Associated Papers
Genetic Variants Associated with Chronic Obstructive Pulmonary Disease Risk: Cumulative Epidemiological Evidence from Meta-Analyses and Genome-Wide Association Studies.
Liu C et al.
Canadian Respiratory Journal, 2022
Whole-Exome Sequencing Analysis of Oral Squamous Cell Carcinoma Delineated by Tobacco Usage Habits.
Patel K et al.
Frontiers in Oncology, 2021
34136393 (PubMed )
Supplement: Table_4.pdf
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia.
Fontana D et al.
Hemasphere, 2020
33196013 (PubMed )
Supplement: hs9-4-e497-s008.xlsx › Sheet1
Interrogating Mutant Allele Expression via Customized Reference Genomes to Define Influential Cancer Mutations.
Grant AD et al.
Scientific Reports, 2019
31484939 (PubMed )
Supplement: 41598_2019_48967_MOESM2_ESM.xls › Supplementary_Variant_File
Extracellular matrix remodeling genes polymorphisms and risk of chronic bronchitis and recurrent pneumonia in children.
Korytina GF et al.
Journal of Human Genetics, 2013
The COPD genetic association compendium: a comprehensive online database of COPD genetic associations.
Castaldi PJ et al.
Human Molecular Genetics, 2010
Single nucleotide polymorphisms of RXRA encoding retinoid X receptor alpha.
Hegele RA et al.
Journal of Human Genetics, 2001
An association study of polymorphisms in the alpha-antichymotrypsin gene for Alzheimer disease in Han-Chinese.
Meng G et al.
Human Mutation, 2000
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