Publications:

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs210139

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs210139

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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Fine-mapping of HLA class I and class II genes identified two independent novel variants associated with nasopharyngeal carcinoma susceptibility.

Cancer Medicine

Wang, Tong-Min TM; Zhou, Ting T; He, Yong-Qiao YQ; Xue, Wen-Qiong WQ; Zhang, Jiang-Bo JB; Zheng, Xiao-Hui XH; Li, Xi-Zhao XZ; Zhang, Shao-Dan SD; Zeng, Yi-Xin YX; Jia, Wei-Hua WH

Publication Date: 2018-12

Variant appearance in text: rs210139

PubMed Link: 30378292

Variant Present in the following documents:

• CAM4-7-6308-s006.xlsx, sheet 1

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Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.

Nature Genetics

Auer, Paul L PL; Teumer, Alexander A; Schick, Ursula U; O'Shaughnessy, Andrew A; Lo, Ken Sin KS; Chami, Nathalie N; Carlson, Chris C; de Denus, Simon S; Dubé, Marie-Pierre MP; Haessler, Jeff J; Jackson, Rebecca D RD; Kooperberg, Charles C; Perreault, Louis-Philippe Lemieux LP; Nauck, Matthias M; Peters, Ulrike U; Rioux, John D JD; Schmidt, Frank F; Turcot, Valérie V; Völker, Uwe U; Völzke, Henry H; Greinacher, Andreas A; Hsu, Li L; Tardif, Jean-Claude JC; Diaz, George A GA; Reiner, Alexander P AP; Lettre, Guillaume G

Publication Date: 2014-06

Variant appearance in text: rs210139

PubMed Link: 24777453

Variant Present in the following documents:

• NIHMS581495-supplement-1.pdf

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Association of genetic markers in the BCL-2 family of apoptosis-related genes with endometrial cancer risk in a Chinese population.

Plos One

Dorjgochoo, Tsogzolmaa T; Xiang, Yong-Bing YB; Long, Jirong J; Shi, Jiajun J; Deming, Sandra S; Xu, Wang-Hong WH; Cai, Hui H; Cheng, Jiarong J; Cai, Qiuyin Q; Zheng, Wei W; Shu, Xiao-Ou XO

Publication Date: 2013

Variant appearance in text: rs210139

PubMed Link: 23637776

Variant Present in the following documents:

• Main text
• pone.0060915.pdf

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A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility.

Human Molecular Genetics

Kanetsky, Peter A PA; Mitra, Nandita N; Vardhanabhuti, Saran S; Vaughn, David J DJ; Li, Mingyao M; Ciosek, Stephanie L SL; Letrero, Richard R; D'Andrea, Kurt K; Vaddi, Madhavi M; Doody, David R DR; Weaver, Joellen J; Chen, Chu C; Starr, Jacqueline R JR; Håkonarson, Håkon H; Rader, Daniel J DJ; Godwin, Andrew K AK; Reilly, Muredach P MP; Schwartz, Stephen M SM; Nathanson, Katherine L KL

Publication Date: 2011-08-01

Variant appearance in text: rs210139

PubMed Link: 21551455

Variant Present in the following documents:

• Main text

View BVdb publication page

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