Publications:

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Selenium, Stroke, and Infection: A Threefold Relationship; Where Do We Stand and Where Do We Go?

Nutrients

Liampas, Andreas A; Zis, Panagiotis P; Hadjigeorgiou, Georgios G; Vavougios, George D GD

Publication Date: 2023-03-15

Variant appearance in text: rs6586282

PubMed Link: 36986135

Variant Present in the following documents:

• Main text
• nutrients-15-01405.pdf

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Effects of Selenium on Chronic Kidney Disease: A Mendelian Randomization Study.

Nutrients

Fu, Shaojie S; Zhang, Li L; Ma, Fuzhe F; Xue, Shuai S; Sun, Tao T; Xu, Zhonggao Z

Publication Date: 2022-10-23

Variant appearance in text: rs6586282

PubMed Link: 36364721

Variant Present in the following documents:

• nutrients-14-04458.pdf

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Genetic association between circulating selenium level and the risk of schizophrenia in the European population: A two-sample Mendelian randomization study.

Frontiers In Nutrition

Deng, Ming-Gang MG; Cui, Han-Tao HT; Nie, Jia-Qi JQ; Liang, Yuehui Y; Chai, Chen C

Publication Date: 2022

Variant appearance in text: rs6586282

PubMed Link: 36082036

Variant Present in the following documents:

• Main text
• fnut-09-969887.pdf

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A Bidirectional Mendelian Randomization Study of Selenium Levels and Ischemic Stroke.

Frontiers In Genetics

Fang, Hui H; Liu, Weishi W; Zhang, Luyang L; Pei, Lulu L; Gao, Yuan Y; Zhao, Lu L; Zhang, Rui R; Yang, Jing J; Song, Bo B; Xu, Yuming Y

Publication Date: 2022

Variant appearance in text: rs6586282

PubMed Link: 35495125

Variant Present in the following documents:

• Main text
• fgene-13-782691.pdf

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Genetic Variation Interacts with Selenium Exposure Regarding Breast Cancer Risk: Assessing Dietary Intake, Serum Levels and Genetically Elevated Selenium Levels.

Nutrients

Sandsveden, Malte M; Bengtsson, Ylva Y; Melander, Olle O; Rosendahl, Ann H AH; Manjer, Jonas J

Publication Date: 2022-02-16

Variant appearance in text: rs6586282

PubMed Link: 35215475

Variant Present in the following documents:

• Main text
• nutrients-14-00826.pdf

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The Effect of Circulating Zinc, Selenium, Copper and Vitamin K1 on COVID-19 Outcomes: A Mendelian Randomization Study.

Nutrients

Sobczyk, Maria K MK; Gaunt, Tom R TR

Publication Date: 2022-01-06

Variant appearance in text: rs6586282

PubMed Link: 35057415

Variant Present in the following documents:

• Main text
• nutrients-14-00233.pdf

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The Effect of Circulating Zinc, Selenium, Copper and Vitamin K1 on COVID-19 Outcomes: A Mendelian Randomization Study.

Nutrients

Sobczyk, Maria K MK; Gaunt, Tom R TR

Publication Date: 2022-01-06

Variant appearance in text: rs6586282

PubMed Link: 35057415

Variant Present in the following documents:

• Main text
• nutrients-14-00233.pdf

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Assessing the Causal Role of Selenium in Amyotrophic Lateral Sclerosis: A Mendelian Randomization Study.

Frontiers In Genetics

He, Di D; Cui, Liying L

Publication Date: 2021

Variant appearance in text: rs6586282

PubMed Link: 34691149

Variant Present in the following documents:

• Main text
• fgene-12-724903.pdf

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Assessing the Role of Selenium in Endometrial Cancer Risk: A Mendelian Randomization Study.

Frontiers In Oncology

Kho, Pik Fang PF; Glubb, Dylan M DM; Thompson, Deborah J DJ; Spurdle, Amanda B AB; O'Mara, Tracy A TA

Publication Date: 2019

Variant appearance in text: rs6586282

PubMed Link: 30972295

Variant Present in the following documents:

• Main text
• fonc-09-00182.pdf

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Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study.

Journal Of Human Genetics

Raffield, Laura M LM; Ellis, Jaclyn J; Olson, Nels C NC; Duan, Qing Q; Li, Jin J; Durda, Peter P; Pankratz, Nathan N; Keating, Brendan J BJ; Wassel, Christina L CL; Cushman, Mary M; Wilson, James G JG; Gross, Myron D MD; Tracy, Russell P RP; Rich, Stephen S SS; Reiner, Alex P AP; Li, Yun Y; Willis, Monte S MS; Lange, Ethan M EM; Lange, Leslie A LA

Publication Date: 2018-03

Variant appearance in text: rs6586282

PubMed Link: 29321517

Variant Present in the following documents:

• Main text
• nihms914904.pdf

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs6586282

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

View BVdb publication page

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Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients.

