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: rs2071002

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition.

Bmc Genomics

Gupta, Hemant H; Chandratre, Khyati K; Sinha, Siddharth S; Huang, Teng T; Wu, Xiaobing X; Cui, Jian J; Zhang, Michael Q MQ; Wang, San Ming SM

Publication Date: 2020-11-30

Variant appearance in text: rs2071002

PubMed Link: 33256598

Variant Present in the following documents:

• 12864_2020_7222_MOESM2_ESM.xlsx, sheet 2

View BVdb publication page

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Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women.

Journal Of Breast Cancer

Sirisena, Nirmala Dushyanthi ND; Adeyemo, Adebowale A; Kuruppu, Anchala Ishani AI; Samaranayake, Nilakshi N; Dissanayake, Vajira Harshadeva Weerabaddana VHW

Publication Date: 2018-06

Variant appearance in text: NQO2: -102A>C; rs2071002

PubMed Link: 29963112

Variant Present in the following documents:

• Main text
• jbc-21-165.pdf

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Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Human Genomics

Karageorgos, Ioannis I; Mizzi, Clint C; Giannopoulou, Efstathia E; Pavlidis, Cristiana C; Peters, Brock A BA; Zagoriti, Zoi Z; Stenson, Peter D PD; Mitropoulos, Konstantinos K; Borg, Joseph J; Kalofonos, Haralabos P HP; Drmanac, Radoje R; Stubbs, Andrew A; van der Spek, Peter P; Cooper, David N DN; Katsila, Theodora T; Patrinos, George P GP

Publication Date: 2015-06-20

Variant appearance in text: rs2071002

PubMed Link: 26092435

Variant Present in the following documents:

• 40246_2015_34_MOESM1_ESM.xlsx, sheet 2

View BVdb publication page

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Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs.

Bmc Genomics

Zhang, Xiaoling X; Gierman, Hinco J HJ; Levy, Daniel D; Plump, Andrew A; Dobrin, Radu R; Goring, Harald H H HH; Curran, Joanne E JE; Johnson, Matthew P MP; Blangero, John J; Kim, Stuart K SK; O'Donnell, Christopher J CJ; Emilsson, Valur V; Johnson, Andrew D AD

Publication Date: 2014-06-27

Variant appearance in text: rs2071002

PubMed Link: 24973796

Variant Present in the following documents:

• Main text
• 12864_2013_Article_6258.pdf

View BVdb publication page

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Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data.

Plos One

Bryzgalov, Leonid O LO; Antontseva, Elena V EV; Matveeva, Marina Yu MY; Shilov, Alexander G AG; Kashina, Elena V EV; Mordvinov, Viatcheslav A VA; Merkulova, Tatyana I TI

Publication Date: 2013

Variant appearance in text: rs2071002

PubMed Link: 24205329

Variant Present in the following documents:

• Main text
• pone.0078833.pdf

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NAD(P)H: quinone oxidoreductase 1 and NRH:quinone oxidoreductase 2 polymorphisms in papillary thyroid microcarcinoma: correlation with phenotype.

Yonsei Medical Journal

Lee, Junguee J; Kim, Koon Soon KS; Lee, Min Ho MH; Kim, Yeon Soo YS; Lee, Min Hee MH; Lee, Seong Eun SE; Kim, Yong Kyung YK; Ryu, Min Jeong MJ; Kim, Soung Jung SJ; Choi, Min Jeong MJ; Jo, Young Suk YS

Publication Date: 2013-09

Variant appearance in text: rs2071002

PubMed Link: 23918565

Variant Present in the following documents:

• Main text
• ymj-54-1158.pdf

View BVdb publication page

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