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记忆力
记忆力
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记忆力
6 个讨论
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嗯，完全记不住东西，各种往事，结果 还是 记忆力不错。。。我是不是被封印了。。
jessica89
• 最后回复
变态的ACTN3
•
2021-11-04 21:00
5322
7
• 来自相关小组
回寄忘了记单号没事吧？
hua2358518
• 最后回复
pony24
•
2018-03-17 12:07
2945
1
• 来自相关小组
啥时候才能出报告啊 等的焦急的一匹
MAIKEBYE
• 最后回复
ouyangke
•
2018-01-28 16:26
2744
3
• 来自相关小组
为什么我的报告里面没有记忆力这项呢？有人知道吗？
何涛
• 最后回复
wuxiang
•
2016-12-17 16:16
3701
3
• 来自相关小组
我的记忆力一直不错，大家的结果如何？
zhengqiang
• 最后回复
谦逊的PKHD1基因
•
2016-10-24 13:37
5755
13
• 来自相关小组
好记忆抵得上烂笔头
zk8848
• 2016-06-29 14:35
2917
0
• 来自相关小组
发起讨论
记忆力
6 个讨论
相关基因
WWC1
位点：RS17070145
COMT
位点：RS4680
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Inoue-Choi M, et al. Genetic Association Between the COMT Genotype and Urinary Levels of Tea Polyphenols and Their Metabolites among Daily Green Tea Drinkers. 1300
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Costas J, et al. Interaction between COMT haplotypes and cannabis in schizophrenia: a case-only study in two samples from Spain. 2011
Malaguti A, et al. Role of COMT, 5-HT(1A) , and SERT genetic polymorphisms on antidepressant response to Transcranial Magnetic Stimulation. 2011
Cerne JZ, et al. Estrogen metabolism genotypes, use of long-term hormone replacement therapy and risk of postmenopausal breast cancer. 2011
Laugsand EA, et al. Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids. 2011
Ancín I, et al. Sensory gating deficit is associated with catechol-O-methyltransferase polymorphisms in bipolar disorder. 2011
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Jugurnauth SK, et al. A COMT gene haplotype associated with methamphetamine abuse. 2011
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Jacobsen LM, et al. The COMT rs4680 Met allele contributes to long-lasting low back pain, sciatica and disability after lumbar disc herniation. 2012
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Barnes A, et al. No association of COMT (Val158Met) genotype with brain structure differences between men and women. 2012
Liang S, et al. Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population. 2012
Martínez-Jauand M, et al. Pain sensitivity in fibromyalgia is associated with catechol-O-methyltransferase (COMT) gene. 2013
Voisey J, et al. A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence: a case control study. 2011
Hill LD, et al. Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome. 2012
Zhang Y, et al. Association between polymorphisms in COMT, PLCH1, and CYP17A1, and non-small-cell lung cancer risk in Chinese nonsmokers. 2013
Bray NJ, et al. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. 2003
Palmatier MA, et al. COMT haplotypes suggest P2 promoter region relevance for schizophrenia. 2004
Chen X, et al. Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families. 2004
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Borroni B, et al. Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease. 2007
Kim H, et al. Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans. 2006
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Cotterchio M, et al. Dietary phytoestrogen intake is associated with reduced colorectal cancer risk. 2006
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Yu R, et al. Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: a case-control study. 2007
Long JR, et al. Genetic polymorphisms in estrogen-metabolizing genes and breast cancer survival. 2007
Zhang K, et al. An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population. 2007
Ton TG, et al. Genetic polymorphisms in dopamine-related genes and smoking cessation in women: a prospective cohort study. 2007
Nunokawa A, et al. No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population. 2007
Yacubian J, et al. Gene-gene interaction associated with neural reward sensitivity. 2007
Zinkstok J, et al. Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia. 2008
Ma X, et al. A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population. 2007
Talkowski ME, et al. Dopamine genes and schizophrenia: case closed or evidence pending? 2007
Gooden KM, et al. Val153Met polymorphism of catechol-O-methyltransferase and prevalence of uterine leiomyomata. 2007
Diaz-Asper CM, et al. Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls. 2008
Vargas-Alarcón G, et al. Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia. 2015
Retz W, et al. Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults. 2007
Juckel G, et al. Association of catechol-O-methyltransferase variants with loudness dependence of auditory evoked potentials. 2008
Fung MM, et al. Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans. 2008
Tander B, et al. Polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase genes: a study on fibromyalgia susceptibility. 2008
Aguilera M, et al. Putative role of the COMT gene polymorphism (Val158Met) on verbal working memory functioning in a healthy population. 2008
