Xiang Qin, Ph.D.
Publications
Variants in genes coding for collagen type IV α-chains are frequent causes of persistent, isolated hematuria during childhood. Pediatr Nephrol. 2023;38(3):687-695.
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An efficient genotyper and star-allele caller for pharmacogenomics. Genome Res. 2023;33(1):61-70.
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CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project. J Mol Diagn. 2022;24(4):337-350.
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Transmission event of SARS-CoV-2 delta variant reveals multiple vaccine breakthrough infections. BMC Med. 2021;19(1):255.
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Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals. PLoS One. 2021;16(8):e0244468.
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Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol). Int J Epidemiol. 2020;49(1):23-24k.
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Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes. Nat Commun. 2018;9(1):828.
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PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation. Pharmacogenet Genomics. 2016;.
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Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines. Pharmacogenomics J. 2016;.
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Convergent evolution of the genomes of marine mammals. Nat Genet. 2015;47(3):272-5.
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Generation and characterization of antibodies against Asian elephant (Elephas maximus) IgG, IgM, and IgA. PLoS One. 2015;10(2):e0116318.
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