Associated Papers
Association of the single-nucleotide polymorphism in the MFG-E8 gene with coronary heart disease in Chinese Han population.
Wang D et al.
Bmc Cardiovascular Disorders, 2025
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.
Narumi S et al.
Nature Genetics, 2024
38714868 (PubMed )
Supplement: 41588_2024_1735_MOESM3_ESM.xlsx › Supplementary_Table_1
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
38277211 (PubMed )
Supplement: elife-89762-supp1.xlsx › Variants
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
37292598 (PubMed )
Supplement: media-1.xlsx › Variants
Identification of Prognostic and Susceptibility Markers in Chronic Myeloid Leukemia Using Next Generation Sequencing.
Shokeen Y et al.
Ethiopian Journal of Health Sciences, 2018
MFGE8 does not influence chorio-retinal homeostasis or choroidal neovascularization in vivo.
Raoul W et al.
Plos One, 2012
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