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Items: 1 to 20 of 22

1.

Association of COMT Val158Met Polymorphism with Psychopathological Symptoms in Patients with Eating Disorders.

Gervasini G, Gonzalez LM, Mota-Zamorano S, Gamero-Villarroel C, Carrillo JA, Flores I, Garcia-Herraiz A.

Curr Mol Med. 2018;18(1):65-70. doi: 10.2174/1566524018666180608090512.

PMID:
29879886
2.

Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies.

Collantoni E, Solmi M, Gallicchio D, Santonastaso P, Meneguzzo P, Carvalho AF, Stubbs B, Clementi M, Pinato C, Forzan M, Cassina M, Fontana F, Piva I, Siani R, Salvo P, Tenconi E, Veronese N, Correll CU, Favaro A.

Eur Eat Disord Rev. 2017 Nov;25(6):524-532. doi: 10.1002/erv.2555.

PMID:
29057600
3.

Dopamine receptor D2 and catechol-O-methyltransferase gene polymorphisms associated with anorexia nervosa in Chinese Han population: DRD2 and COMT gene polymorphisms were associated with AN.

Peng S, Yu S, Wang Q, Kang Q, Zhang Y, Zhang R, Jiang W, Qian Y, Zhang H, Zhang M, Xiao Z, Chen J.

Neurosci Lett. 2016 Mar 11;616:147-51. doi: 10.1016/j.neulet.2016.01.036. Epub 2016 Jan 22.

PMID:
26808641
4.

Clinical and genetic correlates of decision making in anorexia nervosa.

Tenconi E, Degortes D, Clementi M, Collantoni E, Pinato C, Forzan M, Cassina M, Santonastaso P, Favaro A.

J Clin Exp Neuropsychol. 2016;38(3):327-37. doi: 10.1080/13803395.2015.1112878. Epub 2015 Dec 29.

PMID:
26713494
5.

Functional connectivity correlates of response inhibition impairment in anorexia nervosa.

Collantoni E, Michelon S, Tenconi E, Degortes D, Titton F, Manara R, Clementi M, Pinato C, Forzan M, Cassina M, Santonastaso P, Favaro A.

Psychiatry Res Neuroimaging. 2016 Jan 30;247:9-16. doi: 10.1016/j.pscychresns.2015.11.008. Epub 2015 Dec 2.

PMID:
26655584
6.

Catechol-O-methyltransferase activity in erythrocytes from patients with eating disorders.

Amorim-Barbosa T, Serrão MP, Brandão I, Vieira-Coelho MA.

Eat Weight Disord. 2016 Jun;21(2):221-7. doi: 10.1007/s40519-015-0213-0. Epub 2015 Aug 22.

PMID:
26296436
7.

Influence of dopamine polymorphisms on the risk for anorexia nervosa and associated psychopathological features.

Gervasini G, Gordillo I, García-Herráiz A, Flores I, Jiménez M, Monge M, Carrillo JA.

J Clin Psychopharmacol. 2013 Aug;33(4):551-5. doi: 10.1097/JCP.0b013e3182970469.

PMID:
23775054
8.

Catechol-O-methyltransferase genotype modifies executive functioning and prefrontal functional connectivity in women with anorexia nervosa.

Favaro A, Clementi M, Manara R, Bosello R, Forzan M, Bruson A, Tenconi E, Degortes D, Titton F, Di Salle F, Santonastaso P.

J Psychiatry Neurosci. 2013 Jul;38(4):241-8. doi: 10.1503/jpn.120068.

9.

Dopamine in anorexia nervosa: a systematic review.

Kontis D, Theochari E.

Behav Pharmacol. 2012 Sep;23(5-6):496-515. doi: 10.1097/FBP.0b013e328357e115. Review.

PMID:
22854306
10.

Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data.

Brandys MK, Slof-Op't Landt MC, van Elburg AA, Ophoff R, Verduijn W, Meulenbelt I, Middeldorp CM, Boomsma DI, van Furth EF, Slagboom E, Kas MJ, Adan RA.

Psychiatr Genet. 2012 Jun;22(3):130-6. doi: 10.1097/YPG.0b013e328351859e.

PMID:
22366815
11.

Impaired Set-Shifting Ability in Patients with Eating Disorders, Which Is Not Moderated by Their Catechol-O-Methyltransferase Val158Met Genotype.

Kim YR, Kim JE, Kim MH.

Psychiatry Investig. 2010 Dec;7(4):298-301. doi: 10.4306/pi.2010.7.4.298. Epub 2010 Nov 17.

12.

Molecular mechanisms underlying anorexia nervosa: focus on human gene association studies and systems controlling food intake.

Rask-Andersen M, Olszewski PK, Levine AS, Schiöth HB.

Brain Res Rev. 2010 Mar;62(2):147-64. doi: 10.1016/j.brainresrev.2009.10.007. Epub 2009 Nov 18. Review.

PMID:
19931559
13.

The association of catechol-O-methyltransferase genotype with the phenotype of women with eating disorders.

Mikołajczyk E, Grzywacz A, Samochowiec J.

Brain Res. 2010 Jan 11;1307:142-8. doi: 10.1016/j.brainres.2009.10.035. Epub 2009 Oct 21.

PMID:
19852950
14.

The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.

Mukherjee N, Kidd KK, Pakstis AJ, Speed WC, Li H, Tarnok Z, Barta C, Kajuna SL, Kidd JR.

Mol Psychiatry. 2010 Feb;15(2):216-25. doi: 10.1038/mp.2008.64. Epub 2008 Jun 24.

15.

Role of the COMT gene Val158Met polymorphism in mental disorders: a review.

Hosák L.

Eur Psychiatry. 2007 Jul;22(5):276-81. Epub 2007 Apr 6. Review.

PMID:
17419009
16.

Association of eating disorders with catechol-o-methyltransferase gene functional polymorphism.

Mikołajczyk E, Smiarowska M, Grzywacz A, Samochowiec J.

Neuropsychobiology. 2006;54(1):82-6. Epub 2006 Oct 5.

PMID:
17028449
17.

Association of catecholamine-O-methyltransferase and 5-HTTLPR genotype with eating disorder-related behavior and attitudes in females with eating disorders.

Frieling H, Römer KD, Wilhelm J, Hillemacher T, Kornhuber J, de Zwaan M, Jacoby GE, Bleich S.

Psychiatr Genet. 2006 Oct;16(5):205-8.

PMID:
16969275
18.

Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.

Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A.

Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):45-50.

PMID:
16118784
19.

Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa.

Gabrovsek M, Brecelj-Anderluh M, Bellodi L, Cellini E, Di Bella D, Estivill X, Fernandez-Aranda F, Freeman B, Geller F, Gratacos M, Haigh R, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Nacmias B, Ribases M, Remschmidt H, Komel R, Sorbi S, Tomori M, Treasure J, Wagner G, Zhao J, Collier DA.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):68-72.

PMID:
14681918
20.

Heritability, genetics and association findings in anorexia nervosa.

Ben-Dor DH, Laufer N, Apter A, Frisch A, Weizman A.

Isr J Psychiatry Relat Sci. 2002;39(4):262-70. Review.

PMID:
12756858

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