Ettinger U, et al. Catechol-O-methyltransferase (COMT) val158met genotype is associated with BOLD response as a function of task characteristic. 2008
Hirata H, et al. COMT polymorphisms affecting protein expression are risk factors for endometrial cancer. 2008
He C, et al. A prospective study of genetic polymorphism in MPO, antioxidant status, and breast cancer risk. 2009
Bombin I, et al. DRD3, but not COMT or DRD2, genotype affects executive functions in healthy and first-episode psychosis adolescents. 2008
Wray NR, et al. Association study of candidate variants of COMT with neuroticism, anxiety and depression. 2008
Kan T, et al. Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing. 1503
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Hettema JM, et al. Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes. 2008
Shi J, et al. Neurotransmission and bipolar disorder: a systematic family-based association study. 2008
Xing C, et al. Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels. 2007
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Shiels MS, et al. A community-based study of cigarette smoking behavior in relation to variation in three genes involved in dopamine metabolism: Catechol-O-methyltransferase (COMT), dopamine beta-hydroxylase (DBH) and monoamine oxidase-A (MAO-A). 2008
Haraldsson HM, et al. Catechol-O-methyltransferase Val 158 Met polymorphism and antisaccade eye movements in schizophrenia. 2010
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Westberg L, et al. Sex steroid-related candidate genes in psychiatric disorders. 2008
Diergaarde B, et al. Polymorphisms in genes involved in sex hormone metabolism, estrogen plus progestin hormone therapy use, and risk of postmenopausal breast cancer. 2008
Bialecka M, et al. The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications. 2008
Shi J, et al. Genetic associations with schizophrenia: meta-analyses of 12 candidate genes. 2008
Sheldrick AJ, et al. Effect of COMT val158met genotype on cognition and personality. 2008
Tranah GJ, et al. Genetic variation in candidate osteoporosis genes, bone mineral density, and fracture risk: the study of osteoporotic fractures. 2008
Halleland H, et al. Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults. 2009
Tempfer CB, et al. Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis. 2009
Hamaguchi M, et al. Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers. 2008
Huuhka K, et al. Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy. 2008
Biederman J, et al. Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study. 2008
Roffman JL, et al. MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met. 2008
Shrubsole MJ, et al. Drinking green tea modestly reduces breast cancer risk. 2009
Rakvåg TT, et al. Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain. 2008
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Pearce CL, et al. Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium. 2009
Cote ML, et al. Tobacco and estrogen metabolic polymorphisms and risk of non-small cell lung cancer in women. 2009
Need AC, et al. A genome-wide investigation of SNPs and CNVs in schizophrenia. 2009
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Mushlin RA, et al. Clique-finding for heterogeneity and multidimensionality in biomarker epidemiology research: the CHAMBER algorithm. 2009
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Cross DS, et al. Development of a fingerprinting panel using medically relevant polymorphisms. 2009
Benedetti F, et al. Acute antidepressant response to sleep deprivation combined with light therapy is influenced by the catechol-O-methyltransferase Val(108/158)Met polymorphism. 2010
Quednow BB, et al. Sensorimotor gating depends on polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase, but not on neuregulin-1 Arg38Gln genotype: a replication study. 2009
Zhang Z, et al. The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis. 2009
Gadow KD, et al. Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder. 2009
Breitling LP, et al. Variants in COMT and spontaneous smoking cessation: retrospective cohort analysis of 925 cessation events. 2009
Haraldsson HM, et al. COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia. 2009
Ko DC, et al. A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease. 2009
Eisenberg DP, et al. Executive function, neural circuitry, and genetic mechanisms in schizophrenia. 2010
Roe BE, et al. Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene. 2009
Gu Y, et al. Association between COMT gene and Chinese male schizophrenic patients with violent behavior. 2009
Mikołajczyk E, et al. The association of catechol-O-methyltransferase genotype with the phenotype of women with eating disorders. 2010
Doi N, et al. Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint. 2009
Blasi G, et al. Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans. 2009
Benedetti F, et al. Association between catechol-O-methyltransferase Val(108/158)Met polymorphism and psychotic features of bipolar disorder. 2010
Rommelse NN, et al. Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder. 2010
