Associated Papers
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
39991480 (PubMed )
Supplement: mmc5.xlsx › Sheet1
Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
Liu Y et al.
Bmc Oral Health, 2024
38280992 (PubMed )
Supplement: 12903_2024_3888_MOESM2_ESM.xls › Supplementary_Table_1
Molecular characterization of sub-frontal recurrent medulloblastomas reveals potential clinical relevance.
Chen Z et al.
Frontiers in Neurology, 2023
37181548 (PubMed )
Supplement: Data_Sheet_2.xlsx › Germline_mutation-case_1
Molecular characterization and integrative genomic analysis of a panel of newly established penile cancer cell lines.
Zhou QH et al.
Cell Death & Disease, 2018
29880898 (PubMed )
Supplement: 41419_2018_736_MOESM8_ESM.xlsx › Sheet1
Missense Variants in HIF1A and LACC1 Contribute to Leprosy Risk in Han Chinese.
Wang D et al.
American Journal of Human Genetics, 2018
Comprehensive investigating of cytokine and receptor related genes variants in patients with chronic hepatitis B virus infection.
Yu F et al.
Cytokine, 2018
Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits.
Mansilla MA et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies, 2005
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