Publications:

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The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival.

Nutrients

Wang, Yu Y; Du, Meizhi M; Vallis, Jillian J; Shariati, Matin M; Parfrey, Patrick S PS; Mclaughlin, John R JR; Wang, Peizhong Peter PP; Zhu, Yun Y

Publication Date: 2022-11-01

Variant appearance in text: rs9332

PubMed Link: 36364857

Variant Present in the following documents:

• nutrients-14-04594.pdf

View BVdb publication page

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Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research

Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C

Publication Date: 2022-10-21

Variant appearance in text: rs9332

PubMed Link: 36269797

Variant Present in the following documents:

• ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1

View BVdb publication page

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MTRR rs1532268 polymorphism and gastric cancer risk: evidence from a meta-analysis.

The Journal Of International Medical Research

Zhong, Guping G; Luo, Xiaojin X; Li, Ji J; Liao, Yuanhang Y; Gui, Guan G; Sheng, Jianwen J

Publication Date: 2022-05

Variant appearance in text: rs9332

PubMed Link: 35579185

Variant Present in the following documents:

• Main text
• 10.1177_03000605221097486.pdf

View BVdb publication page

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: rs9332

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine

Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM

Publication Date: 2019-12

Variant appearance in text: rs9332

PubMed Link: 31637880

Variant Present in the following documents:

• Main text

View BVdb publication page

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The Length of the Expressed 3' UTR Is an Intermediate Molecular Phenotype Linking Genetic Variants to Complex Diseases.

Frontiers In Genetics

Mariella, Elisa E; Marotta, Federico F; Grassi, Elena E; Gilotto, Stefano S; Provero, Paolo P

Publication Date: 2019

Variant appearance in text: rs9332

PubMed Link: 31475030

Variant Present in the following documents:

• Main text
• fgene-10-00714.pdf

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs9332

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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: rs9332

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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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget

Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S

Publication Date: 2015-06-20

Variant appearance in text: rs9332

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

View BVdb publication page

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One-carbon metabolism pathway gene variants and risk of clear cell renal cell carcinoma in a Chinese population.

Plos One

Zhang, Lei L; Meng, Xiaoxin X; Ju, Xiaobing X; Cai, Hongzhou H; Li, Pu P; Cao, Qiang Q; Shao, Pengfei P; Qin, Chao C; Yin, Changjun C

Publication Date: 2013

Variant appearance in text: rs9332

PubMed Link: 24278388

Variant Present in the following documents:

• Main text
• pone.0081129.pdf

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Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.

Journal Of Cancer Epidemiology

Van Dyke, Alison L AL; Cote, Michele L ML; Wenzlaff, Angela S AS; Abrams, Judith J; Land, Susan S; Iyer, Priyanka P; Schwartz, Ann G AG

Publication Date: 2009

Variant appearance in text: rs9332

PubMed Link: 20445798

Variant Present in the following documents:

• Main text

View BVdb publication page

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Blood leukocyte DNA hypomethylation and gastric cancer risk in a high-risk Polish population.

International Journal Of Cancer

Hou, Lifang L; Wang, Hao H; Sartori, Samantha S; Gawron, Andrew A; Lissowska, Jolanta J; Bollati, Valentina V; Tarantini, Letizia L; Zhang, Fang Fang FF; Zatonski, Witold W; Chow, Wong-Ho WH; Baccarelli, Andrea A

Publication Date: 2010-10-15

Variant appearance in text: rs9332

PubMed Link: 20099281

Variant Present in the following documents:

• Main text

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Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida.

American Journal Of Obstetrics And Gynecology

Martinez, Carla A CA; Northrup, Hope H; Lin, Jone-Ing JI; Morrison, Alanna C AC; Fletcher, Jack M JM; Tyerman, Gayle H GH; Au, Kit Sing KS

Publication Date: 2009-10

Variant appearance in text: rs9332

PubMed Link: 19683694

Variant Present in the following documents:

• Main text

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118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.

Bmc Medical Genetics

Shaw, Gary M GM; Lu, Wei W; Zhu, Huiping H; Yang, Wei W; Briggs, Farren B S FB; Carmichael, Suzan L SL; Barcellos, Lisa F LF; Lammer, Edward J EJ; Finnell, Richard H RH

Publication Date: 2009-06-03

Variant appearance in text: rs9332

PubMed Link: 19493349

Variant Present in the following documents:

• Main text
• 1471-2350-10-49.pdf

View BVdb publication page

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