Bertolino A, et al. Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance. 2010
Pinheiro AP, et al. The Genetics of Anorexia Nervosa: Current Findings and Future Perspectives. 2015
Nemoda Z, et al. Association between dopaminergic polymorphisms and borderline personality traits among at-risk young adults and psychiatric inpatients. 2010
Wang Y, et al. Analysis of association between the catechol-O-methyltransferase (COMT) gene and negative symptoms in chronic schizophrenia. 2010
Kocabas NA, et al. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study. 2010
Cross DS, et al. Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project. 2010
Fijal B, et al. The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder. 2010
Calati R, et al. Catechol-o-methyltransferase gene modulation on suicidal behavior and personality traits: review, meta-analysis and association study. 2011
Demetrovics Z, et al. Association between Novelty Seeking of opiate-dependent patients and the catechol-O-methyltransferase Val(158)Met polymorphism. 2010
Dai F, et al. Association of catechol-O-methyltransferase genetic variants with outcome in patients undergoing surgical treatment for lumbar degenerative disc disease. 2010
Moreno-Galván M, et al. Impact of CYP1A1 and COMT genotypes on breast cancer risk in Mexican women: a pilot study. 2010
Huang CG, et al. Polymorphisms of COMT and XPD and risk of esophageal squamous cell carcinoma in a population of Yili Prefecture, in Xinjiang, China. 2011
Sommerfeldt L, et al. Polymorphisms of adrenergic cardiovascular control genes are associated with adolescent chronic fatigue syndrome. 2011
Munafò MR, et al. Association of COMT Val(108/158)Met genotype and cigarette smoking in pregnant women. 2011
Miller RJ, et al. The impact of the catechol-O-methyltransferase genotype on the acute responsiveness of vascular reactivity to a green tea extract. 2011
Zhang JP, et al. Pharmacogenetics and antipsychotics: therapeutic efficacy and side effects prediction. 2011
Porcelli S, et al. Pharmacogenetics of antidepressant response. 2011
Nixon DC, et al. Interactive effects of DAOA (G72) and catechol-O-methyltransferase on neurophysiology in prefrontal cortex. 2011
Das M, et al. Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands. 2011
Yang SY, et al. EGFR L858R mutation and polymorphisms of genes related to estrogen biosynthesis and metabolism in never-smoking female lung adenocarcinoma patients. 2011
Hill LD, et al. Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. 2011
David SP, et al. Pharmacogenetics of smoking cessation in general practice: results from the patch II and patch in practice trials. 2011
Roten LT, et al. A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2). 2011
Brennan PA, et al. Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes. 2011
Doehring A, et al. Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures. 2011
Armbruster D, et al. Variation in genes involved in dopamine clearance influence the startle response in older adults. 2011
KONG FZ, et al. [An association study of COMT gene polymorphisms with schizophrenia]. 2011
Pivac N, et al. The association between catechol-O-methyl-transferase Val108/158Met polymorphism and suicide. 2011
Christofolini DM, et al. COMT polymorphism and the risk of endometriosis-related infertility. 2011
Doll BB, et al. Dopaminergic genes predict individual differences in susceptibility to confirmation bias. 2011
Massat I, et al. COMT and age at onset in mood disorders: a replication and extension study. 2011
Bhowmik AD, et al. Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability. 2011
Ittiwut R, et al. Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations. 2011
Htun NC, et al. Association of the catechol-O-methyl transferase gene Val158Met polymorphism with blood pressure and prevalence of hypertension: interaction with dietary energy intake. 2011
Desmeules J, et al. Psychological distress in fibromyalgia patients: a role for catechol-O-methyl-transferase Val158met polymorphism. 2012
Gupta M, et al. Diverse facets of COMT: from a plausible predictive marker to a potential drug target for schizophrenia. 2011
Amstadter AB, et al. Genetic associations with performance on a behavioral measure of distress intolerance. 2012
Varga G, et al. Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity. 2012
Hiyoshi M, et al. Association between the catechol-O-methyltransferase (rs4680: Val158Met) polymorphism and serum alanine aminotransferase activity. 2012
Smith CT, et al. Age modulates the effect of COMT genotype on delay discounting behavior. 2012
Brandys MK, et al. Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data. 2012
Butts SF, et al. Joint effects of smoking and gene variants involved in sex steroid metabolism on hot flashes in late reproductive-age women. 2012
Huertas E, et al. C957T polymorphism of the dopamine D2 receptor gene is associated with motor learning and heart rate. 2012
Mitaki S, et al. Impact of five SNPs in dopamine-related genes on executive function. 2013
