A Gibbs sampling approach for genetic linkage parameter estimation 

Genetic and dietary determinants of nonalcoholic fatty liver disease in Hispanic children 

Integrative genomic and epigenomic analysis of human cancer 

Developing and benchmarking computational tools to facilitate T cell receptor repertoire analysis 

Colorectal cancer risks in Singapore Chinese: Polymorphisms in the insulin-like growth factor-1 and the vitamin D receptor 

Statistical methods for family-based gene-association studies 

Study of recombination events causing Charcot -Marie -Tooth disease type IA 

Polymorphisms in ileal sodium-dependent bile acid transporter gene and the risk of colorectal adenomas 

On the fraction of neutral mutations 

Solvation as a driving force for peptide docking to the major histocompatibility complex (MHC) class II molecules 

Engineering genetic tools to illustrate new insights into the homeostatic control of synaptic strength 

Destabilization of the replication fork protection complex is associated with meiotic defects in fission yeast 

Molecular studies of the human galactose-1-phosphate uridyltransferase gene 

Experimental and computational analysis of microsatellite repeat instability in mismatch-repair-deficient mice 

Construction of human linkage maps by sperm typing 

Examining the relationship between common genetic variation, type 2 diabetes and prostate cancer risk in the multiethnic cohort 

Censored survival models for genetic epidemiology: A Gibbs sampling approach 

A population genomics approach to the study of speciation in flowering columbines 

Whole genome amplification from a single cell and mutation analysis of trinucleotide repeats using sperm typing 

Ancestral inference and cancer stem cell dynamics in colorectal tumors 

Genetic architectures of phenotypic capacitance 

etd-YangFan-2235a 

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

Human linkage analysis of pseudoautosomal sequences using single sperm typing 

Quantification of mutations causing achondroplasia: A study of the paternal age effect