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wang jia lin[Author]
(141 results)?
Towards a reference genome that captures global genetic diversity.
Nat Commun. 2020 Oct 30;11(1):5482. doi: 10.1038/s41467-020-19311-w.
Nat Commun. 2020.
PMID: 33127893
Free PMC article.
Identification of an 85-kb Heterozygous 4p Microdeletion With Full Genome Analysis in Autosomal Dominant Charcot-Marie-Tooth Disease.
Hsueh HW, Kao HJ, Chao CC, Hsueh SJ, Huang YN, Lin WJ, Su JP, Shy HT, Yeh TY, Lin CC, Kwok PY, Lee NC, Hsieh ST.
Hsueh HW, et al. Among authors: lin wj.
Neurol Genet. 2023 Jun 16;9(4):e200078. doi: 10.1212/NXG.0000000000200078. eCollection 2023 Aug.
Neurol Genet. 2023.
PMID: 37346931
Free PMC article.
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Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese.
Wei CY, Yang JH, Yeh EC, Tsai MF, Kao HJ, Lo CZ, Chang LP, Lin WJ, Hsieh FJ, Belsare S, Bhaskar A, Su MW, Lee TC, Lin YL, Liu FT, Shen CY, Li LH, Chen CH, Wall JD, Wu JY, Kwok PY.
Wei CY, et al. Among authors: lin wj.
NPJ Genom Med. 2021 Feb 11;6(1):10. doi: 10.1038/s41525-021-00178-9.
NPJ Genom Med. 2021.
PMID: 33574314
Free PMC article.
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Highly efficient capture approach for the identification of diverse inherited retinal disorders.
Kao HJ, Lin TY, Hsieh FJ, Chien JY, Yeh EC, Lin WJ, Chen YH, Ding KH, Yang Y, Chi SC, Tsai PH, Hsu CC, Hwang DK, Tsai HY, Peng ML, Lee SH, Chau SF, Chen CY, Cheang WM, Chen SJ, Kwok PY, Chiou SH, Lu MJ, Huang SP.
Kao HJ, et al. Among authors: lin wj.
NPJ Genom Med. 2024 Jan 9;9(1):4. doi: 10.1038/s41525-023-00388-3.
NPJ Genom Med. 2024.
PMID: 38195571
Free PMC article.
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VarioWatch: providing large-scale and comprehensive annotations on human genomic variants in the next generation sequencing era.
Cheng YC, Hsiao FC, Yeh EC, Lin WJ, Tang CY, Tseng HC, Wu HT, Liu CK, Chen CC, Chen YT, Yao A.
Cheng YC, et al. Among authors: lin wj.
Nucleic Acids Res. 2012 Jul;40(Web Server issue):W76-81. doi: 10.1093/nar/gks397. Epub 2012 May 22.
Nucleic Acids Res. 2012.
PMID: 22618869
Free PMC article.
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