Zhang F, et al. No association of catechol-O-methyltransferase polymorphisms with schizophrenia in the Han Chinese population. 2012
Bakker PR, et al. Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective study. 2012
Olfson E, et al. Convergence of genome-wide association and candidate gene studies for alcoholism. 2012
Miller RJ, et al. The impact of the catechol-O-methyltransferase genotype on vascular function and blood pressure after acute green tea ingestion. 2012
Kim B, et al. The effects of the catechol-O-methyltransferase val158met polymorphism on white matter connectivity in patients with panic disorder. 2013
Ko MK, et al. Association of COMT gene polymorphisms with systemic atherosclerosis in elderly Japanese. 2012
Omair A, et al. Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study. 2012
Pap D, et al. Association between the COMT gene and rumination in a Hungarian sample. 2012
Landi N, et al. The COMT Val/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation. 2013
Mutschler J, et al. Lack of association of a functional catechol-O-methyltransferase gene polymorphism with risk of tobacco smoking: results from a multicenter case-control study. 2013
Teng Y, et al. Catechol-O-methyltransferase and cytochrome P-450 1B1 polymorphisms and endometrial cancer risk: a meta-analysis. 2013
Goetz EL, et al. Genetic moderation of the association between regulatory focus and reward responsiveness: a proof-of-concept study. 2013
Soeiro-De-Souza MG, et al. Association of the COMT Met¹⁵⁸ allele with trait impulsivity in healthy young adults. 2013
Deuker L, et al. Playing nice: a multi-methodological study on the effects of social conformity on memory. 2013
Nikolac Perkovic M, et al. The association between the catechol-O-methyltransferase Val108/158Met polymorphism and hyperactive-impulsive and inattentive symptoms in youth. 2013
Ojeda DA, et al. Common functional polymorphisms in SLC6A4 and COMT genes are associated with circadian phenotypes in a South American sample. 2014
Ghisari M, et al. Genetic polymorphisms in CYP1A1, CYP1B1 and COMT genes in Greenlandic Inuit and Europeans. 2013
Serretti A, et al. No effect of serotoninergic gene variants on response to interpersonal counseling and antidepressants in major depression. 2013
Kontis D, et al. COMT and MTHFR polymorphisms interaction on cognition in schizophrenia: an exploratory study. 2013
Vereczkei A, et al. Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence. 2013
Passarelli MN, et al. No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women. 2014
Baldinger P, et al. Impact of COMT genotype on serotonin-1A receptor binding investigated with PET. 2014
David SP, et al. Influence of a dopamine pathway additive genetic efficacy score on smoking cessation: results from two randomized clinical trials of bupropion. 2013
Kornek M, et al. COMT-Val158Met-polymorphism is not a risk factor for acute kidney injury after cardiac surgery. 2013
Shen Y, et al. Role of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in Han Chinese: a case-control study. 2014
Liu J, et al. Association between maternal COMT gene polymorphisms and fetal neural tube defects risk in a Chinese population. 2014
Pełka-Wysiecka J, et al. BDNF rs 6265 polymorphism and COMT rs 4680 polymorphism in deficit schizophrenia in Polish sample. 6265
Bühler KM, et al. Risky alcohol consumption in young people is associated with the fatty acid amide hydrolase gene polymorphism C385A and affective rating of drug pictures. 2014
Zhang Y, et al. Metabolic syndrome in patients taking clozapine: prevalence and influence of catechol-O-methyltransferase genotype. 2014
Khadzhieva MB, et al. Association of oxidative stress-related genes with idiopathic recurrent miscarriage. 2014
Hopkins SC, et al. Catechol-O-methyltransferase genotype as modifier of superior responses to venlafaxine treatment in major depressive disorder. 2013
Ji Y, et al. Association between the COMTVal158Met Genotype and Alzheimer's Disease in the Han Chinese Population. 2014
Roffman JL, et al. Genetic variation throughout the folate metabolic pathway influences negative symptom severity in schizophrenia. 2013
Thaler L, et al. Epistatic interactions implicating dopaminergic genes in bulimia nervosa (BN): relationships to eating- and personality-related psychopathology. 2012
Soeiro-de-Souza MG, et al. COMT polymorphisms as predictors of cognitive dysfunction during manic and mixed episodes in bipolar I disorder. 2012
Henker RA, et al. The associations between OPRM 1 and COMT genotypes and postoperative pain, opioid use, and opioid-induced sedation. 2013
Tammimäki A, et al. Catechol-O-methyltransferase gene polymorphism and chronic human pain: a systematic review and meta-analysis. 2012
Shashi V, et al. Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms. 2012
Bhakta SG, et al. The COMT Met158 allele and violence in schizophrenia: a meta-analysis. 2012
Carpentier PJ, et al. Shared and unique genetic contributions to attention deficit/hyperactivity disorder and substance use disorders: a pilot study of six candidate genes. 2013
