Whole-Exome Sequencing for the Identification of Susceptibility Genes of Kashin–Beck Disease

CD2AP in mouse and human podocytes controls a proteolytic program that regulates cytoskeletal structure and cellular survival

(2012) Suma Yaddanapudi et al.   JOURNAL OF CLINICAL INVESTIGATION

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

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

(2011) Adam C Naj et al.   NATURE GENETICS

Genome-Wide Gene Expression Analysis Suggests an Important Role of Hypoxia in the Pathogenesis of Endemic Osteochondropathy Kashin-Beck Disease

(2011) Feng Zhang et al.   PLoS One

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

Whole-exome sequencing: a powerful technique for identifying novel genes of complex disorders

(2010) SS Sanders   CLINICAL GENETICS

Exome sequencing: the sweet spot before whole genomes

(2010) J. K. Teer et al.   HUMAN MOLECULAR GENETICS

Rac1 Recruits the Adapter Protein CMS/CD2AP to Cell-Cell Contacts

(2010) Trynette J. van Duijn et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

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

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

Whole exome capture in solution with 3 Gbp of data

(2010) Matthew N Bainbridge et al.   GENOME BIOLOGY

Structure–Function Relations, Physiological Roles, and Evolution of Mammalian ER-Resident Selenoproteins

(2009) Valentina A. Shchedrina et al.   ANTIOXIDANTS & REDOX SIGNALING

SOAP2: an improved ultrafast tool for short read alignment

(2009) R. Li et al.   BIOINFORMATICS

SNP detection for massively parallel whole-genome resequencing

(2009) R. Li et al.   GENOME RESEARCH

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