Publications:

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Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.

Molecular Medicine Reports

Li, Yiqiang Y; Lin, Xuemei X; Zhu, Mingwei M; Li, Jingchun J; Yuan, Zhe Z; Xu, Hongwen H

Publication Date: 2020-09

Variant appearance in text: rs4901706

PubMed Link: 32705272

Variant Present in the following documents:

• Supplementary_Data1.xlsx, sheet 1

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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: rs4901706

PubMed Link: 31637880

Variant Present in the following documents:

• Main text
• CAM4-8-7477.pdf

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: rs4901706

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

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Polymorphisms of microRNA target genes IL12B, INSR, CCND1 and IL10 in gastric cancer.

World Journal Of Gastroenterology

Petkevicius, Vytenis V; Salteniene, Violeta V; Juzenas, Simonas S; Wex, Thomas T; Link, Alexander A; Leja, Marcis M; Steponaitiene, Ruta R; Skieceviciene, Jurgita J; Kupcinskas, Limas L; Jonaitis, Laimas L; Kiudelis, Gediminas G; Malfertheiner, Peter P; Kupcinskas, Juozas J

Publication Date: 2017-05-21

Variant appearance in text: rs4901706

PubMed Link: 28596683

Variant Present in the following documents:

• Main text
• WJG-23-3480.pdf

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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: rs4901706

PubMed Link: 28535796

Variant Present in the following documents:

• 13023_2017_647_MOESM1_ESM.xlsx, sheet 4

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Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma.

Genes

Bradshaw, Gabrielle G; Sutherland, Heidi G HG; Haupt, Larisa M LM; Griffiths, Lyn R LR

Publication Date: 2016-12-17

Variant appearance in text: rs4901706

PubMed Link: 27999330

Variant Present in the following documents:

• Main text
• genes-07-00130.pdf

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A polymorphism at the microRNA binding site in the 3'-untranslated region of C14orf101 is associated with the risk of gastric cancer development.

Experimental And Therapeutic Medicine

Wang, Cuiju C; Zhao, Yufei Y; Ming, Yanming Y; Zhao, Shengnan S; Guo, Zhanjun Z

Publication Date: 2016-09

Variant appearance in text: rs4901706

PubMed Link: 27602096

Variant Present in the following documents:

• Main text

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A polymorphism at the microRNA binding site in the 3' untranslated region of RYR3 is associated with outcome in hepatocellular carcinoma.

Oncotargets And Therapy

Peng, Chenxing C; Guo, Zhanjun Z; Wu, Xiaoyan X; Zhang, Xiao-Lan XL

Publication Date: 2015

Variant appearance in text: rs4901706

PubMed Link: 26309413

Variant Present in the following documents:

• Main text
• ott-8-2075.pdf

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MicroRNA-binding site polymorphisms in hematological malignancies.

Journal Of Hematology & Oncology

Dzikiewicz-Krawczyk, Agnieszka A

Publication Date: 2014-11-25

Variant appearance in text: rs4901706

PubMed Link: 25421940

Variant Present in the following documents:

• Main text
• 13045_2014_Article_83.pdf

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Genetic variation in microRNA networks: the implications for cancer research.

Nature Reviews. Cancer

Ryan, Bríd M BM; Robles, Ana I AI; Harris, Curtis C CC

Publication Date: 2010-06

Variant appearance in text: rs4901706

PubMed Link: 20495573

Variant Present in the following documents:

• Main text

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Aberrant allele frequencies of the SNPs located in microRNA target sites are potentially associated with human cancers.

Nucleic Acids Research

Yu, Zhenbao Z; Li, Zhen Z; Jolicoeur, Normand N; Zhang, Linhua L; Fortin, Yves Y; Wang, Edwin E; Wu, Meiqun M; Shen, Shi-Hsiang SH

Publication Date: 2007

Variant appearance in text: rs4901706

PubMed Link: 17584784

Variant Present in the following documents:

• Main text
• gkm480.pdf

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