Publications:

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A narrative review of precision medicine in neonatal sepsis: genetic and epigenetic factors associated with disease susceptibility.

Translational Pediatrics

Dai, Wenjuan W; Zhou, Wenhao W

Publication Date: 2023-04-29

Variant appearance in text: rs2239815

PubMed Link: 37181024

Variant Present in the following documents:

• Main text
• tp-12-04-749.pdf

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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: rs2239815

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations.

Frontiers In Genetics

Simba, Hannah H; Kuivaniemi, Helena H; Lutje, Vittoria V; Tromp, Gerard G; Sewram, Vikash V

Publication Date: 2019

Variant appearance in text: rs2239815

PubMed Link: 31428123

Variant Present in the following documents:

• Main text
• fgene-10-00642.pdf

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Cumulative evidence for association between genetic polymorphisms and esophageal cancer susceptibility: A review with evidence from meta-analysis and genome-wide association studies.

Cancer Medicine

Tian, Jie J; Liu, Caiyang C; Liu, Guanchu G; Zuo, Chunjian C; Chen, Huanwen H

Publication Date: 2019-03

Variant appearance in text: rs2239815

PubMed Link: 30793520

Variant Present in the following documents:

• Main text

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Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.

Carcinogenesis

Chen, Wenlong C WC; Bye, Hannah H; Matejcic, Marco M; Amar, Ariella A; Govender, Dhiren D; Khew, Yee Wen YW; Beynon, Victoria V; Kerr, Robyn R; Singh, Elvira E; Prescott, Natalie J NJ; Lewis, Cathryn M CM; Babb de Villiers, Chantal C; Parker, M Iqbal MI; Mathew, Christopher G CG

Publication Date: 2019-06-10

Variant appearance in text: rs2239815

PubMed Link: 30753320

Variant Present in the following documents:

• Main text
• bgz026.pdf

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Are mTOR and Endoplasmic Reticulum Stress Pathway Genes Associated with Oral and Bone Diseases?

Caries Research

Bezamat, Mariana M; Deeley, Kathleen K; Khaliq, Shahryar S; Letra, Ariadne A; Scariot, Rafaela R; Silva, Renato M RM; Weber, Megan L ML; Bussaneli, Diego G DG; Trevilatto, Paula C PC; Almarza, Alejandro J AJ; Ouyang, Hongjiao H; Vieira, Alexandre R AR

Publication Date: 2019

Variant appearance in text: rs2239815

PubMed Link: 30205378

Variant Present in the following documents:

• Main text

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Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases

Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ

Publication Date: 2017-05-23

Variant appearance in text: rs2239815

PubMed Link: 28535796

Variant Present in the following documents:

• 13023_2017_647_MOESM1_ESM.xlsx, sheet 4

View BVdb publication page

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs2239815

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

View BVdb publication page

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Integration of VDR genome wide binding and GWAS genetic variation data reveals co-occurrence of VDR and NF-κB binding that is linked to immune phenotypes.

Bmc Genomics

Singh, Prashant K PK; van den Berg, Patrick R PR; Long, Mark D MD; Vreugdenhil, Angie A; Grieshober, Laurie L; Ochs-Balcom, Heather M HM; Wang, Jianmin J; Delcambre, Sylvie S; Heikkinen, Sami S; Carlberg, Carsten C; Campbell, Moray J MJ; Sucheston-Campbell, Lara E LE

Publication Date: 2017-02-06

Variant appearance in text: rs2239815

PubMed Link: 28166722

Variant Present in the following documents:

• Main text
• 12864_2017_Article_3481.pdf

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ADH1B and CDH1 polymorphisms predict prognosis in male patients with non-metastatic laryngeal cancer.

Oncotarget

Li, Daxu D; Zhang, Ruizhi R; Jin, Tianbo T; He, Na N; Ren, Le L; Zhang, Zhe Z; Zhang, Qingna Q; Xu, Ran R; Tao, Hong H; Zeng, Guang G; Gao, Jing J

Publication Date: 2016-11-08

Variant appearance in text: rs2239815

PubMed Link: 27689323

Variant Present in the following documents:

• Main text
• oncotarget-07-73216.pdf

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Genetic variants at 6p21, 10q23, 16q21 and 22q12 are associated with esophageal cancer risk in a Chinese Han population.

International Journal Of Clinical And Experimental Medicine

Jia, Xiaobin X; Liu, Peng P; Zhang, Mingxia M; Feng, Tian T; Tang, Hongtao H; Tang, Zhigang Z; Zhao, Huaqian H; Jin, Tianbo T

Publication Date: 2015

Variant appearance in text: rs2239815

PubMed Link: 26770579

Variant Present in the following documents:

• Main text

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Altered Gene Expression Associated with microRNA Binding Site Polymorphisms.

Plos One

Võsa, Urmo U; Esko, Tõnu T; Kasela, Silva S; Annilo, Tarmo T

Publication Date: 2015

Variant appearance in text: rs2239815

PubMed Link: 26496489

Variant Present in the following documents:

• Main text

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