Associated Papers
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
Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1.
Sung H et al.
Molecular Genetics & Genomic Medicine, 2020
Somatic mutation driven codon transition bias in human cancer.
Son H et al.
Scientific Reports, 2017
29079855 (PubMed )
Supplement: 41598_2017_14543_MOESM1_ESM.pdf
Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.
Shankar GM et al.
Acta Neuropathologica Communications, 2014
25589003 (PubMed )
Supplement: 40478_2014_167_MOESM1_ESM.xlsx › Supplementary_Table_6
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