Publications:

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Association between KRAS gene polymorphisms and genetic susceptibility to breast cancer in a Chinese population.

Journal Of Clinical Laboratory Analysis

Jin, Min M; Lu, Fengke F; Li, Xi X; Zhou, Wei W; Li, Sihui S; Jiang, Yanting Y; Wu, Huiling H; Wang, Jian J

Publication Date: 2022-12-12

Variant appearance in text: rs12587

PubMed Link: 36510353

Variant Present in the following documents:

• Main text
• JCLA-37-e24806.pdf

View BVdb publication page

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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: rs12587

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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: rs12587

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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Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics

Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y

Publication Date: 2022

Variant appearance in text: rs12587

PubMed Link: 35899134

Variant Present in the following documents:

• Table_1.xlsx, sheet 1

View BVdb publication page

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Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer

Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC

Publication Date: 2021-05-29

Variant appearance in text: rs12587

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

View BVdb publication page

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KRAS gene polymorphisms are associated with the risk of glioma: a two-center case-control study.

Translational Pediatrics

Guan, Qian Q; Yuan, Li L; Lin, Ao A; Lin, Huiran H; Huang, Xiaokai X; Ruan, Jichen J; Zhuo, Zhenjian Z

Publication Date: 2021-03

Variant appearance in text: rs12587

PubMed Link: 33850816

Variant Present in the following documents:

• Main text
• tp-10-03-579.pdf

View BVdb publication page

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Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?

European Journal Of Human Genetics : Ejhg

Ferrari, Luca L; Mangano, Eleonora E; Bonati, Maria Teresa MT; Monterosso, Ilaria I; Capitanio, Daniele D; Chiappori, Federica F; Brambilla, Ilaria I; Gelfi, Cecilia C; Battaglia, Cristina C; Bordoni, Roberta R; Riva, Paola P

Publication Date: 2020-10

Variant appearance in text: rs12587

PubMed Link: 32514133

Variant Present in the following documents:

• 41431_2020_658_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs12587

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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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: rs12587

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: rs12587

PubMed Link: 31637880

Variant Present in the following documents:

• Main text

View BVdb publication page

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KRAS rs7973450 A>G increases neuroblastoma risk in Chinese children: a four-center case-control study.

Oncotargets And Therapy

Lin, Ao A; Hua, Rui-Xi RX; Tang, Jue J; Zhu, Jinhong J; Zhang, Ruizhong R; Zhou, Haixia H; Zhang, Jiao J; Cheng, Jiwen J; Xia, Huimin H; He, Jing J

Publication Date: 2019

Variant appearance in text: rs12587

PubMed Link: 31564912

Variant Present in the following documents:

• Main text
• ott-12-7289.pdf

View BVdb publication page

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NRAS and KRAS polymorphisms are not associated with hepatoblastoma susceptibility in Chinese children.

Experimental Hematology & Oncology

Yang, Tianyou T; Wen, Yang Y; Li, Jiahao J; Tan, Tianbao T; Yang, Jiliang J; Pan, Jing J; Hu, Chao C; Yao, Yuxiao Y; Zhang, Jiao J; Xin, Yijuan Y; Li, Suhong S; Xia, Huimin H; He, Jing J; Zou, Yan Y

Publication Date: 2019

Variant appearance in text: rs12587

PubMed Link: 31086727

Variant Present in the following documents:

• Main text

View BVdb publication page

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Additional data support the role of LINC00673 rs11655237 C>T in the development of neuroblastoma.

Aging

Li, Yong Y; Zhuo, Zhen-Jian ZJ; Zhou, Haiyan H; Liu, Jiabin J; Liu, Zan Z; Zhang, Jiao J; Cheng, Jiwen J; Li, Suhong S; Zhou, Haixia H; Zhou, Rong R; He, Jing J; Zhao, Yaowang Y

Publication Date: 2019-04-20

Variant appearance in text: rs12587

PubMed Link: 31005956

Variant Present in the following documents:

• Main text
• aging-11-101920.pdf

View BVdb publication page

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Association of KRAS and NRAS gene polymorphisms with Wilms tumor risk: a four-center case-control study.

Aging

Fu, Wen W; Zhuo, Zhenjian Z; Hua, Rui-Xi RX; Fu, Kai K; Jia, Wei W; Zhu, Jinhong J; Zhang, Jiao J; Cheng, Jiwen J; Zhou, Haixia H; Xia, Huimin H; He, Jing J; Liu, Guochang G

Publication Date: 2019-03-12

Variant appearance in text: rs12587

PubMed Link: 30860980

Variant Present in the following documents:

• Main text
• aging-11-101855.pdf

View BVdb publication page

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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: rs12587

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.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: rs12587

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 1
• oncotarget-08-95841-s002.xlsx, sheet 4

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: rs12587

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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A single-nucleotide polymorphism in the 3'-UTR region of the adipocyte fatty acid binding protein 4 gene is associated with prognosis of triple-negative breast cancer.

Oncotarget

Wang, Wenmiao W; Yuan, Peng P; Yu, Dianke D; Du, Feng F; Zhu, Anjie A; Li, Qing Q; Zhang, Pin P; Lin, Dongxin D; Xu, Binghe B

Publication Date: 2016-04-05

Variant appearance in text: rs12587

PubMed Link: 26959740

Variant Present in the following documents:

• Main text
• oncotarget-07-18984.pdf

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: rs12587

PubMed Link: 25944692

Variant Present in the following documents:

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

View BVdb publication page

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Extensive sequence variation in the 3' untranslated region of the KRAS gene in lung and ovarian cancer cases.

Cell Cycle (Georgetown, Tex.)

Kim, Minlee M; Chen, Xiaowei X; Chin, Lena J LJ; Paranjape, Trupti T; Speed, William C WC; Kidd, Kenneth K KK; Zhao, Hongyu H; Weidhaas, Joanne B JB; Slack, Frank J FJ

Publication Date: 2014

Variant appearance in text: rs12587

PubMed Link: 24552817

Variant Present in the following documents:

• Main text

View BVdb publication page

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Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs.

European Journal Of Human Genetics : Ejhg

Pakstis, Andrew J AJ; Fang, Rixun R; Furtado, Manohar R MR; Kidd, Judith R JR; Kidd, Kenneth K KK

Publication Date: 2012-11

Variant appearance in text: rs12587

PubMed Link: 22535184

Variant Present in the following documents:

• Main text

View BVdb publication page

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