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Items: 1 to 20 of 121

1.

Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.

Spellicy CJ, Northrup H, Fletcher JM, Cirino PT, Dennis M, Morrison AC, Martinez CA, Au KS.

PLoS One. 2012;7(12):e51330. doi: 10.1371/journal.pone.0051330. Epub 2012 Dec 5.

2.

Methylenetetrahydrofolate reductase gene polymorphisms in Turkish children with attention-deficit/hyperactivity disorder.

Ergul E, Sazci A, Kara I.

Genet Test Mol Biomarkers. 2012 Jan;16(1):67-9. doi: 10.1089/gtmb.2011.0062. Epub 2011 Aug 5.

PMID:
21819229
3.
4.

Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems.

Saha T, Chatterjee M, Verma D, Ray A, Sinha S, Rajamma U, Mukhopadhyay K.

Prog Neuropsychopharmacol Biol Psychiatry. 2018 Jun 8;84(Pt A):1-10. doi: 10.1016/j.pnpbp.2018.01.016. Epub 2018 Jan 31.

PMID:
29407547
5.

Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele.

Aneji CN, Northrup H, Au KS.

Birth Defects Res A Clin Mol Teratol. 2012 Feb;94(2):84-90. doi: 10.1002/bdra.22884. Epub 2012 Jan 12.

6.

Altered methyltetrahydrofolate reductase gene polymorphism in mothers of children with attention deficit and hyperactivity disorder.

Baykal S, Batar B, Nalbantoğlu A, Albayrak Y, Hancı H, Potas N, Durankuş F, Beyazyüz M, Karabekiroğlu K.

Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jan 10;88:215-221. doi: 10.1016/j.pnpbp.2018.07.020. Epub 2018 Jul 24.

PMID:
30053573
7.

[Methylenetetrahydrofolate reductase polymorphisms as risk factors for myelomeningocele].

Pardo R, Suazo J, Castillo S, Vargas M, Zalavari A, Santos JL, Blanco R, Rotter K, Solar M, Tapia E.

Rev Med Chil. 2014 May;142(5):587-92. doi: 10.4067/S0034-98872014000500006. Spanish.

8.

Folate pathway and nonsyndromic cleft lip and palate.

Blanton SH, Henry RR, Yuan Q, Mulliken JB, Stal S, Finnell RH, Hecht JT.

Birth Defects Res A Clin Mol Teratol. 2011 Jan;91(1):50-60. doi: 10.1002/bdra.20740. Epub 2010 Dec 1.

9.

Polymorphisms in folate metabolism genes are associated with susceptibility to presbycusis.

Manche SK, Jangala M, Dudekula D, Koralla M, Akka J.

Life Sci. 2018 Mar 1;196:77-83. doi: 10.1016/j.lfs.2018.01.015. Epub 2018 Jan 31.

PMID:
29369772
10.

Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands.

Saha T, Chatterjee M, Sinha S, Rajamma U, Mukhopadhyay K.

J Hum Genet. 2017 Jul;62(7):687-695. doi: 10.1038/jhg.2017.23. Epub 2017 Mar 2.

PMID:
28250422
11.

The human protein kinase C gamma gene (PRKCG) as a susceptibility locus for behavioral disinhibition.

Schlaepfer IR, Clegg HV, Corley RP, Crowley TJ, Hewitt JK, Hopfer CJ, Krauter K, Lessem J, Rhee SH, Stallings MC, Wehner JM, Young SE, Ehringer MA.

Addict Biol. 2007 Jun;12(2):200-9.

PMID:
17508994
12.

Association study of GIT1 gene with attention-deficit hyperactivity disorder in Brazilian children and adolescents.

Salatino-Oliveira A, Genro JP, Chazan R, Zeni C, Schmitz M, Polanczyk G, Roman T, Rohde LA, Hutz MH.

Genes Brain Behav. 2012 Oct;11(7):864-8. doi: 10.1111/j.1601-183X.2012.00835.x. Epub 2012 Sep 7.

13.

Polymorphisms of the folate metabolizing enzymes: Association with SLE susceptibility and in silico analysis.

Salimi S, Keshavarzi F, Mohammadpour-Gharehbagh A, Moodi M, Mousavi M, Karimian M, Sandoughi M.

Gene. 2017 Dec 30;637:161-172. doi: 10.1016/j.gene.2017.09.037. Epub 2017 Sep 22.

PMID:
28943344
14.

Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity.

Liu L, Guan LL, Chen Y, Ji N, Li HM, Li ZH, Qian QJ, Yang L, Glatt SJ, Faraone SV, Wang YF.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):737-48. doi: 10.1002/ajmg.b.31217. Epub 2011 Jul 14.

PMID:
21761555
15.

Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD.

Smoller JW, Biederman J, Arbeitman L, Doyle AE, Fagerness J, Perlis RH, Sklar P, Faraone SV.

Biol Psychiatry. 2006 Mar 1;59(5):460-7. Epub 2005 Sep 28.

PMID:
16197923
16.

Homocysteine, folate, lipid profile and MTHFR genotype and disability in children with myelomeningocele.

Rendeli C, Ausili E, Castorina M, Antuzzi D, Tabacco F, Caldarelli M.

Childs Nerv Syst. 2006 Oct;22(10):1316-21. Epub 2006 Apr 7.

PMID:
16602021
17.

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase, dietary folate intake, and the risk of leukemia in adults.

Liu P, Zhang M, Xie X, Jin J, Holman CD.

Tumour Biol. 2016 Mar;37(3):3265-75. doi: 10.1007/s13277-015-4168-6. Epub 2015 Oct 5.

18.

C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects.

Erdogan MO, Yildiz SH, Solak M, Eser O, Cosar E, Eser B, Koken R, Buyukbas S.

Genet Mol Res. 2010 Jun 22;9(2):1197-203. doi: 10.4238/vol9-2gmr816.

19.

Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data.

Yoshimi A, Aleksic B, Kawamura Y, Takahashi N, Yamada S, Usui H, Saito S, Ito Y, Iwata N, Inada T, Noda Y, Yamada K, Ozaki N.

Schizophr Res. 2010 Dec;124(1-3):216-22. doi: 10.1016/j.schres.2010.07.011. Epub 2010 Aug 7.

PMID:
20692813
20.

Investigations of single nucleotide polymorphisms in folate pathway genes in Chinese families with neural tube defects.

Liu J, Qi J, Yu X, Zhu J, Zhang L, Ning Q, Luo X.

J Neurol Sci. 2014 Feb 15;337(1-2):61-6. doi: 10.1016/j.jns.2013.11.017. Epub 2013 Nov 19.

PMID:
24326202

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