Publications:

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SNPs in miRNAs and Target Sequences: Role in Cancer and Diabetes.

Frontiers In Genetics

Chhichholiya, Yogita Y; Suryan, Aman Kumar AK; Suman, Prabhat P; Munshi, Anjana A; Singh, Sandeep S

Publication Date: 2021

Variant appearance in text: rs9341070

PubMed Link: 34925466

Variant Present in the following documents:

• Main text
• fgene-12-793523.pdf

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Profile of the breast cancer susceptibility marker rs4245739 identifies a role for miRNAs.

Cancer Biology & Medicine

Anwar, Sumadi Lukman SL; Wulaningsih, Wahyu W; Watkins, Johnathan J

Publication Date: 2017-11

Variant appearance in text: rs9341070

PubMed Link: 29372105

Variant Present in the following documents:

• Main text
• cbm-14-4-387.pdf

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Polymorphisms in sex steroid receptors: From gene sequence to behavior.

Frontiers In Neuroendocrinology

Maney, Donna L DL

Publication Date: 2017-10

Variant appearance in text: rs9341070

PubMed Link: 28705582

Variant Present in the following documents:

• Main text

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SNPs in microRNA target sites and their potential role in human disease.

Open Biology

Moszyńska, Adrianna A; Gebert, Magdalena M; Collawn, James F JF; Bartoszewski, Rafał R

Publication Date: 2017-04

Variant appearance in text: rs9341070

PubMed Link: 28381629

Variant Present in the following documents:

• Main text
• rsob-7-170019.pdf

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ESR1 and ESR2 polymorphisms in the BIG 1-98 trial comparing adjuvant letrozole versus tamoxifen or their sequence for early breast cancer.

Breast Cancer Research And Treatment

Leyland-Jones, Brian B; Gray, Kathryn P KP; Abramovitz, Mark M; Bouzyk, Mark M; Young, Brandon B; Long, Bradley B; Kammler, Roswitha R; Dell'Orto, Patrizia P; Biasi, Maria Olivia MO; Thürlimann, Beat B; Harvey, Vernon V; Neven, Patrick P; Arnould, Laurent L; Maibach, Rudolf R; Price, Karen N KN; Coates, Alan S AS; Goldhirsch, Aron A; Gelber, Richard D RD; Pagani, Olivia O; Viale, Giuseppe G; Rae, James M JM; Regan, Meredith M MM; ,

Publication Date: 2015-12

Variant appearance in text: rs9341070

PubMed Link: 26590813

Variant Present in the following documents:

• Main text

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Genetic variation in estrogen and progesterone pathway genes and breast cancer risk: an exploration of tumor subtype-specific effects.

Cancer Causes & Control : Ccc

Nyante, Sarah J SJ; Gammon, Marilie D MD; Kaufman, Jay S JS; Bensen, Jeannette T JT; Lin, Dan Yu DY; Barnholtz-Sloan, Jill S JS; Hu, Yijuan Y; He, Qianchuan Q; Luo, Jingchun J; Millikan, Robert C RC

Publication Date: 2015-01

Variant appearance in text: rs9341070

PubMed Link: 25421376

Variant Present in the following documents:

• Main text

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mrSNP: software to detect SNP effects on microRNA binding.

Bmc Bioinformatics

Deveci, Mehmet M; Catalyürek, Umit V UV; Toland, Amanda Ewart AE

Publication Date: 2014-03-15

Variant appearance in text: rs9341070

PubMed Link: 24629096

Variant Present in the following documents:

• Main text

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MicroRNA-206: a promising theranostic marker.

Theranostics

Novák, Jan J; Kružliak, Peter P; Bienertová-Vašků, Julie J; Slabý, Ondřej O; Novák, Miroslav M

Publication Date: 2014

Variant appearance in text: rs9341070

PubMed Link: 24465270

Variant Present in the following documents:

• Main text
• thnov04p0119.pdf

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MirSNP, a database of polymorphisms altering miRNA target sites, identifies miRNA-related SNPs in GWAS SNPs and eQTLs.

Bmc Genomics

Liu, Chenxing C; Zhang, Fuquan F; Li, Tingting T; Lu, Ming M; Wang, Lifang L; Yue, Weihua W; Zhang, Dai D

Publication Date: 2012-11-23

Variant appearance in text: rs9341070

PubMed Link: 23173617

Variant Present in the following documents:

• Main text
• 1471-2164-13-661.pdf

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MicroRNA binding site polymorphisms as biomarkers of cancer risk.

Expert Review Of Molecular Diagnostics

Pelletier, Cory C; Weidhaas, Joanne B JB

Publication Date: 2010-09

Variant appearance in text: rs9341070

PubMed Link: 20843204

Variant Present in the following documents:

• Main text

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MicroSNiPer: a web tool for prediction of SNP effects on putative microRNA targets.

Human Mutation

Barenboim, Maxim M; Zoltick, Brad J BJ; Guo, Yongjian Y; Weinberger, Daniel R DR

Publication Date: 2010-11

Variant appearance in text: rs9341070

PubMed Link: 20809528

Variant Present in the following documents:

• Main text

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A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.

Cancer Research

Saetrom, Pål P; Biesinger, Jacob J; Li, Sierra M SM; Smith, David D; Thomas, Laurent F LF; Majzoub, Karim K; Rivas, Guillermo E GE; Alluin, Jessica J; Rossi, John J JJ; Krontiris, Theodore G TG; Weitzel, Jeffrey J; Daly, Mary B MB; Benson, Al B AB; Kirkwood, John M JM; O'Dwyer, Peter J PJ; Sutphen, Rebecca R; Stewart, James A JA; Johnson, David D; Larson, Garrett P GP

Publication Date: 2009-09-15

Variant appearance in text: rs9341070

PubMed Link: 19738052

Variant Present in the following documents:

• Main text

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Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.

Human Genetics

Keene, Keith L KL; Mychaleckyj, Josyf C JC; Leak, Tennille S TS; Smith, Shelly G SG; Perlegas, Peter S PS; Divers, Jasmin J; Langefeld, Carl D CD; Freedman, Barry I BI; Bowden, Donald W DW; Sale, Michèle M MM

Publication Date: 2008-09

Variant appearance in text: rs9341070

PubMed Link: 18654799

Variant Present in the following documents:

• Main text

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Comprehensive evaluation of the estrogen receptor alpha gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population.

Human Genetics

Keene, Keith L KL; Mychaleckyj, Josyf C JC; Smith, Shelly G SG; Leak, Tennille S TS; Perlegas, Peter S PS; Langefeld, Carl D CD; Herrington, David M DM; Freedman, Barry I BI; Rich, Stephen S SS; Bowden, Donald W DW; Sale, Michèle M MM

Publication Date: 2008-05

Variant appearance in text: rs9341070

PubMed Link: 18305958

Variant Present in the following documents:

• Main text

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Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes.

American Journal Of Human Genetics

Sethupathy, Praveen P; Borel, Christelle C; Gagnebin, Maryline M; Grant, Gregory R GR; Deutsch, Samuel S; Elton, Terry S TS; Hatzigeorgiou, Artemis G AG; Antonarakis, Stylianos E SE

Publication Date: 2007-08

Variant appearance in text: rs9341070

PubMed Link: 17668390

Variant Present in the following documents:

• Main text

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