Publications:

An EGFR L858R mutation identified in 1862 Chinese NSCLC patients can be a promising neoantigen vaccine therapeutic strategy.

Frontiers In Immunology

Lin, Jing J; Liu, Jun J; Hao, Shi-Guang SG; Lan, Bin B; Zheng, Xiao-Bin XB; Xiong, Jia-Ni JN; Zhang, Ying-Qian YQ; Gao, Xuan X; Chen, Chuan-Ben CB; Chen, Ling L; Huang, Yu-Fang YF; Luo, Hong H; Yi, Yu-Ting YT; Yi, Xin X; Lu, Jian-Ping JP; Zheng, Xiong-Wei XW; Chen, Gang G; Wang, Xue-Feng XF; Chen, Yu Y

Publication Date: 2022

Variant appearance in text: POLE: 2123A>G; H708R

PubMed Link: 36505399

Variant Present in the following documents:

• Table_2.xlsx, sheet 3
• Table_2.xlsx, sheet 2

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Clinical and genomic features of Chinese lung cancer patients with germline mutations.

Nature Communications

Peng, Wenying W; Li, Bin B; Li, Jin J; Chang, Lianpeng L; Bai, Jing J; Yi, Yuting Y; Chen, Rongrong R; Zhang, Yanyan Y; Chen, Chen C; Pu, Xingxiang X; Jiang, Meilin M; Li, Jia J; Zhong, Rui R; Xu, Fang F; Chen, Bolin B; Xu, Li L; Wang, Ning N; Huan, Jiaojiao J; Dai, Pingping P; Guan, Yanfang Y; Yang, Ling L; Xia, Xuefeng X; Yi, Xin X; Wang, Jiayin J; Yu, Fenglei F; Wu, Lin L

Publication Date: 2022-03-10

Variant appearance in text: POLE: 2123A>G; H708R

PubMed Link: 35273153

Variant Present in the following documents:

• 41467_2022_28840_MOESM7_ESM.xlsx, sheet 1

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Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study.

Familial Cancer

Postema, Floor A M FAM; Hopman, Saskia M J SMJ; de Borgie, Corianne A J M CAJM; Aalfs, Cora M CM; Anninga, Jakob K JK; Berger, Lieke P V LPV; Bleeker, Fonnet E FE; Dommering, Charlotte J CJ; van Eijkelenburg, Natasha K A NKA; Hammond, Peter P; van den Heuvel-Eibrink, Marry M MM; Hol, Janna A JA; Kors, Wijnanda A WA; Letteboer, Tom G W TGW; Loeffen, Jan L C M JLCM; Meijer, Lisethe L; Olderode-Berends, Maran J W MJW; Wagner, Anja A; Hennekam, Raoul C RC; Merks, Johannes H M JHM

Publication Date: 2021-10

Variant appearance in text: POLE: 2123A>G; His708Arg

PubMed Link: 33686467

Variant Present in the following documents:

• 10689_2021_Article_237.pdf

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Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study.

Familial Cancer

Postema, Floor A M FAM; Hopman, Saskia M J SMJ; de Borgie, Corianne A J M CAJM; Aalfs, Cora M CM; Anninga, Jakob K JK; Berger, Lieke P V LPV; Bleeker, Fonnet E FE; Dommering, Charlotte J CJ; van Eijkelenburg, Natasha K A NKA; Hammond, Peter P; van den Heuvel-Eibrink, Marry M MM; Hol, Janna A JA; Kors, Wijnanda A WA; Letteboer, Tom G W TGW; Loeffen, Jan L C M JLCM; Meijer, Lisethe L; Olderode-Berends, Maran J W MJW; Wagner, Anja A; Hennekam, Raoul C RC; Merks, Johannes H M JHM

Publication Date: 2021-10

Variant appearance in text: POLE: 2123A>G; His708Arg

PubMed Link: 33686467

Variant Present in the following documents:

• 10689_2021_Article_237.pdf

View BVdb publication page

Finding driver mutations in cancer: Elucidating the role of background mutational processes.

Plos Computational Biology

Brown, Anna-Leigh AL; Li, Minghui M; Goncearenco, Alexander A; Panchenko, Anna R AR

Publication Date: 2019-04

Variant appearance in text: POLE: H708R

PubMed Link: 31034466

Variant Present in the following documents:

• pcbi.1006981.s010.xlsx, sheet 1

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