Publications:

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.

Genome Medicine

Cao, Ye Y; Tokita, Mari J MJ; Chen, Edward S ES; Ghosh, Rajarshi R; Chen, Tiansheng T; Feng, Yanming Y; Gorman, Elizabeth E; Gibellini, Federica F; Ward, Patricia A PA; Braxton, Alicia A; Wang, Xia X; Meng, Linyan L; Xiao, Rui R; Bi, Weimin W; Xia, Fan F; Eng, Christine M CM; Yang, Yaping Y; Gambin, Tomasz T; Shaw, Chad C; Liu, Pengfei P; Stankiewicz, Pawel P

Publication Date: 2019-07-26

Variant appearance in text: KRAS: S171F

PubMed Link: 31349857

Variant Present in the following documents:

• Main text

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Comprehensive targeted super-deep next generation sequencing enhances differential diagnosis of solitary pulmonary nodules.

Journal Of Thoracic Disease

Ye, Mingzhi M; Li, Shiyong S; Huang, Weizhe W; Wang, Chunli C; Liu, Liping L; Liu, Jun J; Liu, Jilong J; Pan, Hui H; Deng, Qiuhua Q; Tang, Hailing H; Jiang, Long L; Huang, Weizhe W; Chen, Xi X; Shao, Di D; Peng, Zhiyu Z; Wu, Renhua R; Zhong, Jing J; Wang, Zhe Z; Zhang, Xiaoping X; Kristiansen, Karsten K; Wang, Jian J; Yin, Ye Y; Mao, Mao M; He, Jianxing J; Liang, Wenhua W

Publication Date: 2018-04

Variant appearance in text: KRAS: Ser171Phe

PubMed Link: 29780628

Variant Present in the following documents:

• Main text

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