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: MTHFD1: I464V

PubMed Link: 35136070

Variant Present in the following documents:

• 41467_2022_28411_MOESM4_ESM.xlsx, sheet 1

View BVdb publication page

Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.

Jama Network Open

Patel, Devanshi D; Mez, Jesse J; Vardarajan, Badri N BN; Staley, Lyndsay L; Chung, Jaeyoon J; Zhang, Xiaoling X; Farrell, John J JJ; Rynkiewicz, Michael J MJ; Cannon-Albright, Lisa A LA; Teerlink, Craig C CC; Stevens, Jeffery J; Corcoran, Christopher C; Gonzalez Murcia, Josue D JD; Lopez, Oscar L OL; Mayeux, Richard R; Haines, Jonathan L JL; Pericak-Vance, Margaret A MA; Schellenberg, Gerard G; Kauwe, John S K JSK; Lunetta, Kathryn L KL; Farrer, Lindsay A LA; ,

Publication Date: 2019-03-01

Variant appearance in text: rs139264994

PubMed Link: 30924900

Variant Present in the following documents:

• jamanetwopen-2-e191350-s001.pdf

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Detecting protein variants by mass spectrometry: a comprehensive study in cancer cell-lines.

Genome Medicine

Alfaro, Javier A JA; Ignatchenko, Alexandr A; Ignatchenko, Vladimir V; Sinha, Ankit A; Boutros, Paul C PC; Kislinger, Thomas T

Publication Date: 2017-07-18

Variant appearance in text: MTHFD1: I464V; rs139264994

PubMed Link: 28716134

Variant Present in the following documents:

• 13073_2017_454_MOESM7_ESM.xlsx, sheet 1

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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Scientific Reports

Chen, Xiaowei Sylvia XS; Reader, Rose H RH; Hoischen, Alexander A; Veltman, Joris A JA; Simpson, Nuala H NH; Francks, Clyde C; Newbury, Dianne F DF; Fisher, Simon E SE

Publication Date: 2017-04-25

Variant appearance in text: MTHFD1: I464V; rs139264994

PubMed Link: 28440294

Variant Present in the following documents:

• srep46105-s2.xls, sheet 8

View BVdb publication page