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: rs1789953

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: rs1789953

PubMed Link: 36364721

Variant Present in the following documents:

• nutrients-14-04458.pdf

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: rs1789953

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM3_ESM.xlsx, sheet 2

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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: rs1789953

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: rs1789953

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: rs1789953

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: rs1789953

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: rs1789953

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: rs1789953

PubMed Link: 30972295

Variant Present in the following documents:

• Main text
• fonc-09-00182.pdf

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Association of Cystathionine β-Synthase Gene Polymorphisms With Preeclampsia.

Clinical And Applied Thrombosis/Hemostasis : Official Journal Of The International Academy Of Clinical And Applied Thrombosis/Hemostasis

de León Bautista, Mercedes Piedad MP; Romero-Valdovinos, Mirza M; Zavaleta-Villa, Beatriz B; Martínez-Flores, Arony A; Olivo-Díaz, Angélica A

Publication Date: 2018-12

Variant appearance in text: rs1789953

PubMed Link: 30380942

Variant Present in the following documents:

• Main text
• 10.1177_1076029618808913.pdf

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Retrospective likelihood-based methods for analyzing case-cohort genetic association studies.

Biometrics

Shen, Yuanyuan Y; Cai, Tianxi T; Chen, Yu Y; Yang, Ying Y; Chen, Jinbo J

Publication Date: 2015-12

Variant appearance in text: rs1789953

PubMed Link: 26177343

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: rs1789953

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: rs1789953

PubMed Link: 25343990

Variant Present in the following documents:

• Main text

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A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.

International Journal Of Pediatric Otorhinolaryngology

Widdershoven, Josine C C JC; Bowser, Mark M; Sheridan, Molly B MB; McDonald-McGinn, Donna M DM; Zackai, Elaine H EH; Solot, Cynthia B CB; Kirschner, Richard E RE; Beemer, Frits A FA; Morrow, Bernice E BE; Devoto, Marcella M; Emanuel, Beverly S BS

Publication Date: 2013-01

Variant appearance in text: rs1789953

PubMed Link: 23121717

Variant Present in the following documents:

• Main text

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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: rs1789953

PubMed Link: 22140583

Variant Present in the following documents:

• pone.0028408.s004.xls, sheet 1

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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: rs1789953

PubMed Link: 21274745

Variant Present in the following documents:

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Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.

Environmental Health Perspectives

Boyles, Abee L AL; Billups, Ashley V AV; Deak, Kristen L KL; Siegel, Deborah G DG; Mehltretter, Lorraine L; Slifer, Susan H SH; Bassuk, Alexander G AG; Kessler, John A JA; Reed, Michael C MC; Nijhout, H Frederik HF; George, Timothy M TM; Enterline, David S DS; Gilbert, John R JR; Speer, Marcy C MC; ,

Publication Date: 2006-10

Variant appearance in text: rs1789953

PubMed Link: 17035141

Variant Present in the following documents:

• Main text
• ehp0114-001547.pdf

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