Disease Markers

Kupcinskiene, Kristina K; Murnikovaite, Martyna M; Varkalaite, Greta G; Juzenas, Simonas S; Trepenaitis, Darius D; Petereit, Ruta R; Maleckas, Almantas A; Kupcinskas, Juozas J; Macas, Andrius A

Publication Date: 2016

Variant appearance in text: rs6586282

PubMed Link: 27999448

Variant Present in the following documents:

• Main text
• DM2016-7853424.pdf

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Polymorphisms of cystathionine beta-synthase gene are associated with susceptibility to sepsis.

European Journal Of Human Genetics : Ejhg

Sponholz, Christoph C; Kramer, Marcel M; Schöneweck, Franziska F; Menzel, Uwe U; Inanloo Rahatloo, Kolsoum K; Giamarellos-Bourboulis, Evangelos J EJ; Papavassileiou, Vassileios V; Lymberopoulou, Korina K; Pavlaki, Maria M; Koutelidakis, Ioannis I; Perdios, Ioannis I; Scherag, André A; Bauer, Michael M; Platzer, Matthias M; Huse, Klaus K

Publication Date: 2016-07

Variant appearance in text: rs6586282

PubMed Link: 26508567

Variant Present in the following documents:

• Main text

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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: rs6586282

PubMed Link: 25575156

Variant Present in the following documents:

• ehp.1307883.s001.508.pdf

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Genome-wide association study of selenium concentrations.

Human Molecular Genetics

Cornelis, Marilyn C MC; Fornage, Myriam M; Foy, Millennia M; Xun, Pengcheng P; Gladyshev, Vadim N VN; Morris, Steve S; Chasman, Daniel I DI; Hu, Frank B FB; Rimm, Eric B EB; Kraft, Peter P; Jordan, Joanne M JM; Mozaffarian, Dariush D; He, Ka K

Publication Date: 2015-03-01

Variant appearance in text: rs6586282

PubMed Link: 25343990

Variant Present in the following documents:

• Main text

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Genome-wide association study identifies loci affecting blood copper, selenium and zinc.

Human Molecular Genetics

Evans, David M DM; Zhu, Gu G; Dy, Veronica V; Heath, Andrew C AC; Madden, Pamela A F PA; Kemp, John P JP; McMahon, George G; St Pourcain, Beate B; Timpson, Nicholas J NJ; Golding, Jean J; Lawlor, Debbie A DA; Steer, Colin C; Montgomery, Grant W GW; Martin, Nicholas G NG; Smith, George Davey GD; Whitfield, John B JB

Publication Date: 2013-10-01

Variant appearance in text: rs6586282

PubMed Link: 23720494

Variant Present in the following documents:

• Main text

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Genetic variant of AMD1 is associated with obesity in urban Indian children.

Plos One

Tabassum, Rubina R; Jaiswal, Alok A; Chauhan, Ganesh G; Dwivedi, Om Prakash OP; Ghosh, Saurabh S; Marwaha, Raman K RK; Tandon, Nikhil N; Bharadwaj, Dwaipayan D

Publication Date: 2012

Variant appearance in text: rs6586282

PubMed Link: 22496743

Variant Present in the following documents:

• Main text

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Folate network genetic variation, plasma homocysteine, and global genomic methylation content: a genetic association study.

Bmc Medical Genetics

Wernimont, Susan M SM; Clark, Andrew G AG; Stover, Patrick J PJ; Wells, Martin T MT; Litonjua, Augusto A AA; Weiss, Scott T ST; Gaziano, J Michael JM; Tucker, Katherine L KL; Baccarelli, Andrea A; Schwartz, Joel J; Bollati, Valentina V; Cassano, Patricia A PA

Publication Date: 2011-11-21

Variant appearance in text: rs6586282

PubMed Link: 22103680

Variant Present in the following documents:

• Main text
• 1471-2350-12-150.pdf

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Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk.

Neurology

Hsu, F-C FC; Sides, E G EG; Mychaleckyj, J C JC; Worrall, B B BB; Elias, G A GA; Liu, Y Y; Chen, W-M WM; Coull, B M BM; Toole, J F JF; Rich, S S SS; Furie, K L KL; Sale, M M MM

Publication Date: 2011-10-18

Variant appearance in text: rs6586282

PubMed Link: 21975197

Variant Present in the following documents:

• Main text

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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: rs6586282

PubMed Link: 21957013

Variant Present in the following documents:

• Main text

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Variation in folate pathway genes and distal colorectal adenoma risk: a sigmoidoscopy-based case-control study.

