Publications:

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: rs3213495

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget

Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH

Publication Date: 2017-11-10

Variant appearance in text: rs3213495

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 1

View BVdb publication page

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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: rs3213495

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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Association between genetic loci linked to HDL-C levels and Indian patients with CAD: a pilot study.

Heart Asia

Stanley, Ashley A; Ponde, C K CK; Rajani, R M RM; Ashavaid, T F TF

Publication Date: 2017

Variant appearance in text: rs3213495

PubMed Link: 28123455

Variant Present in the following documents:

• Main text

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Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio

Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M

Publication Date: 2014

Variant appearance in text: rs3213495

PubMed Link: 24490137

Variant Present in the following documents:

• mmc5.xlsx, sheet 2

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A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies.

International Journal Of Molecular Epidemiology And Genetics

Terry, Kathryn L KL; Vitonis, Allison F AF; Hernandez, Dena D; Lurie, Galina G; Song, Honglin H; Ramus, Susan J SJ; Titus-Ernstoff, Linda L; Carney, Michael E ME; Wilkens, Lynne R LR; Gentry-Maharaj, Aleksandra A; Menon, Usha U; Gayther, Simon A SA; Pharaoh, Paul D PD; Goodman, Marc T MT; Cramer, Daniel W DW; Birrer, Michael J MJ

Publication Date: 2010-07-26

Variant appearance in text: rs3213495

PubMed Link: 21532840

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of single nucleotide polymorphisms in glycosylation genes with risk of epithelial ovarian cancer.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology

Sellers, Thomas A TA; Huang, Yifan Y; Cunningham, Julie J; Goode, Ellen L EL; Sutphen, Rebecca R; Vierkant, Robert A RA; Kelemen, Linda E LE; Fredericksen, Zachary S ZS; Liebow, Mark M; Pankratz, V Shane VS; Hartmann, Lynn C LC; Myer, Jeff J; Iversen, Edwin S ES; Schildkraut, Joellen M JM; Phelan, Catherine C

Publication Date: 2008-02

Variant appearance in text: rs3213495

PubMed Link: 18268124

Variant Present in the following documents:

• Main text

View BVdb publication page

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