Clinical implications of copy number variations in autoimmune disorders
Seon-Hee Yim, Seung-Hyun Jung, Boram Chung, Yeun-Jun Chung
Korean J Intern Med. 2015;30(3):294-304. Published online 2015 Apr 29 DOI: https://doi.org/10.3904/kjim.2015.30.3.294
Citations to this article as recorded by 
Guardians of Immunity: Advances in Primary Immunodeficiency Disorders and Management
Nikhil Chowdary Peddi, Sravya Vuppalapati, Himabindu Sreenivasulu, Sudheer kumar Muppalla, Apeksha Reddy Pulliahgaru
Cureus.2023;[Epub] CrossRef
The pseudogenes of eukaryotic translation elongation factors (EEFs): Role in cancer and other human diseases
Luigi Cristiano
Genes & Diseases.2022; 9(4): 941. CrossRef
An Update Evolving View of Copy Number Variations in Autoimmune Diseases
Rong-hua Song, Chao-qun Gao, Jing Zhao, Jin-an Zhang
Frontiers in Genetics.2022;[Epub] CrossRef
Role of genetics and epigenetics in male infertility
Sezgin Gunes, Sandro C. Esteves
Andrologia.2021;[Epub] CrossRef
Detecting pathogenic variants in autoimmune diseases using highâthroughput sequencing
Matt A Field
Immunology & Cell Biology.2021; 99(2): 146. CrossRef
A cross-comparison of cognitive ability across 8 genomic disorders
Michael Mortillo, Jennifer G Mulle
Current Opinion in Genetics & Development.2021; 68: 106. CrossRef
MCKAT: a multi-dimensional copy number variant kernel association test
Nastaran Maus Esfahani, Daniel Catchpoole, Javed Khan, Paul J. Kennedy
BMC Bioinformatics.2021;[Epub] CrossRef
Genomic alterations driving psoriasis pathogenesis
S. Singh, D. Pradhan, P. Puri, V. Ramesh, S. Aggarwal, A. Nayek, A.K. Jain
Gene.2019; 683: 61. CrossRef
Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease
Svetlana Frenkel, Charles N. Bernstein, Michael Sargent, Qin Kuang, Wenxin Jiang, John Wei, Bhooma Thiruvahindrapuram, Elizabeth Spriggs, Stephen W. Scherer, Pingzhao Hu, Vincenzo De Luca
PLOS ONE.2019; 14(6): e0217846. CrossRef
De novo vs. inherited copy number variations in multiple sclerosis susceptibility
Kalthoum Tizaoui
Cellular & Molecular Immunology.2018; 15(9): 812. CrossRef
Using low-coverage whole genome sequencing technique to analyze the chromosomal copy number alterations in the exfoliative cells of cervical cancer
Tong Ren, Jing Suo, Shikai Liu, Shu Wang, Shan Shu, Yang Xiang, Jing-He Lang
Journal of Gynecologic Oncology.2018;[Epub] CrossRef
Association between FCGR3B copy number variations and susceptibility to autoimmune diseases: a meta-analysis
Young Ho Lee, Sang-Cheol Bae, Young Ho Seo, Jae-Hoon Kim, Sung Jae Choi, Jong Dae Ji, Gwan Gyu Song
Inflammation Research.2015; 64(12): 983. CrossRef