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PUBMED FOR HANDHELDS

Journal Abstract Search

217 related items for PubMed ID: 25101272

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  • 4. Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: an association study.
    Jönsson EG, Larsson K, Vares M, Hansen T, Wang AG, Djurovic S, Rønningen KS, Andreassen OA, Agartz I, Werge T, Terenius L, Hall H.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Sep 05; 147B(6):976-82. PubMed ID: 18165967
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  • 6. The T Allele of MTHFR c.C677T and Its Synergism with G (Val 158) Allele of COMT c.G472A Polymorphism Are Associated with the Risk of Bipolar I Disorder.
    Rahimi Z, Kakabaraee K, Garavand A, Rahimi Z.
    Genet Test Mol Biomarkers; 2016 Sep 05; 20(9):510-5. PubMed ID: 27447284
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  • 8. Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia.
    Vares M, Saetre P, Deng H, Cai G, Liu X, Hansen T, Rasmussen HB, Werge T, Melle I, Djurovic S, Andreassen OA, Agartz I, Hall H, Terenius L, Jönsson EG.
    Am J Med Genet B Neuropsychiatr Genet; 2010 Mar 05; 153B(2):610-618. PubMed ID: 19746410
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  • 10. Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene with schizophrenia: association is significant in men but not in women.
    Sazci A, Ergul E, Kucukali I, Kara I, Kaya G.
    Prog Neuropsychopharmacol Biol Psychiatry; 2005 Sep 05; 29(7):1113-23. PubMed ID: 16084002
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  • 11. Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and age of onset in schizophrenia: a combined analysis of independent samples.
    Saetre P, Vares M, Werge T, Andreassen OA, Arinami T, Ishiguro H, Nanko S, Tan EC, Han DH, Roffman JL, Muntjewerff JW, Jagodzinski PP, Kempisty B, Hauser J, Vilella E, Betcheva E, Nakamura Y, Regland B, Agartz I, Hall H, Terenius L, Jönsson EG.
    Am J Med Genet B Neuropsychiatr Genet; 2011 Mar 05; 156(2):215-24. PubMed ID: 21302350
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  • 12. Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet's disease.
    Messedi M, Frigui M, Chaabouni Kh, Turki M, Neifer M, Lahiyani A, Messaouad M, Bahloul Z, Ayedi F, Jamoussi K.
    Gene; 2013 Sep 15; 527(1):306-10. PubMed ID: 23827456
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  • 14. Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population.
    Kalkan G, Yigit S, Karakuş N, Ateş O, Bozkurt N, Ozdemir A, Pancar GŞ.
    Gene; 2013 Nov 01; 530(1):109-12. PubMed ID: 23954881
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  • 19. Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and susceptibility to acute lymphoblastic leukemia in a cohort of Egyptian children.
    Mosaad YM, Abousamra NK, Elashery R, Fawzy IM, Eldein OA, Sherief DM, El Azab HM.
    Leuk Lymphoma; 2015 Nov 01; 56(9):2699-705. PubMed ID: 25629981
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  • 20. Study of C677T variant of methylene tetrahydrofolate reductase gene in autistic spectrum disorder Egyptian children.
    Ismail S, Senna AA, Behiry EG, Ashaat EA, Zaki MS, Ashaat NA, Salah DM.
    Am J Med Genet B Neuropsychiatr Genet; 2019 Jul 01; 180(5):305-309. PubMed ID: 31033224
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