Publications:

A prognostic risk model for glioma patients by systematic evaluation of genomic variations.

Iscience

Zhang, Baifeng B; Wan, Weiqing W; Li, Zibo Z; Gao, Zhixian Z; Ji, Nan N; Xie, Jian J; Wang, Junmei J; Wang, Bin B; Lai-Wan Kwong, Dora D; Guan, Xinyuan X; Gao, Shengjie S; Zhao, Yuanli Y; Lu, Youyong Y; Zhang, Liwei L; Rodland, Karin D KD; Tsang, Shirley X SX

Publication Date: 2022-12-22

Variant appearance in text: RPL3L: V360M

PubMed Link: 36536675

Variant Present in the following documents:

• mmc3.xls, sheet 1

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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: RPL3L: V360M

PubMed Link: 35136070

Variant Present in the following documents:

• 41467_2022_28411_MOESM4_ESM.xlsx, sheet 1

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Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.

Communications Biology

Thorolfsdottir, Rosa B RB; Sveinbjornsson, Gardar G; Sulem, Patrick P; Nielsen, Jonas B JB; Jonsson, Stefan S; Halldorsson, Gisli H GH; Melsted, Pall P; Ivarsdottir, Erna V EV; Davidsson, Olafur B OB; Kristjansson, Ragnar P RP; Thorleifsson, Gudmar G; Helgadottir, Anna A; Gretarsdottir, Solveig S; Norddahl, Gudmundur G; Rajamani, Sridharan S; Torfason, Bjarni B; Valgardsson, Atli S AS; Sverrisson, Jon T JT; Tragante, Vinicius V; Holmen, Oddgeir L OL; Asselbergs, Folkert W FW; Roden, Dan M DM; Darbar, Dawood D; Pedersen, Terje R TR; Sabatine, Marc S MS; Willer, Cristen J CJ; Løchen, Maja-Lisa ML; Halldorsson, Bjarni V BV; Jonsdottir, Ingileif I; Hveem, Kristian K; Arnar, David O DO; Thorsteinsdottir, Unnur U; Gudbjartsson, Daniel F DF; Holm, Hilma H; Stefansson, Kari K

Publication Date: 2018

Variant appearance in text: RPL3L: Val360Met; rs140116056

PubMed Link: 30271950

Variant Present in the following documents:

• 42003_2018_68_MOESM1_ESM.pdf

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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: RPL3L: V360M

PubMed Link: 25356899

Variant Present in the following documents:

• pgen.1004772.s004.xlsx, sheet 38

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NCI-60 whole exome sequencing and pharmacological CellMiner analyses.

Plos One

Reinhold, William C WC; Varma, Sudhir S; Sousa, Fabricio F; Sunshine, Margot M; Abaan, Ogan D OD; Davis, Sean R SR; Reinhold, Spencer W SW; Kohn, Kurt W KW; Morris, Joel J; Meltzer, Paul S PS; Doroshow, James H JH; Pommier, Yves Y

Publication Date: 2014

Variant appearance in text: RPL3L: V360M; rs140116056

PubMed Link: 25032700

Variant Present in the following documents:

• pone.0101670.s004.xlsx, sheet 1

View BVdb publication page