Deletion Variants ofRABGAP1L, 10q21.3, andC4Are Associated With the Risk of Systemic Lupus Erythematosus in Korean Women

CNVRuler: a copy number variation-based case–control association analysis tool

(2012) Ji-Hong Kim et al.   BIOINFORMATICS

Copy Number Analysis of Complement C4A, C4B and C4A Silencing Mutation by Real-Time Quantitative Polymerase Chain Reaction

(2012) Riitta Paakkanen et al.   PLoS One

Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms

(2011) Catarina D. Campbell et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic analyses of interferon pathway-related genes reveal multiple new loci associated with systemic lupus erythematosus

(2011) Paula S. Ramos et al.   ARTHRITIS AND RHEUMATISM

Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population

(2011) Yongmei Lv et al.   RHEUMATOLOGY INTERNATIONAL

The potential role of VPREB1 gene copy number variation in susceptibility to rheumatoid arthritis

(2010) Seon-Hee Yim et al.   MOLECULAR IMMUNOLOGY

Genetic susceptibility to systemic lupus erythematosus in the genomic era

(2010) Yun Deng et al.   Nature Reviews Rheumatology

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

(2010) Andrew E. Dellinger et al.   NUCLEIC ACIDS RESEARCH

Copy number variants in genetic susceptibility and severity of systemic lupus erythematosus

(2009) T. Ptacek et al.   CYTOGENETIC AND GENOME RESEARCH

NA-Seq: A Discovery Tool for the Analysis of Chromatin Structure and Dynamics during Differentiation

(2009) Gaetano Gargiulo et al.   DEVELOPMENTAL CELL

Copy number variations in East-Asian population and their evolutionary and functional implications

(2009) S.-H. Yim et al.   HUMAN MOLECULAR GENETICS

FCGR3B copy number variation is not associated with lupus nephritis in a Chinese population

(2009) J. Lv et al.   LUPUS

RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome

(2009) Maria Cristina Roberti et al.   VIRCHOWS ARCHIV

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

(2008) Steven A McCarroll et al.   NATURE GENETICS