPK1) are Associated with Birth Weight
Ethnic differences in interleukin 6 (IL-6) and IL6 receptor genes in spontaneous preterm birth and effects on amniotic fluid protein levels
Screening of the endothelin1 gene (EDN1) in a cohort of patients with essential left ventricular hypertrophy.
The use of Meta-Analysis Risk Estimates for Candidate Genes in Combination to Predict Coronary Heart Disease Risk
Interaction of Genetic Risk Factors Confers Higher Risk for Thrombotic Stroke in Male Chinese
Association Between Human Polymorphic DNA Markers and Hypoxia Adaptation in Sherpa Detected by a Preliminary Genome Scan
Investigation of the PARK10 Gene in Parkinson Disease
Evidence for an Association of the Dopamine D5 Receptor Gene on Age at Onset of Attention Deficit Hyperactivity Disorder
Multivariate Linkage Analysis of Specific Language Impairment (SLI)
Deconstructing Jaco
Application of multi-locus analytical methods to identify interacting loci in case-control studies
On the Usage of HWE for Identifying Genotyping Errors
The Reply of Zou & Donner to Teo's Commentary on their Manuscript