Linkage disequilibrium and its application to mapping in Arabidopsis thaliana 

Modeling and analyzing novel genetic data: Single -feature polymorphisms and polony sequences 

The role of genetic variation in insulin -like growth factors in prostate cancer risk: The multiethnic cohort 

Association testing of polymorphisms in the vitamin D metabolism and signaling pathway with multiple sclerosis across multiple populatuions 

Analysis of SNP differential expression and allele-specific expression in gestational trophoblastic disease using RNA-seq data 

Best practice development for RNA-Seq analysis of complex disorders, with applications in schizophrenia 

Association mapping in Arabidopsis thaliana 

Cytolytic T-lymphocyte recognition of class I molecules 

Integrative genomic and epigenomic analysis of human cancer 

Genetic risk factors in breast cancer susceptibility: The multiethnic cohort 

From risk mitochondrial and metabolic phenotype towards a precision medicine approach for Alzheimer's disease 

danbing-tk: a computational genetics framework for studying variable number tandem repeats 

Variation in insulin-like growth factor-2 binding protein 2 interacts with adiposity to alter insulin sensitivity in Mexican Americans 

Common immune-related factors and risk of non-Hodgkin lymphomy 

Diploid genome reconstruction from shotgun sequencing 

Human linkage analysis of pseudoautosomal sequences using single sperm typing 

Colorectal cancer: genomic variations in insulin-like growth factor-1 and -2 

The role of inflammation in non-Hodgkin lymphoma etiology 

Markov chain Monte Carlo methods in population genetics 

Statistical methods for family-based gene-association studies 

Genetic variations in gene from the cytochrome P450 family may account for differential response to pioglitazone therapy in the Hispanic women 

Essays in health economics 

Application of machine learning methods in genomic data analysis 

Estimating recombination rates from single nucleotide polymorphisms using summary statistics. 

The fit of the genetic relative risk models of the human leucocyte antigen (HLA) in the risk of insulin-dependent diabetes mellitus in the Finnish population