Cancer Causes & Control : Ccc

Levine, A Joan AJ; Lee, Won W; Figueiredo, Jane C JC; Conti, David V DV; Vandenberg, David J DJ; Davis, Brian D BD; Edlund, Christopher K CK; Henning, Susanne M SM; Heber, David D; Stern, Mariana C MC; Haile, Robert W RW

Publication Date: 2011-04

Variant appearance in text: rs6586282

PubMed Link: 21274745

Variant Present in the following documents:

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Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Genetic Epidemiology

Locke, Adam E AE; Dooley, Kenneth J KJ; Tinker, Stuart W SW; Cheong, Soo Yeon SY; Feingold, Eleanor E; Allen, Emily G EG; Freeman, Sallie B SB; Torfs, Claudine P CP; Cua, Clifford L CL; Epstein, Michael P MP; Wu, Michael C MC; Lin, Xihong X; Capone, George G; Sherman, Stephanie L SL; Bean, Lora J H LJ

Publication Date: 2010-09

Variant appearance in text: rs6586282

PubMed Link: 20718043

Variant Present in the following documents:

• Main text

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Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults.

Human Molecular Genetics

Lange, Leslie A LA; Croteau-Chonka, Damien C DC; Marvelle, Amanda F AF; Qin, Li L; Gaulton, Kyle J KJ; Kuzawa, Christopher W CW; McDade, Thomas W TW; Wang, Yunfei Y; Li, Yun Y; Levy, Shawn S; Borja, Judith B JB; Lange, Ethan M EM; Adair, Linda S LS; Mohlke, Karen L KL

Publication Date: 2010-05-15

Variant appearance in text: rs6586282

PubMed Link: 20154341

Variant Present in the following documents:

• Main text

View BVdb publication page

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Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.

Circulation. Cardiovascular Genetics

Paré, Guillaume G; Chasman, Daniel I DI; Parker, Alexander N AN; Zee, Robert R Y RR; Mälarstig, Anders A; Seedorf, Udo U; Collins, Rory R; Watkins, Hugh H; Hamsten, Anders A; Miletich, Joseph P JP; Ridker, Paul M PM

Publication Date: 2009-04

Variant appearance in text: rs6586282

PubMed Link: 20031578

Variant Present in the following documents:

• Main text

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Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.

Human Molecular Genetics

Hazra, Aditi A; Kraft, Peter P; Lazarus, Ross R; Chen, Constance C; Chanock, Stephen J SJ; Jacques, Paul P; Selhub, Jacob J; Hunter, David J DJ

Publication Date: 2009-12-01

Variant appearance in text: rs6586282

PubMed Link: 19744961

Variant Present in the following documents:

• Main text

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Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study.

Blood

Mälarstig, Anders A; Buil, Alfonso A; Souto, Juan Carolos JC; Clarke, Robert R; Blanco-Vaca, Francisco F; Fontcuberta, Jordi J; Peden, John J; Andersen, Malin M; Silveira, Angela A; Barlera, Simona S; Seedorf, Udo U; Watkins, Hugh H; Almasy, Laura L; Hamsten, Anders A; Soria, José Manuel JM; ,

Publication Date: 2009-08-13

Variant appearance in text: rs6586282

PubMed Link: 19525478

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.

American Journal Of Human Genetics

Tanaka, Toshiko T; Scheet, Paul P; Giusti, Betti B; Bandinelli, Stefania S; Piras, Maria Grazia MG; Usala, Gianluca G; Lai, Sandra S; Mulas, Antonella A; Corsi, Anna Maria AM; Vestrini, Anna A; Sofi, Francesco F; Gori, Anna Maria AM; Abbate, Rosanna R; Guralnik, Jack J; Singleton, Andrew A; Abecasis, Goncalo R GR; Schlessinger, David D; Uda, Manuela M; Ferrucci, Luigi L

Publication Date: 2009-04

Variant appearance in text: rs6586282

PubMed Link: 19303062

Variant Present in the following documents:

• Main text

View BVdb publication page

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Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants.

Plos One

Velez, Digna R DR; Fortunato, Stephen J SJ; Thorsen, Poul P; Lombardi, Salvatore J SJ; Williams, Scott M SM; Menon, Ramkumar R

Publication Date: 2008-09-26

Variant appearance in text: rs6586282

PubMed Link: 18818748

Variant Present in the following documents:

• Main text
• pone.0003283.pdf

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