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Items: 1 to 20 of 71


Copy number variations in Saudi family with intellectual disability and epilepsy.

Naseer MI, Chaudhary AG, Rasool M, Kalamegam G, Ashgan FT, Assidi M, Ahmed F, Ansari SA, Zaidi SK, Jan MM, Al-Qahtani MH.

BMC Genomics. 2016 Oct 17;17(Suppl 9):757.


Catechol-O-methyltransferase val(158)met Polymorphism Interacts with Sex to Affect Face Recognition Ability.

Lamb YN, McKay NS, Singh SS, Waldie KE, Kirk IJ.

Front Psychol. 2016 Jun 27;7:965. doi: 10.3389/fpsyg.2016.00965.


Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.

Duarte RR, Troakes C, Nolan M, Srivastava DP, Murray RM, Bray NJ.

Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):806-14. doi: 10.1002/ajmg.b.32445.


Catechol-O-Methyltransferase Val158Met Polymorphism and Clinical Response to Antipsychotic Treatment in Schizophrenia and Schizo-Affective Disorder Patients: a Meta-Analysis.

Huang E, Zai CC, Lisoway A, Maciukiewicz M, Felsky D, Tiwari AK, Bishop JR, Ikeda M, Molero P, Ortuno F, Porcelli S, Samochowiec J, Mierzejewski P, Gao S, Crespo-Facorro B, Pelayo-Terán JM, Kaur H, Kukreti R, Meltzer HY, Lieberman JA, Potkin SG, Müller DJ, Kennedy JL.

Int J Neuropsychopharmacol. 2016 Apr 29;19(5). pii: pyv132. doi: 10.1093/ijnp/pyv132.


Sex differences in the locus coeruleus-norepinephrine system and its regulation by stress.

Bangasser DA, Wiersielis KR, Khantsis S.

Brain Res. 2016 Jun 15;1641(Pt B):177-88. doi: 10.1016/j.brainres.2015.11.021. Review.


Molecular genetic mechanisms of allelic specific regulation of murine Comt expression.

Segall SK, Shabalina SA, Meloto CB, Wen X, Cunningham D, Tarantino LM, Wiltshire T, Gauthier J, Tohyama S, Martin LJ, Mogil JS, Diatchenko L.

Pain. 2015 Oct;156(10):1965-77. doi: 10.1097/j.pain.0000000000000258.


The role of epigenetics in personalized medicine: challenges and opportunities.

Rasool M, Malik A, Naseer MI, Manan A, Ansari S, Begum I, Qazi MH, Pushparaj P, Abuzenadah AM, Al-Qahtani MH, Kamal MA, Gan S.

BMC Med Genomics. 2015;8 Suppl 1:S5. doi: 10.1186/1755-8794-8-S1-S5. Review.


The enzymatic activities of brain catechol-O-methyltransferase (COMT) and methionine sulphoxide reductase are correlated in a COMT Val/Met allele-dependent fashion.

Moskovitz J, Walss-Bass C, Cruz DA, Thompson PM, Hairston J, Bortolato M.

Neuropathol Appl Neurobiol. 2015 Dec;41(7):941-51. doi: 10.1111/nan.12219.


Genome-wide association studies using haplotypes and individual SNPs in Simmental cattle.

Wu Y, Fan H, Wang Y, Zhang L, Gao X, Chen Y, Li J, Ren H, Gao H.

PLoS One. 2014 Oct 20;9(10):e109330. doi: 10.1371/journal.pone.0109330.


Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain.

Smith SB, Reenilä I, Männistö PT, Slade GD, Maixner W, Diatchenko L, Nackley AG.

Pain. 2014 Nov;155(11):2390-9. doi: 10.1016/j.pain.2014.09.009.


Interactions among catechol-O-methyltransferase genotype, parenting, and sex predict children's internalizing symptoms and inhibitory control: Evidence for differential susceptibility.

Sulik MJ, Eisenberg N, Spinrad TL, Lemery-Chalfant K, Swann G, Silva KM, Reiser M, Stover DA, Verrelli BC.

Dev Psychopathol. 2015 Aug;27(3):709-23. doi: 10.1017/S0954579414000807.


Methionine sulfoxide reductase regulates brain catechol-O-methyl transferase activity.

Moskovitz J, Walss-Bass C, Cruz DA, Thompson PM, Bortolato M.

Int J Neuropsychopharmacol. 2014 Oct;17(10):1707-13. doi: 10.1017/S1461145714000467.


COMT Genetic Reduction Produces Sexually Divergent Effects on Cortical Anatomy and Working Memory in Mice and Humans.

Sannino S, Gozzi A, Cerasa A, Piras F, Scheggia D, Managò F, Damiano M, Galbusera A, Erickson LC, De Pietri Tonelli D, Bifone A, Tsaftaris SA, Caltagirone C, Weinberger DR, Spalletta G, Papaleo F.

Cereb Cortex. 2015 Sep;25(9):2529-41. doi: 10.1093/cercor/bhu053.


Gene-sex interactions in schizophrenia: focus on dopamine neurotransmission.

Godar SC, Bortolato M.

Front Behav Neurosci. 2014 Mar 6;8:71. doi: 10.3389/fnbeh.2014.00071. Review.


Catechol-O-methyltransferase Val158Met polymorphism on the relationship between white matter hyperintensity and cognition in healthy people.

Liu ME, Huang CC, Yang AC, Tu PC, Yeh HL, Hong CJ, Liou YJ, Chen JF, Chou KH, Lin CP, Tsai SJ.

PLoS One. 2014 Feb 13;9(2):e88749. doi: 10.1371/journal.pone.0088749.


Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer.

Kambur O, Kaunisto MA, Tikkanen E, Leal SM, Ripatti S, Kalso EA.

Anesthesiology. 2013 Dec;119(6):1422-33. doi: 10.1097/ALN.0000000000000013.


Catecholaminergic gene variants: contribution in ADHD and associated comorbid attributes in the eastern Indian probands.

Ghosh P, Sarkar K, Bhaduri N, Ray A, Sarkar K, Sinha S, Mukhopadhyay K.

Biomed Res Int. 2013;2013:918410. doi: 10.1155/2013/918410.


Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.

Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, Ren-Patterson R, Lipska BK, Carmel M, Kolachana B, Weizman A, Weinberger DR.

Biol Psychiatry. 2014 Mar 1;75(5):406-13. doi: 10.1016/j.biopsych.2013.07.021.


Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision.

Bortsov AV, Diatchenko L, McLean SA.

Neuromolecular Med. 2014 Mar;16(1):83-93. doi: 10.1007/s12017-013-8255-9.

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