K. Hao

发表

Genome-wide selection of tag SNPs using multiple-marker correlation

K. Hao, 2007 .

Familial aggregation of airway responsiveness: a community-based study.

Xiping Xu, Bin-yan Wang, Z. Fang, 2005, Annals of epidemiology.

Novel pheochromocytoma susceptibility loci identified by integrative genomics.

M. Pujana, C. Stiles, N. Aronin, 2005, Cancer research.

Placental Gene Transcript Proportions are Altered in the Presence of In Utero Arsenic and Cadmium Exposures, Genetic Variants, and Birth Weight Differences

C. Marsit, Shouneng Peng, M. Deyssenroth, 2022, Frontiers in Genetics.

Electrocardiographic left ventricular hypertrophy, β3 adrenergic receptor polymorphism and endpoint of ACEI treatment of hypertension

T. Niu, Xiping Xu, A. Ronnenberg, 2004 .

A candidate gene association study on preterm delivery: application of high-throughput genotyping technology and advanced statistical methods.

Tianhua Niu, Xiping Xu, Xin Xu, 2004, Human molecular genetics.

Single-nucleotide polymorphisms of the KCNS3 gene are significantly associated with airway hyperresponsiveness

T. Niu, Xiping Xu, Z. Fang, 2005, Human Genetics.

SNPkit: an efficient approach to systematic evaluation of candidate single nucleotide polymorphisms in public databases.

T Niu, T. Niu, J Li, 2002, BioTechniques.

beta(3) Adrenergic receptor polymorphism and obesity-related phenotypes in hypertensive patients.

T. Niu, Xiping Xu, A. Ronnenberg, 2004, Obesity research.

Correction: Inferring Loss-of-Heterozygosity from Unpaired Tumors Using High-Density Oligonucleotide SNP Arrays

M. Meyerson, W. Sellers, M. Rubin, 2007, PLoS Comput. Biol..

Inferring Loss-of-Heterozygosity from Unpaired Tumors Using High-Density Oligonucleotide SNP Arrays

Wing Hung Wong, Rameen Beroukhim, Levi A Garraway, 2006, PLoS Comput. Biol..

Inferring Loss-of-Heterozygosity From Tumor-only Samples Using High-Density Oligonucleotide SNP Arrays

Wing Hung Wong, Rameen Beroukhim, Edward A. Fox, 2022 .

Estimation of genotype error rate using samples with pedigree information--an application on the GeneChip Mapping 10K array.

Cheng Li, Carsten Rosenow, C. Rosenow, 2004, Genomics.

Erratum: Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays (PLoS Computational Biology 2, 5, doi:10.1371/journal.pcbi.0020041)

Rameen Beroukhim, Edward A. Fox, Mark A. Rubin, 2007 .

Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data

Wing Hung Wong, Carsten Rosenow, W. Wong, 2005, BMC Genetics.

Hypertensive patients from two rural Chinese counties respond differently to benazepril: the Anhui Hypertension Health Care Study.

T. Niu, Xiping Xu, A. Ronnenberg, 2004, Annals of epidemiology.

Detect and adjust for population stratification in population-based association study using genomic control markers: an application of Affymetrix Genechip® Human Mapping 10K array

W. Wong, C. Rosenow, Cheng Li, 2004, European Journal of Human Genetics.

Heart rate-corrected QT interval duration is significantly associated with blood pressure in Chinese hypertensives.

Xiping Xu, Jianping Li, Yan Zhang, 2006, Journal of electrocardiology.

Power estimation of multiple SNP association test of case‐control study and application

Xiping Xu, Xin Xu, Xiping Xu, 2004, Genetic epidemiology.

Genome-wide selection of tag SNPs using multiple-marker correlation

K. Hao, K. Hao, 2007, Bioinform..

GIGSEA: genotype imputed gene set enrichment analysis using GWAS summary level data

Yuan Shen, Jing Yu, Ke Hao, 2018, Bioinform..

β2 Adrenergic Receptor Gene Arg16Gly Polymorphism is Associated with Therapeutic Efficacy of Benazepril on Essential Hypertension in Chinese

T. Niu, Xiping Xu, Jianping Li, 2004, Clinical and experimental hypertension.

Incorporating Individual Error Rate into Association Test of Unmatched Case-Control Design

Ke Hao, Xiaobin Wang, K. Hao, 2005, Human Heredity.

A sparse marker extension tree algorithm for selecting the best set of haplotype tagging single nucleotide polymorphisms

T. Niu, Simin Liu, K. Hao, 2005, Genetic epidemiology.