BHMT c.477+52C>T

Variant ID: 5-78416416-C-T

NM_001713.2(BHMT):c.477+52C>T

This variant was identified in 20 publications

View GRCh38 version.




Publications:


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: rs567754
PubMed Link: 36364721
Variant Present in the following documents:
  • nutrients-14-04458.pdf
View BVdb publication page



Association and Interaction Effect of BHMT Gene Polymorphisms and Maternal Dietary Habits with Ventricular Septal Defect in Offspring.

Nutrients
Luo, Manjun M; Wang, Tingting T; Huang, Peng P; Zhang, Senmao S; Song, Xinli X; Sun, Mengting M; Liu, Yiping Y; Wei, Jianhui J; Shu, Jing J; Zhong, Taowei T; Chen, Qian Q; Zhu, Ping P; Qin, Jiabi J
Publication Date: 2022-07-28

Variant appearance in text: rs567754
PubMed Link: 35956270
Variant Present in the following documents:
  • Main text
  • nutrients-14-03094.pdf
View BVdb publication page



Folate Related Pathway Gene Analysis Reveals a Novel Metabolic Variant Associated with Alzheimer's Disease with a Change in Metabolic Profile.

Metabolites
Miyan, Jaleel J; Buttercase, Charlotte C; Beswick, Emma E; Miyan, Salma S; Moshkdanian, Ghazaleh G; Naz, Naila N
Publication Date: 2022-05-24

Variant appearance in text: rs567754
PubMed Link: 35736408
Variant Present in the following documents:
  • metabolites-12-00475.pdf
View BVdb publication page



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: rs567754
PubMed Link: 35215475
Variant Present in the following documents:
  • Main text
  • nutrients-14-00826.pdf
View BVdb publication page



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: rs567754
PubMed Link: 34691149
Variant Present in the following documents:
  • Main text
  • fgene-12-724903.pdf
View BVdb publication page



Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.

Frontiers In Cell And Developmental Biology
Martinelli, Marcella M; Palmieri, Annalisa A; Carinci, Francesco F; Scapoli, Luca L
Publication Date: 2020

Variant appearance in text: rs567754
PubMed Link: 33195260
Variant Present in the following documents:
  • Main text
  • fcell-08-592271.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: BHMT: 477+52C>T; rs567754
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
View BVdb publication page



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: rs567754
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Conditionally reprogrammed normal and primary tumor prostate epithelial cells: a novel patient-derived cell model for studies of human prostate cancer.

Oncotarget
Timofeeva, Olga A OA; Palechor-Ceron, Nancy N; Li, Guanglei G; Yuan, Hang H; Krawczyk, Ewa E; Zhong, Xiaogang X; Liu, Geng G; Upadhyay, Geeta G; Dakic, Aleksandra A; Yu, Songtao S; Fang, Shuang S; Choudhury, Sujata S; Zhang, Xueping X; Ju, Andrew A; Lee, Myeong-Seon MS; Dan, Han C HC; Ji, Youngmi Y; Hou, Yong Y; Zheng, Yun-Ling YL; Albanese, Chris C; Rhim, Johng J; Schlegel, Richard R; Dritschilo, Anatoly A; Liu, Xuefeng X
Publication Date: 2017-04-04

Variant appearance in text: rs567754
PubMed Link: 28009986
Variant Present in the following documents:
  • oncotarget-08-22741-s003.xlsx, sheet 1
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs567754
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



Genetic variants in one-carbon metabolism genes and breast cancer risk in European American and African American women.

International Journal Of Cancer
Gong, Zhihong Z; Yao, Song S; Zirpoli, Gary G; David Cheng, Ting-Yuan TY; Roberts, Michelle M; Khoury, Thaer T; Ciupak, Gregory G; Davis, Warren W; Pawlish, Karen K; Jandorf, Lina L; Bovbjerg, Dana H DH; Bandera, Elisa V EV; Ambrosone, Christine B CB
Publication Date: 2015-08-01

Variant appearance in text: rs567754
PubMed Link: 25598430
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs567754
PubMed Link: 25343990
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.

International Journal Of Molecular Epidemiology And Genetics
Moore, Amy A; Enquobahrie, Daniel A DA; Sanchez, Sixto E SE; Ananth, Cande V CV; Pacora, Percy N PN; Williams, Michelle A MA
Publication Date: 2012

Variant appearance in text: rs567754
PubMed Link: 23205182
Variant Present in the following documents:
  • Main text
View BVdb publication page



Folate pathway and nonsyndromic cleft lip and palate.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Blanton, Susan H SH; Henry, Robin R RR; Yuan, Quiping Q; Mulliken, John B JB; Stal, Samuel S; Finnell, Richard H RH; Hecht, Jacqueline T JT
Publication Date: 2011-01

Variant appearance in text: rs567754
PubMed Link: 21254359
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genes and abdominal aortic aneurysm.

Annals Of Vascular Surgery
Hinterseher, Irene I; Tromp, Gerard G; Kuivaniemi, Helena H
Publication Date: 2011-04

Variant appearance in text: rs567754
PubMed Link: 21146954
Variant Present in the following documents:
  • Main text
View BVdb publication page



Betaine-homocysteine methyltransferase: human liver genotype-phenotype correlation.

Molecular Genetics And Metabolism
Feng, Qiping Q; Kalari, Krishna K; Fridley, Brooke L BL; Jenkins, Gregory G; Ji, Yuan Y; Abo, Ryan R; Hebbring, Scott S; Zhang, Jianping J; Nye, Monica D MD; Leeder, J Steven JS; Weinshilboum, Richard M RM
Publication Date: 2011-02

Variant appearance in text: rs567754
PubMed Link: 21093336
Variant Present in the following documents:
  • Main text
View BVdb publication page



118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.

Bmc Medical Genetics
Shaw, Gary M GM; Lu, Wei W; Zhu, Huiping H; Yang, Wei W; Briggs, Farren B S FB; Carmichael, Suzan L SL; Barcellos, Lisa F LF; Lammer, Edward J EJ; Finnell, Richard H RH
Publication Date: 2009-06-03

Variant appearance in text: rs567754
PubMed Link: 19493349
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-49.pdf
View BVdb publication page



Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study.

Genetic Epidemiology
Boyles, Abee L AL; Wilcox, Allen J AJ; Taylor, Jack A JA; Shi, Min M; Weinberg, Clarice R CR; Meyer, Klaus K; Fredriksen, Ase A; Ueland, Per Magne PM; Johansen, Anne Marte W AM; Drevon, Christian A CA; Jugessur, Astanand A; Trung, Truc Nguyen TN; Gjessing, Håkon K HK; Vollset, Stein Emil SE; Murray, Jeffrey C JC; Christensen, Kaare K; Lie, Rolv T RT
Publication Date: 2009-04

Variant appearance in text: rs567754
PubMed Link: 19048631
Variant Present in the following documents:
  • Main text
View BVdb publication page



Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization.

Molecular Genetics And Metabolism
Li, Fang F; Feng, Qiping Q; Lee, Candace C; Wang, Shuzhan S; Pelleymounter, Linda L LL; Moon, Irene I; Eckloff, Bruce W BW; Wieben, Eric D ED; Schaid, Daniel J DJ; Yee, Vivien V; Weinshilboum, Richard M RM
Publication Date: 2008-07

Variant appearance in text: rs567754
PubMed Link: 18457970
Variant Present in the following documents:
  • Main text
View BVdb publication page