CBS c.316+224C>T

Variant ID: 21-44488395-G-A

NM_000071.2(CBS):c.316+224C>T

This variant was identified in 12 publications

View GRCh38 version.




Publications:


Genetics and Epigenetics of One-Carbon Metabolism Pathway in Autism Spectrum Disorder: A Sex-Specific Brain Epigenome?

Genes
Tisato, Veronica V; Silva, Juliana A JA; Longo, Giovanna G; Gallo, Ines I; Singh, Ajay V AV; Milani, Daniela D; Gemmati, Donato D
Publication Date: 2021-05-20

Variant appearance in text: rs234715
PubMed Link: 34065323
Variant Present in the following documents:
  • Main text
  • genes-12-00782.pdf
View BVdb publication page



Multifactorial Origin of Neurodevelopmental Disorders: Approaches to Understanding Complex Etiologies.

Toxics
De Felice, Alessia A; Ricceri, Laura L; Venerosi, Aldina A; Chiarotti, Flavia F; Calamandrei, Gemma G
Publication Date: 2015-03-23

Variant appearance in text: rs234715
PubMed Link: 29056653
Variant Present in the following documents:
  • Main text
  • toxics-03-00089.pdf
View BVdb publication page



New Perspective on Impact of Folic Acid Supplementation during Pregnancy on Neurodevelopment/Autism in the Offspring Children - A Systematic Review.

Plos One
Gao, Yunfei Y; Sheng, Chao C; Xie, Ri-Hua RH; Sun, Wen W; Asztalos, Elizabeth E; Moddemann, Diane D; Zwaigenbaum, Lonnie L; Walker, Mark M; Wen, Shi Wu SW
Publication Date: 2016

Variant appearance in text: rs234715
PubMed Link: 27875541
Variant Present in the following documents:
  • Main text
  • pone.0165626.pdf
View BVdb publication page



The Relationship between Folic Acid and Risk of Autism Spectrum Disorders.

Healthcare (Basel, Switzerland)
Neggers, Yasmin Y
Publication Date: 2014-10-23

Variant appearance in text: rs234715
PubMed Link: 27429286
Variant Present in the following documents:
  • Main text
  • healthcare-02-00429.pdf
View BVdb publication page



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: rs234715
PubMed Link: 25575156
Variant Present in the following documents:
  • ehp.1307883.s001.508.pdf
View BVdb publication page



Increasing prevalence, changes in diagnostic criteria, and nutritional risk factors for autism spectrum disorders.

Isrn Nutrition
Neggers, Yasmin H YH
Publication Date: 2014

Variant appearance in text: rs234715
PubMed Link: 24967269
Variant Present in the following documents:
  • Main text
  • ISRN.NUTRITION2014-514026.pdf
View BVdb publication page



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: rs234715
PubMed Link: 21748308
Variant Present in the following documents:
  • Main text
View BVdb publication page



Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism.

Epidemiology (Cambridge, Mass.)
Schmidt, Rebecca J RJ; Hansen, Robin L RL; Hartiala, Jaana J; Allayee, Hooman H; Schmidt, Linda C LC; Tancredi, Daniel J DJ; Tassone, Flora F; Hertz-Picciotto, Irva I
Publication Date: 2011-07

Variant appearance in text: rs234715
PubMed Link: 21610500
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs234715
PubMed Link: 20718043
Variant Present in the following documents:
  • Main text
View BVdb publication page



Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma.

Molecular Vision
Fan, Bao Jian BJ; Chen, Teresa T; Grosskreutz, Cynthia C; Pasquale, Louis L; Rhee, Douglas D; DelBono, Elizabeth E; Haines, Jonathan L JL; Wiggs, Janey L JL
Publication Date: 2008

Variant appearance in text: rs234715
PubMed Link: 19112534
Variant Present in the following documents:
  • Main text
View BVdb publication page



Predictive genomics of cardioembolic stroke.

Stroke
Ramoni, Rachel Badovinac RB; Himes, Blanca E BE; Sale, Michele M MM; Furie, Karen L KL; Ramoni, Marco F MF
Publication Date: 2009-03

Variant appearance in text: rs234715
PubMed Link: 19064790
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs234715
PubMed Link: 17035141
Variant Present in the following documents:
  • Main text
  • ehp0114-001547.pdf
View BVdb publication page