Białecka M, et al. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease. 2012
Lanni C, et al. Influence of COMT Val158Met polymorphism on Alzheimer's disease and mild cognitive impairment in Italian patients. 2015
Lancaster TM, et al. COMT val158met predicts reward responsiveness in humans. 2012
Poletti S, et al. Catechol-O-methyltransferase (COMT) genotype biases neural correlates of empathy and perceived personal distress in schizophrenia. 2013
Martínez-Ramírez OC, et al. Polymorphisms of catechol estrogens metabolism pathway genes and breast cancer risk in Mexican women. 2013
Pap D, et al. Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: relevance for major depression. 2012
Creese B, et al. No association of COMT val158met polymorphism and psychotic symptoms in Lewy body dementias. 2012
Suarez-Kurtz G, et al. Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin. 2012
Gaysina D, et al. The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence. 2013
Zhang X, et al. Prefrontal white matter impairment in substance users depends upon the catechol-o-methyl transferase (COMT) val158met polymorphism. 2013
Spronk DB, et al. DBH -1021C>T and COMT Val108/158Met genotype are not associated with the P300 ERP in an auditory oddball task. 2013
Landau R, et al. The effect of OPRM1 and COMT genotypes on the analgesic response to intravenous fentanyl labor analgesia. 2013
Hatzimanolis A, et al. Potential role of membrane-bound COMT gene polymorphisms in female depression vulnerability. 2013
Klebe S, et al. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. 2013
Wang Y, et al. COMT rs4680 Met is not always the 'smart allele': Val allele is associated with better working memory and larger hippocampal volume in healthy Chinese. 2013
Seok JH, et al. Effect of the COMT val158met polymorphism on white matter connectivity in patients with major depressive disorder. 2013
Niitsu T, et al. Pharmacogenetics in major depression: a comprehensive meta-analysis. 2013
Cargnin S, et al. An opposite-direction modulation of the COMT Val158Met polymorphism on the clinical response to intrathecal morphine and triptans. 2013
González-Castro TB, et al. Distribution of the Val108/158Met polymorphism of the COMT gene in healthy Mexican population. 2013
Soeiro-De-Souza MG, et al. Gender effects of the COMT Val 158 Met genotype on verbal fluency in healthy adults. 2013
Woods JS, et al. Genetic polymorphisms of catechol-O-methyltransferase modify the neurobehavioral effects of mercury in children. 2014
Park S, et al. Catechol-O-methyltransferase Val158-Met polymorphism and a response of hyperactive-impulsive symptoms to methylphenidate: A replication study from South Korea. 2014
Shen Y, et al. A multicenter case-control study on screening of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in han chinese. 2014
Jiménez-Jiménez FJ, et al. COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis. 2014
Carmel M, et al. Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects. 2014
Liu X, et al. Association study of polymorphisms in the alpha 7 nicotinic acetylcholine receptor subunit and catechol-o-methyl transferase genes with sensory gating in first-episode schizophrenia. 2013
Wan GX, et al. The Catechol-O-Methyltransferase Val158Met Polymorphism Contributes to the Risk of Breast Cancer in the Chinese Population: An Updated Meta-Analysis. 2014
Parasuraman R, et al. Interactive effects of the COMT gene and training on individual differences in supervisory control of unmanned vehicles. 2014
Zozulinsky P, et al. Dopamine system genes are associated with orienting bias among healthy individuals. 2014
Park S, et al. Interactions Between Early Trauma and Catechol-O-Methyltransferase Genes on Inhibitory Deficits in Children With ADHD. 2014
Baeken C, et al. The influence of COMT Val¹⁵⁸Met genotype on the character dimension cooperativeness in healthy females. 2014
Iwasaki M, et al. Green tea consumption and breast cancer risk in Japanese women: a case-control study. 2013
Smith SB, et al. Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain. 2014
Noohi F, et al. Association of COMT val158met and DRD2 G>T genetic polymorphisms with individual differences in motor learning and performance in female young adults. 2014
Du JZ, et al. Lack of association between the COMT rs4680 polymorphism and ovarian cancer risk: evidence from a meta-analysis of 3,940 individuals. 2015
Shibata N, et al. Association between the catechol-O-methyltransferase polymorphism Val158Met and Alzheimer's disease in a Japanese population. 2015
Shin SY, et al. An atlas of genetic influences on human blood metabolites. 2014
Niarchou M, et al. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. 2014
Vercammen A, et al. Common polymorphisms in dopamine-related genes combine to produce a 'schizophrenia-like' prefrontal hypoactivity. 2014
Moreau C, et al. Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease. 2015
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