Genome-wide copy number variation study and gene expression analysis identify ABI3BP as a susceptibility gene for Kashin–Beck disease

Association of TNF-α and Fas gene promoter polymorphism with the risk of Kashin–Beck disease in Northwest Chinese population

(2012) Quan-ming Zhao et al.   CLINICAL RHEUMATOLOGY

Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study

(2012) Yan-Fang Guo et al.   HUMAN GENETICS

Copy Number Variation on Chromosome 10q26.3 for Obesity Identified by a Genome-Wide Study

(2012) Tie-Lin Yang et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD

(2011) Evangelia Stergiakouli et al.   AMERICAN JOURNAL OF PSYCHIATRY

Genetic variants in the HLA-DRB1 gene are associated with Kashin-Beck disease in the Tibetan population

(2011) Yi Shi et al.   ARTHRITIS AND RHEUMATISM

SNP and mRNA expression for glutathione peroxidase 4 in Kashin-Beck disease

(2011) Xiao Hong Du et al.   BRITISH JOURNAL OF NUTRITION

Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies

(2011) Dalin Li et al.   GENETIC EPIDEMIOLOGY

Comparative analysis of gene expression profiles between primary knee osteoarthritis and an osteoarthritis endemic to Northwestern China, Kashin-Beck disease

(2010) Chen Duan et al.   ARTHRITIS AND RHEUMATISM

Kashin–Beck disease and Sayiwak disease in China: Prevalence and a comparison of the clinical manifestations, familial aggregation, and heritability

(2010) A.L. Lü et al.   BONE

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis

(2010) Ivonne Jarick et al.   HUMAN MOLECULAR GENETICS

The effect of Kashin-Beck disease-affected feed and T-2 toxin on the bone development of Wistar rats

(2010) Denglu YAN et al.   International Journal of Rheumatic Diseases

Association study between polymorphisms in selenoprotein genes and susceptibility to Kashin-Beck disease

(2010) Y.M. Xiong et al.   OSTEOARTHRITIS AND CARTILAGE

Heritability estimates and linkage analysis of 23 short tandem repeat loci on chromosomes 2, 11, and 12 in an endemic osteochondropathy in China

(2010) XW Shi et al.   SCANDINAVIAN JOURNAL OF RHEUMATOLOGY

Inferring weak population structure with the assistance of sample group information

(2009) MELISSA J. HUBISZ et al.   Molecular Ecology Resources

A Medical Mystery in Middle China

(2009) R. Stone   SCIENCE

Osteo-Chondroprogenitor–Specific Deletion of the Selenocysteine tRNA Gene, Trsp, Leads to Chondronecrosis and Abnormal Skeletal Development: A Putative Model for Kashin-Beck Disease

(2009) Charlene M. Downey et al.   PLoS Genetics

Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis

(2008) Tie-Lin Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Integrated detection and population-genetic analysis of SNPs and copy number variation

(2008) Steven A McCarroll et al.   NATURE GENETICS

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS

Comparative analysis of gene expression profiles between the normal human cartilage and the one with endemic osteoarthritis

(2008) W.Z. Wang et al.   OSTEOARTHRITIS AND CARTILAGE