Publications:

SMAP is a pipeline for sample matching in proteogenomics.

Nature Communications

Li, Ling L; Niu, Mingming M; Erickson, Alyssa A; Luo, Jie J; Rowbotham, Kincaid K; Guo, Kai K; Huang, He H; Li, Yuxin Y; Jiang, Yi Y; Hur, Junguk J; Liu, Chunyu C; Peng, Junmin J; Wang, Xusheng X

Publication Date: 2022-02-08

Variant appearance in text: TRDN: A367T

PubMed Link: 35136070

Variant Present in the following documents:

• 41467_2022_28411_MOESM4_ESM.xlsx, sheet 1

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TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw.

Nature Communications

Gomes, Carolina Cavalieri CC; Gayden, Tenzin T; Bajic, Andrea A; Harraz, Osama F OF; Pratt, Jonathan J; Nikbakht, Hamid H; Bareke, Eric E; Diniz, Marina Gonçalves MG; Castro, Wagner Henriques WH; St-Onge, Pascal P; Sinnett, Daniel D; Han, HyeRim H; Rivera, Barbara B; Mikael, Leonie G LG; De Jay, Nicolas N; Kleinman, Claudia L CL; Valera, Elvis Terci ET; Bassenden, Angelia V AV; Berghuis, Albert M AM; Majewski, Jacek J; Nelson, Mark T MT; Gomez, Ricardo Santiago RS; Jabado, Nada N

Publication Date: 2018-11-01

Variant appearance in text: TRDN: A367T

PubMed Link: 30385747

Variant Present in the following documents:

• 41467_2018_6690_MOESM8_ESM.xlsx, sheet 1

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Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer.

Ebiomedicine

Yu, Xian-Jun XJ; Yang, Min-Jun MJ; Zhou, Bo B; Wang, Gui-Zhen GZ; Huang, Yun-Chao YC; Wu, Li-Chuan LC; Cheng, Xin X; Wen, Zhe-Sheng ZS; Huang, Jin-Yan JY; Zhang, Yun-Dong YD; Gao, Xiao-Hong XH; Li, Gao-Feng GF; He, Shui-Wang SW; Gu, Zhao-Hui ZH; Ma, Liang L; Pan, Chun-Ming CM; Wang, Ping P; Chen, Hao-Bin HB; Hong, Zhi-Peng ZP; Wang, Xiao-Lu XL; Mao, Wen-Jing WJ; Jin, Xiao-Long XL; Kang, Hui H; Chen, Shu-Ting ST; Zhu, Yong-Qiang YQ; Gu, Wen-Yi WY; Liu, Zi Z; Dong, Hui H; Tian, Lin-Wei LW; Chen, Sai-Juan SJ; Cao, Yi Y; Wang, Sheng-Yue SY; Zhou, Guang-Biao GB

Publication Date: 2015-06

Variant appearance in text: TRDN: A367T

PubMed Link: 26288819

Variant Present in the following documents:

• mmc5.xlsx, sheet 2

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De novo mutations in moderate or severe intellectual disability.

Plos Genetics

Hamdan, Fadi F FF; Srour, Myriam M; Capo-Chichi, Jose-Mario JM; Daoud, Hussein H; Nassif, Christina C; Patry, Lysanne L; Massicotte, Christine C; Ambalavanan, Amirthagowri A; Spiegelman, Dan D; Diallo, Ousmane O; Henrion, Edouard E; Dionne-Laporte, Alexandre A; Fougerat, Anne A; Pshezhetsky, Alexey V AV; Venkateswaran, Sunita S; Rouleau, Guy A GA; Michaud, Jacques L JL

Publication Date: 2014-10

Variant appearance in text: TRDN: A367T

PubMed Link: 25356899

Variant Present in the following documents:

• pgen.1004772.s004.xlsx, sheet 19

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