Publications:

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Associations of Polymorphisms Localized in the 3'UTR Regions of the KRAS, NRAS, MAPK1 Genes with Laryngeal Squamous Cell Carcinoma.

Genes

Insodaite, Ruta R; Smalinskiene, Alina A; Liutkevicius, Vykintas V; Ulozas, Virgilijus V; Poceviciute, Roberta R; Bielevicius, Arunas A; Kucinskas, Laimutis L

Publication Date: 2021-10-23

Variant appearance in text: rs7973450

PubMed Link: 34828284

Variant Present in the following documents:

• Main text
• genes-12-01679.pdf

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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: rs7973450

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

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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: rs7973450

PubMed Link: 33850816

Variant Present in the following documents:

• Main text
• tp-10-03-579.pdf

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Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications

Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A

Publication Date: 2021-01-08

Variant appearance in text: rs7973450

PubMed Link: 33420045

Variant Present in the following documents:

• 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 2

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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: rs7973450

PubMed Link: 32514133

Variant Present in the following documents:

• 41431_2020_658_MOESM2_ESM.xlsx, sheet 1

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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: rs7973450

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

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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: rs7973450

PubMed Link: 31564912

Variant Present in the following documents:

• Main text
• ott-12-7289.pdf

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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: rs7973450

PubMed Link: 31086727

Variant Present in the following documents:

• Main text
• 40164_2019_Article_135.pdf

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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: rs7973450

PubMed Link: 30860980

Variant Present in the following documents:

• Main text
• aging-11-101855.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: rs7973450

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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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: rs7973450

PubMed Link: 26959740

Variant Present in the following documents:

• Main text
• oncotarget-07-18984.pdf

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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: rs7973450

PubMed Link: 24552817

Variant Present in the following documents:

• Main text

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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: rs7973450

PubMed Link: 22535184

Variant Present in the following documents:

• Main text

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