Publications:

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: rs6586281

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM10_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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Gene-arsenic interaction in longitudinal changes of blood pressure: Findings from the Health Effects of Arsenic Longitudinal Study (HEALS) in Bangladesh.

Toxicology And Applied Pharmacology

Farzan, Shohreh F SF; Karagas, Margaret R MR; Jiang, Jieying J; Wu, Fen F; Liu, Mengling M; Newman, Jonathan D JD; Jasmine, Farzana F; Kibriya, Muhammad G MG; Paul-Brutus, Rachelle R; Parvez, Faruque F; Argos, Maria M; Scannell Bryan, Molly M; Eunus, Mahbub M; Ahmed, Alauddin A; Islam, Tariqul T; Rakibuz-Zaman, Muhammad M; Hasan, Rabiul R; Sarwar, Golam G; Slavkovich, Vesna V; Graziano, Joseph J; Ahsan, Habibul H; Chen, Yu Y

Publication Date: 2015-10-01

Variant appearance in text: rs6586281

PubMed Link: 26220686

Variant Present in the following documents:

• Main text

View BVdb publication page

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Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study.

Environmental Health Perspectives

Wu, Fen F; Jasmine, Farzana F; Kibriya, Muhammad G MG; Liu, Mengling M; Cheng, Xin X; Parvez, Faruque F; Islam, Tariqul T; Ahmed, Alauddin A; Rakibuz-Zaman, Muhammad M; Jiang, Jieying J; Roy, Shantanu S; Paul-Brutus, Rachelle R; Slavkovich, Vesna V; Islam, Tariqul T; Levy, Diane D; VanderWeele, Tyler J TJ; Pierce, Brandon L BL; Graziano, Joseph H JH; Ahsan, Habibul H; Chen, Yu Y

Publication Date: 2015-05

Variant appearance in text: rs6586281

PubMed Link: 25575156

Variant Present in the following documents:

• ehp.1307883.s001.508.pdf

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A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis.

Plos One

Marini, Nicholas J NJ; Hoffmann, Thomas J TJ; Lammer, Edward J EJ; Hardin, Jill J; Lazaruk, Katherine K; Stein, Jason B JB; Gilbert, Dennis A DA; Wright, Crystal C; Lipzen, Anna A; Pennacchio, Len A LA; Carmichael, Suzan L SL; Witte, John S JS; Shaw, Gary M GM; Rine, Jasper J

Publication Date: 2011

Variant appearance in text: rs6586281

PubMed Link: 22140583

Variant Present in the following documents:

• pone.0028408.s004.xls, sheet 1

View BVdb publication page

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Genetic studies of the cystathionine beta-synthase gene and myelomeningocele.

Birth Defects Research. Part A, Clinical And Molecular Teratology

Tilley, Melissa M MM; Northrup, Hope H; Au, Kit Sing KS

Publication Date: 2012-01

Variant appearance in text: rs6586281

PubMed Link: 21957013

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia.

Cancer Causes & Control : Ccc

Metayer, Catherine C; Scélo, Ghislaine G; Chokkalingam, Anand P AP; Barcellos, Lisa F LF; Aldrich, Melinda C MC; Chang, Jeffrey S JS; Guha, Neela N; Urayama, Kevin Y KY; Hansen, Helen M HM; Block, Gladys G; Kiley, Vincent V; Wiencke, John K JK; Wiemels, Joseph L JL; Buffler, Patricia A PA

Publication Date: 2011-09

Variant appearance in text: rs6586281

PubMed Link: 21748308

Variant Present in the following documents:

• Main text

View BVdb publication page

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